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在牛感染口蹄疫病毒持续期,检测各种体液和组织中的口蹄疫病毒序列。

Detection of foot-and-mouth disease viral sequences in various fluids and tissues during persistence of the virus in cattle.

作者信息

Bergmann I E, Malirat V, Augé de Mello P, Gomes I

机构信息

Pan American Foot-and-Mouth Disease Center, Rio de Janeiro, Brazil.

出版信息

Am J Vet Res. 1996 Feb;57(2):134-7.

PMID:8633795
Abstract

OBJECTIVE

To assess whether foot-and-mouth disease virus (FMDV)-specific sequences could be identified in tissues from persistently virus-infected animals.

DESIGN

Cattle with experimentally induced persistent FMDV infections were slaughtered at 750 days after viral exposure. Experimentally infected pigs were slaughtered at 28 days after FMDV inoculation. Postmortem specimens were asceptically removed.

ANIMALS

Three bovids and 3 pigs were studied, as well as 1 control animal for each species.

PROCEDURE

Various tissues were examined for the presence of FMDV-specific sequences by dot-blot hybridization assay, using a molecularly cloned FMDV cDNA corresponding to the polymerase coding region.

RESULTS

The FMDV-specific genomic sequences were only detected in RNA from spleen, lung, larynx, tonsils, pancreas, liver, esophagus, and WBC of bovids.

CONCLUSIONS

It was established that, at late stages of the persistent infection, when virus isolation was not possible, cattle may carry FMDV-specific sequences in different tissues. Retention of viral sequences could not be demonstrated in specimens from experimentally infected swine, 28 days after viral inoculation.

摘要

目的

评估在持续病毒感染动物的组织中是否能鉴定出口蹄疫病毒(FMDV)特异性序列。

设计

对实验诱导的FMDV持续感染牛在病毒暴露后750天进行屠宰。对实验感染猪在FMDV接种后28天进行屠宰。无菌采集死后标本。

动物

研究了3头牛科动物和3头猪,以及每个物种的1只对照动物。

方法

使用对应于聚合酶编码区的分子克隆FMDV cDNA,通过斑点杂交试验检测各种组织中FMDV特异性序列的存在情况。

结果

仅在牛科动物的脾脏、肺、喉、扁桃体、胰腺、肝脏、食管和白细胞的RNA中检测到FMDV特异性基因组序列。

结论

已证实,在持续感染后期,当无法进行病毒分离时,牛可能在不同组织中携带FMDV特异性序列。在病毒接种28天后,实验感染猪的标本中未证实病毒序列的留存。

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