首页> 外文期刊>Comparative Medicine >Temporal transmission studies of mouse parvovirus 1 in BALB/c and C.B-17/Icr-Prkdcscid mice.
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Temporal transmission studies of mouse parvovirus 1 in BALB/c and C.B-17/Icr-Prkdcscid mice.

机译:小鼠细小病毒1在BALB / c和C.B-17 / Icr-Prkdcscid小鼠中的时间传播研究。

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Faecal shedding and transmission of mouse parvovirus 1 (MPV) to naive sentinels, breeding mates, and progeny were assessed. Neonatal SCID and BALB/c mice inoculated with MPV were evaluated over 24 wk; several mice from each strain were mated once during this period. Faecal MPV loads for each cage were determined weekly by quantitative polymerase chain reaction (PCR) analysis, and all mice were evaluated by quantitative PCR analysis of lymphoid tissues and seroconversion to MPV antigens in immunocompetent mice. Results indicated persistently high faecal shedding of MPV in SCID mice throughout the evaluation period sufficient to allow transmission to sentinels, naive breeding partners, and the progeny of infected male mice and naive partners. Lymphoid tissue viral loads in the progeny of infected female SCID mice were high at weaning but low at 6 wk of age. Infected BALB/c mice shed high levels of MPV in faeces for 3 wk postinoculation, with seroconversion only in sentinels exposed during the first 2 wk postinoculation. Thereafter the faeces of infected BALB/c mice and the lymphoid tissues of sentinels, naive breeding partners, and progeny intermittently contained extremely low levels of MPV DNA. Although pregnancy and lactation did not increase viral shedding in BALB/c mice, MPV exposure levels were sufficient to induce productive infection in some BALB/c progeny. These data indicate that the adaptive immune response suppresses, but does not eliminate, MPV shedding; this suppression is sufficient to inhibit infection of weanling and adult mice but allows productive infection of some progeny..
机译:粪便脱落和小鼠细小病毒1(MPV)的传播到幼稚的前哨,繁殖的伴侣和后代进行了评估。接种MPV的新生SCID和BALB / c小鼠在24周内进行了评估;在此期间,将每种菌株的几只小鼠交配一次。每周通过定量聚合酶链反应(PCR)分析确定每个笼子的粪便MPV载量,并通过对免疫组织小鼠的淋巴组织进行定量PCR分析和血清转化为MPV抗原来评估所有小鼠。结果表明,在整个评估期内,SCID小鼠中MPV的粪便排泄率持续较高,足以传播至前哨,幼稚的繁殖伴侣以及被感染的雄性小鼠和幼稚的伴侣的后代。感染的雌性SCID小鼠后代中的淋巴组织病毒载量在断奶时较高,但在6周龄时较低。感染后的BALB / c小鼠在接种后3周内粪便中的MPV含量较高,仅在接种后2周内暴露于前哨的患者才发生血清转化。此后,被感染的BALB / c小鼠的粪便以及前哨,幼稚的繁殖伴侣和后代的淋巴组织间歇地含有极低水平的MPV DNA。尽管妊娠和哺乳期并未增加BALB / c小鼠的病毒脱落,但MPV暴露水平足以在某些BALB / c后代中引起生产性感染。这些数据表明,适应性免疫反应可以抑制但不能消除MPV脱落。这种抑制足以抑制断奶和成年小鼠的感染,但允许某些子代的生产性感染。

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