도축돈에서의 Actinobacillus pleuropneumoniae 분리, 동정 및 감염률 조사
Isolation, identification and serological investigation of Actinobacillus pleuropneumoniae in slaughtered pigs
0
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
This study was conducted to isolate the Actinobacillus pleuropneumoniae (APP) and to find out the dis-tribution of 15 serovars mainly in southern Gyeonggi province, Korea. From July 2011 to Nov. 2012, a total of 2,204 slaughter pigs (110 herds) were inspected for evaluation of APP like pneumonic lesions. 48 (33.8%) APP strains were isolated from the 142 lungs and identified using PCR assays (cps, apx/omlA, biovar). Consequently, the serotype ratio were as in the following; type2 41.7% (n=20), type5 33.3% (n=16), type12 10.4% (n=5), type1 6.2% (n=3), type4 and 7 2.1% (n=1) and unknown 4.2% (n=2). Also serological test was implemented for 452 (83 herds) serum samples randomly collected from above slaughter pigs using commercial ELISA kits. The positive ratio of each serotype for tested pigs were 19.1% (77/404) on [2], 7.1% (32/452) on [3, 6, 8], 6.9% (28/404) on [5a, 5b], 6.2% (28/452) on [4, 7], 2.8% (9/320) on [12], 2.0% (9/452) on [1, 9, 11] and 0.0% (0/452) on [10]. And 49.3% (223/452) of pigs were positive on apxⅣ antibody. On the basis of latter screening test, the infected farm ratio accounted for 71.1% (59/83) and that was much higher than previously reported data.
Abstract
This study was conducted to isolate the Actinobacillus pleuropneumoniae (APP) and to find out the dis-tribution of 15 serovars mainly in southern Gyeonggi province, Korea. From July 2011 to Nov. 2012, a total of 2,204 slaughter pigs (110 herds) were inspected for evaluation of APP like pneumonic lesions. 48 (33.8%) APP strains were isolated from the 142 lungs and identified using PCR assays (cps, apx/omlA, biovar). Consequently, the serotype ratio were as in the following; type2 41.7% (n=20), type5 33.3% (n=16), type12 10.4% (n=5), type1 6.2% (n=3), type4 and 7 2.1% (n=1) and unknown 4.2% (n=2). Also serological test was implemented for 452 (83 herds) serum samples randomly collected from above slaughter pigs using commercial ELISA kits. The positive ratio of each serotype for tested pigs were 19.1% (77/404) on [2], 7.1% (32/452) on [3, 6, 8], 6.9% (28/404) on [5a, 5b], 6.2% (28/452) on [4, 7], 2.8% (9/320) on [12], 2.0% (9/452) on [1, 9, 11] and 0.0% (0/452) on [10]. And 49.3% (223/452) of pigs were positive on apxⅣ antibody. On the basis of latter screening test, the infected farm ratio accounted for 71.1% (59/83) and that was much higher than previously reported data.
참고문헌 (18)
- 국립수의과학검역원, "동물질병 표준검사법", 국립수의과학검역원 예규 제 65호, ~ (2008)
- Angen Ø, "Development of a multiplex PCR test for identification of Actinobacillus pleuropneumoniae serovars 1, 7, and 12", Vet Microbiol, 132, pp.312~318 (2008)
- Branka V, "Selective media for the isolation of Actinobacillus pleuropneumoniae from the pig", Acta Veterinaria, 54, pp.395~401 (2004)
- Fery J, "Detection, identification, and subtyping of Actinobacillus pleuropneumoniae", Methods Mol Biol, 216, pp.87~95 (2003)
- Gottschalk M, "Actinobacillosis, In Disease of Swine. 10th ed", pp.653~669 (2012), Wiley-Blackwell
- Gram T, "Improved diagnostic PCR assay for Actinobacillus pleuropneumoniae based on the nucleotide sequence of an outer membrane lipoprotein", J Clin Microbiol, 36, pp.443~448 (1998)
- Gram T, "An Actinobacillus pleuropneumoniae PCR typing system based on the apx and omlA genes–evaluation of isolates from lungs and tonsils of pigs", Vet Microbiol, 75, pp.43~57 (2000)
- Jessing SG, "Evaluation of a multiplex PCR test for simultaneous identification and serotyping of Actinobacillus pleuropneumoniae serotypes 2, 5, and 6", J Clin Microbiol, 41, pp.4095~4100 (2003)
- Jung BY, "Biochemical characteristics and serotypes of Actinobacillus pleuropneumoniae isolated from pneumonic lungs of pigs", Korean J Vet Res, 36, pp.181~186 (1996)
- 정지열, "돼지에서 분리한 Actinobacillus pleuropneumoniae의 혈청형 분포 및 항생제 감수성", 대한수의학회지, 52(3), pp.177~181 (2012), 대한수의학회
- Lee JH, "Studies on serotyping and detection of Actinobacillus pleuropneumoniae by multiplex PCR techniques and immunodiffusion test", Kor J Anim Sci, 41, pp.387~396 (1999)
- Mittal KR, "An evaluation of agglutination and coagglutination techniques for serotyping of Haemophilus pleuropneumoniae isolates", American J Vet Res, 48, pp.219~226 (1987)
- Evaluation of Actinobacillus pleuropneumoniae diagnostic test using samples from naturally and experimentally infected pigs, "Oliveira S", NPB, ~, pp.Pork checkoff NPB #08-095 (2009)
- Schaller A, "Characterization of apxIVA, a new RTX determinant of Actinobacillus pleuropneumoniae", Microbiology, 145, pp.2105~2116 (1999)
- Schuchert JA, "Detection and identification of Actinobacillus pleuropneumoniae serotypes 1, 2, and 8 by multiplex PCR", J Clin Microbiol, 42, pp.4344~4348 (2004)
- Serrano-Rubio LE, "Identification of Actinobacillus pleuropneumoniae biovars 1 and 2 in pigs using a PCR assay", Mol Cell Probes, 22, pp.305~312 (2008)
- 신동호, "돼지 흉막폐렴균의 유행 혈청형과 biofilm 분포도", 예방수의학회지, 35(1), pp.7~12 (2011), 한국예방수의학회
- Tonpitak W, "Isolation of Actinobacillus pleuropneumoniae serotype 15-like strain from a porcine tonsil in Thailand: A case report", Thai J Vet Med, 40, pp.343~348 (2010)
