Literature DB >> 34626576

Expanded Histopathology and Tropism of Ebola Virus in the Rhesus Macaque Model: Potential for Sexual Transmission, Altered Adrenomedullary Hormone Production, and Early Viral Replication in Liver.

David X Liu1, Timothy K Cooper2, Donna L Perry2, Louis M Huzella2, Amanda M W Hischak2, Randy J Hart2, Nejra Isic2, Russell Byrum2, Danny Ragland2, Marisa St Claire2, Kurt Cooper2, Rebecca Reeder2, James Logue2, Peter B Jahrling2, Michael R Holbrook2, Richard S Bennett2, Lisa E Hensley3.   

Abstract

The pathogenesis of Ebola virus disease (EVD) is still incomplete, in spite of the availability of a nonhuman primate modelfor more than 4 decades. To further investigate EVD pathogenesis, a natural history study was conducted using 27 Chinese-origin rhesus macaques. Of these, 24 macaques were exposed intramuscularly to Kikwit Ebola virus and euthanized at predetermined time points or when end-stage clinical disease criteria were met, and 3 sham-exposed macaques were euthanized on study day 0. This study showed for the first time that Ebola virus causes uterine cervicitis, vaginitis, posthitis, and medullary adrenalitis. Not only was Ebola virus detected in the interstitial stromal cells of the genital tract, but it was also present in the epididymal and seminal vesicular tubular epithelial cells, ectocervical and vaginal squamous epithelial cells, and seminal fluid. Furthermore, as early as day 3 after exposure, Ebola virus replicative intermediate RNA was detected in Kupffer cells and hepatocytes. These findings in the nonhuman model provide additional insight into potential sexual transmission, possible disruption of sympathetic hormone production, and early virus replication sites in human EVD patients. Published by Elsevier Inc.

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Year:  2021        PMID: 34626576      PMCID: PMC8759036          DOI: 10.1016/j.ajpath.2021.09.009

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


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