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本文引用的文献

1
A PCR-based strategy for detection of mouse parvovirus.一种基于聚合酶链反应的小鼠细小病毒检测策略。
J Am Assoc Lab Anim Sci. 2009 May;48(3):263-7.
2
Molecular detection of murine norovirus from experimentally and spontaneously infected mice.从实验性和自然感染小鼠中检测小鼠诺如病毒的分子方法。
Exp Anim. 2009 Apr;58(2):135-40. doi: 10.1538/expanim.58.135.
3
Primary high-dose murine norovirus 1 infection fails to protect from secondary challenge with homologous virus.原发性高剂量鼠诺如病毒1感染无法抵御同源病毒的二次攻击。
J Virol. 2009 Jul;83(13):6963-8. doi: 10.1128/JVI.00284-09. Epub 2009 Apr 29.
4
Murine norovirus infection has no significant effect on adaptive immunity to vaccinia virus or influenza A virus.鼠诺如病毒感染对痘苗病毒或甲型流感病毒的适应性免疫没有显著影响。
J Virol. 2009 Jul;83(14):7357-60. doi: 10.1128/JVI.00623-09. Epub 2009 Apr 29.
5
A serological survey to evaluate contemporary prevalence of viral agents and Mycoplasma pulmonis in laboratory mice and rats in western Europe.一项血清学调查,以评估西欧实验小鼠和大鼠中病毒病原体和肺炎支原体的当代流行情况。
Lab Anim (NY). 2009 May;38(5):161-5. doi: 10.1038/laban0509-161.
6
Kinetics of transmission, infectivity, and genome stability of two novel mouse norovirus isolates in breeding mice.两种新型小鼠诺如病毒分离株在繁殖小鼠中的传播动力学、感染性及基因组稳定性
Comp Med. 2009 Feb;59(1):27-36.
7
Murine norovirus: an intercurrent variable in a mouse model of bacteria-induced inflammatory bowel disease.鼠诺如病毒:细菌诱导的炎症性肠病小鼠模型中的一个并发变量
Comp Med. 2008 Dec;58(6):522-33.
8
Immune mechanisms responsible for vaccination against and clearance of mucosal and lymphatic norovirus infection.负责针对黏膜和淋巴系统诺如病毒感染进行疫苗接种及清除感染的免疫机制。
PLoS Pathog. 2008 Dec;4(12):e1000236. doi: 10.1371/journal.ppat.1000236. Epub 2008 Dec 12.
9
The use of cross-foster rederivation to eliminate murine norovirus, Helicobacter spp., and murine hepatitis virus from a mouse colony.采用交叉寄养重衍生法从一个小鼠种群中清除小鼠诺如病毒、幽门螺杆菌和小鼠肝炎病毒。
J Am Assoc Lab Anim Sci. 2008 Nov;47(6):19-24.
10
Contemporary prevalence of infectious agents in laboratory mice and rats.实验室小鼠和大鼠中感染因子的当代流行情况。
Lab Anim. 2009 Apr;43(2):165-73. doi: 10.1258/la.2008.008009. Epub 2008 Nov 17.

小鼠诺如病毒感染对小鼠细小病毒感染的影响。

Effect of murine norovirus infection on mouse parvovirus infection.

作者信息

Compton Susan R, Paturzo Frank X, Macy James D

机构信息

Section of Comparative Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.

出版信息

J Am Assoc Lab Anim Sci. 2010 Jan;49(1):11-21.

PMID:20122310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2824961/
Abstract

Enzootic infection with mouse parvovirus (MPV) remains a common problem in laboratory colonies, and diagnosis of MPV infection is complicated by viral and host factors. The effect of an underlying viral infection on MPV infection has not previously been investigated. We assessed the effect of murine norovirus (MNV) infection, the most prevalent infectious agent in laboratory mice, on MPV shedding, tissue distribution and transmission. Fecal MPV shedding persisted longer in BALB/c mice infected with MNV 1 wk prior to MPV infection than in mice infected with MPV only, but transmission of MPV to soiled-bedding sentinels was not prolonged in coinfected mice. MPV DNA levels in coinfected BALB/c mice were higher in mesenteric lymph nodes and spleens at 1 and 2 wk after inoculation and in small intestines at 1 wk after inoculation compared with levels in mice infected with MPV only. In C57BL/6 mice, fecal shedding was prolonged, but no difference in soiled bedding transmission or MPV DNA levels in tissues was detected between singly and coinfected mice. MPV DNA levels in singly and coinfected SW mice were similar. MPV DNA levels were highest in SW, intermediate in BALB/c and lowest in C57BL/6 mice. MPV DNA levels in mesenteric lymph nodes of BALB/c and SW mice exceeded those in small intestines and feces, whereas the inverse occurred in C57BL/6 mice. In conclusion, MNV infection increased the duration of MPV shedding and increased MPV DNA levels in tissues of BALB/c mice.

摘要

小鼠细小病毒(MPV)的地方性感染在实验动物群体中仍然是一个常见问题,并且MPV感染的诊断因病毒和宿主因素而变得复杂。先前尚未研究过潜在病毒感染对MPV感染的影响。我们评估了实验室小鼠中最普遍的感染因子——小鼠诺如病毒(MNV)感染对MPV排泄、组织分布和传播的影响。在MPV感染前1周感染MNV的BALB/c小鼠中,粪便中MPV的排泄持续时间比仅感染MPV的小鼠更长,但在共感染的小鼠中,MPV向污染垫料哨兵的传播并未延长。与仅感染MPV的小鼠相比,共感染的BALB/c小鼠在接种后1周和2周时肠系膜淋巴结和脾脏中的MPV DNA水平较高,在接种后1周时小肠中的MPV DNA水平也较高。在C57BL/6小鼠中,粪便排泄时间延长,但在单感染和共感染的小鼠之间,未检测到污染垫料传播或组织中MPV DNA水平的差异。单感染和共感染的SW小鼠中的MPV DNA水平相似。MPV DNA水平在SW小鼠中最高,在BALB/c小鼠中居中,在C57BL/6小鼠中最低。BALB/c和SW小鼠肠系膜淋巴结中的MPV DNA水平超过小肠和粪便中的水平,而在C57BL/6小鼠中则相反。总之,MNV感染增加了BALB/c小鼠中MPV的排泄持续时间,并增加了组织中的MPV DNA水平。