Scientific Program

Conference Series Ltd invites all the participants across the globe to attend 6th World Congress on Control and Prevention of HIV/AIDS, STDs & STIs Hilton Zurich Airport, Zurich, Switzerland.

Day 1 :

Keynote Forum

Reza Nassiri

Michigan State University
USA

Keynote: Emerging antibiotic resistance: A threat to modern medicine

Time : 09:20-09:50

Conference Series STD-HIV AIDS 2018 International Conference Keynote Speaker Reza Nassiri photo
Biography:

Reza Nassiri is a former Associate Dean of Global Health at the Michigan State University (MSU). He also served as MSU director of Institute of International Health. He is currently Professor of Pharmacology and Toxicology, Professor of Family and Community Medicine, and, lecturer in Global Health, Infectious Diseases and Tropical Medicine. He currently works on international public health issues relating to chronic diseases and has expertise in global health. He has made contributions in various fields of medical sciences including clinical investigation and health education. On the basis of his extensive experience and expertise in chronic infectious diseases including HIV/AIDS, TB as well as antimicrobial resistance and human gut microbiome, he developed clinical research programs in Brazil, South Africa, Haiti, Dominican Republic and Mexico.

Abstract:

Global consumption of antibiotics has increased nearly 40% in the last decade. The incredible rapid resistance of antibiotic resistance which is taking place worldwide is not only a serious threat to the practice of modern medicine, but equally important, a threat to global public health. This urgent issue is so alarming that it caught the attention of G-20 Summit in both China (2016) and Germany (2017), let alone the U.N. Assembly in 2016 had called for a special meeting of “superbugs” which focused on the escalating drug resistance with respect to the sexually transmitted disease gonorrhea and carbapenem resistant Enterobacteriaceae. While

the causes of antibiotic resistance are complex, certainly human behavior play a significant role in the spread of antibiotic resistant genes. In addition to the human behavior, the drivers of resistance include agriculture sector, animal husbandry, household and industry – these factors contribute significantly to the spread of the resistant genes within the ecosystem. Such resistant mechanisms are continuously emerging globally, which threatens our ability to treat common infections, resulting in increased death, disability and costs. Since the development and clinical use of penicillins, nearly 1000 resistant-related beta-lactamases that inactivate various types of antibiotics have been identified. There is also a global concern about the emergence of antibiotic resistant carried by the healthy individuals, the commensal bacteria. The CDC and WHO surveillance data shows that the resistance in E. coli is generally and consistently the highest for antibacterial agents in both human and veterinary medicine. Within communities, resistant bacteria circulate from person to person or from animals and environment to person, or vice versa. With 1 billion people travelling each year, bacteria is becoming more mobile. The bacterial resistance can kill 700,000 worldwide each year and it’s been estimated to kill 10 million by 2050. The WHO estimates 78 million people a year get gonorrhea, an STD that can infect the genitals, rectum and throat - there is a widespread resistance to the first-line medicine ciprofloxacin as well as increasing resistance to azithromycin.

The emergence of resistance to last-resort treatments known as extended-spectrum cephalosporins (ESCs) is now eminent. The five riskiest superbugs are recognized as (1) the original one: Staphylococcus Aureus (MRSA), (2) the hospital lurkers: Clostridium Difficile and Acinetobacter, (3) the food borne pathogens: Escherichia Coli and Salmonella, (4) The sexually-transmitted infections: Gonorrhea and Chlamydia, and (5) TB. India is a typical example of encountering the deadly bacterial resistance. The discovery of the New Delhi metallo-beta-lactamase-1 (NDM-1) which disables almost all antibiotics directed against it, was turning point in the rapid emergence of blaNDM-1 gene which was first identified in 2008 in people who had traveled in India or sought medical care in South Asia. The gene for NDM-1 travels on a plasmid, an extra-chromosomal loop of DNA that can be traded freely among bacteria. So far, it has been found a variety of bacterial species that carry NDM-1 particularly in the gut bacteria, can cause serious infections in vulnerable hospital patients in India, South Asia, South Africa and the UK. There are two major routes of spread for the bacteria; hospital and the community. In hospital infections, bacteria carrying NDM-1 move from person to person when patients who have received many antibiotics, develop diarrhea and traces of feces contaminate surfaces, equipment and healthcare workers' hands. In community infections, the bacteria carrying the enzyme passes from person to person when traces of feces contaminate municipal water supplies – and with a large percentage of the population lacking any access to sanitation. Public Health Foundation

of India believes that 60,000 infants per year are dying of drug-resistant infections due to NDM-1. In addition, tourists can pick up antibiotic-resistance genes in just 2-3 days. Currently, India is facing with two antibiotic resistant genes what carry NDM-1; E. coli and Klebsiella. The discovery mrc-1 gene in China which is being transferred between Klesbsiella pneumoniae and E. Coli further compounded the global burden of antibiotic resistance, which has already spread to the neighboring countries. In the animal husbandry and agricultural sectors of China, the demand for the antibiotics to reach almost 12,000 tons per year. The high prevalence

of the mrc-1 gene in E. Coli samples both in animals and raw meat, with the number of positive-testing samples are increasing each year in China. On average, more than 20 percent of bacteria in the animal samples and 15 percent of the raw meat samples carried the mrc-1 gene. Numerous European countries have reported the existence of mrc-1 gene in the isolates from human, isolates from animals used for food, isolates from food, and isolated from the environment. In conclusion, pathogens rapidly develop mutations that render current treatments ineffective – resistance to carbapenems, one of the ‘last lines’ of antibiotics, is widespread and has been observed in numerous countries. Therefore, there is an urgent need between research universities and industry aimed at developing novel antimicrobial agents to save the practice of modern medicine.

Keynote Forum

Thierry Troussier

Head of UNESCO Chair Sexual Health & Human Rights
Paris Diderot University
France

Keynote: Why it is important to integrate the SDGs in a sexual and reproductive health education to improve the HIV and STIs results and to achieve the SDGs?

Time : 09:50-10:20

Conference Series STD-HIV AIDS 2018 International Conference Keynote Speaker Thierry Troussier photo
Biography:

Thierry Troussier is currently working at the Health Directorate General of the French Ministry of Health. Since 2018, in charge of sexual health promotion strategies, 2001– 2017 Coordinator of the national program for HIV-AIDS and STIs prevention for Metropolitan France and the five French Overseas Territories.

Abstract:

Background: The UNESCO Chair for sexual health & human rights is engaged in the implementation of the sustainable developmentgoals (SDGs). Strategically, she uses a global perspective them to advance her advocacy on sexual reproductive health and rights(SRHR).Methods: For increase understanding and exchange experiences on sexual reproductive health and rights, the UNESCO Chair proposes a chart developing targets for 17 SDGs, in relation with SRHR. This chart on “Sexual Health and Rights” in the 2030 Agenda NU, is presented for this symposium. Results: The aim of this chart is to describe the relation between the SDGs, human rights and sexual health in order to: facilitatepeople’s access to information and lifelong learning on their sexual heath and reproductive health; promote health and sexual wellbeingfor living better and longer; ensuring universal access to sexual and reproductive health-care services and ending the HIV and

STIs epidemics; include a focus on the general population and specific population groups like migrants, LGBTI, handicapped andelderly people; challenge pervasive stigmatization and discrimination and; to promote a people-centered approach, gender equalityand health equity. The final objective of this chart is to strengthen and advance our advocacy on sexual and reproductive health andsexual rights on the ground, among healthcare professionals, social and legal professionals, as well as with the decision makers.Conclusion & Discussion: To achieve in 2030, the sustainable development goals 3.3 (end the HIV and STIs epidemics) as well asthe targets of goal 2 (zero hunger), goal 6 (clean water and sanitation) and goal 7 (clean and affordable energy), this requires thatgoal 17 be fully realized indeed the partnerships between the countries, the regions of the world and between the private and public organizations is essential to solve financial and human needs.

Conference Series STD-HIV AIDS 2018 International Conference Keynote Speaker Kristine McCluskey photo
Biography:

Kristine McCluskey is lead PA and both a pathology residency and a pathologists’ Assistant Program Instructor with expertise in acroscopic pathology. She received the Baylor College of Medicine’s Fulbright and Jaworksi, LLP Faculty Excellence Award in Teaching and  Evaluation. She conducts monthly workshops and directed her first symposium for continuing medical education credit accredited by the American Society for Clinical Pathology pertaining to macroscopic  disease at a local and national level. She has spoken at national conferences regarding her field in academic medicine and surgical specimen processing. Her educational tools have been published andshe plans to pursue a doctorate in health science education. Her research interests include medical education curriculum development and breast cancer.

Abstract:

Since 2016, United States (US) Zika virus (ZIKV) transmission provoked our pathology residents, and pathologists' assistant students to follow fetal and placental tissue sampling protocols recommended by the Center for Disease Control (CDC). As tissue collection increased at our institution located in Texas, an ongoing local transmitter and inundated by Hurricane Harvey which offered additional breeding grounds for vectors, unpublished data emerged at our insitution suggesting viral presence in fetal and placental tissue without maternal viral positivity implying the importance of adequate training regarding prosection and sampling. Current research demonstrated that ZIKV persisted in fetal tissue resulting in Congenital Zika Syndrome. Unbeknownst of recent findings, learners procuring samples required repeated updated protocol review and often questioned purpose behind submission to the CDC. In response, we designed two traditional algorithms combining our work flow and resources beginning with identifying presumed ZIKV transmitted specimens to receiving verification of ZIKV infection and the repercussions thereafter. This systematic approach was presented during resident and pathologists' assistant student orientation and reviewed during macrosopic inspection and prosection, known as grossing, of placentas, products of conception and autopsy organ blocks. As a result, residents and pathologists' assistant students proffered adequate sampling and understood its gravity. In our lab, all past medical histories of received specimens were evaluated by pathology staff without relying only upon the submitting physician’s direction to retain tissue. More suspected tissue was sequestered for possible studies when, in the past, this tissue may have otherwise been disposed of following standard final diagnosis. In conclusion, our algorithms became indispensable learning devices for our trainees and will remain as a dynamic teaching tool . By generating a well-defined, customized, condensed ZIKV transmitted tissue protocol specific to our institution to include current emerging discoveries, gross inspectors and autopsy prosectors will remain updated and continue their vital role in continuity of care for those afflicted by ZIKV.

Conference Series STD-HIV AIDS 2018 International Conference Keynote Speaker Sharwani Vijayshree Lal, photo
Biography:

Sharwani Vijayshree Lal is currently working as a Medical Officer at a Central Government Hospital in the capital of India. She has developed sharp acumen and insight ineffective clinical judgement. Her passion for meticulous and comprehensive management of a case has matured during her rewarding exposure to healthcare in hospitals and educational institutions over the years. This study, capturing profile of opportunistic infections in patients with HIV, effectively demonstrates the significance of sound assessment and diligent handling of a case.

Abstract:

Statement of the Problem: India has 21.17 lakh people living with HIV/AIDS (PLHIV) in 2015. Although mortality has decreased substantially but the course of HIV is still frequently complicated by various opportunistic infections which are still the most common cause of death amongst these patients. Methodology: It was a cross sectional, observational study done over a span of one year at PGIMER, Dr. RML Hospital, New Delhi. Patients were evaluated for any pre-existing opportunistic infections by clinical, radiological and laboratory parameters. Results: A total of 651 patients were started on ART (64% males and 36% females). The most common route of transmission was heterosexual (95%) followed by intravenous drug abuse (3%) and 2% couldn’t elicit any cause. 32, 13 and 24 patients were positive for HBsAg, Anti-HCV and VDRL respectively. The mean CD4 counts of 651 patients were 264/μL. 130 (20%) patients amongst  these 651 developed or had opportunistic infections at the time of initiation of ART and their mean CD4 counts were 95/μL. All of them were on 1st line ART as per NACO guidelines (2NRTI + 1NNRTI). 95% compliance was seen in >90% of these patients. 80% of these opportunistic infections manifested after ART was started (Immune Reconstitution Inflammatory Syndrome - IRIS). The most common opportunistic infection was tuberculosis (74%) out of which 61 (45%) patients had extra pulmonary TB and 39 (29%) had pulmonary TB. 16 (12%), 11 (8%), 3 (2%), 3 (2%) had candidiasis, diarrhea, herpes zoster, cryptococcal meningitis respectively,and 1 case each of toxoplasmosis, LRTI and molluscum contagiosum. 14 patients died of these infections, 6 were lost for follow up.Conclusion: Opportunistic infections especially TB is very common in PLHIV in India. Many of these infections occur as a part of IRIS, where a thorough clinical judgement and expert management is of utmost importance.

Conference Series STD-HIV AIDS 2018 International Conference Keynote Speaker Natalie Borg photo
Biography:

Natalie Borg has completed her PhD from the University of Melbourne and postdoctoral studies from Monash University Department of Biochemistry and Molecular Biology. She is an ARC Future Fellow and Heads the Immunity and Infection Laboratory at the leading Australian University, Monash University. She has published 29 papers in premier journals including Nature and Nature Structural and Molecular Biology.

Abstract:

Hendra virus (HeV) is a paramyxovirus that causes severe disease and a high incidence of fatality in infected humans. Despite recurrent outbreaks and potential for human lethality no vaccine or anti-viral agent is available to prevent or treat human HeV infection. Key to HeV pathogenicity is the viral phosphoprotein (P) gene, which also encodes the V and W proteins as distinct products. V modulates the host response to infection by targeting numerous host proteins. Here, we show nuclear transport receptors are amongst those targeted by HeV V. We characterize the interactions and identify key residues in V that mediate the interaction.Finally, we report specific inhibitors of nuclear transport prevent interaction with host transporters, and reduce HeV infection. These findings broaden our understanding of HeV-host interactions and have implications for the design of novel anti-HeV therapeutics.

Conference Series STD-HIV AIDS 2018 International Conference Keynote Speaker Kristina M. Miller photo
Biography:

Kristina Miller holds a PhD from Stanford University (1992) and is currently the Head of Genetics and Genomics at Fisheries and Oceans Canada. She is also an adjunct professor at UBC. Dr. Miller is on the editorial board for Immuno genetics, Facets and Coastal Marine Fisheries Journal. She has over 120 primary publications in the fields of genetics, genomics, immune genetics, and disease.

Abstract:

Climate change enhances vulnerability of organisms to stress and disease, which can result in volatility in survival and ultimately population decline for many species. Emerging infectious diseases have been resolved in some cases, but understanding their disease etiology can be difficult in instances where morbidity and mortality are not readily observable. Sensitive technologies to detect early stages of disease development in live-sampled organisms, and the ability to differentiate pathogen carrier states from active disease states are required to demonstrate impacts of infectious diseases in wild populations. We present the discovery and validation of host transcriptional biomarkers capable of distinguishing the presence of an active viral disease state (VDD) from latent viral infections, and viral versus bacterial disease states in salmon. Biomarker discovery was conducted through meta-analysis of published and in-house microarray data, and validation performed on independent datasets including disease challenge studies and farmed diagnoses of various viral, bacterial, and parasitic diseases. We demonstrate that the VDD biomarker panel is predictive of disease development across RNA-viral species, salmon species, and salmon tissues, and can recognize a viral disease state in cultured and wild-migrating salmon. Application of this technology has led to the discovery of eight novel salmon viruses in British Columbia alone. Biomarkers resolved in our study on salmon were highly overlapping with those based on similar human viral influenza research, suggesting a highly conserved suite of host genes associated with viral disease that may be applicable across a broad range of vertebrate taxa.

  • Recent Emerging Diseases
    Sexually Transmitted Infectious Diseases
    Pediatric Infectious Diseases
    Diagnostic Tools
Location: Zurich, Switzerland
Speaker

Chair

Reza Nassiri

Michigan State University
USA

Speaker

Co-Chair

Qingzhong Kong

Case Western Reserve University
USA

Speaker
Biography:

Qingzhong Kong has completed his PhD at the University of Massachusetts at Amherst and postdoctoral studies at Yale University. He is currently an Associate Professor of Pathology, Neurology and Regenerative Medicine, Associate Director, National Prion Disease Pathology Surveillance Center, Case Western Reserve University School of Medicine. He has published over 50 original research papers in reputable journals (including Science Translational Medicine, Journal of Clinical Investigations, PNAS, Cell Reports, and Plant Cells) and has been serving as an Editorial Board Member on multiple scientific journals.

Abstract:

Chronic wasting disease (CWD) is the prion disease found in several cervid species (mule deer, white-tailed deer, American elk, moose, and reindeer). CWD prions are among the most infectious and highly transmissible between cervids. It has reached epidemic levels in many regions of USA and parts of Canada. Recent detection of CWD in wild moose and reindeer in Norway confirmed its spread to the European continent. The continued spread of CWD and popular hunting and consumption of cervid meat and other products raise serious public health concerns. The discovery of novel CWD strains further complicates the issue since prion strains are known to influence prion transmission barrier between species. However, human susceptibility to CWD prions is still unclear, especially on the difference in zoonotic potential among various CWD prion strains. We have been working to address the CWD zoonosis question for well over a decade. We used CWD samples from multiple cervid species collected at various geographic locations to inoculate transgenic mice expressing human or elk prion protein (PrP). We found infectious prions in the spleen or brain in a small fraction of CWD-inoculated transgenic mice expressing human prion protein, which is consistent with a recent report of CWD transmission in macaques (a nonhuman primate model) and indicates that humans are not completely resistant to CWD prions. This finding has significant ramifications on the public health impact of CWD prions. The influence of key cervid prion protein polymorphisms, the prion strain dependence of CWD-to-human transmission barrier, and the characterization of experimental human CWD prions will be discussed. Preliminary examination of human prion cases with a history of cervid hunting and/or consumption will be presented.

Speaker
Biography:

Maria José Figueras is a PhD from University of Barcelona in 1986. Since 1979, she is a Lecturer at the Medical School of the University Rovira i Virgili, Reus, Spain and Professor of Microbiology since 2001. She has been working in the microbiological contamination of water since 1990. She is the advisor on the management of the risk derived from contaminated bathing water to the World Health Organization (WHO), the United Nations Environmental Programme (UNEP), and the European Commission. She is involved in the European research projects aqua-chip, healthy-water, epibathe and aquavalens. Director of 8 PhDs on the taxonomy and epidemiology of the emerging pathogens Aeromonas and Arcobacter and author of 170 papers.

Abstract:

At least 10 of the species included in the genus Aeromonas can be considered emerging pathogens to humans because they are able to produce a broad spectrum of infections. Since the earlier association of aeromonads with human disease, gastroenteritis, bacteremia and wound infections have remained the dominating presentations. The role of Aeromonas as etiological agent of diarrhea has been questioned for several years. However, recenty using dose response models of microbial infection we estimated that the median Aeromonas dose required for producing diarrhoeal cases (1%) ranged from 1.24 x 104 cfu to 0.9 cfu for low and highly susceptible individuals, repectively. Cases of mixed infections have been investigated and reveal important interactions among the recovered strains that impact the development of the infection. New findings evidenced that Aeromonas activate a strong immune response in a human monocytic cell line (THP-1) producing cell damage. Aeromonas are associated to other infections that can affect the respiratory tract, the bone and/or joints, the urinary tract and also necrotizing fasciitis mainly in patients with cirrhosis or hepatobiliary disease. We can predict that Aeromonas infections will remain a health problem in the near future considering the increase on the life span that will result in more elderly persons with potential undelaying diseases. Recognition of the Aeromonas infections at the clinical setting have and will improve with the used of the MALDI-TOF identification system, avoiding classical errors like the overestimation of Aeromonas hydrophila. However, there is a strong need for improving the database.

  • Vector Borne Infections
    Microbial Genomics
    Host and Microbial Genetics
    HIV/AIDS
    Diagnostic Tools for Immunological and Virological Monitoring of HIV Infection
Location: Zurich, Switzerland
Speaker

Chair

Shih-Yen Chen

Taipei Medical University, Shuang Ho Hospital
Taiwan

Speaker

Co-Chair

Dibyendu Banerjee

Calcutta National Medical College
India

Speaker
Biography:

Sheikh Ajaz Rasool, Professor, Chairman, Dean Faculty of Science (August 2006 – February 2007) and has been a senior most Professor of Karachi University in the department of Microbiology, University of Karachi. He pursued his M.Sc. in Microbiology, PhD in Bacterial-Molecular Genetics from Moscow State University and Post-doc. from England. He has been awarded with many awards like British Council Postdoc. Award 1990, Best Karachi University Scientist Award 1996, Best University Teacher HEC-Award 2004 and Presidential Award of Academic Excellence 2007. He has supervised more than 50 research thesis, published more than 120 research papers and holds a membership of more than 20 Scientific/Academic bodies.

Abstract:

Super drug resistance (PDR / EDR) in microbial strains has been a continuous phenomenon in nosocomial and miscellaneous infections. The load of these bugs has inflated ever since worldwide. Microbes evolve such phenomena involving mutational processes, hyper performance of pumping out systems, synthesis of secretory saccharides, bioaccumulation and directed flagella based shifting resulting out of hypo-doses of drug stimulation. Further, the prevalence of Enterobacteriaceae member strains has been witnessed producing Extended Spectrum β-Lactamases (ESBLs). Drug resistance in viral entities has also posed challenge for public health programs. About 20% of the deaths are caused due to viral hepatitis in one of the provinces of Pakistan. A counter malarial acrine drug is being tried against proteinaceous infectious particles (causing many transmissible neuro-diseases). These epigenetically agents have been a source of concern for our planet regarding food safety issues (e.g. infected meat). A UN Report about multiple NGOs involvement in ‘sex for food’ scandal in Haiti is alarming. No doubt man has made significant achievements in effective and neo-antimicrobials research, one wonders not any infectious agent has been completely knocked out. Our group has been focusing on ascertaining the basis of antibiotic deferring processes acquired by (indigenous) clinical strains. Accordingly, sub-lethal doses of the drug result in development of hyper-resistances. The presentation shall involve the molecular genetically basis (and other parameters) for acquiring the resistance. Achievable problem shooting way outs will also be discussed.

 

 

Speaker
Biography:

Lisa Becherer studied chemistry (BSc and MSc) and is currently working on her PhD in Microsystems Engineering at the University of Freiburg at the Laboratory for MEMS Applications, IMTEK. Her research involve nucleic acid analysis with focus on isothermal amplification and digital amplification on centrifugal microfluidic cartridges.

Abstract:

Nucleic acid amplification tests (NAAT) are not only a powerful tool for early diagnosis of HIV infections, NAAT are also a reliable method for HIV viral load measurements during the monitoring of antiretroviral therapy. Additionally, NAAT allow simultaneous (multiplex) detection of different targets enabling the detection of HIV/HTLV co infections. Loopmediated isothermal amplification (LAMP) [1, 2] emerges as a convenient alternative to polymerase chain reaction (PCR) for rapid amplification of target DNA and RNA. As an isothermal NAAT, LAMP does not require expensive equipment for thermo cycling and is therefore especially suitable for point-of-care testing [3]. However, available multiplex detection techniques for LAMP suffer from elaborate assay design as well as time-consuming optimization work. Here we present the first multiplex reverse transcription (RT) LAMP for identification of HIV/HTLV co-infections [4]. The quantitative real-time assay is based on universal mediator and reporter molecules [5] generating a fluorescence signal in the presence of target sequences. During amplification of target DNA the mediator is displaced (step 1, Figure 1). The released mediator hybridizes to the reporter generating a fluorescence signal (step 2, Figure 1) which can be detected.

Speaker
Biography:

Sharwani Vijayshree Lal is currently working as a Medical Officer at a Central Government Hospital in the capital of India. She has developed sharp acumen and insight in effective clinical judgement. Her passion for meticulous and comprehensive management of a case has matured during her rewarding exposure to healthcare in hospitals and educational institutions over the years. This study, capturing profile of opportunistic infections in patients with HIV, effectively demonstrates the significance of sound assessment and diligent handling of a case.

Abstract:

Statement of the Problem: 40 years old male with fever and constitutional symptoms for ≥2 months who concealed his diagnosis of HIV/AIDS and developed zidovudine induced lactic acidosis with pancreatitis and myopathy. Methodology: Patient presented with c/o weakness, body ache, weight loss (8 kg), pain abdomen since ≥2 months, and intractable vomiting and breathlessness since last 1 week. He was prescribed antibiotics, PPIs, prokinetics earlier by previous doctors but to no relief. Findings: General physical examination was unremarkable expect for toxic looks, dehydration and extensive oral thrush. HIV testing was advised but he refused to consent. On repeated counseling and questioning his wife accepted the patient being a case of HIV/AIDS on ART (zidovudine, lamivudine and nevirapine) for past one year. This fact was willingly concealed by patient to all previous doctors. CECT head and abdomen, and routine laboratory reports were normal except serum amylase which was 350U/L (Normal: 30-125 U/L), serum lipase was 210 U/L (Normal: 10-150 U/L) serum lactate was 7 mmol/L (Normal: 0.5-1.0 mmol/L), CPK was 320 U/L (Normal: 25-200 U/L), CD4 cell counts were 224/µL. ABG was suggestive of high anion gap metabolic acidosis. A provisional diagnosis of AIDS with zidovudine induced lactic acidosis with pancreatitis and myopathy was made. ART was immediately stopped and appropriate treatment was started. He was discharged after 10 days in satisfactory condition on tenofovir, lamivudine and efavirenz. Conclusion & Significance: This case explains the importance of detailed history taking (including concomitant medicine exposure) and vigilant physical examination (oral candidiasis in our case) especially in India to reach a diagnosis where HIV/ AIDS is a social stigma and its status is not willingly disclosed by the patient. Other fact being that zidovudine can also cause lactic acidosis and pancreatitis (which is more commonly associated with stavudine) and that too with no bone marrow toxicity (more often a hallmark of zidovudine).

Speaker
Biography:

Shih Yen Chen is currently a Chief of Department of Pediatrics, Taipei Medical University, Shuang Ho Hospital, Taiwan. He received his Doctor of Medicine degree from Taipei Medical College, and Doctor of Philosophy degree from Chang Gung University College of Medicine.

Abstract:

Background: Norovirus (NoV) is an emerging enteric pathogen worldwide. NoV plays an increasingly important role in enteric infections. The rapid transmission of NoV via person-to-person contact makes infection control difficult. A quantitative method is even more important in the management of NoV infection in immunocompromised hosts, including transplant and cancer patients. Materials & Methods: Fecal specimens were collected from previously healthy children with NoV gastroenteritis confirmed by RT-PCR. The transcript of VP2 gene was reverse transcribed into cDNA and dissolved in DNase-free distilled water. The cDNA quantity was equivalent, approximately, to 4.12×1012 copy numbers according to EndMemo number calculation. The standard curve using 10-fold serial dilution of the cDNA was obtained (10-1-10-10). The equivalent copy numbers in 53 fecal samples from NoV-infected patients were counted. The clinical presentations of the patients were retrospectively collected and analyzed by GraphPad Prism 6.0 (GraphPad Software, Inc.). The NoV was also genotyped using methods as described earlier. Fisher exact test was used to determine differences between clinical features. Statistical significance was analyzed using a nonparametric Mann-Whitney U test for two independent samples. Results: A total of 53 fecal samples from NoV-infected hospitalized children age range, 8 months to 5 years were collected for analysis of viral load with the time for sample collection varied from day 1 to day 19 after the onset of the illness. We identified a longer shedding period in 21 febrile patients (6.75±3.14 days after disease onset) than in 32 afebrile ones (5.7±3.4 days after disease onset) (p=0.03); however, there is no significant difference between the 37 older patients (≥1 years old, 6.5±3.9 days after illness onset) and the 16 younger ones (<1 years old, 5.8±2.6 days after illness onset) in terms of viral shedding. Furthermore, we found a significantly longer shedding period in patients infected by NoV GII.4 Sydney strain (30 cases; 6.9±3.1 days after illness onset) than those infected by non-GII.4 Sydney strains (23 cases; 5.7±3.7 days after disease onset) (p<0.01). Discussion: In this study, we used the SYBR green-based real-time RT-PCR to measure NoV viral load in the feces of patients with NoV infection. SYBR green real-time RT-PCR showed a higher sensitivity in viral load calculation as the detection limit of the technique was at 50 RNA copies/ml in a previous study. With this method, we found febrile NoV GII.4 Sydney strain-infected children have a longer viral shedding. In the previous study indicate that Norovirus infection induced immune response in the patients, and inflammation may drive viral replication, leading to a longer shedding period following the onset of the illness. Conclusion: In conclusion, we devised a sensitive method for quantification of NoV viral load in patients and successful established the model of NoV viral shedding. This method is useful for devising efficient infection control measures for NoV infection, investigating outbreaks, and monitoring viral transmission and evolution.

Speaker
Biography:

Dibyendu Banerjee completed his MBBS from J S S Medical College and Hospital, Mysore and MD in Medical Microbiology from Institute of Postgraduate Medical Education and Research, Kolkata in 2006. He was trained from SGPGI, Lucknow. He is presently an Associate Professor in Department of Medical Microbiology, CNMC with many PGTs doing thesis work under him. He acted as external examiners in different parts of the country. He has 15 research papers published in indexed medical journals, including one review article on anthrax and is Reviewer of three indexed journals including Indian Journal of Public Health (indexed in MEDLINE).

Abstract:

Acinetobacter baumannii is now a formidable emerging pathogen. It is being increasingly isolated in clinical settings and from a wide range of infections. It is known that A. baumannii shows presence of dormant cells, a characteristic feature rarely found in other gram negative bacteria. This explains its environmental persistence as well as its ability to survive for a long time on abiotic surfaces under desiccated conditions. This ability to colonise and to grow as a biofilm has an important role in its persistence and spread in hospital environment. But whether the level or strength of biofilm formation varies with infection of different organs is not yet known. If an association can be found out between strength of biofilm formation and its variation according to different sites of infection, it can give a clue that pathogenesis of biofilm formation may have an intimate link with organotropism of different isolates. Multiple isolates of A. baumannii were taken from different clinical materials. Biofilm forming reference strains of A. baumannii (ATCC19606) and non biofilm forming reference strains of E. coli (ATCC25922) were used as positive and negative controls respectively. The strength of biofilm forming capacity (high/ medium/none) of each isolate was measured by microtitre plate method with primary filter of ELISA plate reader set at 570 nm. It was found that strength of biofilm formation varied for different sources of infection. The present study was a hospital based observational cross sectional study.

Speaker
Biography:

Usman Lodhi is a Provincial MDR-TB Coordinator/Focal Person for DRTB/PTP-Punjab, Pakistan. Currently he is involved in two more research studies related to DRTB in Punjab. He also supported implementation of National Guidelines for PMDT in Punjab along with technical assistance regarding regimen selection especially on new drugs and short term regimen for MDR-TB. Before joining PTP, he also worked with Association for Social Development as a Regional Coordinator and MDR Physician. Since 2013 he is working in public health intervention program related to Drug Resistant TB.

Abstract:

Tuberculosis still the deadliest infectious disease among all communicable infections and drug resistant tuberculosis patients (DRTB) remains an evil for low income countries like Pakistan. Irrational use of second line drugs including fluoroquinolones and second line injections along with lack of proper awareness to both level community and treatment provider, less number of diagnostic and treatment centers, poor adherence to treatment, primary default, infection prevention and lack of technical resources in Punjab may lead to rise in incidence of DRTB. To find out treatment outcomes and their associations with type of resistance among DRTB patients in Punjab, retrospective cohort analysis was done. Of the total bacteriologically confirmed DRTB registered patients at various programmatic management of drug resistant tuberculosis (PMDT) sites across Punjab, n=2046 patient’s records were analyzed. Bivariate analysis shows a significant positive association (relative risk [RR] 1.7 & p-value ≤ 0.001) between type of resistance and treatment outcome in DRTB patients. Overall treatment success rate for DRTB in Punjab was 61.14% and favorable outcomes including cured and treatment completed were 59.4% and 1.7% respectively. While the unfavorable treatment outcomes including died, LTFU, not evaluated, treatment failure were 22.3%, 9.7%, 3.5%, and 2.7% respectively. Scale up DRTB surveillance activities, contact screening, integration of DRTB with other public health programs, active case finding among populations will have a positive impact on drug resistance tuberculosis case notification and control over spread of diseases.

Speaker
Biography:

Kristina Miller holds a PhD from Stanford University (1992) and is currently the Head of Genetics and Genomics at Fisheries and Oceans Canada.  She is also an adjunct professor at UBC.  Dr. Miller is on the editorial board for Immunogenetics, Facets and Coastal Marine Fisheries Journal.  She has over 120 primary publications in the fields of genetics, genomics, immunogenetics, and diseases.

Abstract:

Piscine orthoreovirus Strain PRV-1 is the causative agent of heart and skeletal muscle inflammation (HSMI) in Atlantic salmon (Salmo salar). Given its high prevalence in net pen salmon, debate has arisen on whether PRV poses a risk to migratory salmon, especially in British Columbia (BC) where commercially important wild Pacific salmon are in decline. Various strains of PRV have been associated with diseases in Pacific salmon, including erythrocytic inclusion body syndrome (EIBS), HSMI-like disease, jaundice syndrome, and jaundice/anemia in Japan, Norway, Chile and Canada. Herein, we examine the developmental pathway of HSMI and jaundice/anemia associated with PRV-1 in farmed Atlantic and Chinook (Oncorhynchus tshawytscha) salmon in BC, respectively. A molecular viral disease development (VDD) biomarker panel differentiated fish that were merely viral carriers from those in an active viral disease state, and  In situ hybridization (ISH) localized PRV-1 within developing lesions in both diseases. The two diseases showed dissimilar pathological pathways, as indicated by the preponderance of inflammatory lesions in heart and skeletal muscle in Atlantic salmon, and the development of degenerative-necrotic lesions in kidney and liver in Chinook salmon. However, our data indicate that a species-related difference in PRV load tolerance in red blood cells can explain these differences. Moreover, complete viral genome sequencing revealed no consistent differences in the sequence of PRV-1 variants intimately involved in the development of both diseases, suggesting that migratory Chinook salmon may be at more than a minimal risk of disease from exposure to the high levels of PRV occurring on salmon farms.

Speaker
Biography:

Paulo Antonio Rodrigues Gouveia is currently working as a Project Director Mutamba MGU against HIV, Brazil. He is graduated from the Science Center: ITPAC - Institute Tocantinense. President Antonio Carlos (ITPAC), from Araguaina in 2007, as Doctorate in medicine. He worked at Regional Hospital of Araguaína from 2007 to 2011. From 2011 to the present, he is an active member of ITPAC Medical University Institute. His research mainly focuses on HealthCare, Biological/Pharmacology Sciences.

Abstract:

This study aims to analyze the therapeutic use of Guazulma ulmifolia lam extract as an AIDS treatment, describing the management of treatment performed in a clinical report. This work was a literature review. The case reported was a 35-year-old Mozambican, diagnosed with HIV virus in 2008. In March of 2017, she started using Guazulma ulmifolia lam extract for 30 days, and has since received successive negative HIV test results. It was concluded that the efficacy of Guazulma ulmifolia has been increasingly proven for the treatment of AIDS, with the advantages being a natural remedy, without any side effects, and there is no ethical-moral impediment to be applied in infected population.

Speaker
Biography:

Nebiyu Ler Alaro is a graduate of Texila America University Guyana PHD Public Health 2018 July. He took up Education as a career after majoring in Nursing. He completed Master’s education 2015 and starting PHD Public Health 2016. I am currently living and working South Sudan Doctors with Africa CUAMM as Health Project Manager.

Abstract:

As one of the main goals of the partnership framework (PF) between the Government of Ethiopia (GoE) and the US Government (USG), Ethiopia has set a national target of reducing new HIV infections by 50% by the end of 2014 (National Target). Funded by the USG, The PF provides a five-year joint strategic plan (2010-2014) for cooperation to support Ethiopia’s national HIV/AIDS response (PEPFAR, 2010). Ethiopia has an estimated adult prevalence of 1.5% and about a million people living with HIV/AIDS (PLWHA) (ECSA & IFC, 2012), among countries most affected by the epidemic. The International Labor Organization (ILO) projection for 2015 indicates that as much as 8.5% of the Ethiopian labor force loss will be due to HIV/AIDS deaths (World Learning, 2012). On the other hand, Since the PF took effect, USG funding to the program has been in constant decline. Moreover, the PF does not fully take into account context and development barriers due to the prevailing social, political, economic and development policies in the country. Participation of the private sector, independent civil societies and media in the development process has been severely curtailed. Contextual factors have been seriously challenging the prevention of mother-to-child transmissions (PMTCT) efforts. Furthermore, the country lacks a comprehensive strategy to fully address the issue of most-at-risk population (MARP) as drivers of the HIV epidemic; and the HIV/AIDS response excludes men who have sex with men (MSM), A “Significant Unacknowledged” but fast growing transmission route of HIV (Tadele, 2008). Drawing from literature review and practicum experience in Ethiopia, this paper examines the feasibility of Ethiopia’s national target. The main problem in the HIV/AIDS discourse in Ethiopia appears to be behavioral change, but not lack of knowledge. In addition, contrary to the widespread public belief that homosexuality is not Ethiopian; there exists a flourishing underground male-sex trade in Addis Ababa.