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柯萨奇病毒B3心肌炎变异株在近交系小鼠中的差异效应。心脏组织损伤的病理学特征。

Differential effects of myocarditic variants of Coxsackievirus B3 in inbred mice. A pathologic characterization of heart tissue damage.

作者信息

Chow L H, Gauntt C J, McManus B M

机构信息

Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha.

出版信息

Lab Invest. 1991 Jan;64(1):55-64.

PMID:1990209
Abstract

The histopathologic features reflecting the influence of virus genotype and host differences on myocarditis were evaluated in six inbred mouse strains (C57BL/6, B10.D2, BALB/c, DBA/2, A/J, and C3H/HeJ) inoculated with four respective variants of coxsackievirus B3 (CVB3-CG, -SH, -ST, or -NR). The most severe and most prevalent histologic lesions occurred after infection with CVB3-SH or -CG variants, regardless of mouse strain. In general, C57BL/6 mice showed the lowest susceptibility to myocarditis while A/J or C3H/HeJ animals had the highest susceptibility, whether early (7 days) or late (21 days) after CVB3 inoculation. Lesion size and calcification depended to an extent on disease severity, but calcification in the C3H/HeJ myocardium was notably sparse. Lesions clustered distinctly in the midthird of the ventricular wall in some animals, particularly in DBA/2 mice. Extensive pericarditis occurred exclusively in BALB/c and DBA/2 animals and predominated over the right ventricle anterolaterally. Virus titer in the heart did not account for disease susceptibility among mouse strains. These characteristics reflect differences in pathogenicity and are important considerations in the study of mechanisms in CVB3-induced myocarditis in mice.

摘要

在接种柯萨奇病毒B3(CVB3)四种不同变体(CVB3 - CG、- SH、- ST或 - NR)的六种近交系小鼠品系(C57BL / 6、B10.D2、BALB / c、DBA / 2、A / J和C3H / HeJ)中,评估了反映病毒基因型和宿主差异对心肌炎影响的组织病理学特征。无论小鼠品系如何,感染CVB3 - SH或 - CG变体后出现的组织学病变最为严重且最为普遍。一般来说,C57BL / 6小鼠对心肌炎的易感性最低,而A / J或C3H / HeJ动物的易感性最高,无论是在接种CVB3后的早期(7天)还是晚期(21天)。病变大小和钙化在一定程度上取决于疾病严重程度,但C3H / HeJ心肌中的钙化明显较少。在一些动物中,病变明显聚集在心室壁的中三分之一处,特别是在DBA / 2小鼠中。广泛的心包炎仅发生在BALB / c和DBA / 2动物中,且主要位于右心室前外侧。心脏中的病毒滴度不能解释小鼠品系之间的疾病易感性。这些特征反映了致病性的差异,是研究CVB3诱导的小鼠心肌炎机制时的重要考虑因素。

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