International Conference on Microbial Pathogenesis,Infectious Diseases & Control August 23-24 , 2017 Toronto, Canada
Avail Upto 11 CME Credits

Biography:

Carole Creuzenet has completed her PhD in Biochemistry at the University of Nantes and The National Institute for Agronomical Research (France). She has completed her Post-doctoral studies at the Massachusetts Institute of Technology (USA) and the University of Guelph (Canada). She is Associate Professor at the University of Western Ontario (London, Canada) where her lab focuses on virulence factors from bacterial gastrointestinal pathogens such as Campylobacter jejuni, Helicobacter pylori and Yersinia pseudotuberculosis. Her focus is on glycolipids and glycoproteins as well as on novel secreted proteins and their folding partners. She has published 38 papers in reputed journals.          

Abstract:

H. pylori causes gastritis, gastric ulcers and cancers but the mechanisms of virulence are not fully understood. It produces secreted proteins which may play a role in eliciting gastric inflammation, including the helicobacter cysteine rich protein HcpE (HP0235) whose biological function is unknown. Our goal was to investigate if HcpE is secreted by H. pylori and is involved in host/pathogen interactions, and identify components essential for its production. Using a combination of anti-HcpE ELISA and western blots, knockout mutagenesis, phenotypic analyses and biochemical assays, we demonstrate that HcpE is secreted by many strains as a soluble protein and in association with outer membrane vesicles. We show that infected patients produce anti-HcpE antibodies, indicating in situ HcpE production. We show that HcpE comprises many disulfide bonds and identify DsbK (HP0231) as a folding factor necessary for HcpE production, and show that recombinant DsbK can refold unprocessed, reduced HcpE in vitro. This highlights the first biologically relevant substrate for DsbK. Furthermore, we show that DsbK has disulfide bond (Dsb) forming activity on reduced lysozyme and has DsbA-like activity upon expression in E. coli, despite its similarity with DsbG. Also, we show a role of DsbK in redox homeostasis in H. pylori. Finally, we show an important role for DsbK and HcpE in host-pathogen interactions, including murine gastric colonization and pro-inflammatory cytokine production in human gastric explants and in murine splenocytes. Both proteins will be investigated as therapeutic targets to treat H. pylori infections and prevent gastric ulcers and cancers.

Biography:

Louis Bengyella has expertise in fungal-plant, virus-plant and insect-plant interactions and he is interested in plant health and increased crop production. He has completed his PhD at the University of Burdwan, India and Post-doctoral studies from the University of the Witwatersrand School of Cell and Molecular Biology and Department of Biotechnology in Vaal University of Technology, South Africa. He has published more than 30 papers in reputed journals and has been serving as an Editorial Board Member for Springer, Elsevier, Science alert and Academic publishers.

Abstract:

It is established that Cochliobolus lunatus secretes a myriad of proteins to break plant primary defense (i.e. cuticle and cell walls) and degrade complex carbohydrates for nutrients acquisition. Many larger secreted proteins with potential roles in pathogenicity include predicted cutinases, peptidases, glucanases, fungal transporters belonging to the major facilitator super-family (MFS), and ATP-binding cassette (ABC) group proteins, and carbohydrates active enzymes. But major physiological pathways affected in potato during C. lunatus colonization are unknown during incitement of brown-to-black leaf spot disease. Using proteomics approach, it is shown that C. lunatus significantly (P<0.05) suppressed the host functional proteome at 96 h after infection, predominantly affecting the expression of ribulose bisphosphate carboxylase enzyme, plastid aldolase enzyme, alcohol dehydrogenase 2 and photosystem II protein prior to the formation of brown-to-black leaf spot disease. Robust host–response was observed at 24 h after infection associated by 307 differentially expressed peptide spots concurring with the active phase of production of infectious hyphae. Importantly, C. lunatus differentially down-regulate StNPR1 transcript by 8.19-fold by 24 h after infection. We also observed that C. lunatus transiently down-regulate the expression of StNPR1 at the onset of infection. Put together, the infection negatively affects the expression of proteome modules involved in photosynthesis, carbon fixation and light assimilation. This study contributes towards better understanding of the mechanism underlining the invasion strategies of C. lunatus.

Biography:

Arghavan Alisoltani has her expertise in Computational Biology and Genetic Studies of Model Plants and Animals. She has completed her PhD at the Shahrekord University, Iran. She is currently pursuing her Post-doctoral research in Department of Biotechnology, The Vaal University of Technology, South Africa. Her scientific productivity is publishing several research papers in high ranked journals.

Abstract:

Metagenomic analysis based on high throughput sequencing is a newly developed approach, widely been applied to identify the microbial composition and diversity of ruminant animals. Despite attempts have been done to depict the microbial composition of rumen in various animals, the little attention has been devoted to finding core-bacterial composition of ruminant animals, pathogenic species. Due to integrative analysis of different datasets is expected to be more informative, in the present study, microbial composition of different animals was evaluated, using integrative analysis of metagenomic data aim to obtain holistic overview of core-bacterial population. In total, 12 datasets were analyzed using the CLC Microbial Genomics Module in CLC Genomics Workbench 9.1 (CLC Bio, Qiagen). SILVA.123 database (97%) was used for detection of operational taxonomic units (OTUs) with the similarity percentage of 97%. In total 3,471 OTUs are found based on SILVA.123 database. Bacteroidetes was the most abundant phylum across all samples (42.57%), followed by Firmicutes (36.25%), and Proteobacteria (13.43%). In addition, Prevotella1 (21.4%), Rikenellaceae RC9 gut group (5.9), and Veillonellaceae UCG-001 (4.5%) were recorded as dominant genera across all studied animals. Functional profiling of OTUs has been provided good clues about the potential role of bacterial population in ruminants. We found that high amounts of OTUs were related to human diseases such as different cancers. Taken together, our findings provided an overall insight about the core-bacterial composition and function of ruminant animals, human disease related bacteria.

Biography:

Mallika Lavania has completed her PhD from Agra University. She is the Senior Research Scientist of Stanley Browne Laboratory, The Leprosy Mission Trust, India, a premier organization which works with individuals and communities disadvantaged by leprosy, irrespective of caste, creed and religion, by addressing their physical, mental, social and spiritual needs to uphold human dignity and eradicate leprosy. She has published more than 30 papers in reputed journals and has been serving as an Editorial Board Member of BMC Infectious Diseases.

Abstract:

Leprosy caused by multidrug-resistant Mycobacterium leprae is an emerging public health concern worldwide. Global efforts to control leprosy by intensive chemotherapy have led to a significant decrease in the number of registered patients. Current recommended control measures for treating leprosy with MDT are designed to prevent the spread of drug-resistant M. leprae. However, drug resistance has been reported since 1964 for dapsone, 1976 for rifampicin and 1996 for ofloxacin. We report here the identification of a multidrug-resistant strain of M. leprae from relapsed leprosy patients from an endemic region in India. The drug resistant profiles of the isolated strains were confirmed by the identification of mutations in genes previously shown to be associated with resistance to each drug (Rifampicin, Dapsone and Ofloxacin). Two hundred and fifty slit- skin smears samples were collected from relapse leprosy cases from different hospitals of The Leprosy Mission across India between 2009 and 2016. DNAs were extracted from these samples and analyzed for PCR targeting genes associated with drugs (Rifampicin, Dapsone and Ofloxacin) in M. leprae. Thai-53 (Wild-type) and Zensko 4 (MDR) strains were used as reference strains. Twelve strains showed representative mutations in more than two genes and two strain showed mutation in all three genes responsible for rifampicin, dapsone and ofloxacin. Among these eleven strains 9 strains were showed mutation in rifampicin and dapsone and 3 showed in dapsone and ofloxacin. The study showed occurrence of MDR strains of M.leprae in MDT treated leprosy patients from endemic regions of India.

Biography:

Mahnoush Momeni specialized in General Surgery from Tehran Medical University in 2003 and has been working in the Burn and Trauma Center with the plastic surgery team ever since. She is involved in research about burns, wounds and plastic surgery. She is also a member of Burn Research Center at Iran Medical University

Abstract:

A double -stranded DNA virus of family of Para Pox causes Orf disease. Human infection mostly is because of occupational hazard and infected animals handling.

Our patient was an 18 year old woman who was burned in 2015. One week after admission in the hospital she has been undergone skin graft of upper extremity however vegetative granulomatous ulceration was appeared on wound hence grafted area was failed. With careful History investigation we noticed that the water which had been used to turn out the flame was drinking bottle for sheeps.

With the suspecting of Orf disease we disinfected all the wounds and dressing tools with Dakin’s solution. We waited about 12 days to do skin graft and most of skin grafted area was taken afterwards .PCR test for Para pox viruses was positive.

Conclusion:

In burn patient with a history of probable contamination, the Orf disease should be considered.

Manipulation of the disease in early stages in burn wound could potentially spread it and change the degree of the wound. For prevention of nosocomial outbreak of orf, wound care and wound disinfection should be done perfectly .Isolation and disinfection of all the dressing tool should be considered. The education of wound care providers in burn hospital and perfect wound disinfection would protect the patient from cross contamination and following this phase all the graft would be taken.

Biography:

Luciene Airy Nagashima has completed her MD and PhD in Microbiology at the State University of Londrina, Brazil. Her research is focused on immune response to fungal infection, especially with experimental infection with Arthrographis kalrae and its hemolytic factors. She is currently working as an Industrial Biotechnology Analyst in the Institute of Technology of Parana (Brazil), with the production of antigens for the diagnosis of bovine brucellosis, tuberculosis and enzootic bovine leukosis.

Abstract:

Bovine tuberculosis is a chronic disease caused primarily by Mycobacterium bovis. This zoonotic disease constitutes a public health issue and causes damage to the agricultural industry. In Brazil, the National Program for the Control and Eradication of Brucellosis and Tuberculosis establishes mandatory measures such as the diagnosis tests in animals. The standard method for detection of bovine tuberculosis is the tuberculin test, which uses the purified protein derivate (PPD) as antigen. The bovine tuberculin PPD is a complex mixture of proteins derived from the cultivation of M. bovis. Its composition and mechanisms involved in the immune response of the tuberculin test are not entirely clear. In the present work, bovine tuberculins which had low reactivity in the skin test in sensitized guinea pigs compared to a reference preparation, and tuberculins with positive results in potency test were analyzed by immune enzymatic assay (ELISA) and by western blot. The results showed differences in reactivity of the antibodies to the different samples of tuberculin, in both tests. The tuberculins with lower potencies revealed low intensity bands, especially below 30 kDa, which indicates that the proteins in these bands may be essential to the immunogenicity of the product. The identification of these proteins could help to elucidate which proteins are effective in intradermal reaction, enabling the development of more specific tests.