DETECTION OF SIMIAN T-LYMPHOTROPIC VIRUS TYPE-I USING THE POLYMERASE CHAIN-REACTION

被引:15
作者
DEZZUTTI, CS
LAZO, A
YEE, JY
BLAKESLEE, JR
MATHES, LE
BROWN, BG
LAIRMORE, MD
机构
[1] OHIO STATE UNIV,DEPT VET ANAT & CELLULAR BIOL,COLUMBUS,OH 43210
[2] CTR RETROVIRUS RES,COLUMBUS,OH
[3] UNIV CALIF DAVIS,DEPT MED PATHOL,DAVIS,CA 95616
[4] CTR DIS CONTROL,CTR INFECT DIS,ATLANTA,GA 30333
关键词
D O I
10.1002/ijc.2910500524
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To develop the polymerase chain reaction (PCR) for the detection of simian T-lymphotropic virus type I (STLV-I) infection, cell lines or peripheral-blood mononuclear cells (PBMC) from 2 non-human primate species [African green monkeys (AGM), Cercopithecus aethiops; baboon, Papio cynocephalus] were evaluated for their STLV-I status using oligonucleotide primer pairs and probes specific for the tax and pol gene regions of the closely related human T-lymphotropic virus type I (HTLV-I). These PCR results were compared with serologic (Western blot assay) and viral culture (p24-antigen capture assay) data. PCR products for both gene regions were detected in established baboon, Japanese macaque and rhesus macaque STLV-I-producing cell lines. STLV-I tax and pol products were also detected in PBMC from 4 of 4 infected AGM and 4 of 4 infected baboons, each of which were also Western-blot-positive and p24-antigen-capture-positive. Of the remaining AGM (n = 7) and baboon (n = 1) which were PCR-negative, each was also Western-blot-negative and p24-antigen-capture-negative. Two seronegative and virus-culture-negative AGM were classified as PCR indeterminate with weak reactivity using tax primers. These primer pairs failed to amplify DNA from uninfected human PBMC, an uninfected human lymphoid cell line, a simian immunodeficiency virus macaque (SIV(mac)251)-infected cell line and a simian-retrovirus-type-D(SRV-D)-infected cell line. HTLV-II-pol-specific primer pairs failed to amplify DNA from STLV-I-infected cell lines and PBMC from STLV-I-infected monkeys. Further, HTLV-I pol and tax primer pairs successfully amplified RNA from HTLV-I- and STLV-I-infected cell lines by reverse transcriptase (RT)-PCR. We have demonstrated excellent specificity in the detection of STLV-I by PCR using these HTLV-I-derived primers and probes. Additionally, our data suggest that the tax and pol gene regions are conserved between HTLV-I and STLV-I strains found among these diverse species of non-human primates.
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页码:805 / 810
页数:6
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