scholarly journals Mesenchymoproliferative Enteropathy Associated With Dual Simian Polyomavirus and Rhesus Cytomegalovirus Infection in a Simian Immunodeficiency Virus–Infected Rhesus Macaque (Macaca mulatta)

2012 ◽  
Vol 50 (4) ◽  
pp. 715-721 ◽  
Author(s):  
S. Cummings Macri ◽  
H. L. Knight ◽  
A. D. Miller
1997 ◽  
Vol 46 (1) ◽  
pp. 83-87 ◽  
Author(s):  
Yuji FUJII ◽  
Ryouzaburou MUKAI ◽  
Yuichi MURAYAMA ◽  
Hirofumi AKARI ◽  
Makoto MACHIDA ◽  
...  

2005 ◽  
Vol 42 (3) ◽  
pp. 391-396 ◽  
Author(s):  
H. Bielefeldt-Ohmann ◽  
D. H. Barouch ◽  
A. M. Bakke ◽  
A. G. Bruce ◽  
M. Durning ◽  
...  

Multifocal submucosal stromal tumors were diagnosed in a 5.5-year-old rhesus macaque ( Macaca mulatta) experimentally infected with simian immunodeficiency virus, strain SIVsmE660, and CD4+ T cell depleted. The animal was negative for simian retroviruses, SRV-1, -2, and -5. Polymerase chain reaction analysis of DNA from tumor and spleen tissue revealed abundant, preferential presence of retroperitoneal fibromatosis herpesvirus, the macaque homologue of the Kaposi sarcoma-associated herpesvirus (human herpesvirus-8), in the tumors. This was corroborated by demonstration of viral latent nuclear antigen-1 in the nuclei of a majority of the spindeloid tumor cells. Low levels of an additional macaque herpesvirus, rhesus rhadinovirus, were also detected in the spleen and tumor tissues. The spindeloid cells labeled positively for vimentin and CD117 but were negative for CD31, CD68, desmin, and smooth muscle cell actin. Collectively, these findings suggest a relation to but not absolute identity with simian mesenchymoproliferative disorders (MPD) or typical gastrointestinal stromal tumors (GISTs).


2001 ◽  
Vol 21 (3) ◽  
pp. 173-180 ◽  
Author(s):  
Luis D. Giavedoni ◽  
Jennifer D. Imhoof ◽  
M. Cristina Velasquillo ◽  
Laura M. Parodi ◽  
Vida L. Hodara

PLoS ONE ◽  
2019 ◽  
Vol 14 (11) ◽  
pp. e0224082
Author(s):  
Michael Winkler ◽  
Sabine Gärtner ◽  
Lara Markus ◽  
Markus Hoffmann ◽  
Inga Nehlmeier ◽  
...  

2001 ◽  
Vol 75 (8) ◽  
pp. 3753-3765 ◽  
Author(s):  
Jennifer L. Greenier ◽  
Christopher J. Miller ◽  
Ding Lu ◽  
Peter J. Dailey ◽  
Fabien X. Lü ◽  
...  

ABSTRACT A better understanding of the host and viral factors associated with human immunodeficiency virus (HIV) transmission is essential to developing effective strategies to curb the global HIV epidemic. Here we used the rhesus macaque-simian immunodeficiency virus (SIV) animal model of HIV infection to study the range of viral genotypes that are transmitted by different routes of inoculation and by different types of viral inocula. Analysis of transmitted variants was undertaken in outbred rhesus macaques inoculated intravenously (IV) or intravaginally (IVAG) with a genetically heterogeneous SIVmac251 stock derived from a well-characterized rhesus macaque viral isolate. In addition, we performed serial IV and IVAG passage experiments using plasma from SIV-infected macaques as the inoculum. We analyzed the V1-V2 region of the SIV envelope gene from virion-associated RNA in plasma from infected animals by the heteroduplex mobility assay (HMA) and by DNA sequence analysis. We found that a more diverse population of SIV genetic variants was present in the earliest virus-positive plasma samples from all five IV SIVmac251-inoculated monkeys and from two of five IVAG SIVmac251-inoculated monkeys. In contrast, we found a relatively homogeneous population of SIV envelope variants in three of five monkeys inoculated IVAG with SIVmac251 stock and in two monkeys infected after IVAG inoculation with plasma from an SIV-infected animal. In some IVAG-inoculated animals, the transmitted SIV variant was the most common variant in the inoculum. However, a specific viral variant in the SIVmac251 stock was not consistently transmitted by IVAG inoculation. Thus, it is likely that host factors or stochastic processes determine the specific viral variants that infect an animal after IVAG SIV exposure. In addition, our results clearly demonstrate that the route of inoculation is associated with the extent and breadth of the genetic complexity of the viral variant population in the earliest stages of systemic infection.


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