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创伤弧菌的签名标签诱变

Signature-tagged mutagenesis of Vibrio vulnificus.

作者信息

Yamamoto Mai, Kashimoto Takashige, Tong Ping, Xiao Jianbo, Sugiyama Michiko, Inoue Miyuki, Matsunaga Rie, Hosohara Kohei, Nakata Kazue, Yokota Kenji, Oguma Keiji, Yamamoto Koichiro

机构信息

Department of Nutritional Science, Okayama Prefectural University, Soja, Okayama 719-1197, Japan.

出版信息

J Vet Med Sci. 2015 Jul;77(7):823-8. doi: 10.1292/jvms.14-0655. Epub 2015 Mar 9.

Abstract

Vibrio vulnificus is the causative agent of primary septicemia, wound infection and gastroenteritis in immunocompromised people. In this study, signature-tagged mutagenesis (STM) was applied to identify the virulence genes of V. vulnificus. Using STM, 6,480 mutants in total were constructed and divided into 81 sets (INPUT pools); each mutant in a set was assigned a different tag. Each INPUT pool was intraperitoneally injected into iron-overloaded mice, and in vivo surviving mutants were collected from blood samples from the heart (OUTPUT pools). From the genomic DNA of mixed INPUT or OUTPUT pools, digoxigenin-labeled DNA probes against the tagged region were prepared and used for dot hybridization. Thirty tentatively attenuated mutants, which were hybridized clearly with INPUT probes but barely with OUTPUT probes, were negatively selected. Lethal doses of 11 of the 30 mutants were reduced to more than 1/100; of these, the lethal doses of 2 were reduced to as low as 1/100,000. Transposon-inserted genes in the 11 attenuated mutants were those for IMP dehydrogenase, UDP-N-acetylglucosamine-2-epimerase, aspartokinase, phosphoribosylformylglycinamidine cyclo-ligase, malate Na (+) symporter and hypothetical protein. When mice were immunized with an attenuated mutant strain into which IMP dehydrogenase had been inserted with a transposon, they were protected against V. vulnificus infection. In this study, we demonstrated that the STM method can be used to search for the virulence genes of V. vulnificus.

摘要

创伤弧菌是免疫功能低下人群原发性败血症、伤口感染和肠胃炎的病原体。在本研究中,采用基因标签诱变技术(STM)来鉴定创伤弧菌的毒力基因。利用STM共构建了6480个突变体,并将其分为81组(输入池);每组中的每个突变体都被赋予一个不同的标签。将每个输入池腹腔注射到铁过载小鼠体内,并从心脏采集的血液样本中收集体内存活的突变体(输出池)。从混合的输入池或输出池的基因组DNA中,制备针对标签区域的地高辛标记DNA探针,并用于点杂交。30个初步减毒的突变体被阴性选择,这些突变体与输入探针杂交清晰,但与输出探针杂交微弱。30个突变体中有11个的致死剂量降低到1/100以上;其中,2个的致死剂量降低到低至1/100000。11个减毒突变体中插入转座子的基因分别是IMP脱氢酶、UDP-N-乙酰葡糖胺-2-表异构酶、天冬氨酸激酶、磷酸核糖甲酰甘氨脒环化连接酶、苹果酸Na(+)同向转运体和假定蛋白。当用转座子插入IMP脱氢酶的减毒突变株免疫小鼠时,它们受到了创伤弧菌感染的保护。在本研究中,我们证明了STM方法可用于寻找创伤弧菌的毒力基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa4f/4527504/cee6404e97f5/jvms-77-823-g001.jpg

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