Revised definition of Actinobacillus sensu stricto isolated from animals -: A review with special emphasis on diagnosis

被引:59
作者
Christensen, H [1 ]
Bisgaard, M [1 ]
机构
[1] Royal Vet & Agr Univ, Dept Vet Microbiol, DK-1870 Frederiksberg C, Denmark
关键词
taxonomy; Actinobacillus; diagnostic tests; 16S rRNA; PCR;
D O I
10.1016/j.vetmic.2003.12.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The taxonomy of the members of the genus Actinobacillus associated with animals has been reviewed with focus on classification and identification including molecular based characterization, typing and identification. Out of the 22 species or species like taxa reported as Actinobacillus, 19 are associated with animals. When classified on the basis of 16S rRNA sequence based phylogenetic analysis, DNA-DNA hybridizations and phenotypic analysis, Actinobacillus sensu stricto is restricted to include A. lignieresii, A. pleuropneumoniae, A. equuli subsp. equuli, A. equuli subsp. haemolyticus (taxon 11 of Bisgaard), A. hominis, A. suis, A. ureae, A. arthritidis (taxon 9 of Bisgaard), Actinobacillus genomospecies I and 2 and the taxa 8 and 26 of Bisgaard. The remaining I I species of Actinobacillus are unrelated to A. sensu stricto and should consequently be grouped with other genera or be renamed as new genera depending on new data. Identification of members of Actinobacillus at species level is possible through phenotypic characterization combined with information on host of isolation. PCR tests are available for specific detection of A. pleuropneumoniae. Only A. pleuropneumoniae is presently considered as a primary pathogen. Based on different types of RTX genes it is possible to PCR type A. pleuropneumoniae to serotype level. PCR might also be used for the specific detection of A. equili subsp. haemolyticus. Epidemiological investigations and surveillance have so far included serotyping, multi,locus enzyme electrophoresis (MLEE), ribotyping and restriction fragment length profiling. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:13 / 30
页数:18
相关论文
共 106 条
[1]   Proposal of Histophilus somni gen. nov., sp nov for the three species incertae sedis 'Haemophilus somnus', 'Haemophilus agni' and 'Histophilus ovis' [J].
Angen, O ;
Ahrens, P ;
Kuhnert, P ;
Christensen, H ;
Mutters, R .
INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY, 2003, 53 :1449-1456
[2]   Taxonomic relationships of the [Pasteurella] haemolytica complex as evaluated by DNA-DNA hybridizations and 16S rRNA sequencing with proposal of Mannheimia haemolytica gen. nov., comb, nov., Mannheimia granulomatis comb, nov., Mannheimia glucosida sp. nov., Mannheimia ruminalis sp. nov., and Mannheimia varigena sp. nov. [J].
Angen, O ;
Mutters, R ;
Caugant, DA ;
Olsen, JE ;
Bisgaard, M .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1999, 49 :67-86
[3]  
[Anonymous], COWANS STEELS MANUAL
[4]   ACTINOBACILLOSIS IN JOINTS OF RABBITS [J].
ARSECULERATNE, SN .
JOURNAL OF COMPARATIVE PATHOLOGY AND THERAPEUTICS, 1962, 72 (01) :33-&
[5]   Iron acquisition by Actinobacillus suis:: identification and characterization of transferrin receptor proteins and encoding genes [J].
Bahrami, F ;
Ekins, A ;
Niven, DF .
VETERINARY MICROBIOLOGY, 2003, 94 (01) :79-92
[6]   Association of Actinobacillus pleuropneumoniae capsular polysaccharide with virulence in pigs [J].
Bandara, AB ;
Lawrence, ML ;
Veit, HP ;
Inzana, TJ .
INFECTION AND IMMUNITY, 2003, 71 (06) :3320-3328
[7]  
BAUM KH, 1984, J AM VET MED ASSOC, V185, P792
[8]   RTX TOXIN GENOTYPES AND PHENOTYPES IN ACTINOBACILLUS-PLEUROPNEUMONIAE FIELD STRAINS [J].
BECK, M ;
VANDENBOSCH, JF ;
JONGENELEN, IMCA ;
LOEFFEN, PLW ;
NIELSEN, R ;
NICOLET, J ;
FREY, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (11) :2749-2754
[9]   TOXICITY OF HEMOPHILUS-PLEUROPNEUMONIAE FOR PORCINE LUNG MACROPHAGES, PERIPHERAL-BLOOD MONOCYTES, AND TESTICULAR CELLS [J].
BENDIXEN, PH ;
SHEWEN, PE ;
ROSENDAL, S ;
WILKIE, BN .
INFECTION AND IMMUNITY, 1981, 33 (03) :673-676
[10]   BIOLOGICAL CHARACTERIZATION OF ACTINOBACILLUS SPECIES AND PASTEURELLA-UREAE [J].
BERCOVIER, H ;
ESCANDE, F ;
GRIMONT, PAD .
ANNALES DE MICROBIOLOGIE, 1984, A135 (02) :203-218