Ansai T, Yu W, Urnowey S, Barik S, Takehara T
Department of Preventive Dentistry, Kyushu Dental College, Manazuru, Kitakyushu, Japan.
Oral Microbiol Immunol. 2003 Dec;18(6):398-400. doi: 10.1046/j.0902-0055.2003.00080.x.
Porphyromonas gingivalis has been isolated from lesions of advanced adult periodontitis, and implicated as a periodontal pathogen. We have previously cloned a novel endopeptidase, designated PepO, from P. gingivalis 381, which exhibited significant homology to human endothelin-converting enzyme (ECE)-1. In order to determine the nature and function of the PepO in the host, a pepO gene-deficient mutant strain was constructed by allelic exchange mutagenesis using the ermF-ermAM cassette. No endopeptidase activity was detected in the pepO-deficient mutant. In addition, adherent HeLa (HEp-2) cells were infected with the mutant and the two wild-type strains for assessment of bacterial invasion by an antibiotic protection assay. The invasion efficiency of the mutant strain was about a quarter of the wild type strains. These results suggest that PepO is involved in the first step, i.e. invasion/lysis of mammalian cell membrane, which affects the kinetics of rate of invasion.
牙龈卟啉单胞菌已从晚期成人牙周炎病变中分离出来,并被认为是一种牙周病原体。我们之前从牙龈卟啉单胞菌381中克隆了一种新型内肽酶,命名为PepO,它与人内皮素转换酶(ECE)-1具有显著同源性。为了确定宿主中PepO的性质和功能,使用ermF-ermAM盒通过等位基因交换诱变构建了pepO基因缺陷突变株。在pepO缺陷突变体中未检测到内肽酶活性。此外,用该突变体和两种野生型菌株感染贴壁的HeLa(HEp-2)细胞,通过抗生素保护试验评估细菌的侵袭情况。突变株的侵袭效率约为野生型菌株的四分之一。这些结果表明PepO参与了第一步,即哺乳动物细胞膜的侵袭/裂解,这影响了侵袭速率的动力学。