Leukotoxin confers beta-hemolytic activity to Actinobacillus actinomycetemcomitans

被引:73
作者
Balashova, NV [1 ]
Crosby, JA [1 ]
Al Ghofaily, L [1 ]
Kachlany, SC [1 ]
机构
[1] Univ Med & Dent New Jersey, Dept Oral Biol, New Jersey Dent Sch, Newark, NJ 07103 USA
关键词
D O I
10.1128/IAI.74.4.2015-2021.2006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Actinobacillus actinomycetemcomitans is the etiologic agent of localized aggressive periodontitis, a rapidly progressing oral disease that occurs in adolescents. A. actinomycetemcomitans can also cause systemic disease, including infective endocarditis. In early work on A. actitiontyceteincomitans workers concluded that this bacterium is not beta-hemolytic. More recent reports have suggested that A. actinomycetemcomitans does have the potential to be beta-hemolytic. While growing A. actinomycetemcomitans on several types of growth media, we noticed a beta-hemolytic reaction on media from one manufacturer. Beta-hemolysis occurred on Columbia agar from Accumedia with either sheep or horse blood, but not oil similar media from other manufacturers. A surprising result was that mutants of A. actinomycetemcomitans defective for production of leukotoxin, a toxin that is reportedly highly specific for only human and primate white blood cells, are not beta-hemolytic. Purified leukotoxin was able to lyse sheep and human erythrocytes in vitro. This work showed that in contrast to the accepted view, A. actinomycetemcomitans leukotoxin can indeed destroy erythrocytes and that the production of this toxin results in beta-hemolytic colonies oil solid medium. In light of these results, the diagnostic criteria for clinical identification of A. actinomycetemcomitans and potentially related bacteria should be reevaluated. Furthermore, in studies on A. actinomycetemcomitans leukotoxin workers should now consider this toxin's ability to destroy red blood cells.
引用
收藏
页码:2015 / 2021
页数:7
相关论文
共 42 条
[1]  
Avila-Campos Mario Julio, 1995, Revista do Instituto de Medicina Tropical de Sao Paulo, V37, P215, DOI 10.1590/S0036-46651995000300006
[2]   Periodontal disease and coronary heart disease - A reappraisal of the exposure [J].
Beck, JD ;
Eke, P ;
Heiss, G ;
Madianos, P ;
Couper, D ;
Lin, DM ;
Moss, K ;
Elter, J ;
Offenbacher, S .
CIRCULATION, 2005, 112 (01) :19-24
[3]   Infective endocarditis due to unusual or fastidious microorganisms [J].
Berbari, EF ;
Cockerill, FR ;
Steckelberg, JM .
MAYO CLINIC PROCEEDINGS, 1997, 72 (06) :532-542
[4]  
BERGEY DH, 1994, BERGEYS MANUAL DETE
[5]   ELECTRON IMMUNOCYTOCHEMICAL LOCALIZATION OF ACTINOBACILLUS-ACTINOMYCETEMCOMITANS LEUKOTOXIN [J].
BERTHOLD, P ;
FORTI, D ;
KIEBA, IR ;
ROSENBLOOM, J ;
TAICHMAN, NS ;
LALLY, ET .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 1992, 7 (01) :24-27
[6]   Nonspecific adherence and fibril biogenesis by Actinobacillus actinomycetemcomitans:: TadA protein is an ATPase [J].
Bhattacharjee, MK ;
Kachlany, SC ;
Fine, DH ;
Figurski, DH .
JOURNAL OF BACTERIOLOGY, 2001, 183 (20) :5927-5936
[7]   Taxonomy and virulence of oral spirochetes [J].
Chan, ECS ;
McLaughlin, R .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 2000, 15 (01) :1-9
[8]   Infective endocarditis caused by HACEK microorganisms [J].
Das, M ;
Badley, AD ;
Cockerill, FR ;
Steckelberg, JM ;
Wilson, WR .
ANNUAL REVIEW OF MEDICINE, 1997, 48 :25-33
[9]   Phenotypic variation in Actinobacillus actinomycetemcomitans during laboratory growth:: implications for virulence [J].
Fine, DH ;
Furgang, D ;
Schreiner, HC ;
Goncharoff, P ;
Charlesworth, J ;
Ghazwan, G ;
Fitzgerald-Bocarsly, P ;
Figurski, DH .
MICROBIOLOGY-SGM, 1999, 145 :1335-1347
[10]   Tenacious adhesion of Actinobacillus actinomycetemcomitans strain CU1000 to salivary-coated hydroxyapatite [J].
Fine, DH ;
Furgang, D ;
Kaplan, J ;
Charlesworth, J ;
Figurski, DH .
ARCHIVES OF ORAL BIOLOGY, 1999, 44 (12) :1063-1076