Zhang Xiaoyan, Jiang Xiaowu, Yang Ling, Fang Lihua, Shen Hongxia, Lu Xingmeng, Fang Weihuan
Institute of Preventive Veterinary Medicine and Zhejiang Provincial Key Laboratory of Preventive Veterinary Medicine, Zhejiang University, Hangzhou 310058, P.R. China.
J Microbiol Biotechnol. 2015 Jun;25(6):771-81. doi: 10.4014/jmb.1408.08085.
To examine if the molecular chaperone DnaK operon proteins of Streptococcus suis type 2 (SS2) are involved in adhesion to host cells, the abundance values of these proteins from the surface of two SS2 strains of different adhesion capability were compared. Their roles in growth and adhesion to human laryngeal epithelial cell line HEp-2 cells were investigated on SS2 strain HA9801 and its mutants with DnaK operon genes partially knocked-out (PKO mutant) under heat stress. The major difference was that DnaJ was more abundant in strain HA9801 than in strain JX0811. Pretreatment of the bacteria with hyperimmune sera to DnaJ, but not with those to other proteins, could significantly reduce SS2 adhesion to HEp-2 cells. PKO of dnaJ g ene resulted in decreased SS2 growth at 37 °C and 42 °C, and reduced its adhesion to HEp-2 cells. The wild-type strain stressed at 42 °C had increased expression of DnaJ on its surface and elevated adhesion to HEp-2 cells, which was also inhibitable by DnaJ specific antiserum. These results indicate that the DnaJ of S. suis type 2 is important not only for thermotolerance but also for adhesion to host cells. Because DnaJ expression is increased upon temperature upshift with increased exposure on the bacterial surface, the febrile conditions of the cases with systemic infections might help facilitate bacterial adhesion to host cells. DnaJ could be one of the potential candidates as a subunit vaccine because of its good immunogenicity.
为了研究猪链球菌2型(SS2)的分子伴侣DnaK操纵子蛋白是否参与对宿主细胞的黏附,比较了来自两种黏附能力不同的SS2菌株表面这些蛋白的丰度值。在热应激条件下,对SS2菌株HA9801及其DnaK操纵子基因部分敲除的突变体(PKO突变体)研究了它们在生长以及对人喉上皮细胞系HEp-2细胞黏附方面的作用。主要差异在于,DnaJ在菌株HA9801中比在菌株JX0811中更丰富。用抗DnaJ的超免疫血清预处理细菌,而不是用抗其他蛋白的血清预处理,可显著降低SS2对HEp-2细胞的黏附。dnaJ基因的PKO导致SS2在37℃和42℃下生长减少,并降低其对HEp-2细胞的黏附。在42℃应激的野生型菌株其表面DnaJ表达增加,对HEp-2细胞的黏附增强,这也可被DnaJ特异性抗血清抑制。这些结果表明,猪链球菌2型的DnaJ不仅对耐热性很重要,而且对宿主细胞黏附也很重要。由于温度升高时DnaJ表达增加且在细菌表面的暴露增加,全身性感染病例的发热状况可能有助于促进细菌对宿主细胞的黏附。由于DnaJ具有良好的免疫原性,它可能是亚单位疫苗的潜在候选之一。