Herrington D A, Hall R H, Losonsky G, Mekalanos J J, Taylor R K, Levine M M
Department of Medicine, University of Maryland School of Medicine, Baltimore 21201.
J Exp Med. 1988 Oct 1;168(4):1487-92. doi: 10.1084/jem.168.4.1487.
Isogenic mutant strains of V. cholerae O1 lacking elements of a genetic regulon controlled by toxR and implicated in virulence were tested in volunteers. A deletion mutation in ctxA, the gene encoding the A subunit of cholera toxin, markedly attenuated disease symptoms without affecting intestinal colonization. Deletion of toxR, the gene encoding the cholera toxin-positive regulatory protein resulted in a diminution in colonizing capacity. A deletion mutation in tcpA, encoding the major subunit of the toxin coregulated pilus (regulated by toxR), abolished the colonizing capacity of this strain. These results show for the first time the role of a specific pilus structure in colonization of the human intestine by V. cholerae O1 and exemplify the significance of a genetic regulon in pathogenesis.
对缺乏由toxR控制且与毒力有关的遗传调控子元件的霍乱弧菌O1同基因突变菌株在志愿者身上进行了测试。ctxA(编码霍乱毒素A亚基的基因)中的缺失突变显著减轻了疾病症状,而不影响肠道定植。toxR(编码霍乱毒素阳性调节蛋白的基因)的缺失导致定植能力下降。tcpA(编码毒素共调节菌毛主要亚基,受toxR调节)中的缺失突变消除了该菌株的定植能力。这些结果首次表明了特定菌毛结构在霍乱弧菌O1定植人肠道中的作用,并例证了遗传调控子在发病机制中的重要性。