Darmstadt G L, Mentele L, Podbielski A, Rubens C E
Departments of Pediatrics, University of Washington School of Medicine, Seattle, Washington 98105, USA.
Infect Immun. 2000 Mar;68(3):1215-21. doi: 10.1128/IAI.68.3.1215-1221.2000.
To evaluate the role of putative group A streptococcal virulence factors in the initiation of skin infections, we compared the adherence of a wild-type M49-protein skin-associated strain to that of a series of 16 isogenic mutants created by insertional inactivation of virulence genes. None of the mutants, including the M-protein-deficient (emm mutant) strain, displayed reduced adherence to early-passage cultured human keratinocytes, but adherence of the mutant lacking hyaluronic acid capsule expression (has mutant) was increased 13-fold. In contrast, elimination of capsule expression in M2-, M3-, and M18-protein has mutants increased adherence only slightly (1.3- to 2.3-fold) compared to their respective wild-type strains. A mutant with inactivation of both emm and has displayed high-level adherence (34.9 +/- 4.1%) equal to that of the has mutant strain (40.7 + 8.0%), confirming the lack of involvement of M49 protein in attachment. Moreover, adherence of the M49-protein-deficient (emm mutant) and wild-type strains was increased to the same level (57 and 55%, respectively) following enzymatic digestion of their hyaluronic acid capsule. Adherence of mutants lacking oligopeptide permease (Opp) expression was increased 3.8- to 5.5-fold, in association with decreased cell-associated hyaluronic acid capsule. Finally, soluble CD46 failed to inhibit adherence of M49- and M52-serotype skin strains. We conclude that (i) bacterial M protein and keratinocyte CD46 do not mediate adherence of M49 skin-associated Streptococcus pyogenes to epidermal keratinocytes, (ii) hyaluronic acid capsule impedes the interaction of bacterial adhesins with keratinocyte receptors, (iii) modulation of capsule expression may be important in the pathogenesis of skin infections, and (iv) the molecular interactions in attachment of skin strains of S. pyogenes to keratinocytes are unique and remain unidentified.
为评估推定的A组链球菌毒力因子在皮肤感染起始中的作用,我们比较了野生型M49蛋白皮肤相关菌株与通过毒力基因插入失活产生的一系列16个同基因突变体的黏附情况。包括M蛋白缺陷(emm突变体)菌株在内的所有突变体,对早期传代培养的人角质形成细胞的黏附均未降低,但缺乏透明质酸荚膜表达的突变体(has突变体)的黏附增加了13倍。相比之下,M2 -、M3 -和M18蛋白has突变体中荚膜表达的消除与各自野生型菌株相比,仅使黏附略有增加(1.3至2.3倍)。一个emm和has均失活的突变体表现出高水平的黏附(34.9 +/- 4.1%),与has突变体菌株(40.7 + 8.0%)相当,证实M49蛋白不参与黏附。此外,M49蛋白缺陷(emm突变体)和野生型菌株的透明质酸荚膜经酶消化后,黏附增加到相同水平(分别为57%和55%)。缺乏寡肽通透酶(Opp)表达的突变体的黏附增加了3.8至5.5倍,同时细胞相关的透明质酸荚膜减少。最后,可溶性CD46未能抑制M49和M52血清型皮肤菌株的黏附。我们得出结论:(i)细菌M蛋白和角质形成细胞CD46不介导M49皮肤相关化脓性链球菌与表皮角质形成细胞的黏附;(ii)透明质酸荚膜阻碍细菌黏附素与角质形成细胞受体的相互作用;(iii)荚膜表达调控在皮肤感染发病机制中可能很重要;(iv)化脓性链球菌皮肤菌株与角质形成细胞黏附中的分子相互作用是独特的,仍未明确。