scholarly journals Optimization of PCR for quantification of simian immunodeficiency virus genomic RNA in plasma of rhesus macaques (Macaca mulatta ) using armored RNA

2013 ◽  
Vol 43 (1) ◽  
pp. 31-43 ◽  
Author(s):  
C.J. Monjure ◽  
C.D. Tatum ◽  
A.T. Panganiban ◽  
M. Arainga ◽  
V. Traina-Dorge ◽  
...  
2014 ◽  
Vol 43 (6) ◽  
pp. 468-476
Author(s):  
Keiko Y. Petrosky ◽  
Heather L. Knight ◽  
Susan V. Westmoreland ◽  
Andrew D. Miller

2001 ◽  
Vol 103 (1) ◽  
pp. 79-88 ◽  
Author(s):  
Franz-Josef Kaup ◽  
Juan Antonio Boga ◽  
Savio Freire Bruno ◽  
Andrea Didier ◽  
Katrin Hermann ◽  
...  

Virology ◽  
1996 ◽  
Vol 216 (2) ◽  
pp. 444-450 ◽  
Author(s):  
WOLFGANG LÜKE ◽  
CHEICK COULIBALY ◽  
ULF DITTMER ◽  
GERALD VOSS ◽  
REINHARD OESTERLE ◽  
...  

2001 ◽  
Vol 356 (1410) ◽  
pp. 845-847 ◽  
Author(s):  
Philippe Lena ◽  
Paul Luciw

Trace amounts of simian immunodeficiency virus (SIV) proviral DNA were detected in monolayers of primary kidney cells from two rhesus macaques ( Macaca mulatta ) heavily infected with the highly pathogenic strain SIVmac251. There was no detectable infectious SIV in the supernatant from the kidney cell cultures obtained from either monkey. However, infectious SIV was rescued by co–culture of kidney cells with a permissive lymphoid cell line. Macrophages, present in these cultures, may be the reservoir for the proviral genomes.


2005 ◽  
Vol 42 (1) ◽  
pp. 19-29 ◽  
Author(s):  
I. Kondova ◽  
M. A. Simon ◽  
S. A. Klumpp ◽  
J. MacKey ◽  
G. Widmer ◽  
...  

2000 ◽  
Vol 124 (10) ◽  
pp. 1480-1484
Author(s):  
Laura V. Chalifoux ◽  
Angela Carville ◽  
Douglas Pauley ◽  
Brendon Thompson ◽  
Andrew A. Lackner ◽  
...  

Abstract Context.—Enterocytozoon bieneusi is the most frequent microsporidian parasite of human patients with acquired immunodeficiency syndrome and is a significant cause of diarrhea and wasting. Recently, this organism has also been recognized as a spontaneous infection of several species of captive macaques. As in humans, E bieneusi frequently causes enteropathy and cholangiohepatitis in immunodeficient simian immunodeficiency virus (SIV)–infected macaques. Objective.—To examine E bieneusi as an etiologic agent of nonsuppurative proliferative serositis in immunodeficient rhesus macaques (Macaca mulatta). Design.—Retrospective analysis of necropsy material obtained from immunodeficient SIV-infected rhesus macaques. Results.—Examination of SIV-infected rhesus macaques (n = 225) revealed E bieneusi proliferative serositis in 7 of 16 cases of peritonitis of unknown origin. The organism could be identified by in situ hybridization and polymerase chain reaction in sections of pleura and peritoneum obtained at necropsy. Serositis was always accompanied by moderate-to-severe infection of the alimentary tract, and morphologic evidence suggested dissemination through efferent lymphatics. Colabeling experiments revealed most infected cells to be cytokeratin positive and less frequently positive for the macrophage marker CD68. Sequencing of a 607–base pair segment of the small subunit ribosomal gene revealed 100% identity to sequences obtained from rhesus macaques (Genbank accession AF023245) and human patients (Genbank accession AF024657 and L16868). Conclusions.—These findings indicate that E bieneusi disseminates in immunodeficient macaques and may be a cause of peritonitis in the immunocompromised host.


2017 ◽  
Vol 4 (1) ◽  
pp. 107-115
Author(s):  
Matthias Mietsch ◽  
Ulrike Sauermann ◽  
Kerstin Mätz-Rensing ◽  
Antonina Klippert ◽  
Maria Daskalaki ◽  
...  

Abstract. Human immunodeficiency virus (HIV) comorbidities have become clinically more important due to antiretroviral therapy. Although therapy increases life expectancy, it does not completely suppress immune activation and its associated complications. The simian immunodeficiency virus (SIV)-infected rhesus macaque (Macaca mulatta) represents a valuable model for the investigation of SIV-associated diseases. Although cardiovascular (CV) changes are common in HIV-infected patients, there are only a few reports on the incidence of CV findings in SIV-infected animals. In addition, potential associations between pathohistological findings and hematological parameters are still unclear. We therefore conducted a retrospective analysis of 195 SIV-infected rhesus macaques that were euthanized with AIDS-related symptoms at the German Primate Center, Goettingen, over a 25-year period. Pathological findings were correlated with hematological data. The main findings included myocarditis (12.8 %), endocarditis (9.7 %), and arteriopathy (10.3 %) in various organs. Thrombocytopenia occurred more frequently in macaques with endocarditis or arteriopathy than in macaques without CV disease (80 % in animals with endocarditis, 60 % in animals with arteriopathy, p < 0. 0001 and p = 0. 0016, respectively). Further investigations of the interaction between coagulation markers, proinflammatory cytokines, and biomarkers associated with endothelial dysfunction (e.g., D-dimers) and histological data (vascular wall structure) may unravel the mechanisms underlying HIV/SIV-associated CV comorbidities.


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