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利用聚合酶链反应检测跳蚤中鼠疫耶尔森菌进行鼠疫监测的新方法。

New method for plague surveillance using polymerase chain reaction to detect Yersinia pestis in fleas.

作者信息

Hinnebusch J, Schwan T G

机构信息

Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, Hamilton, Montana 59840.

出版信息

J Clin Microbiol. 1993 Jun;31(6):1511-4. doi: 10.1128/jcm.31.6.1511-1514.1993.

Abstract

Yersinia pestis, the plague bacillus, infects a variety of mammals throughout the world and is transmitted by fleas. We developed a polymerase chain reaction (PCR) test using primers designed from the Y. pestis plasminogen activator gene to directly detect plague-infected fleas. As few as 10 Y. pestis cells were detected, even in the presence of flea tissue, by PCR and then agarose gel electrophoresis and ethidium bromide staining. The feasibility of the assay was demonstrated by using naturally infected Xenopsylla cheopis fleas. The detection of Y. pestis in fleas by PCR provides a rapid and sensitive way to monitor plaque in wild animal populations, allowing public health officials to better assess the potential risk of transmission to humans.

摘要

鼠疫杆菌耶尔森氏菌可感染全球多种哺乳动物,并通过跳蚤传播。我们利用从耶尔森氏菌纤溶酶原激活基因设计的引物开发了一种聚合酶链反应(PCR)检测方法,以直接检测感染鼠疫的跳蚤。通过PCR,然后进行琼脂糖凝胶电泳和溴化乙锭染色,即使在存在跳蚤组织的情况下,也能检测到低至10个耶尔森氏菌细胞。使用自然感染的印鼠客蚤证明了该检测方法的可行性。通过PCR检测跳蚤中的耶尔森氏菌提供了一种快速且灵敏的方法来监测野生动物群体中的鼠疫,使公共卫生官员能够更好地评估向人类传播的潜在风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e68/265569/d69894c33c53/jcm00018-0125-a.jpg

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