Pedersen N C, Yamamoto J K, Ishida T, Hansen H
Department of Medicine, School of Veterinary Medicine, University of California, Davis 95616.
Vet Immunol Immunopathol. 1989 May;21(1):111-29. doi: 10.1016/0165-2427(89)90134-7.
Feline immunodeficiency virus (FIV) (formerly feline T-lymphotropic lentivirus or FTLV) was first isolated from a group of cats in Petaluma, California in 1986. The virus is a typical lentivirus in gross and structural morphology. It replicates preferentially but not exclusively in feline T-lymphoblastoid cells, where it causes a characteristic cytopathic effect. The major structural proteins are 10, 17 (small gag), 28 (major core), 31 (endonuclease?), 41 (transmembrane?), 52 (core precursor polyprotein), 54/62 (reverse transcriptase?), and 110/130 (major envelope) kilodaltons in size. The various proteins are antigenically distinguishable from those of other lentiviruses, although serum from EIAV-infected horses will cross-react with some FIV antigens. Kittens experimentally infected with FIV manifest a transient (several days to 2 weeks) fever and neutropenia beginning 4 to 8 weeks after inoculation. This is associated with a generalized lymphadenopathy that persists for up to 9 months. Most cats recover from this initial phase of the disease and become lifelong carriers of the virus. Complete recovery does not occur to any extent in nature or in the laboratory setting. One experimentally infected cat died from a myeloproliferative disorder several months after infection. The terminal AIDS-like phase of the illness has been seen mainly in naturally infected cats. It appears a year or more following the initial infection in an unknown proportion of infected animals. FIV has been identified in cats from all parts of the world. It is most prevalent in high density populations of free roaming cats (feral and pet), and is very uncommon in closed purebred catteries. Male cats are twice as likely to become infected as females. Older male cats adopted as feral or stray animals are at the highest risk of infection, therefore. The infection rate among freely roaming cats rises throughout life, and reaches levels ranging from less than 1% to 12% or more depending on the area. Clinically affected cats tend to be 5 years or older at the time of hospitalization. Experimental and seroepidemiologic studies suggest that FIV is transmitted mainly by bites. Intimate, non-traumatic contact (mutual grooming, shared use of food, water and litter pans) is inefficient in transmitting the infection. In utero and venereal transmission could not be demonstrated in laboratory settings. There is no statistical linkage between FIV and feline leukemia virus (FeLV) infections in nature. The FeLV infection rate in FIV-infected animals is the same as it is for non-FIV-infected cats.(ABSTRACT TRUNCATED AT 400 WORDS)
猫免疫缺陷病毒(FIV)(以前称为猫T淋巴细胞嗜性慢病毒或FTLV)于1986年首次从加利福尼亚州佩塔卢马的一组猫中分离出来。该病毒在总体和结构形态上是一种典型的慢病毒。它优先但并非唯一地在猫T淋巴母细胞样细胞中复制,在那里它会引起特征性的细胞病变效应。主要结构蛋白的大小分别为10、17(小gag)、28(主要核心)、31(核酸内切酶?)、41(跨膜?)、52(核心前体多聚蛋白)、54/62(逆转录酶?)和110/130(主要包膜)千道尔顿。尽管感染马传染性贫血病毒(EIAV)的马的血清会与一些FIV抗原发生交叉反应,但各种蛋白质在抗原性上与其他慢病毒的蛋白质是可区分的。实验感染FIV的小猫在接种后4至8周开始出现短暂(几天至2周)的发热和中性粒细胞减少。这与持续长达9个月的全身性淋巴结病有关。大多数猫从疾病的初始阶段恢复过来,并成为该病毒的终身携带者。在自然或实验室环境中都不会出现完全恢复的情况。一只实验感染的猫在感染几个月后死于骨髓增殖性疾病。疾病的终末期艾滋病样阶段主要见于自然感染的猫。在初始感染后一年或更长时间,在未知比例的感染动物中出现。FIV已在世界各地的猫中被鉴定出来。它在自由放养的高密度猫群(野猫和宠物猫)中最为普遍,在封闭的纯种猫舍中非常罕见。雄性猫感染的可能性是雌性猫的两倍。因此,作为野猫或流浪动物收养的老年雄性猫感染风险最高。自由放养的猫的感染率在一生中都会上升,根据地区不同,感染率从不到1%到12%或更高不等。临床受影响的猫在住院时往往年龄在5岁或以上。实验和血清流行病学研究表明,FIV主要通过咬伤传播。亲密的、无创伤的接触(相互梳理毛发、共用食物、水和猫砂盆)在传播感染方面效率低下。在实验室环境中未证实子宫内传播和性传播。在自然环境中,FIV与猫白血病病毒(FeLV)感染之间没有统计学关联。FIV感染动物中的FeLV感染率与未感染FIV的猫相同。(摘要截取自400字)