Meet Inspiring Speakers and Experts at our 3000+ Global Conference Series LLC LTD Events with over 1000+ Conferences, 1000+ Symposiums
and 1000+ Workshops on Medical, Pharma, Engineering, Science, Technology and Business.

Explore and learn more about Conference Series LLC LTD : World’s leading Event Organizer

Back

8th World Congress on Virology

San Antonio, USA

Shubhada Bopegamage

Shubhada Bopegamage

Slovak Medical University, Slovak Republic

Title: Are Peyer’s Patches the primary site of Coxsackievirus B infection?

Biography

Biography: Shubhada Bopegamage

Abstract

Enterovirus infections are often asymptomatic or appear as undifferentiated febrile illnesses, yet they are associated with a broad range of diseases. Most of the knowledge concerning the spread of enteroviruses in the human body is based on experimental studies of poliovirus infections in monkeys. From these studies it is generally believed that local infection of the mucosa is followed by a regional infection in the lymphatic tissues such as tonsils and Peyer’s patches leading to the belief that the primary sites of replication are the epithelial cells of the small intestines and the Peyer’s patches. The spread of Coxsackie B viruses (CVB) after oral infection is expected to follow a similar route. Our aim was to study the duration as well as the localization of viral markers in the murine intestine after oral and intraperitoneal (i.p.) route of infection. Transverse sections of the small intestines were chosen for this purpose. Swiss albino and CD1 male (outbred) mice were infected via oral and i.p. route of infection with different strains of CVB. Interferon alpha was localized by immunohistochemistry, whereas viral markers were assessed by viral protein VP1 immunohistochemical analysis, in situ hybridization and detection of CVB3e-GFP in cryosections. Irrespective of the virus strain and dose of infection, the small intestines showed enlarged Peyer’s patches, with enlarged germinating centers. Prolonged presence of virus was observed in the smooth muscle of the small intestines after oral infection, but not after i.p. infection and was confirmed by PCR. Interferon alpha was detected in the Peyer’s patches and in the mucosal layer of the small intestine. We observed a total absence of VP1, 3A and the e-GFP in the Peyer’s patches at all stages of infection irrespective of the virus strain used. In conclusion, infection of the epithelial cells was observed in the small intestine but not in murine Peyer’s patches. Therefore, based on a mouse model of CVB3 infection, our results do not support the hypothesis of viral replication or even presence of CVB in the Peyer’s patches.