Russo T A, Sharma G, Brown C R, Campagnari A A
Department of Medicine, State University of New York at Buffalo 14215.
Infect Immun. 1995 Apr;63(4):1263-9. doi: 10.1128/iai.63.4.1263-1269.1995.
The O-specific antigen in extraintestinal isolates of Escherichia coli is believed to be an important virulence factor. To assess its role in the pathogenic process, proven isogenic derivatives with either a complete (CP921) or nearly complete (CP920) deficiency of the O4 antigen were obtained by TnphoA'1-mediated transposon mutagenesis of an O4/K54/H5 blood isolate (CP9). By utilizing a previously reported isogenic K54 capsule-deficient derivative (CP9.137), additional isogenic derivatives deficient in both the K54 capsular antigen and either all (CP923) or nearly all (CP922) of the O4 antigen were also constructed. These strains and their wild-type parent were evaluated in vitro for serum sensitivity and in vivo by intraperitoneal challenge of outbred mice. The complete or nearly complete loss of the O4 antigen (CP920 and CP921) resulted in only a minor increase in serum sensitivity. In contrast, CP9.137 had a significant increase in serum sensitivity, and CP922 and CP923 were extremely serum sensitive. When tested in vivo, the complete or nearly complete loss of the O4 antigen resulted in a small but significant increase (P < or = 0.05), not the expected decrease, in virulence compared with its wild-type parent. In contrast, CP9.137 and CP922 were significantly less virulent (P < or = 0.05). These studies do not exclude a role for the O4 antigen moiety of lipopolysaccharide in the pathogenesis of extraintestinal E. coli infection; however, they demonstrate that the O4 antigen plays only a minor role in serum resistance in vitro and that its loss does not diminish and perhaps enhances the virulence of CP9 in vivo after intraperitoneal challenge.
大肠杆菌肠外分离株中的O特异性抗原被认为是一种重要的毒力因子。为了评估其在致病过程中的作用,通过对一株O4/K54/H5血源分离株(CP9)进行TnphoA'1介导的转座子诱变,获得了O4抗原完全缺失(CP921)或几乎完全缺失(CP920)的经证实的同基因衍生物。利用先前报道的K54荚膜缺失同基因衍生物(CP9.137),还构建了同时缺失K54荚膜抗原和全部(CP923)或几乎全部(CP922)O4抗原的其他同基因衍生物。对这些菌株及其野生型亲本进行了体外血清敏感性评估,并通过对远交系小鼠进行腹腔注射来评估其体内情况。O4抗原的完全或几乎完全缺失(CP920和CP921)仅导致血清敏感性略有增加。相比之下,CP9.137的血清敏感性显著增加,而CP922和CP923对血清极为敏感。在体内试验时,与野生型亲本相比,O4抗原的完全或几乎完全缺失导致毒力有小幅但显著的增加(P≤0.05),而不是预期的降低。相比之下,CP9.137和CP922的毒力显著降低(P≤0.05)。这些研究并不排除脂多糖的O4抗原部分在肠外大肠杆菌感染发病机制中的作用;然而,它们表明O4抗原在体外血清抗性中仅起次要作用,并且其缺失不会降低,甚至可能增强CP9在腹腔注射后的体内毒力。