中国畜牧兽医 ›› 2021, Vol. 48 ›› Issue (12): 4597-4606.doi: 10.16431/j.cnki.1671-7236.2021.12.028

• 预防兽医 • 上一篇    下一篇

鼠伤寒沙门菌Hfq依赖型sRNA GcvB对Ⅲ型分泌系统相关基因调控作用的研究

段世宇1,2, 杨阳1,2, 张家莉1,2, 潘永1,2, 杨琦1,2,3, 周碧君1,2,3   

  1. 1. 贵州大学动物科学学院, 贵阳 550025;
    2. 贵州省动物疫病研究室, 贵阳 550025;
    3. 贵州省动物疫病与兽医公共卫生重点实验室, 贵阳 550025
  • 收稿日期:2021-04-12 出版日期:2021-12-20 发布日期:2021-12-02
  • 通讯作者: 杨琦 E-mail:yangqinmg@163.com
  • 作者简介:段世宇(1995-),女,贵州盘州人,硕士,研究方向:病原微生物学,E-mail:1440740962@qq.com
  • 基金资助:
    国家自然科学基金(31760740、31602065)

Study on Hfq Dependent sRNA GcvB of Salmonella Typhimurium on the Regulation of Type Ⅲ Secretory System Related Genes

DUAN Shiyu1,2, YANG Yang1,2, ZHANG Jiali1,2, PAN Yong1,2, YANG Qi1,2,3, ZHOU Bijun1,2,3   

  1. 1. College of Animal Science, Guizhou University, Guiyang 550025, China;
    2. Laboratory of Animal Diseases in Guizhou Province, Guiyang 550025, China;
    3. Key Laboratory of Animal Diseases and Veterinary Public Health of Guizhou Province, Guiyang 550025, China
  • Received:2021-04-12 Online:2021-12-20 Published:2021-12-02

摘要: 试验旨在研究鼠伤寒沙门菌伴侣蛋白Hfq依赖型sRNA GcvB对spaPinvC基因 mRNA所具有的调控作用。利用λ-Red同源重组技术构建spaPinvC基因LacZ融合菌株,并利用P22噬菌体转导技术分别构建GcvBHfq基因单缺失和双缺失菌株及GcvB功能区域缺失株,通过β-半乳糖苷酶活性试验测定在伴侣蛋白Hfq、sRNA GcvB及Hfq & GcvB缺失株中spaPinvC基因β-半乳糖核苷酶活性;实时荧光定量PCR测定spaPinvC基因mRNA表达量。结果显示,利用P22噬菌体转导技术成功构建出ΔGcvB(696 bp)、ΔHfq(2 369 bp)、ΔGcvBΔHfq(2 369/696 bp)、GcvBΔR1(757 bp)、GcvBΔR2(951 bp)、GcvBΔR3(986 bp)缺失株;β-半乳糖苷酶活性检测结果显示,与野生型菌株相比,spaP基因β-半乳糖核苷酶活性在缺失株GcvBΔR2、GcvBΔR3中极显著下调(P<0.01),在缺失株ΔGcvB、ΔHfq、ΔGcvBΔHfq、GcvBΔR1中极显著上调(P<0.01);而invC基因β-半乳糖核苷酶活性在缺失株GcvBΔR2、GcvBΔR3中极显著下调(P<0.01),在缺失株GcvBΔR1中显著下调(P<0.05),在缺失株ΔGcvB、ΔHfq、ΔGcvBΔHfq中极显著上调(P<0.01)。实时荧光定量PCR结果显示,与野生型菌株相比,spaP基因在ΔGcvB、ΔHfq、ΔGcvBΔHfq和GcvBΔR1缺失菌株中转录水平极显著上调(P<0.01),而GcvBΔR2缺失菌株转录水平极显著下调(P<0.01),GcvBΔR3缺失菌株转录水平显著下调(P<0.05),invC基因ΔGcvB、ΔHfq、ΔGcvBΔHfq缺失菌株转录水平极显著上调(P<0.01),GcvBΔR1、GcvBΔR2缺失菌株均极显著下调(P<0.01),GcvBΔR3缺失菌株均显著下调(P<0.05)。通过以上试验结果得出,sRNA GcvB及伴侣蛋白Hfq对invCspaP基因存在一定的调控作用。本试验结果为sRNA GcvB及伴侣蛋白Hfq调控提供了理论依据,丰富了GcvB的靶基因数目。

关键词: 鼠伤寒沙门菌; sRNA; 同源重组; Hfq; Ⅲ型分泌系统

Abstract: The purpose of this experiment was to study the regulatory effect of Salmonella Typhimurium chaperone protein Hfq-dependent sRNA GcvB on spaP and invC gene mRNA.λ-Red homologous recombination technology was used to construct spaP and invC genes LacZ fusion strains, P22 phage transduction technology was used to construct GcvB and Hfq genes single deletion and double deletion strains and GcvB functional region deletion strains.β-galactosinosidase activity experiment was performed to determine the protein expression activity of spaP and invC genes in chaperone proteins Hfq, sRNA GcvB and Hfq & GcvB deletion strains.Real-time PCR was used to determine the mRNA expression of spaP and invC genes.The results showed that P22 phage transduction technology successfully constructed ΔGcvB (696 bp), ΔHfq (2 369 bp), ΔGcvBΔHfq (2 369/696 bp), GcvBΔR1 (757 bp), GcvBΔR2 (951 bp), GcvBΔR3 (986 bp) deletion strains.β-galactosinosidase activity test results showed that compared with wild-type strains, the β-galactosinosidase activity of spaP gene was extremely significantly down-regulated in the deleted strains GcvBΔR2 and GcvBΔR3 (P<0.01), and the β-galactosinosidase activity of the invC gene was extremely significantly up-regulated in the deleted strains ΔGcvB, ΔHfq, ΔGcvBΔHfq and GcvBΔR1 (P<0.01).The invC gene was extremely significantly down-regulated in the deletion strain GcvBΔR2 and GcvBΔR3 protein activity (P<0.01), and the GcvBΔR1 protein activity was significantly down-regulated in the deletion strain (P<0.05).The protein activity in the deletion strains ΔGcvB, ΔHfq and ΔGcvBΔHfq was extremely significantly up-regulated (P<0.01).Real-time PCR results showed that compared with the wild-type strain, the transcription level of the spaP gene in ΔHfq, ΔGcvB, ΔGcvBΔHfq and GcvBΔR1 deletion strains was extremely significantly up-regulated (P<0.01), while the transcription level of GcvBΔR2 deletion strain was extremely significantly down-regulated (P<0.01).The transcription level of GcvBΔR3 deletion strains was significantly down-regulated (P<0.05), the transcription level of invC gene ΔHfq, ΔGcvBΔHfq and ΔGcvB deletion strains was extremely significant up-regulated (P<0.01), GcvBΔR1 and GcvBΔR2 deletion strains were all extremely significantly downward-regulated (P<0.01), GcvBΔR3 deletion strains were all significant down-regulated (P<0.05).According to the above experimental results, sRNA GcvB and chaperonin Hfq had a certain regulatory effect on invC and spaP genes.This experiment provided a theoretical basis for the regulation of sRNA GcvB and chaperonin Hfq, and enriched the number of target genes of GcvB.

Key words: Salmonella Typhimurium; sRNA; homologous recombination; Hfq; type Ⅲ secretion system

中图分类号: