首页> 外文期刊>Infection and immunity >Characterization of porin and ompR mutants of a virulent strain of Salmonella typhimurium: ompR mutants are attenuated in vivo.
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Characterization of porin and ompR mutants of a virulent strain of Salmonella typhimurium: ompR mutants are attenuated in vivo.

机译:鼠伤寒沙门氏菌强毒株的孔蛋白和ompR突变体的表征:ompR突变体在体内减弱。

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The ompC, ompD, and ompF genes encode the three major porins of Salmonella typhimurium. ompR encodes a positive regulator required for the expression of ompC and ompF. Transposon-generated mutations in ompC, ompD, ompF, and ompR were introduced into the S. typhimurium mouse virulent strain SL1344 by P22-mediated transduction. Following preliminary characterization in vitro, the strains were used to challenge BALB/c mice by using the oral or intravenous route. Strains harboring ompC or ompF mutations were as virulent as SL1344 after oral challenge. Strains harboring ompD mutations had a slight reduction in virulence. In contrast, ompR mutants failed to kill BALB/c mice after oral challenge and the intravenous 50% lethal dose was reduced by approximately 10(5). The ompR mutants persisted in murine tissues for several weeks following oral or intravenous challenge. Furthermore, mice orally immunized with these ompR mutant strains were well protected against challenge with virulent SL1344.
机译:ompC,ompD和ompF基因编码鼠伤寒沙门氏菌的三种主要孔蛋白。 ompR编码表达ompC和ompF所需的正调节子。转座子在ompC,ompD,ompF和ompR中产生的突变通过P22介导的转导被引入鼠伤寒沙门氏菌鼠毒性菌株SL1344。在体外初步表征后,通过口服或静脉内途径将菌株用于攻击BALB / c小鼠。口服攻击后,带有ompC或ompF突变的菌株的毒力与SL1344一样。带有ompD突变的菌株的毒力略有降低。相反,ompR突变体在口服攻击后未能杀死BALB / c小鼠,静脉内50%致死剂量降低了约10(5)。口服或静脉内攻击后,ompR突变体在鼠类组织中持续存在数周。此外,用这些ompR突变株口服免疫的小鼠得到了很好的保护,可以抵抗强毒SL1344的攻击。

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