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内源性嗜亲性小鼠白血病病毒Akv的产前传播及致病性

Prenatal transmission and pathogenicity of endogenous ecotropic murine leukemia virus Akv.

作者信息

Hesse I, Luz A, Kohleisen B, Erfle V, Schmidt J

机构信息

Institute of Molecular Virology, GSF-National Research Center for Environment and Health, Neuherberg, Germany.

出版信息

Lab Anim Sci. 1999 Oct;49(5):488-95.

Abstract

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.

摘要

目的

携带内源性嗜亲性鼠白血病病毒(MuLV)的小鼠品系能够终生表达感染性病毒。MuLV经胎盘传播的风险引发了对胚胎感染和致病效应诱导的担忧,且出生后MuLV感染可能导致肿瘤发生。

方法

将内源性嗜亲性MuLV阴性的SWR/J胚胎植入感染Akv的病毒血症SWR/J小鼠、自发表达前病毒的AKR/J小鼠以及未感染的SWR/J对照小鼠体内;在妊娠14天时研究病毒整合和病毒表达情况。对肿瘤发展进行18个月的监测。

结果

从感染Akv的SWR/J小鼠体内回收的111个胚胎中,20个(18%)发育正常的胚胎被感染。在从感染Akv的SWR/J小鼠体内回收的11(9%)个胚胎以及从AKR/J小鼠体内回收的60个(3%)胚胎中的2个中检测到新的前病毒;均未表达病毒蛋白。从感染Akv的SWR/J小鼠体内回收的127个胚胎中,16个(13%)死亡;5个中的4个(80%)被感染并表达病毒蛋白。从AKR/J小鼠体内回收的71个胚胎中,11个(15%)死亡,2个中的[此处原文有误,应为2个中的2个]有病毒整合;未检测到病毒表达。与非病毒血症SWR/J对照小鼠相比,从经实验感染的病毒血症SWR/J小鼠和自发表达内源性MuLV的AKR/J小鼠体内回收的死亡胚胎数量显著更高,且胚胎致死率与产前前病毒表达显著相关。出生后接种Akv在24只SWR/J小鼠中的15只(61%)诱导发生淋巴细胞性淋巴瘤,平均潜伏期±标准差为14±2.4个月。39只对照小鼠中只有3只(8%)发生淋巴瘤(P<0.005)。

结论

MuLV病毒血症母鼠体内的胚胎容易被感染,且致白血病内源性逆转录病毒的不适当产前表达可能在嗜亲性前病毒阳性小鼠品系的胚胎致死率和繁殖性能下降中起关键作用。

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