Scientific Program

Conference Series Ltd invites all the participants across the globe to attend 4th International Congress on Bacteriology and Infectious Diseases San Antonio, Texas, USA.

Day 2 :

Keynote Forum

Kei Amemiya

US Army Medical Research Institute of Infectious Diseases, USA

Keynote: Host-pathogen interactions by clinical strains of Burkholderia pseudomallei in a murine model of melioidosis

Time : 10.00AM

Conference Series Bacteriology 2016 International Conference Keynote Speaker Kei Amemiya photo

Dr. Kei Amemiya is a Principal Investigator in the Bacteriology Division at the US Army Medical Reseach Institute of Infectious Diseases. He has been at USAMRIID since 1999 and has been involved in developing vaccine candidates against plague, glanders, and melioidosis. His interest has been in studying the host’s immune response to the pathogen and vaccines in small and large animal models. Before coming to USAMRIID, he was at the National Institutes of Health and Georgetown University, where he was studying the host response to bacterial and viral pathogens or autoimmune diseases in humans.


Melioidosis, which is caused by Burkholderia pseudomallei, is endemic in South-East Asia and Northern Austrialia, but it is not well known in other parts of the world. It is the third leading cause of disease in the endemic area behind tuberculosis and HIV. Pneumonia is the most frequent clinical presentation observed in melioidosis patients, and diabetes is the most common risk factor for the disease. The high susceptibility of these latter patients to infection by B. pseudomallei is an enigma that appears to be associated with an immunocompromised immune system, but it does not make HIV/AIDS patients more susceptible to melioidosis. One problem with diagnosis of melioidosis is that the clinical presentation may mimic other chronic infections like tuberculosis. There appears to be many different strains of B. pseudomallei that can cause melioidosis, and they may display different clinical presentations that make diagnosis more difficult. In addition, the pathogen tends to be highly drug resistant that makes treatment of the disease uncertain. Because of these inherent complications, we have been evaluating different human clinical isolates of B. pseudomallei in murine models of melioidosis to characterize their virulence. We see two different types of host response to infection by the strains of B. pseudomallei, depending on the strain of mice used in the studies. BALB/c mice are more easily acutely infected by the pathogen, while C57BL/6 mice tend to be much more resistant to infection. These differences in the host will be presented as well as the host’s response to the pathogen in chronically infected mice.