Classic AIDS in a sooty mangabley after an 18-year natural infection

被引:82
作者
Ling, BH
Apetrei, C
Pandrea, I
Veazey, RS
Lackner, AA
Gormus, B
Marx, PA
机构
[1] Tulane Univ, Ctr Hlth Sci, Tulane Natl Primate Res Ctr, Covington, LA 70433 USA
[2] Tulane Univ, Sch Med, Dept Microbiol & Immunol, Covington, LA 70433 USA
[3] Tulane Univ, Sch Med, Dept Pathol, Covington, LA 70433 USA
[4] Tulane Univ, Sch Publ Hlth & Trop Med, Dept Trop Med, New Orleans, LA 70112 USA
关键词
D O I
10.1128/JVI.78.16.8902-8908.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Prevailing theory holds that simian immunodeficiency virus (SIV) infections are nonpathogenic in their natural simian hosts and that lifelong infections persist without disease. Numerous studies have reported that SIV-infected sooty mangabeys (SMs; Cercocebus atys) remain disease free for up to 24 years despite relatively high levels of viral replication. Here, we report that classic AIDS developed after an 18-year incubation in an SM (E041) with a natural SIVsm infection. Unlike that described in previous reports of SIV-related disease in SMs, the SIVsm infecting E041 was not first passaged through macaques; moreover, SM E041 was simian T-cell leukemia virus antibody negative. SM E041 was euthanized in 2002 after being diagnosed with severe disseminated B-cell lymphoma. The plasma virus load had been approximately the same for 16 years when a 100-fold increase in virus load occurred in years 17 and 18. Additional findings associated with AIDS were CD4(+)-cell decline, loss of p27 core antibody, and loss of control of SIVsm replication with disseminated giant cell disease. These findings suggest that the time to development of AIDS exceeds the average lifetime of SMs in the wild and that the principal adaptation of SIV to its natural African hosts does not include complete resistance to disease. Instead, AIDS may develop slowly, even in the presence of high virus loads. However, a long-term relatively high virus load, such as that in SM E041, is consistent with AIDS development in less than 18 years in humans and macaques. Therefore, the results also suggest that SMs have a special mechanism for resisting AIDS development.
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页码:8902 / 8908
页数:7
相关论文
共 46 条
[1]   The history of SIVS and AIDS: Epidemiology, phylogeny and biology of isolates from naturally SIV infected non-human primates (NHP) in Africa [J].
Apetrei, C ;
Robertson, DL ;
Marx, PA .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2004, 9 :225-254
[2]   Simian immunodeficiency virus of African green monkeys is apathogenic in the newborn natural host [J].
Beer, B ;
Denner, J ;
Brown, CR ;
Norley, S ;
zur Megede, J ;
Coulibaly, C ;
Plesker, R ;
Holzammer, S ;
Baier, M ;
Hirsch, VM ;
Kurth, R .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY, 1998, 18 (03) :210-220
[3]   Simian immunodeficiency virus replicates to high levels in naturally infected African green monkeys without inducing immunologic or neurologic disease [J].
Broussard, SR ;
Staprans, SI ;
White, R ;
Whitehead, EM ;
Feinberg, MB ;
Allan, JS .
JOURNAL OF VIROLOGY, 2001, 75 (05) :2262-2275
[4]   Normal T-cell turnover in sooty mangabeys harboring active simian immunodeficiency virus infection [J].
Chakrabarti, LA ;
Lewin, SR ;
Zhang, LQ ;
Gettie, A ;
Luckay, A ;
Martin, LN ;
Skulsky, E ;
Ho, DD ;
Cheng-Mayer, C ;
Marx, PA .
JOURNAL OF VIROLOGY, 2000, 74 (03) :1209-1223
[5]   Primary SIVsm isolates use the CCR5 coreceptor from sooty mangabeys naturally infected in west Africa: A comparison of coreceptor usage of primary SIVsm, HIV-2, and SIVmac [J].
Chen, ZW ;
Gettie, A ;
Ho, DD ;
Marx, PA .
VIROLOGY, 1998, 246 (01) :113-124
[6]   Genetic characterization of new west African simian immunodeficiency virus SIVsm: Geographic clustering of household-derived SIV strains with human immunodeficiency virus type 2 subtypes and genetically diverse viruses from a single feral sooty mangabey troop [J].
Chen, ZW ;
Telfer, P ;
Gettie, A ;
Reed, P ;
Zhang, LQ ;
Ho, DD ;
Marx, PA .
JOURNAL OF VIROLOGY, 1996, 70 (06) :3617-3627
[7]   High levels of viral replication during primary simian immunodeficiency virus SIVagm infection are rapidly and strongly controlled in African green monkeys [J].
Diop, OM ;
Gueye, P ;
Dias-Tavares, M ;
Kornfeld, C ;
Faye, A ;
Ave, P ;
Huerre, M ;
Corbet, S ;
Barre-Sinoussi, F ;
Müller-Trutwin, MC .
JOURNAL OF VIROLOGY, 2000, 74 (16) :7538-7547
[8]   IDENTIFICATION OF A NEF ALLELE THAT CAUSES LYMPHOCYTE-ACTIVATION AND ACUTE DISEASE IN MACAQUE MONKEYS [J].
DU, ZJ ;
LANG, SM ;
SASSEVILLE, VG ;
LACKNER, AA ;
ILYINSKII, PO ;
DANIEL, MD ;
JUNG, JU ;
DESROSIERS, RC .
CELL, 1995, 82 (04) :665-674
[9]  
FULTZ PN, 1990, DEV BIOLOGICALS, V72, P253
[10]   ISOLATION OF A T-LYMPHOTROPIC RETROVIRUS FROM NATURALLY INFECTED SOOTY MANGABEY MONKEYS (CERCOCEBUS-ATYS) [J].
FULTZ, PN ;
MCCLURE, HM ;
ANDERSON, DC ;
SWENSON, RB ;
ANAND, R ;
SRINIVASAN, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (14) :5286-5290