Scientific Program

Conference Series Ltd invites all the participants across the globe to attend 4th International Conference on Antimicrobials, Multiple Drug Resistance & Antibiotics Resistance Las Vegas, Nevada, USA.

Day 2 :

Keynote Forum

Hideko Kaji

Professor,Thomas Jefferson University, USA

Keynote: Lethal effect of denatured ribosome recycling factor at lag phase

Time : 09:45-10:30

Conference Series Antibiotics Resistance 2018 International Conference Keynote Speaker Hideko Kaji photo
Biography:

Dr. Hideko Kaji obtained her Ph.D from Purdue University. He had faculty positions at Vanderbilt School of Medicine, The Johns Hopkins Medical School, and Fox Chase Cancer Research Institute. Currently she is a professor of biochemistry and molecular biology at Jefferson Medical College, Thomas Jefferson University.

Abstract:

Ribosome recycling factor (RRF) is an essential protein factor responsible for disassembly of the post-termination complex. Protein synthesis consists of 4 steps, initiation, elongation of peptide chain, termination and the ribosome recycling step. RRF catalyzes the fourth step of protein synthesis in bacteria.  It was known that inactivation of temperature sensitive RRF (tsRRF) at lag phase resulted in lethal effect (Janosi, Mottagui-Tabar et al. 1998)while at log and stationary phase it has bacteriostatic effect. In this paper, we tried to elucidate the beginning of physiological and cellular changes due to the inactivation of RRF so that we have a glimpse of the possible mechanism of lethal effect of inactivation of tsRRF at lag phase only. We found under the condition where the lethal effect is observed that a large amount of 40S particles were formed containing 16S rRNA. Within hour of the appearance of this 40S particles cells start dying. Measures such as inhibition of protein chain elongation stopped the lethal effect of tsRRF at the non-permissive temperature. All such measures eliminated the appearance of the 40S particles. We conclude that the 40S particle is essential for lethal effect of tsRRF at the lag phase. Our proteomics data showed upregulation of alternate ribosome rescue factor (ArfA) at the non-permissive temperature provide evidence about RRF essentiality. Effect of various antibiotics on the formation of the 40S particles and on the lethal effect of tsRRF will be described.

Keynote Forum

John J S Cadwell

FiberCell Systems Inc, USA

Keynote: The hollow fiber infection model: Principles and practice

Time : 09:00-09:40

Conference Series Antibiotics Resistance 2018 International Conference Keynote Speaker John J S Cadwell photo
Biography:

John J.S. Cadwell received his degree in pharmacology from the University of Miami in 1981. He spent additional time studying at the University of Nottingham and the National Institute of Medical Research at Mill Hill, U.K.. In 2000 he founded FiberCell Systems Inc., a company specializing in the research and supply of hollow fiber bioreactors. He has over 10 publications in the field and three patents relating to hollow fiber systems and is considered a world expert in the field.

Abstract:

Emerging antibiotic resistance presents a serious global health threat. 2 million people in the United States were infected with antibiotic resistant bacteria in 2014 and more than 20,000 died as a direct result of these infections, many more from complications. Antimicrobial resistance has been identi ed as one of the three greatest threats to human health [1]. Antibiotic discovery and development require static susceptibility testing to screen compounds, in vitro pharmacodynamics/ pharmacokinetic (PK/PD) studies to model drug dynamics and efficacy, and testing in animal models to provide critical information prior to the clinical evaluation of new antibiotics.

The one compartment PK/PD model typically consists of an open central reservoir containing the organism of interest, a source of diluent and a waste reservoir. 1) Open system, not bio safe 2)Bacteria numbers change over time 3)Large volume requires large amount of drug and diluent 4) Rapid changes in drug concentration not possible, cannot model short half-lives 


Animal models have many shortcomings though they have served as a primary development tool for many years: 1) PK/PD may not match human values
2)Cannot sample same animal over time
3)Difficult to study large numbers of bacteria to reveal resistance 4) Many infections cannot be modeled in a mouse or other animal

To address these shortcomings the two-compartment in vitro pharmacokinetic model utilizing hollow ber bioreactors was developed, the Hollow ber infection model (HFIM). The advantages of the HFIM are as follows: 1) Closed, bio-safe system
2) Large number of organism can be tested, revealing resistance
3) Precisely simulates human PK/PD
4) Repetitive sampling over time, both drug and organism
5) Total kill can be determined
6) Single use, disposable, reproducible 7) Two drug models can be tested
8) Can model both dosing curve and elimination curve
9) Can look at bacteria in different growth phases and in combination with cells


The clinical utility of the HFIM has been demonstrated and is now endorsed by the EMA. An overview of historic pk/pd models is presented and the utility of the system as it relates to antibiotics and other drugs are discussed.

Keynote Forum

Oluwadapo Oluwaseun J

Doctor at BIOS Specialist Hospital

Keynote: ANTIMICROBIALS INFECTIOUS AND INFECTIVE ENDOCARDITIS

Time : 11:20-12:20

Conference Series Antibiotics Resistance 2018 International Conference Keynote Speaker  Oluwadapo Oluwaseun J photo
Biography:

Workshop

Oluwadapo Oluwaseun J was working as a doctor at BIOS Specialist hospital in Nigeria. He published two books (1) Natural Medicine (2) Cardiovascular Diseases and a graduate of Medicine and surgery. University of Ibadan. Also, a member of National Journals Board.

 

 

Abstract:

INTRODUCTION:

Coronary artery disease had historically been considered to be uncommon in the sub-Saharan African of Negro Origin. This assertion may not be totally true considering the rising trend of cardiac death in the region while coronary artery disease is not a common cause of syncope we report a case of Nigeria who presented with history of recurrent syncope. He underwent coronary angiogram as part of his evaluation and was diagnosed to have coronary artery disease a significant single vessel disease (LAD).

 

CASE OF PRESENTATION

A 45 year old normotensive,EU glyceamic,non-smoker and non-alcoholic was referred from peripheral hospital to cardiology unit of bios specialist hospital, Nigeria for evaluation of recurrent syncope. He had two episodes of syncope with 72 hour occurring exercise preceded by dizziness, no chest palpations or dyspnoea .initial routine electrocardiogram (ECG) and 24 hour holter (EEG) were essentially normal. Another episode of syncope warranted further investigation. An immediate electrocardiogram taken showed deeply inverted symmetrical T-wave at the anterior leads. He underwent coronary angiogram at institute of cardiovascular Disease (ICVD),madras medical mission, India which revealed distal left main disease and 70-80% stenosis of the proximal (LAD). Circumflex artery was non dominant with normal right coronary artery. He subsequently had PTCA + STENT to LAD. Post revasculation course has been satisfactory with no recurrence syncope

 

CONCLUSION

In view of the rising trend of cardiac death in the country, there is the need for high index of suspicion for coronary artery and thorough evaluation of patients with syncope.

Therefore, endocarditis -is the term given to microbial intention of the heart valve or endocardium.

 

WHAT TO DISCUSSED:

In the conference centre we shall discussed on*

#Antimicrobials Infectious and infective endocarditis

#Clinical features of the sub acute illness& investigation.

# Chemo prophylaxis

#Antibiotic treatment regimen in infective endocarditis

#Complications and prognosis

 

Keynote Forum

John J S Cadwell

FiberCell Systems Inc., USA

Keynote: 3-D Cell based Pk/Pd assays in hollow fi ber bioreactors

Time : 09:00-09:45

Conference Series Antibiotics Resistance 2018 International Conference Keynote Speaker John J S Cadwell photo
Biography:

John J S Cadwell has received his Degree in Pharmacology from the University of Miami in 1981. He spent additional time studying at the University of Nottingham and the National Institute of Medical Research at Mill Hill, UK. In 2000, he founded Fiber Cell Systems Inc., a company specializing in the research and supply of hollow fi ber bioreactors. He has over 10 publications in the fi eld and three patents relating to hollow fi ber systems and is considered a world expert in the field.

Abstract:

Many drug eff ects are dependent upon not just concentration, but also time. Cell based assays and in vitro testing methods are a useful, time and cost eff ective tools for drug discovery. However, it is generally accepted that many of the available assays are not eff ective for examining the eff ects of both time and concentration, and do not closely mimic physiologic kinetics or the complex environment required for virus or parasite testing. Static cell based assays in plates, fl asks or other formats do not readily permit changes in drug concentration as would be seen in human Pk/Pd. Animal models generally do not provide the same drug kinetics as would be found in humans and can be diffi cult to quantitate. Hollow fi ber (HF) bioreactors can mimic complex, 3-D and multi-cellular structures and environments required for virus and parasite culture in vitro. HF cartridges have continuous medium circulation supporting dynamic control of drug concentration over time and resulting in
the mimicking of dynamic tissue drug concentrations. A high surface-area-to-volume ratio permits extremely rapid exchange
of metabolites and pharmacoactive molecules between the central reservoir and cells growing in the relatively small ECS of the
cartridge. Furthermore, the volume of this central reservoir can be easily adjusted to permit rapid and reproducible changes in drug concentration. Simulation of the kinetics of multiple drugs can also be accomplished so drug/drug interactions and combination therapies can readily be modeled. The system is compact enough that multiple cartridges can be conveniently manipulated in a relatively small space, providing multiplexed or parallel and higher throughput type assays. Such systems can be configured for cell based assays employing either a single-cell type or multi-cell in co-cultivation. Th ese assays can generate data that is not available in any other manner, and bridge an important gap between animal studies and phase I clinical trials. Large number of cells can be assayed over a pharmacologically relevant period of time. Drug concentrations can be controlled in a dynamic fashion and both adsorption and elimination curves can be modeled. Multiple tests can be performed on the same cell population. Th ree dimensional cultures of multiple cell types can model complex processes such as virus infections in tissues, parasite infections, hematopoiesis, cancer cell propagation, cancer cell metastasis, and the blood brain barrier.

Keynote Forum

Hideko Kaji

Thomas Jefferson University, USA

Keynote: Lethal effect of denatured ribosome recycling factor at lag phase

Time : 09:45-10:30

Conference Series Antibiotics Resistance 2018 International Conference Keynote Speaker Hideko Kaji photo
Biography:

Hideko Kaji has obtained her PhD from Purdue University. She had faculty positions at Vanderbilt School of Medicine, The Johns Hopkins Medical School, and Fox Chase Cancer Research Institute. Currently, she is a Professor of Biochemistry and Molecular Biology at Jefferson Medical college, Thomas Jefferson University.

Abstract:

Ribosome recycling factor (RRF) is an essential protein factor responsible for disassembly of the post-termination complex. Protein synthesis consists of four steps, initiation, elongation of peptide chain, termination and the ribosome recycling step. RRF catalyzes the fourth step of protein synthesis in bacteria. It was known that inactivation of temperature sensitive RRF (tsRRF) at lag phase resulted in lethal eff ect (Janosi, Mottagui-Tabar et al. 1998) while at log and stationary phase it  has bacteriostatic eff ect. In this paper, we tried to elucidate the beginning of physiological and cellular changes due to the inactivation of RRF so that we have a glimpse of the possible mechanism of lethal eff ect of inactivation of tsRRF at lag phase only. We found under the condition where the lethal eff ect is observed that a large amount of 40S particles were formed
containing 16S rRNA. Within hour of the appearance of this 40S particles cells start dying. Measures such as inhibition of protein chain elongation stopped the lethal eff ect of tsRRF at the non-permissive temperature. All such measures eliminated the appearance of the 40S particles. We conclude that the 40S particle is essential for lethal eff ect of tsRRF at the lag phase. Our proteomics data showed upregulation of alternate ribosome rescue factor (ArfA) at the non-permissive temperature provide evidence about RRF essentiality. Eff ect of various antibiotics on the formation of the 40S particles and on the lethal eff ect of tsRRF will be described.

Conference Series Antibiotics Resistance 2018 International Conference Keynote Speaker Helieh S Oz photo
Biography:

Dr Helieh Oz has a DVM, MS (U. IL); PhD (U. MN) and clinical translational research certifi cate (U.KY). Dr Oz is an active member of American Association of Gastroenterology (AGA) and AGA Fellow (AGAF) and associate in Rome Foundation (Functional Gastrointestinal Diseases). she is a Microbiologist with expertise in
infectious and infl ammatory diseases, drugs discovery, pathogenesis, innate/mucosal Immunity, molecular biology, and micronutrient. she has over 90 publications in the areas of chronic infl ammatory disorders, microbial and infectious diseases. she has served as Lead Editor for special issues including Gut infl ammatory,
infectious diseases and nutrition 2018 (Mediators of Infl ammation); Gastrointestinal infl ammation, repair: role of microbiome, infection, nutrition (Gastroenterology Research Practice), J Nutrient and guest Editor for J. Pediatric Infectious Disease. she is a member of different editorial board and an avid reviewer for journals. she recently visited Sun Yat Sen University in Guangzhou and 5th Affi liated University Hospitals in Zhuhai to give lectures in Tropical and Infectious Diseases.

Abstract:

Neglected tropical diseases include microbial, parasitic and viral diseases. Toxoplasmosis is number one cause of foodborne hospitalization and congenital diseases aff ecting 60 million people in USA and 1/3rd of global population. About 1700 patients suff er from Malaria in USA each year, and millions are infected in South Asia and Africa. It is estimated that 600-800 million people worldwide to be infected with hookworms which cause severe anemia, growth retardation and eosinophilic enteritis. Dengue (break back) hemorrhagic fever is endemic in Far East and back again in Southern States and Hawaii. HIV/AIDS aff ects about 1.1 million in USA and another 1 million in China. About 1 million people suff er from multidrug resistant Mycobacterium tuberculosis in China, and it has become a major public health problem. Th e estimated cost to treat a multidrug resistant patient is over 200 times more than those infected with non-resistant tuberculosis. Th e funding for global neglected tropical diseases was started in 2006 with $15 million supported by USA. Th is funding has increased to $100 million in 2017 and current requested budget is $75 million for 2018. Th is integrative presentation will discuss a recent visit to Sun Yat Sen University Medical Center and Zhuhai Affi liated Hospitals located in the exotic tropical Southern China and some of the neglected tropical diseases endemic in the area. In addition, the presentation aims to alarm the need for scientific collaboration between 2 countries to advance the knowledge of tropical and infectious diseases in developing eff ective  therapeutic antimicrobial, preventive measures and diagnostic tools, in order to end the humans’ suff erings.

Keynote Forum

Ghassan Matar

American University of Beirut, Lebanon

Keynote: Combating antimicrobial resistance – Utility of antimicrobial combination therapy and/or inhibitors

Time : 11:35-12:20

Conference Series Antibiotics Resistance 2018 International Conference Keynote Speaker Ghassan Matar photo
Biography:

Dr. Ghassan M. Matar is a Professor and Vice Chairperson in the Department of Experimental Pathology, Immunology & Microbiology, American University of Beirut. To present he published 101 articles in refereed international journals and received funding from various extramural sources. His research interests deal mainly with molecular mechanisms of resistance to antimicrobial agents in pathogenic bacteria, namely carbapenem resistance in ESBL and non-ESBL producing Enterobacteriaceae and assessment of combination using antimicrobial therapy with and without inhibitors or natural products, in infections caused by carbapenem
resistant Enterobacteriaceae harboring various carbapenemase encoding genes.

Abstract:

The range of antimicrobial agents that can be used to treat bacterial infections is becoming limited with the constant increase in antimicrobial resistance (AMR). Several genetic factors underlie AMR, including β-lactamase-encoding genes such as blaCTXM-15 that confers resistance to third-generation cephalosporins, and blaOXA-48, blaNDM-1, and blaKPC-2 that confer resistance
to carbapenems. Remaining treatment approaches for such resistant infections include antimicrobial combination therapy and the use of β-lactamase inhibitors. Th is study assesses the molecular eff ects of such treatment approaches on antimicrobial resistantEnterobacteriaceae clinical isolates in vitro and in vivo. Nine clinical Enterobacteriaceae isolates were included in the study. One harboring blaCTXM-15, one harboring blaOXA-48, one harboring blaKPC-2, two harboring blaNDM-1 and blaCTXM-15,
and four harboring blaOXA-48 and blaCTXM-15. Minimal inhibitory concentrations were determined for carbapenems with
β-lactamase inhibitors: avibactam, Ca-EDTA, and relebactam. Synergism between antibiotic combinations was determined by
double disc diff usion when using colistin with several antibiotics. In vitro and in vivo gene expression levels were done on these combinations with and without inhibitors. Th e use of meropenem, imipenem, and ertapenem with the selected β-lactamase inhibitors restored isolate susceptibility in 100%, 87.5%, and 25% of the cases, respectively. Antimicrobial synergism was mostly detected between colistin and meropenem, fosfomycin, or tigecycline. Survival studies revealed the survival of most mice receiving antimicrobial combination therapy with inhibitors as compared to the controls. Overall gene expression levels of resistance genes were variable depending on treatment. Th e threat of antibiotic resistant bacterial infections remains viable; however, diff erent approaches to therapy are available

  • Origins and Types of Antibiotic and Antimicrobials

Session Introduction

Helieh S. Oz

American Association of Gastroenterology

Title: Overuse of Antibiotics in food Animal Industry and Infectious and Inflammatory Complications in Humans

Time : 12:00-13:00

Speaker
Biography:

Workshop

Dr Helieh Oz has a DVM, MS (U. IL); PhD (U. MN) and clinical translational research certificate (U.KY). Dr Oz is an active member of American Association of Gastroenterology (AGA) and AGA Fellow (AGAF) and associate in Rome Foundation (Functional Gastrointestinal Diseases). Dr Oz is a Microbiologist with expertise in infectious and inflammatory diseases, drugs discovery, pathogenesis, innate/mucosal Immunity, molecular biology, and micronutrient. Dr. Oz has over 90 publications in the areas of chronic inflammatory disorders, microbial and infectious diseases. Dr Oz has served as Lead Editor for special issues including Gut inflammatory, infectious diseases and nutrition 2017 (Mediators of Inflammation); gastrointestinal inflammation, repair: role of microbiome, infection, nutrition (Gastroenterology Research Practice), J. Nutrient and guest Editor for J. Pediatric Infectious Disease. Dr Oz is a member of different editorial board and an avid reviewer for journals. 

Abstract:

Pathogens cause dysregulated immune and inflammatory response. Microbiome in the gastrointestinal tract (GI) acts as a protector of health from disease. Microbiota helps absorption of nutrients and guards against invasive pathogens to dwell in GI. While, antibiotics are required to fight pathogens and infectious diseases, overuse and abuse as well as unintentional consumption of food contaminated with antibiotics affect GI to alter the composition of microbiome. Further, antibiotics shift equilibrium from health into disease status as in infections with Clostridium spp. Infectious protozoan and microbial diseases are transmitted from animals and cause GI inflammation and diarrhea in man. The common preventive practice for infectious diseases and growth promoter in farm animals are continued use (overuse) of antibiotics which enter blood circulation and contaminate eggs, milk, and meat products. Antibiotics are entered food chain and consumed by humans with possible allergic, antibiotic resistance, and other enigmatic side effects. It is estimated that over 80% of antimicrobials are used for prevention and growth promotion in swine, cattle and chickens compared to only 20% used in human therapies. This presentation will aim to discuss unintentional consumption of antibiotic residues in contaminated food products with possible side effects. Association between overuse and abuse of antibiotics in food animal industry will be discussed with outbreaks of major infectious foodborne diseases, altered gut microbiota and dysbiosis with serious complications. In addition, different preventive measures will be discussed including possible applications of new agents as surrogates to substitute antibiotics in food animals.

Speaker
Biography:

Alessandro Pini is Associate Professor of Biochemistry at the University of Siena, Italy. He has a degree in Biology, a PhD in Biotechnology, and a postgraduate degree in Clinical Biochemistry. He was visiting researcher at the Centre of Protein Engineering, MRC, Cambridge, UK, and at the Swiss Federal Institute for Research (ETH), Zurich, Switzerland.
He is founder and president of the company SetLance, based in Siena. SetLance has a special focus in the identification and early development of peptide-based drugs. He is author of dozens of publications and inventor in 12 patents regarding antibodies and peptides and their applications.

Abstract:

The peptide SET-M33 is currently under preclinical development for the set up of a new antibacterial agent against the most important Gram-negative pathogens (Brunetti et al. 2016, Sci Reports). It is a synthestic molecule produced in tetrabranched form, that makes the peptide particularly stable for in vivo use.
SET-M33 has a potent activity against a large panel of Gram-negative bacteria, with MIC90 below 1.5 μM for multiresistant strains of Pseudomonas aeruginosa and Klebsiella pneumoniae. Its mechanism of action involves LPS binding and membrane permeation (van der Weide et al. 2017, Biochim Biophys Acta). In in-vivo models of P. aeruginosa infections the peptide enabled a survival percentage of 60-80% in sepsis and lung infections when injected i.v. or by nebulization. The peptide is also able to neutralize LPS thus inhibiting the expression of inflammatory cytokines. This produces a strong anti-inflammatory effect as demonstrated in vivo in models of pulmonary infections (Brunetti et al. 2016, J Biol Chem). Plasma clearance, biodistribution, acute toxicity, synergistic activity with traditional drugs, and resistance selection profiles in comparison with molecules already used in the clinical practice, have been evaluated.
The conjugation of SET-M33 to nanoparticles based on different carriers (dextran, poly-lactide-co-glycolide, and others) is under evaluation for the improved delivery and slow release of the molecule administerd by aereosol or systemically.
Preclinical tests including ADME, safety pharmacology and manufacturing processes are in the last stages of development, thus SET-M33 is expected to enter into clinical trials in the next 18 months.
 

Speaker
Biography:

Antoine Abou Fayad has completed his PhD at the age of 26 years from Univeristy of St Andrews, UK, and postdoctoral studies from Helmholtz Institute for Pharmaceutical Research in Saarland, Germany. He is currently a junior group leader and an instructor at the department of experimental pathology, immunology and microbiology at the faculty of medicine in the American University of Beirut. He has published more than 12 papers in the field of AMR in reputed journals and has 2 pending patent applications. 

Abstract:

Antimicrobial resistance (AMR) is a life threatening urgent global health problem. There is increasing concern about the alarming emergence of multidrug-resistant superbugs. Infections resulting from such superbugs are barely responsive to treatment with few if any currently available antibiotics, reviving memories of the pre-antibiotic era and raising concerns regarding a post-antibiotic era. Given the complexity of the AMR challenge and concerns about issues at the interface of human health, animal health, and the environment, it seems particularly important to emphasize the role of a One Health approach in addressing the problem. Priorities should not only consist of strengthened human and animal health surveillance and monitoring for resistant organisms, antimicrobial stewardship programs, infection-control courses, and development of rapid diagnostic tests, but also should include, development and validation of new antimicrobial agents. As noticed, since combination therapeutic strategies will reach a dead-end very soon, novel antimicrobials with unexploited targets are highly needed in a timely manner. Soil microorganisms produce natural products as a significant number of drugs in clinical use are derived from these metabolites. Actinomycetes and Myxobacteria are mainly soil dwelling microorganisms that produce secondary metabolites to be screened for antibacterial activity. More than 80% of clinically utilized antibiotics are either natural products or natural product-derived molecules such as vancomycin, teicoplanin, daptomycin, tetracycline and many others. Our aim is to demonstrate the progress on isolating and identifying novel antimicrobials from  new Actinomycetes and Myxobacteria from Lebanon. 

Speaker
Biography:

Prof. Hak-Ryul Kim has completed his PhD from Auburn University in Auburn, Alabama and postdoctoral studies from University of Maryland, School of Pharmacy in Baltimore, Maryland. He is a professor and Chairman of School of Food Science and Biotechnology, Kyungpook Nartional University in Daegu Korea. He has published more than 65 papers in reputed journals and has been serving as a board member of the International Society of Biocatalysis and Agricultureal Biotechnology. 

Abstract:

Structural modification of natural lipids by biocatalysis can change their properties or even create novel functionalities. Hydroxy fatty acid, one of oxylipins, can be produced from the microbial bioconversion of natural vegetable oils. Recently 7,10-dihydroxy-8(E)-octadecenoic acid (DOD) was produced with high yield from olive oil containing oleic acid by bacterial strain Pseudomonas aeruginosa PR3, and further study confirmed that DOD contained strong antimicrobial activities against broad range of microorganisms. In this study we tried to modify DOD molecules by physical reaction to create new functionality or to enhance the antimicrobial activity of DOD. After the harsh heat-treatment, a novel furan fatty acid (EODA) was produced from DOD. We confirmed that EODA presented strong antibacterial activity against multidrug-resistant Staphylococcus aureus and also EODA showed a recuperative effect of the beta-lactam antibiotics activity against methicillin-resistant Staphylococcus aureus.

Temedie-Asogwa Tarilate

Nnamdi Azikiwe University, Nigeria

Title: Antibiotic Utilisation Review in a Nigerian Tertiary Hospital

Time : 15:50-16:20

Speaker
Biography:

Temedie-Asogwa Tarilate is a 29 year old pharmacist. She completed her B-Pharm degree at the age of 21 years from Niger Delta University, Wilberforce Island, Nigeria. She holds a masters degree in Clinical Pharmacy from Nnamdi Azikiwe University, Awka, Nigeria. She has an eight (8) years cumulative work experience as a Pharmacist. She has for 5 years now worked as a clinical Pharmacist at the University of Port Harcourt Teaching Hospital.and currently head the geriatrics pharmacy unit of the hospital. She has published two papers in reputable journals and also functions as a preceptor and co-supervise undergraduate pharmacy students.

Abstract:

Inappropriate use of medicines is widespread in teaching hospitals. The study aims to assess antibiotic use pattern among hospitalised patients in University of Port Harcourt Teaching Hospital (UPTH), Nigeria. A cross-sectional survey was conducted in medical, surgical, paediatrics, and obstetrics and gynaecology wards from October 2015 to March 2016 using seventeen (17) core antimicrobial drug use indicators developed under the Rational Pharmaceutical Management Plus (RPM-Plus) Program of Management Sciences for Health and revised under the Strengthening Pharmaceutical Systems (SPS) Program. A total of 2356 patients’ folders were reviewed retrospectively and data obtained statistically analysed. Additionally, sixteen inpatient physicians were interviewed to understand the reason behind the antibiotic prescribing practice observed. Antibiotics were prescribed in 68.8 percent of hospitalizations. Only 84.2 percent appeared on the essential drug list, 60.4 percent were injections and 39.9 percent were prescribed in generics. Each patient was prescribed 2.74 antibiotics at ₦13,632.00 cost averagely per hospitalization. Cephalosporin antibiotics were most commonly prescribed. The percentage of prescribed antibiotics actually administered was 87.4 percent, while 88.5% were empirically prescribed. About 35.0 percent of antibiotics were prescribed for Respiratory Tract Infections. Only 62.2 percent of key antibiotics were available and there was no systems regulating antibiotics use at UPTH. Physicians reported certain factors influenced the antibiotic use pattern observed. Antibiotics use in UPTH did not conform to acceptable standards. Establishment of local protocols and systems regulating antibiotics use including an antibiotic stewardship programme could improve rational antibiotic use; curtail cost and result in substantial savings.

Speaker
Biography:

Zajeba Tabashsum is a second year Graduate student at the Department of Animal and Avian Sciences in University of Maryland- College Park. Her research area is focused on natural antimicrobials and their implications. She has already published 4 papers in reputed journals and submitted one book chapter. Recently one of her abstract has got accepted for oral presentation and has presented posters in different national/international coferences. 

Abstract:

With growing trend of back yard, mixed crop-livestock or pasture/organic farming system, cross-contamination of produce specifically leafy-vegetables with enteric pathogens including Salmonella, Listeria and Escherichia coli is a major concern. Again produce-borne infections in the US are rising faster than ever causing thousands of hospitalizations and deaths yearly. It is also huge economic burden and major reason to recall produce products. So post-harvest processing is necessary to decrease contamination by enteric pathogens for safer products. As organic-farmers cannot use synthetic chemicals/antibiotic, they are desperately needed a natural-alternative to eliminate contaminants from produces.  As an alternative approach, we verified the efficacy of berry pomace extract (BPE) which is high in phenolic compounds including flavan, flavanone, glucuronides, glucosides, quinolones, catechol, tannins, quercetin, chlorogenic acid, gallic acid, and xanthoxic acid as sanitizer in controlling enteric pathogen Salmonella from fresh produces. For this purpose spinach and celery were decontaminated for any natural contamination and spiked with Salmonella enterica serovar Typhimurium   (ATCC® 14028™) and dipped into BPE or water for same time period and reduction in bacterial load and alteration in virulent-gene expression level was determined. There was significant reduction in bacterial number from 0.5-3.5 log with BPE treatments when compared to dipping into water also reduced bacterial number but not as efficiently. The expression of virulent-genes were also altered significantly by BPE treatments. Our findings indicated that BPE can be a potential natural alternative to replace synthetic chemical sanitizer to eliminate/reduce major enteric bacterial pathogens particularly Salmonella in produces and limit salmonellosis in human.

Nataliya Roth

University of Natural Resources and Life Sciences, Austria

Title: Role of feed additives in the strategy to reduce the prevalence of antimicrobial resistance in broilers

Time : 16:50-17:20

Speaker
Biography:

Nataliya Roth has completed her MSc in Academy of Veterinary Medicine in Lviv, Ukraine and MSc at the University of Natural Resources and Life Sciences in Vienna, Austria. Last 10 years she was working in R&D of feed additives producer Biomin Holding GmbH. Last four years she was working on her PhD about antibiotic use, resistance and strategies to overcome resistance on University of Natural Resources and Life Sciences in Vienna.

Abstract:

The application of antibiotics for the treatment of disease, disease prevention and growth promotion in food-producing animals provides favorable conditions for the selection, persistence and spread of antibiotic-resistant bacteria and their resistance determinants at the farm level. Increasing antibiotic resistance is a major public health concern. Fluoroquinolones are used to treat and prevent poultry diseases worldwide. Fluoroquinolone resistance rates are high in their countries of use. The aim of this study was to evaluate the effect of an acid-based feed additive, as well as fluoroquinolone antibiotics, on the prevalence of antibiotic-resistant E. coli. To study the emergence of antibiotic resistance in Gram-negative bacteria, E. coli are widely accepted as indicator bacteria. A total of 480 broiler chickens (Ross 308) were randomly assigned to three treatments: a control group receiving a basal diet; a group receiving a feed additive (FA) based on formic acid, acetic acid and propionic acid; and an antibiotic enrofloxacin (AB) group given the same diet, but supplemented with enrofloxacin in water. A pooled fecal sample of one-day-old chicks was collected upon arrival at the experimental farm. On day 17 and day 38 of the trial, cecal samples from each of the eight pens were taken, and the count of E. coli and antibiotic-resistant E.coli was determined.

The results of the study show a high prevalence of antibiotic-resistant E. coli in one-day-old chicks. Supplementation of the diet with FA and treatment of broilers with AB did not have a significant influence on the total number of E. coli in the cecal content on day 17 and day 38 of the trial. Supplementation with FA contributed to better growth performance and to a significant decrease (P ≤ 0.05) in E. coli resistant to ampicillin and tetracycline compared to the control and AB groups, as well as to a decrease (P ≤ 0.05) in sulfamethoxazole and ciprofloxacin-resistant E. coli compared to the AB group. Treatment with AB increased (P ≤ 0.05) the average daily weight compared to the control group and increased (P ≤ 0.05) the number of E. coli resistant to ciprofloxacin, streptomycin, sulfamethoxazole and tetracycline; it also decreased (P ≤ 0.05) the number of E. coli resistant to cefotaxime and extended spectrum beta-lactamase-(ESBL)-producing E. coli in the ceca of broilers. 

Speaker
Biography:

Dr. Bernard C. Silvala is the current Department Head of the Medical Laboratory Technology Program at the University of Tabuk. He is an  Assistant Professor in Microbiology. He has published numerous works in Microbiological assays, educational manuals and scientific articles. Also a member of editorial board reviewer of reputable journals.

Abstract:

Panton-valentine leukocidin (PV-luk) toxin is a very potent toxin responsible for severe and fatal form of Staphylococcal infections. This study aimed to determine the frequency of PV-luk producing methicillin resistant S. aureus (MRSA) and compare the conventional against real time PCR for identification of MRSA. A total number of 47 MRSA isolates were enrolled in the study. All are identified and typed using VITEK system. DNA was extracted and subject to conventional and real time PCR (RT-PCR) for the detection of mecA, luk-PV, orfX, mecA/mecC SCC/orfX junction genes. Forty-five isolates (95.7%) confirmed as MRSA and 2 isolated showed a mixed infection of Methicillin sensitive S. aureus (MSSA) and Methicillin resistant coagulase negative Staphylococci (MRCoNS).  Fifteen out of forty-seven (31.9%) have Panton – Valentine Leukocidin gene (luk-PV) gene.  PV-luk was detected in one third of tested MRSA emerging the possibility to have a potent superbug. In addition to, diagnosis of MRSA is highly accurate when using multiplex real time PCR rather than conventional PCR.

 

  • Antimicrobial resistance and its emergence of animals

Session Introduction

Richard M Beteck

Rhodes University, South Africa

Title: Metronidazole schiff base hybrids: Synthesis and in vitro anti-trichomonocidal evaluation

Time : 12:20-12:50

Speaker
Biography:

Richard Mbi Beteck has completed his PhD at the age of 28 years from North-West University, Potchefstroom campus and is currently a postdoctoral fellow at Rhodes University.

Abstract:

Trichomoniasis is a neglected venereal infection affecting almost 43 million people in Africa and almost 4 million people in the United states of America. It is a very common disease with high prevalence of up to 40 % in some regions in Africa. It is caused by Trichomonas vaginalis, a parasitic protozoan which is transmitted from person to persons during sex. It has been established that infection with T. Vaginalis increases the chances of acquiring and transmitting HIV. It also amplifies the progression of other sexually transmitted diseases. Treatment of Trichomoniasis rely solely on metronidazole and tinidazole, with metronidazole being the mainstay therapy. These agents are effective and safe at low doses required to treat susceptible strains of the parasite. However, serious side effects arose when large doses are used to manage metronidazole tolerant and resistant strains of T. Vaginalis.  With metronidazole tolerant and resistant strains of T. Vaginalis well documented, it is imperative to develop new trichomonacidal agents. Methodology & Theoretical Orientation: Our approach is to develop novel agents that can potentially probe new targets in the parasite and can still be reduced in the parasite hydrogenosome to generate reactive radicals (as does metronidazole). To this effect, we conceptualised and synthesise target compounds containing a metronidazole (MTZ) unit flagged by Schiff bases of varied lipophilicities and hydrogen bonding properties. Findings: Target compounds were screened in vitro against drug susceptible strains of the parasite for preliminary investigation and were established to be potent, with almost 80 % of target compounds exhibiting 100 % parasite inhibition at 10 µM. Conclusion & Significance: There is currently no treatment for metronidazole resistant trichomoniasis. Our approach has delivered very potent agents having the potential to probe additional targets to that of MTZ. They are promising templates to overcome the issue of resistance.
 

Samuel Kesse

China Pharmaceutical University, China

Title: New antibiotics on the market and how to effectively use them

Time : 13:50-14:15

Speaker
Biography:

NA

Abstract:

NA

Biography:

Mengfei is at his last stage of PhD study in the University of Maryland, and he will finish his PhD in May 2018. His research area is focusing on applying modern techniques of microbiology in improving human gut microbiome as well as preventing foodborne enteric diseases. So far he has published 3 book chapters and 10 papers in reputed journals, and he has presented 3 oral talks and more than 10 posters in top-level conferences.

Abstract:

Microbial horizontal gene transfer is a continuous process and it shapes especially bacterial genomes. However, the niches of microbial ecology as well as synthetic antibiotics or natural antimicrobials in the influence on the evolution of this biological networks are not fully understood yet. So far, very little attention has been paid on how dosages of antibiotics utilized in farm animal production contributes to the overall problem of antibiotic resistance. In this study, we investigated the mechanisms of sub-therapeutic and therapeutic dosages of synthetic antibiotics that foster the exchange of genetic materials in the microbial community in various components of farm animal production system using marked conventional and organic farm isolated Salmonella enterica serovar Typhimurium strains. The relatedness among the S. Typhimurium isolates from this study was investigated based on genome-wide SNP comparisons and the draft genome contigs have been submitted to NCBI. The antibiotic resistant S. Typhimurium isolates from conventional farm cultured in both conventional and organic soils failed to lose their tetracycline resistance, whereas highly sensitive S. Typhimurium strains isolated from organic farm gradually acquired higher tetracycline MICs over time under both types of soils. None of the isolated S. Typhimurium strains developed or lost sulfamethoxazole/trimethoprim resistance in soil environment. The qRT-PCR analysis indicated that differential expression of genes involved in antibiotic resistance in S. Typhimurium isolates was artificially inoculated under antibiotic pressure. The findings suggest some basic patterns in mechanism of S. Typhimurium antibiotic-resistance development in farm-related microbial ecosystems.

Pramod Jog

D.Y.Patil Medical College, Pune

Title: Use and abuse of antibiotics

Time : 14:40-15:05

Biography:

NA

Abstract:

NA

Rahul M Lokhande

BJ Govt Medical College, India

Title: DRUG RESISTANT TUBERCULOSIS-CHALLENGES UNFOLDED

Time : 15:05-15:30

Speaker
Biography:

       Dr Rahul Lokhande  , MD in Pulmonary Medicine. Working as Associate Professor in Chest department of BJ Govt Medical college Pune  India. Member of Drug Resistant Tuberculosis Board of Aundh Chest Hospital . He is one of Fogarty Scholar with collaboration with John Hopkins University , Baltimore  USA. Working on  many studies and trial  conducted in BJ government College  along with CTU unit , in field of HIV , Tuberculosis and diabeties , upcoming trials on vaccines for tuberculosis .   Presently working on “Factors for Unfavorable Outcome of Drug Resistant Tuberculosis  “.   

Abstract:

              Antibiotic resistance is an important concern for the public health authorities at global level. Community based researches in developing countries have shown increase in burden of antimicrobial resistance.  In 1993 World Health Organization (WHO) declared Tuberculosis as a global emergency and promoted directly observed treatment short course (DOTS) in 1995. Millions of lives have been saved compare with the pre DOTS era, high cure rates have been achieved in most of countries worldwide. Global incidence of tuberculosis has been in a slow decline since the early 2000’s. However, the emergence and spread of Multidrug resistant (MDR) tuberculosis, extensively drug resistant ( XDR ) tuberculosis pose a threat to global tuberculosis control .

  Genotypic  and Phenotypic changes in Mycobacterium Tuberculosis ,with lack of adequate laboratory facilities in most of tuberculosis endemic countries leads to missing the diagnosis. Multidrug resistant tuberculosis and XDR tuberculosis greatly complicate patient management within resource poor national tuberculosis program , reducing  treatment  efficacy  and increasing  the cost of treatment .

         Despite nearly 20 years  of WHO promoting activity and >12 years of MDR tuberculosis specific activity , has the country response  to the drug resistant tuberculosis  epidemic been so in effectual ? The current dilemmas, challenges and priority needs for global drug resistance screening and surveillance, improving treatment regimens, and management of outcomes and prevention of drug resistance will be discussed

 

Speaker
Biography:

Samir Jaoua, PhD from the University of Technology of Compiegne (UTC, France), is currently Professor at the Department of Biological and Environmental Sciences (CAS, QU). He is also Qualified Professor of France Universities “Section 64: Molecular Biology and Biochemistry” and Professor at the University of Sfax (Tunisia) and having been previously Director of Laboratory at the Center of Biotechnology of Sfax (University of Sfax- Tunisia). He is molecular and microbial geneticist, having more than 30 years of experience in the fields of molecular and microbial Biotechnology in different countries: France, Switzerland, Belgium, Germany, Tunisia and Qatar. He is the author of 118 publications with impact factors; H-index: 30 and served as member, Chair, and General Chair of a number of conferences. 

Abstract:

Bacillus thuringiensis strain BUPM4 is known for its ability to produce a bacteriocin, called Bacthuricin F4 (BF4), which inhibits the growth of several Gram-positive bacteria and particularly Bacillaceae. This study aimed to use the insertional transposon mutagenesis approach for disrupting and thus identifying genes associated with BF4 synthesis. Here, the mini-Tn10 transposon was used to generate a library of B. thuringiensis mutants. Twenty thousand clones were screened for the search of mutants with affected bacteriocin synthesis. Bymolecular hybridization, it was demonstrated that the mini-Tn10 transposition occurred in different sites. Clone MB1, containing a mini-Tn10 single-copy insertion, lost the BF4 synthesis, but maintained its immunity to BF4. The flanking sequences surrounding the mini-Tn10 insertion were cloned and sequenced. The bacteriocinogenic plasmid pIBF4 from Bacillus thuringiensis responsible of Bacthuricin F4 synthesis was isolated and characterized. It has a molecular weight of 19.1 kb. Ninety-five percent of cells retained the pIBF4 plasmid after 200 generations, demonstrating its high stability. pIBF4 was successfully transferred to Bacillus thuringiensis HD1CryB strain with a transfer frequency of 10-8 transconjugants per donor cell. The study of the recipient host range revealed that pIBF4 is specifically transferable to Bacillus thuringiensis strains with variable transfer frequencies depending on the recipient host strain. 

  • Evolution and Mechanisms of Antibiotics and Antimicrobials Resistance | Antimicrobial Resistance and its Emergence of Animals | Antimicrobial Resistance: Emergence and its Eccentricity | Antibiotics: Types and Prognosis
Speaker

Chair

Hideko Kaji

Thomas Jefferson University, USA

Speaker
Biography:

Alessandro Pini is Associate Professor of Biochemistry at the University of Siena, Italy. He has a degree in Biology, a PhD in Biotechnology, and a Postgraduate
degree in Clinical Biochemistry. He was a Visiting Researcher at the Centre of Protein Engineering, MRC, Cambridge, UK, and at the Swiss Federal Institute for
Research (ETH), Zurich, Switzerland. He is the Founder and President of the company SetLance, based in Siena. He is author of dozens of publications and
inventor in 12 patents regarding antibodies and peptides and their applications.

Abstract:

The peptide SET-M33 is currently under preclinical development for the setup of a new antibacterial agent against the most important Gram-negative pathogens (Brunetti et al. 2016, Sci Reports). It is a synthetic molecule produced in tetra branched form, that makes the peptide particularly stable for in vivo use. SET-M33 has a potent activity against a large panel of Gram-negative bacteria, with MIC90 below 1.5μM for multi resistant strains of Pseudomonas aeruginosa and Klebsiella pneumoniae. Its mechanism of action involves LPS binding and membrane permeation (van der Weide et al. 2017, Biochim Biophys Acta). In in-vivo models of P. aeruginosa infections the peptide enabled a survival percentage of 60-80% in sepsis and lung infections when injected I.V or by nebulization. Th e peptide is also able to neutralize LPS thus inhibiting the expression of infl ammatory cytokines. Th is produces a strong anti-infl ammatory eff ect as demonstrated in vivo in models of pulmonary
infections (Brunetti et al. 2016, J Biol Chem). Plasma clearance, biodistribution, acute toxicity, synergistic activity with traditional drugs, and resistance selection profi les in comparison with molecules already used in the clinical practice, have been evaluated. The conjugation of SET-M33 to nanoparticles based on diff erent carriers (dextran, poly-lactide-co-glycoside, and others) is under evaluation for the improved delivery and slow release of the molecule administered by aerosol or systemically. Preclinical tests including ADME, safety pharmacology and manufacturing processes are in the last stages of development, thus SET-M33 is expected to enter into clinical trials in the next 18 months.

Nataliya Roth

University of Natural Resources and Life Sciences, Austria

Title: Role of feed additives in the strategy to reduce the prevalence of antimicrobial resistance in broilers

Time : 14:00-14:30

Speaker
Biography:

Nataliya Roth has completed her MS in Academy of Veterinary Medicine in Lviv, Ukraine and at the University of Natural Resources and Life Sciences in Vienna,
Austria. For last 10 years, she has been working in R&D of feed additives producer Biomin Holding GmbH. For last four years, she was working on her PhD about antibiotic use, resistance and strategies to overcome resistance on University of Natural Resources and Life Sciences in Vienna.

Abstract:

The application of antibiotics for the treatment of disease, disease prevention and growth promotion in food-producing animals provides favorable conditions for the selection, persistence and spread of antibiotic-resistant bacteria and their resistance determinants at the farm level. Increasing antibiotic resistance is a major public health concern. Fluoroquinolones are used to treat and prevent poultry diseases worldwide. Fluoroquinolone resistance rates are high in their countries of use. The aim of this study was to evaluate the eff ect of an acid-based feed additive, as well as fl uoroquinolone antibiotics, on the prevalence of antibiotic-resistant E. coli. To study the emergence of antibiotic resistance in Gram-negative bacteria, E. coli are widely accepted as indicator bacteria. A total of 480 broiler chickens (Ross 308) were randomly assigned to three treatments: a control group receiving a basal diet; a group receiving a feed additive (FA) based on formic acid, acetic acid and propionic acid; and an antibiotic enrofl oxacin (AB) group given the same diet but supplemented with enrofl oxacin in water. A pooled
fecal sample of one-day-old chicks was collected upon arrival at the experimental farm. On day 17 and day 38 of the trial, cecal samples from each of the eight pens were taken, and the count of E. coli and antibiotic-resistant E. coli was determined. The results of the study show a high prevalence of antibiotic-resistant E. coli in one-day-old chicks. Supplementation of the diet with FA and treatment of broilers with AB did not have a signifi cant infl uence on the total number of E. coli in the cecal content on day 17 and day 38 of the trial. Supplementation with FA contributed to better growth performance and to a significant decrease (P≤0.05) in E. coli resistant to ampicillin and tetracycline compared to the control and AB groups, as well as to a decrease (P≤0.05) in sulfamethoxazole and ciprofl oxacin-resistant E. coli compared to the AB group. Treatment with AB increased (P≤0.05) the average daily weight compared to the control group and increased (P≤0.05) the number of E. coli resistant to ciprofl oxacin, streptomycin, sulfamethoxazole and tetracycline; it also decreased (P≤0.05) the number of E. coli resistant to cefotaxime and extended spectrum beta-lactamase-(ESBL)-producing E. coli in the ceca of broilers.

Speaker
Biography:

Richard Mbi Beteck has completed his PhD from North-West University, Potchefstroom Campus and is currently a Postdoctoral Fellow at Rhodes University.

Abstract:

Introduction: Trichomoniasis is a neglected venereal infection aff ecting almost 43 million people in Africa and almost 4 million people in the United states of America. It is a very common disease with high prevalence of up to 40% in some regions in Africa. It is caused by Trichomonas vaginalis, a parasitic protozoan which is transmitted from person to persons during sex. It has been established that infection with T. vaginalis increases the chances of acquiring and transmitting HIV. It also amplifi es the progression of other sexually transmitted diseases. Treatment of Trichomoniasis rely solely on metronidazole and tinidazole, with metronidazole being the mainstay therapy. Th ese agents are eff ective and safe at low doses required to treat susceptible strains of the parasite. However, serious side eff ects arose when large doses are used to manage metronidazole tolerant and resistant strains of T. vaginalis. With metronidazole tolerant and resistant strains of T. vaginalis well documented, it is imperative to develop new trichomonacidal agents.
 
Methodology & Th eoretical Orientation: Our approach is to develop novel agents that can potentially probe new targets in the parasite and can still be reduced in the parasite hydrogenosome to generate reactive radicals (as does metronidazole). To this eff ect, we conceptualised and synthesise target compounds containing a metronidazole (MTZ) unit fl agged by Schiff bases of varied lipophilicities and hydrogen bonding properties.
 
Findings: Target compounds were screened in vitro against drug susceptible strains of the parasite for preliminary investigation and were established to be potent, with almost 80% of target compounds exhibiting 100% parasite inhibition at 10μM.
 
Conclusion & Signifi cance: Th ere is currently no treatment for metronidazole resistant trichomoniasis. Our approach has delivered very potent agents having the potential to probe additional targets to that of MTZ. Th ey are promising templates to overcome the issue of resistance.

Speaker
Biography:

Hak-Ryul Kim has completed his PhD from Auburn University in Auburn, Alabama and Postdoctoral studies from University of Maryland, School of Pharmacy in Baltimore, Maryland. He is a Professor and Chairman of School of Food Science and Biotechnology, Kyungpook Nartional University in Daegu Korea. He has published more than 65 papers in reputed journals and has been serving as a Board Member of the International Society of Biocatalysis and Agricultureal Biotechnology.

Abstract:

Structural modifi cation of natural lipids by biocatalysis can change their properties or even create novel functionalities. Hydroxy fatty acid, one of oxylipins, can be produced from the microbial bioconversion of natural vegetable oils. Recently 7,10-dihydroxy-8(E)-octadecenoic acid (DOD) was produced with high yield from olive oil containing oleic acid by bacterial strain Pseudomonas aeruginosa PR3, and further study confi rmed that DOD contained strong antimicrobial activities against broad range of microorganisms. In this study we tried to modify DOD molecules by physical reaction to create new functionality or to enhance the antimicrobial activity of DOD. Aft er the harsh heat-treatment, a novel furan fatty acid (EODA) was produced from DOD. We confi rmed that EODA presented strong antibacterial activity against multi drug-resistant Staphylococcus aureus and also EODA showed a recuperative eff ect of the b-lactam antibiotics activity against methicillinresistant Staphylococcus aureus.

Speaker
Biography:

Alessandro Pini is Associate Professor of Biochemistry at the University of Siena, Italy. He has a degree in Biology, a PhD in Biotechnology, and a postgraduate degree in Clinical Biochemistry. He was visiting researcher at the Centre of Protein Engineering, MRC, Cambridge, UK, and at the Swiss Federal Institute for Research (ETH), Zurich, Switzerland. He is founder and president of the company SetLance, based in Siena. SetLance has a special focus in the identifi cation and early development of peptide-based drugs. He is author of dozens of publications and inventor in 12 patents regarding antibodies and peptides and their applications.

Abstract:

Sepsis is a clinical syndrome caused by the body's immune and coagulation systems. Septic shock is a life-threatening condition that is characterized by low blood pressure despite adequate fl uid replacement, and organ dysfunction or failure. Sepsis is an important cause of death in people of all ages (Perner et al, 2017, Intensive Care Med). It is triggered by bacterial infections and by the release of LPS and LTA from bacterial surfaces (Ianaro et al, 2009 Mini Rev Med Chem; Kang et al, 2016 Arch Pharm Res).Here it will be described the construction of a new device for the selective removal of LPS and LTA from blood of patient with sepsis. Th is medical device is based on a resin conjugated with SET-M33 (Brunetti et al. 2016, Sci Reports), a synthetic peptide capable to strongly bind LPS and LTA from Gram-negative and Gram-positive bacteria, respectively. Th e device is able to remove selectively LPS and LTA from human blood samples without aff ecting serum protein content. It is currently under development for the clinical use in Intensive Care Units where sepsis is among the most imporant cause of death worldwide

  • Modern Antibiotics for Various Diseases and Infections | Antibiotics: Market Analysis & Business Opportunities | Alternative Strategies for Antimicrobial Resistance Worldwide | Analytical Strategies for Antimicrobials & Antibiotics
Speaker

Chair

Akira Kaji

University of Pennsylvania, USA

Speaker

Co-Chair

Chair 2-Tore Midtvedt

Karolinska Institute, Sweden

Session Introduction

Nataliya Roth

University of Natural Resources and Life Sciences, Austria

Title: Prevalence of antibiotic resistant bacteria in animals -A global perspective farm environments

Time : 13:30-14:00

Speaker
Biography:

Nataliya Roth has completed her MS in Academy of Veterinary Medicine in Lviv, Ukraine and at the University of Natural Resources and Life Sciences in Vienna,
Austria. From past 10 years, she has been working in R&D of feed additives producer Biomin Holding GmbH. From past four years, she was working on her PhD about antibiotic use, resistance and strategies to overcome resistance at University of Natural Resources and Life Sciences in Vienna.

Abstract:

The increase in antibiotic resistance is a global concern for human and animal health. Resistant microorganisms can move between food-producing animals and humans by direct contact, through the food chain or in the environment. An overview of antibiotic use and resistance in food producing animals from diff erent countries provides an essential tool to fi nding solutions to prevent the spread of antibiotic resistance. Th e monitoring of antimicrobial use together with resistance rates of indicator E. coli provides an overview, allowing the identifi cation of further regulatory and research needs. Th e established national surveillance of antibiotic resistance is essential in providing comparable data. Scientifi c work provides some AR data
for countries that lack national monitoring, which indicates the prevalence of resistant bacteria. Available data from the US, China, the United Kingdom and Germany indicate minor diff erences in resistance rates among E. coli isolated from chickens on farms, from slaughterhouses and from retail meat. Th e resistance rates to fl uoroquinolones and quinolones are lower in US in comparison to other large poultry producers that allow that use of  fluoroquinolones. Th ese fi ndings demonstrate the possibility to produce poultry without fluoroquinolones, which results in low resistance rates. Th e resistance rates in E. coli to representatives of several antibiotic classes, e.g., tetracycline, sulfamethoxazole, streptomycin and ampicillin, are rather high in large poultry producing countries, with the exception of ampicillin resistance in the US.

Speaker
Biography:

Helieh S Oz is an active Member of American Association of Gastroenterology (AGA) and AGA Fellow (AGAF) and an Associate in Rome Foundation (Functional Gastrointestinal Diseases). She is a Microbiologist with expertise in infectious and infl ammatory diseases, drugs discovery, pathogenesis, innate/mucosal immunity, molecular biology, and micronutrient. She has over 90 publications in the areas of chronic infl ammatory disorders, microbial and infectious diseases. She has served as Lead Editor for special issues including Gut infl ammatory, infectious diseases and nutrition 2017 (Mediators of Infl ammation); gastrointestinal infl ammation, repair: role of microbiome, infection, nutrition (Gastroenterology Research Practice), J. Nutrient and guest Editor for J. Pediatric Infectious Disease. She is a member of different Editorial Board and an avid reviewer for journals.

Abstract:

Pathogens cause dysregulated immune and infl ammatory response. Microbiome in the gastrointestinal tract (GI) acts as a protector of health from disease. Microbiota helps absorption of nutrients and guards against invasive pathogens to dwell in GI. While, antibiotics are required to fi ght pathogens and infectious diseases, overuse and abuse as well as unintentional consumption of food contaminated with antibiotics aff ect GI to alter the composition of microbiome. Further, antibiotics shift equilibrium from health into disease status as in infections with Clostridium Spp. Infectious protozoan and microbial diseases are transmitted from animals and cause GI infl ammation and diarrhea in man. Th e common preventive practice for infectious diseases and growth promoter in farm animals are continued use (overuse) of antibiotics which enter blood circulation and contaminate eggs, milk, and meat products. Antibiotics are entered food chain and consumed by humans
with possible allergic, antibiotic resistance, and other enigmatic side eff ects. It is estimated that over 80% of antimicrobials are used for prevention and growth promotion in swine, cattle and chickens compared to only 20% used in human therapies. This presentation will aim to discuss unintentional consumption of antibiotic residues in contaminated food products with possible
side eff ects. Association between overuse and abuse of antibiotics in food animal industry will be discussed with outbreaks of major infectious foodborne diseases, altered gut microbiota and dysbiosis with serious complications. In addition, different preventive measures will be discussed including possible applications of new agents as surrogates to substitute antibiotics in food animals.

Speaker
Biography:

Yeon-Jung Lee is a graduate student in School of Food Science and Biotechnology, Kyungpook National University in Daegu Korea.

Abstract:

Hydroxy fatty acids have been widely studied because they have various biological properties that can be utilized in many industries, compared with other types of fatty acids. Among the hydroxy fatty acids, our research group focused on 7,10-dihydroxy-8(E)-octadecenoic acid (DOD). We confi rmed that the strong antibacterial activities of DOD against foodborne pathogenic bacteria and plant pathogenic bacteria. Saccharide–fatty acid esters are important biodegradable emulsifiers in foods, cosmetics, and pharmaceuticals, hence, we focused on enzymatic synthesis of DOD-saccharide esters for industrial utilization of DOD. Several saccharides were screened as a substrate for esterifi cation with DOD. As a result, DOD xylitol ester was successfully produced at 50 with stirring at 200rpm for 24 hours in the presence of lipozyme RMIM as enzyme, and t-butyl alcohol as solvent. Its structure was confi rmed by GC/MS.

Poster 2: Adailton Pereira dos Santos

Federal University of Goias, Brazil

Title: Resistance of Pseudomonas aeruginosa against betalactamics

Time : 15:00-16:00

Speaker
Biography:

Adailton Pereira dos Santos has graduated in Biology from the Pontifi cal Catholic University of Goiás (2002). He has a Specialization in Teacher Training in the area of Environmental Education by the Pontifi cal Catholic University of Goiás (2002-2003). He currently teaches at Dom Pedro I State College (2014-2017) and Severina Maria de Jesus State College (2003-2017). He has experience in General Biology, with emphasis in General Biology, mainly in the following subjects: Ecotoxicology, Danio rerio, Industrial Effl uents and Bioindicators.

Abstract:

The emergence and spread of antimicrobial resistance are problems of big global importance. Th e Β-lactamases are enzymes that hydrolyze the β-lactams ring; this prevents the action of β-lactams antimicrobials. Th e objective of this work was to diagnose phenotypically and molecularly 15 beta-lactamase resistance genes. Sixty samples of Pseudomonas aeruginosa were
selected, and the antibiogram test was done for resistance test against beta-lactams class. A literature review was performed and discovered many genes that present resistance to beta-lactams in Pseudomonas aeruginosa bacteria. Aft er the literature revision, molecular tests of PCR SYBR Green method, to amplify of the genes corresponding to the resistances found in phenotyping
were performed. Following the antibiograms of the samples, they found that 24/60 (40%) were resistant to aztreonam, 15/60 (25%) to gentamicin, 6/60 (10%) to ceft azidime, 4/60 (6%), ciprofl oxacin, 4/60 (6.6%) to imepenem and 2/60 (3.3%) to piperacillin + tazobactam. No sample showed positive results for ESBL, metallo-β-lactamase neither to carbapenemase. The isolates of P. aeruginosa from our study showed a high production rate of AmpC. Among the preliminary results, we found data of correlation between beta-lactam antibiotics and resistance genes. Th e blaVIM, blaIMP, blaCTX-M, blaKPC, blaGIM, blaSPM genes presented resistant to piperacillin + tazobactan, ciprofl oxacin, aztreonam and ceft azidime. According the criteria established by the Institute of Clinical and Laboratory Standards, this work presents the same beta-lactamases resistance shown by literature.

Poster 3-Andressa Liberal Santos

Federal University of Goias, Brazil

Title: Beta-lactamics antimicrobial resistance from Enterobacteriaceae

Time : 15:00-16:00

Biography:

Santos A L has completed her graduation in Microbiology and Immunology from Universidade Federal do Rio de Janeiro. Currently, she is pursuing her Master’s
degree in Biology of parasite-host relationships of Universidade Federal de Goiás in Brazil

Abstract:

Antimicrobial resistance is a worldwide problem. Resistance is generated by the acquisition of genes that encode methods of evasion to the mechanisms of action of antimicrobials. Strains with resistance to multiple classes of antibiotics emerged among the major Gram-negative species, including the family Enterobacteriaceae. Among the antibiotics, frequently used are beta-lactams and resistance to this class has also increased. Th e objective of this work was identifi ed Enterobacteriaceae resistance by phenotypic method and to standardize a molecular diagnostic method for 15 beta-lactam resistance genes. The Kirby and Bauer methods were used to verify the phenotypic resistance to beta-lactams and the molecular tracing of resistance  genes was done using the real-time polymerase chain reaction (qPCR) method using the SYBR Green System. Among the results, the study also showed the phenotyic resistance of beta-lactams following the criteria established by the Institute of Clinical and Laboratory Standards, in which the samples had a total of 118 resistances, being 5.08% in K. pneumoniae, 0.84%
in P. mirabilis, 3.38% in C. freundii, 19.49% in S. enterica, 23.72% in E. aerogenes, 16.94% in E. agglomerans, 1.69% in R terrigenes, 5.93% in P. stuartii, 10.16% in M. morganii and 7.62% in H. alvei. Aft er, a bibliographic research was carried out on resistance genes, antimicrobial and Enterobacteriaceae like Klebsiella pneumoniae, Proteus mirabilis, Citrobacter freundii,
Enterobacter cloacae, Enterobacter aerogenes, Enterobacter agglomerans, Serratia marcescens, Salmonella enterica, Raoultella terrigenes, Providencia stuartii, Morganella morganii and Hafnia alvei. Subsequently. Th e work presents bibliographic data on the relationship between beta-lactams and resistance genes studied, as well as the relation of these and Enterobacteriaceae, all of clinical origin in Brazil. Finally, molecular resistance profi les were screened on the bacteria studied, there is a
correlation of phenotype data with the genes studied. A molecular diagnostic method for 15 beta-lactams resistance genes in Enterobacteriaceae was standardized via qPCR.

Biography:

Célia Regina Malveste Ito has completed her Bachelor's degree in Biological Sciences from the Pontifi cal Catholic University of Goiás (2008) and a Master's degree in Health Sciences from the Federal University of Goiás in 2017, doing research in the area of Microbiology. Currently, she is a Supervisor and Technician of the Eye Bank of the Federal University of Goiás. She has experience in the fi eld of General Biology, with emphasis on evaluation and preservation of human tissues.

Abstract:

Introduction: Gentamicin is the most eff ective antibiotic for the decontamination of donor eyes before enucleation and preserved corneas for transplantation, being the most used in the composition of commercial preservation media. It is important to detect trends of microbial resistance to the antibiotics of choice in most presently used corneal preservation solutions.
 
Objective: Th e objective of the present study was to analyze the susceptibility of the isolated microbiota in donor eyes for corneal transplantation to gentamicin.
 
Result: In relation to the antimicrobial action of gentamicin, of the 335 bacterial samples isolated, antibiotic test against gentamicin was performed in 305 samples, of which 88% (268/305) were sensitive to the antibiotic and 12% (37/305) were antibiotic-resistant. Of these, 12% of gentamicin-resistant strains, 5% were Gram-negative bacteria and 7% were Gram-positive bacteria, most of which were Staphylococcus Coagulase Negative (SCN).
 
Discussion: Th is sensitivity rate is still worrying, since there is no adequate antisepsis of Ocular tissues prior to preservation, microorganisms resistant to the antibiotic contained in the preservation medium may remain in the corneal tissue at the time of transplantation, resulting in a corneal receptor endophthalmitis.
 
Conclusion: Although some strains resistant to gentamicin have been found, the corneal preservation medium containing gentamicin as an antibiotic complements tissue decontamination procedure and provides greater safety for the preservation of corneal tissue for transplantation.

Speaker
Biography:

Ji-Sun Moon is a graduate student in School of Food Science and Biotechnology, Kyungpook National University in Daegu Korea..

Abstract:

Structural modifi cation of natural lipids by biocatalysis can change their properties or even create novel functionalities.
Hydroxy fatty acid, one of oxylipins, can be produced from the microbial bioconversion of natural vegetable oils. Recently
7,10-dihydroxy-8(E)-octadecenoic acid (DOD) was produced with high yield from olive oil containing oleic acid by bacterial strain Pseudomonas aeruginosa PR3, and further study confi rmed that DOD contained strong antimicrobial activities against broad range of microorganisms. In this study, we tried to modify DOD molecules by physical reaction to create new functionality or to enhance the antimicrobial activity of DOD. Aft er the harsh heat-treatment, a novel furan fatty acid (EODA) was produced from DOD. We confi rmed that EODA presented strong antibacterial activity against multidrug-resistant
Staphylococcus aureus and also EODA showed a recuperative eff ect of the beta-lactam antibiotics activity against methicillinresistant Staphylococcus aureus