The challenge of detecting herds sub-clinically infected with Actinobacillus pleuropneumoniae

被引:62
作者
Gottschalk, Marcelo [1 ]
机构
[1] Univ Montreal, Fac Vet Med, Dept Pathol & Microbiol, Swine & Poultry Infect Dis Ctr CRIPA,Grp Rech Mal, St Hyacinthe, PQ J2S 2M2, Canada
关键词
Actinobacillus pleuropneumoniae; Carrier animals; Serology; Serotyping; Direct detection; ELISA; PCR; LINKED-IMMUNOSORBENT-ASSAY; POLYMERASE-CHAIN-REACTION; OUTER-MEMBRANE LIPOPROTEIN; CAPSULAR POLYSACCHARIDE ANTIGENS; INDEPENDENT ELISA ANTIGENS; MULTIPLEX PCR ASSAY; APXIVA GENE; PIG HERDS; ANTIMICROBIAL RESISTANCE; PASTEURELLA-MULTOCIDA;
D O I
10.1016/j.tvjl.2015.06.016
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The introduction into a naive herd of animals sub-clinically infected with Actinobacillus pleuropneumoniae (App) is frequently the cause of clinical pleuropneumonia and the identification of such infected herds is a priority in the control of disease. Different serological tests for App have been developed and a number of these are routinely used. Some are species-specific whereas others identify more specifically the serotype/serogroup involved which requires updated information about important serotypes recovered from diseased pigs in a given area/country. Serotyping methods based on molecular techniques have been developed lately and are ready to be used by most diagnostic laboratories. When non-conclusive serological results are obtained, direct detection of App from tonsils is sometimes attempted. This review addresses different techniques and approaches used to monitor herds sub-clinically infected by this important pathogen. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:30 / 38
页数:9
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