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Induction of deletion mutation onompR gene ofSalmonella enterica serovar Typhi isolates from asymptomatic typhoid carriers to evolve attenuated strains for vaccine development

机译:诱导无症状伤寒沙门氏菌鼠伤寒沙门氏菌的突变突变型onompR基因进化为疫苗开发用减毒株

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Objective:To develop attenuated strains ofSalmonella enterica serovar Typhi(S. typhi) for the candidate vaccine by osmolar stress.Methods:S. typhiSS3 andSS5 strains were isolated from asymptomatic typhoid carriers inNamakkal,TamilNadu,India.Both strains were grown inLB (LuriaBertani) medium supplemented with various concentration ofNaCl(0.1-0.7M) respectively. The effect of osmolar stress was determined at molecular level byPCR usingMGR06 andMGR 07 primers corresponding to ompR with chromosomalDNA of S. typhiSS3 andSS5 strains. Attenuation by osmolar stress results in deletion mutation of theS. typhi strains was determined by agglutination assays, precipitation method,SDSPAGE analysis and by animal models. Results:The799 bp amplifiedompRgene product from wild typeS. typhiSS3 andSS5 illustrate the presence of virulent gene.Interestingly, there was only a282 bp amplified product fromS. typhiSS3 andSS5 grown in the presence of0.5,0.6 and0.7MNaCl.This illustrates the occurrence of deletion mutation inompRgene at high concentration ofNaCl.Furthermore, both the wild-type and mutantS. typhi outer membraneSDS-PAGE profile reveals the differences in the expression ofompF,ompC andompA proteins.In mice, wild type and mutant strains lethal dose (LD50) were determined.The mice died within72 h when both the wild type strains were injected intraperitoneally with3 logCFU.mL-1.When the mice were injected with the mutants in same dosage, no clinical symptoms were observed; whereas the serum antibody titre was elicited within two weeks indicated that the mutants have the ability to induce protective humoral immune response.These results suggest thatS. typhiSS3 andSS5 may be used as good candidate strains for the development of live attenuated vaccine against salmonellosis.Conclusions:This study demonstrates that theS. typhistrains were attenuated and could be good vaccine candidates in future.
机译:目的:通过渗透压法研制减毒鼠伤寒沙门氏菌伤寒沙门氏菌作为候选疫苗。从印度泰米尔纳德邦纳马卡尔的无症状伤寒携带者中分离出typhiSS3和SS5菌株。两种菌株均在分别添加了不同浓度NaCl(0.1-0.7M)的LB(LuriaBertani)培养基中生长。使用与鼠伤寒沙门氏菌SS3和SS5菌株的染色体DNA对应的ompR的MGR06和MGR 07引物,通过PCR在分子水平上确定了渗透压的影响。渗透压应力引起的衰减导致S的缺失突变。通过凝集分析,沉淀法,SDSPAGE分析和动物模型确定伤寒菌株。结果:来自野生型S的799bp扩增的ompR基因产物。 typhiSS3和SS5证明了有毒基因的存在。有趣的是,只有S282的282 bp扩增产物。 typhiSS3和SS5在0.5、0.6和0.7MNaCl的存在下生长。这说明在高浓度的NaCl中出现了inompR基因的缺失突变。此外,野生型和突变型S都存在。伤寒外膜SDS-PAGE图谱显示了ompF,ompC和ompA蛋白表达的差异。测定了小鼠的野生型和突变株致死剂量(LD50)。在两种野生型菌株腹膜内注射3 logCFU后72小时内死亡。 .mL-1。当给小鼠注射相同剂量的突变体时,未观察到临床症状;而在两周之内引起的血清抗体滴度表明该突变体具有诱导保护性体液免疫反应的能力。 typhiSS3和SS5可以作为开发抗沙门氏菌减毒活疫苗的良好候选菌株。伤寒菌减毒了,将来可能成为很好的疫苗候选者。

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  • 来源
    《亚太热带医药杂志(英文版)》 |2014年第012期|933-939|共7页
  • 作者单位

    Centre for Biotechnology, Muthayammal College of Arts & Science, Rasipuram-637 408, Tamil Nadu, India;

    Department of Marine Biotechnology, Bharathidasan University, Tiruchirappalli-620 024, Tamil Nadu, India;

    Department of Biotechnology, Vivekanandha College of Engineering for Women, Tiruchengode-637 205. Tamil Nadu, India;

    Department of Zoology, Arignar Anna Government Arts College, Namakkal-637 001, Tamil Nadu, India;

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