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DOI 10.1089/vbz.2015.1917

Медицинская библиотека · Vector borne and zoonotic diseases (Larchmont, N.Y.) · 2016

An Early Passage Human Isolate of Kyasanur Forest Disease Virus Shows Acute Neuropathology in Experimentally Infected CD-1 Mice.

Basu Atanu, Yadav Pragya, Prasad Sharda, Badole Sachin, Patil Dilip, Kohlapure Rajendra Motilal, Mourya Devendra T

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Kyasanur Forest disease virus (KFDV) is a tick-borne Flavivirus that causes a severe illness in humans. Disease spectrum can vary from subclinical infection to fatal cases with hemorrhagic complications. The pathology of KFDV remains incompletely understood.

METHODS

This study describes the histopathologic and immunohistochemical findings in experimentally infected infant CD-1 mice with an early passage human KFDV isolate.

RESULTS

Acute histological changes were primarily seen in the brain. The spectrum of changes included gliosis, inflammatory response, necrosis, neural loss, and syncytium formation in mid and hind brain structures. Microscopic lesions observed in the liver were mainly necrosis and vacuolation of hepatocytes and in small intestine, prominent epithelial cell necrosis. KFDV antigens could be stained by a sensitive immunohistochemical labeling in the same organs.

CONCLUSIONS

Findings from this study are suggestive of neuropathology as the main manifestation of an early passaged human KFDV isolate. Importantly, this suggests that KFDV may be causing primarily a neurologic disease and secondary organ damage could be because of disease pathology per se. The use of primary low passage human isolates and neuropathology profile could also be more apt in developing a challenge model for testing potential antivirals and therapeutic agents.

Для цитирования: Basu Atanu, Yadav Pragya, Prasad Sharda, Badole Sachin, Patil Dilip, Kohlapure Rajendra Motilal, Mourya Devendra T. An Early Passage Human Isolate of Kyasanur Forest Disease Virus Shows Acute Neuropathology in Experimentally Infected CD-1 Mice.. Vector borne and zoonotic diseases (Larchmont, N.Y.). 2016. DOI: 10.1089/vbz.2015.1917.

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