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在鸭疫里默氏菌中开发标记基因随机突变技术以鉴定生存和致病性必需基因。

Development of signature-tagged mutagenesis in Riemerella anatipestifer to identify genes essential for survival and pathogenesis.

机构信息

Shanghai Veterinary Research Institute, the Chinese Academy of Agricultural Sciences, 518 Ziyue Road, Shanghai 200241, China.

Shanghai Veterinary Research Institute, the Chinese Academy of Agricultural Sciences, 518 Ziyue Road, Shanghai 200241, China.

出版信息

Vet Microbiol. 2020 Nov;250:108857. doi: 10.1016/j.vetmic.2020.108857. Epub 2020 Sep 19.

Abstract

Riemerella anatipestifer causes epizootic infectious disease in ducks, geese, turkeys and other birds, and serious economic losses especially to the duck industry. However, little is known about the molecular basis of its pathogenesis. In this study, signature-tagged transposon mutagenesis based on Tn4351 was developed in R. anatipestifer to identify genes essential for survival and pathogenesis. Seventeen tagged Tn4351 random mutation libraries of the R. anatipestifer strain WJ4 containing 5100 mutants were screened for survive using a duckling infection model. Twenty mutants that could not be recovered from the infected ducklings, were identified, and 17 mutated genes were identified by inverse PCR or genome-walking PCR. Of these genes, FIP52_03215, FIP52_04350 and FIP52_09345, were inserted into two mutant strains, and FIP52_03215 and FIP52_03175 were found exclusively on the chromosome of serotype 1 R. anatipestifer strains. Twelve out of 17 genes encoding for proteins were predicted to be involved in amino acid, nucleotide, coenzyme, or lipid transport and metabolism, one gene was predicted to be involved in signal transduction, one gene was predicted to be involved in DNA replication, recombination and repair, the other three genes had an unknown function. Animal experiments showed that the virulence of mutants 16-284, 7-295, 24-231, 9-232 and 19-214 were significantly attenuated compared to that of the wild-type WJ4. Moreover, the median lethal dose of mutant 16-284 was greater than 10 CFU, and its virulence to ducklings was partially restored when it was complemented with the shuttle expression plasmid pRES-FIP52_09345. The results in this study will be helpful to further study the molecular mechanisms of the pathogenesis of R. anatipestifer infection.

摘要

鸭疫里默氏杆菌引起鸭、鹅、火鸡和其他鸟类的爆发性传染病,给养鸭业造成严重的经济损失。然而,人们对其发病机制的分子基础知之甚少。本研究基于 Tn4351 发展了鸭疫里默氏杆菌的标记转座子突变技术,以鉴定生存和发病所必需的基因。利用雏鸭感染模型筛选了包含 5100 个突变体的鸭疫里默氏杆菌 WJ4 菌株的 17 个标记 Tn4351 随机突变文库,以筛选存活的突变体。从感染雏鸭中无法恢复的 20 个突变体被鉴定出来,通过反向 PCR 或基因组步行 PCR 鉴定了 17 个突变基因。其中,FIP52_03215、FIP52_04350 和 FIP52_09345 被插入到两个突变株中,FIP52_03215 和 FIP52_03175 仅存在于 1 型鸭疫里默氏杆菌血清型菌株的染色体上。17 个编码蛋白的基因中,有 12 个预测参与氨基酸、核苷酸、辅酶或脂质的运输和代谢,1 个预测参与信号转导,1 个预测参与 DNA 复制、重组和修复,其他 3 个基因功能未知。动物实验表明,与野生型 WJ4 相比,突变体 16-284、7-295、24-231、9-232 和 19-214 的毒力显著降低。此外,突变体 16-284 的半数致死剂量大于 10 CFU,当用穿梭表达质粒 pRES-FIP52_09345 进行互补时,其对雏鸭的毒力部分恢复。本研究结果将有助于进一步研究鸭疫里默氏杆菌感染发病机制的分子机制。

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