Kachlany S C, Fine D H, Figurski D H
Department of Microbiology, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.
Infect Immun. 2000 Nov;68(11):6094-100. doi: 10.1128/IAI.68.11.6094-6100.2000.
Actinobacillus actinomycetemcomitans, the etiologic agent for localized juvenile periodontitis and certain other human infections, such as endocarditis, expresses a leukotoxin that acts on polymorphonuclear leukocytes and macrophages. Leukotoxin is a member of the highly conserved repeat toxin (RTX) family of bacterial toxins expressed by a variety of pathogenic bacteria. While the RTX toxins of other bacterial species are secreted, the leukotoxin of A. actinomycetemcomitans is thought to remain associated with the bacterial cell. We have examined leukotoxin production and localization in rough (adherent) and smooth (nonadherent) strains of A. actinomycetemcomitans. We found that leukotoxin expressed by the rough, adherent, clinical isolate CU1000N is indeed cell associated, as expected. However, we were surprised to find that smooth, nonadherent strains of A. actinomycetemcomitans, including Y4, JP2 (a strain expressing a high level of toxin), and CU1060N (an isogenic smooth variant of CU1000N), secrete an abundance of leukotoxin into the culture supernatants during early stages of growth. After longer times of incubation, leukotoxin disappears from the supernatants, and its loss is accompanied by the appearance of a number of low-molecular-weight polypeptides. The secreted leukotoxin is active, as evidenced by its ability to kill HL-60 cells in vitro. We found that the growth phase and initial pH of the growth medium significantly affect the abundance of secreted leukotoxin, and we have developed a rapid (<2 h) method to partially purify large amounts of leukotoxin. Remarkably, mutations in the tad genes, which are required for tight nonspecific adherence of A. actinomycetemcomitans to surfaces, cause leukotoxin to be released from the bacterial cell. These studies show that A. actinomycetemcomitans has the potential to secrete abundant leukotoxin. It is therefore appropriate to consider a possible role for leukotoxin secretion in the pathogenesis of A. actinomycetemcomitans.
伴放线放线杆菌是局限性青少年牙周炎及某些其他人类感染(如心内膜炎)的病原体,它表达一种作用于多形核白细胞和巨噬细胞的白细胞毒素。白细胞毒素是多种病原菌表达的高度保守的重复毒素(RTX)家族的成员。虽然其他细菌物种的RTX毒素是分泌型的,但人们认为伴放线放线杆菌的白细胞毒素仍与细菌细胞相关。我们研究了伴放线放线杆菌粗糙(黏附性)菌株和平滑(非黏附性)菌株中白细胞毒素的产生和定位。我们发现,正如预期的那样,粗糙、黏附性临床分离株CU1000N表达的白细胞毒素确实与细胞相关。然而,我们惊讶地发现,伴放线放线杆菌的平滑、非黏附性菌株,包括Y4、JP2(一种表达高水平毒素的菌株)和CU1060N(CU1000N的同基因平滑变体),在生长早期会向培养上清液中分泌大量白细胞毒素。培养较长时间后,白细胞毒素从上清液中消失,其消失伴随着一些低分子量多肽的出现。分泌的白细胞毒素具有活性,体外杀伤HL-60细胞的能力证明了这一点。我们发现生长阶段和生长培养基的初始pH值显著影响分泌的白细胞毒素的丰度,并且我们开发了一种快速(<2小时)方法来部分纯化大量白细胞毒素。值得注意的是,伴放线放线杆菌紧密非特异性黏附于表面所需的tad基因发生突变会导致白细胞毒素从细菌细胞中释放出来。这些研究表明,伴放线放线杆菌有分泌大量白细胞毒素的潜力。因此,有必要考虑白细胞毒素分泌在伴放线放线杆菌致病机制中可能发挥的作用。