Hara Masayuki, Kikuchi Toshihiko, Ono Fumiko, Takano Jun-ichirou, Ageyama Naohide, Fujimoto Koji, Terao Keiji, Baba Tadashi, Mukai Ryozaburo
Tsukuba Primate Center for Medical Science National Institute Infectious Diseases (NIID), 1 Hachimandai, Tsukuba, 305-0843 Japan.
Comp Med. 2005 Apr;55(2):145-9.
The exogenous simian type D retroviruses (SRV/Ds) are prevalent in macaque monkeys and sometimes cause immunodeficiency with anemia, weight loss, and persistent unresponsive diarrhea. SRV/D isolates are classified as subtypes 1 to 6, and the entire sequences of the gag region of SRV/D-1, -2, and -3 and SRV/D-Tsukuba (SRV/D-T) have been determined. We designed specific primers in the gag region of SRV/D-T that enabled us to directly detect by polymerase chain reaction (PCR) SRV/D-T proviral DNA sequences in DNA extracted from whole blood. Using this assay and another PCR assay that detects multiple SRV/D subtypes, we performed a survey for SRV/D infection in our specific pathogen-free (SPF) and conventional colonies at Tsukuba Primate Center (TPC). In the SPF colony, no SRV/D signal was detected in any animal. On the other hand, SRV/D-T was detected in 11 of 49 animals (22.5%) in the conventional colony. SRV/D-T was the only SRV/D subtype detected. Consequently, SRV/D-T is the major SRV/D subtype present in cynomolgus monkeys at TPC.
外源性猿猴D型逆转录病毒(SRV/Ds)在猕猴中普遍存在,有时会导致免疫缺陷,并伴有贫血、体重减轻和持续性无反应性腹泻。SRV/D分离株被分为1至6个亚型,并且已经确定了SRV/D-1、-2和-3以及筑波猿猴D型逆转录病毒(SRV/D-T)的gag区域的完整序列。我们在SRV/D-T的gag区域设计了特异性引物,这使我们能够通过聚合酶链反应(PCR)直接检测从全血中提取的DNA中的SRV/D-T前病毒DNA序列。使用该检测方法以及另一种检测多种SRV/D亚型的PCR检测方法,我们在筑波灵长类动物中心(TPC)的无特定病原体(SPF)和常规猴群中进行了SRV/D感染调查。在SPF猴群中,未在任何动物中检测到SRV/D信号。另一方面,在常规猴群的49只动物中有11只(22.5%)检测到SRV/D-T。SRV/D-T是检测到的唯一SRV/D亚型。因此,SRV/D-T是TPC食蟹猴中存在的主要SRV/D亚型。