内源性嗜生态小鼠白血病病毒Akv的产前传播和致病性。

Laboratory animal science Pub Date : 1999-10-01
I Hesse, A Luz, B Kohleisen, V Erfle, J Schmidt
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引用次数: 0

摘要

目的:研究携带内源性嗜生态小鼠白血病病毒(MuLV)的小鼠品系终生表达感染性病毒的能力。MuLV经胎盘传播的风险引起了对胚胎感染和诱导致病作用的关注,并且产后MuLV感染可能导致肿瘤发生。方法:内源性嗜生态mulv阴性的SWR/J胚胎分别植入akv感染的病毒血症型SWR/J小鼠、自发表达原病毒的AKR/J小鼠和未感染的SWR/J对照小鼠;在妊娠14天检测病毒整合和病毒表达。监测肿瘤发展超过18个月。结果:111只正常发育的受akv感染的SWR/J小鼠胚胎中,有20只(18%)被感染。在111只感染akv的SWR/J小鼠胚胎中有10只(9%)检测到新的原病毒,在60只AKR/J小鼠胚胎中有2只(3%)检测到新的原病毒;没有表达病毒蛋白。从akv感染的SWR/J小鼠中回收的127个胚胎中,16个(13%)死亡;5例中有4例(80%)感染并表达病毒蛋白。71个AKR/J小鼠胚胎中,11个(15%)死亡,2个有病毒整合;未检测到病毒表达。实验感染、病毒血症SWR/J小鼠和自发内源性表达mulv的AKR/J小鼠的死亡胚胎数量明显高于非病毒血症SWR/J小鼠,胚胎死亡率与产前原病毒表达显著相关。24只(61%)SWR/J小鼠中有15只在出生后接种Akv诱导淋巴母细胞淋巴瘤,平均+/- SD潜伏期为14 +/- 2.4个月。39只对照小鼠中只有3只(8%)发生了淋巴瘤(P < 0.005)。结论:mulv病毒坝的胚胎容易被感染,产前不适当的白血病内源逆转录病毒表达可能在嗜生态病毒阳性小鼠株的胚胎死亡和繁殖性能下降中起关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prenatal transmission and pathogenicity of endogenous ecotropic murine leukemia virus Akv.

Objective: Mouse strains carrying endogenous ecotropic murine leukemia viruses (MuLV) are capable of expressing infective virus throughout life. Risk of transplacental transmission of MuLV raises concerns of embryo infection and induction of pathogenic effects, and postnatal MuLV infection may lead to tumorigenesis.

Methods: Endogenous ecotropic MuLV-negative SWR/J embryos were implanted into Akv-infected viremic SWR/J mice, into spontaneously provirus-expressing AKR/J mice, and into noninfected SWR/J control mice; virus integration and virus expression were investigated at 14 days' gestation. Tumor development was monitored over 18 months.

Results: Of 111 embryos, 20 (18%) recovered from Akv-infected SWR/J mice, which had developed normally, were infected. New proviruses were detected in 10 of 111 (9%) embryos from Akv-infected SWR/J mice, and in 2 of 60 (3%) embryos from AKR/J mice; none expressed viral protein. Of 127 embryos recovered from Akv-infected SWR/J mice, 16 (13%) were dead; 4 of 5 (80%) were infected and expressed viral protein. Of 71 embryos from AKR/J mice, 11 (15%) were dead, and 2 of 2 had virus integration; virus expression was not detected. Numbers of dead embryos recovered from experimentally infected, viremic SWR/J mice and from spontaneously endogenous MuLV-expressing AKR/J mice were significantly higher, compared with numbers from nonviremic SWR/J control mice, and embryo lethality was significantly associated with prenatal provirus expression. Postnatal inoculation of Akv induced lymphoblastic lymphomas in 15 of 24 (61%) SWR/J mice within mean +/- SD latency of 14 +/- 2.4 months. Only 3 of 39 (8%) control mice developed lymphomas (P < 0.005).

Conclusion: Embryos in MuLV-viremic dams are readily infected, and inappropriate prenatal expression of leukemogenic endogenous retroviruses may play a critical role in embryo lethality and decreased breeding performance in ecotropic provirus-positive mouse strains.

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