alexa Immunohistochemical and Molecular Detection of pH1N1 in NecropsiedPulmonary Tissues of Fatal Cases with Indeterminate Conventional Testing

Journal of Forensic Pathology
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Short Communication

Immunohistochemical and Molecular Detection of pH1N1 in NecropsiedPulmonary Tissues of Fatal Cases with Indeterminate Conventional Testing

Shelke V1, Potdar V2, Chadha M2, Kolhapure R1, Prasad S1, Jain P1 and Basu A1*

1Department of Electron Microscopy and Histopathology Group, National Institute of Virology, Pune, India

2Deparment of Influenza Group, National Institute of Virology, Pune, India

*Corresponding Author:
Atanu Basu
Electron Microscopy and Histopathology Group
National Institute of Virology
Pune, India
Tel: 9120 26006217
E-mail: [email protected]

Received date: February 1, 2016; Accepted date: March 16, 2016; Published date: April 10, 2016

Citation: Shelke V, Potdar V, Chadha M, Kolhapure R, Prasad S, et al. (2016) Immunohistochemical and Molecular Detection of pH1N1 in Necropsied Pulmonary Tissues of Fatal Cases with Indeterminate Conventional Testing. J Foren Path 1:101. doi:10.4172/JFP.1000101

Copyright: © 2016 Shelke V, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

The rapid emergence of a novel influenza A/ H1N1 virus designated pH1N1 2009 caused one of the fastest pandemics of the twentieth century. The rapid development of an accurate detection test for this pandemic virus using reverse transcription-real time polymerase chain reaction (rRT-PCR) helped in timely diagnosis. In India this pandemic peaked between August to October 2009.The r-RT PCR for pH1N1 2009 was the main diagnostic test used on throat/nasopharyngeal swabs in all cases. While in majority of the cases this test provided reliable confirmation of the virus, it gave negative or indeterminate results in a subset of cases meeting the standard case definition for the pandemic infection and negative for seasonal flu. In the present study we examined 4 such fatal cases where microscopic pathology of the lung was consistent with viral bronchopneumonia for the presence of pH1N1 2009 using r-RT PCR on nucleic acid extracted from the paraffin sections that showed presence of viral antigens by immunohistochemistry. In all 4 cases pH1N1 sequences could be identified. These findings therefore emphasize the important role of microscopic pathology techniques in conjunction with molecular tools in the diagnostic confirmation of novel agents during a public health emergency.

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