Neglected zoonotic agents in cattle abortion: tackling the difficult to grow bacteria

被引:49
作者
Vidal, Sara [1 ,2 ]
Kegler, Kristel [3 ]
Greub, Gilbert [4 ,5 ]
Aeby, Sebastien [4 ,5 ]
Borel, Nicole [6 ]
Dagleish, Mark P. [7 ]
Posthaus, Horst [3 ]
Perreten, Vincent [1 ]
Rodriguez-Campos, Sabrina [1 ]
机构
[1] Univ Bern, Inst Vet Bacteriol, Vetsuisse Fac, Laenggassstr 122, CH-3012 Bern, Switzerland
[2] Univ Bern, Grad Sch Cellular & Biomed Sci, Theodor Kocher Inst, Freiestr 1, CH-3001 Bern, Switzerland
[3] Univ Bern, Inst Anim Pathol, Vetsuisse Fac, Laenggassstr 122, CH-3012 Bern, Switzerland
[4] Univ Hosp Ctr, Inst Microbiol, Bugnon 48, CH-1011 Lausanne, Switzerland
[5] Univ Lausanne, Bugnon 48, CH-1011 Lausanne, Switzerland
[6] Univ Zurich, Inst Vet Pathol, Vetsuisse Fac, Winterthurerstr 270, CH-8057 Zurich, Switzerland
[7] Moredun Res Inst, Pentlands Sci Pk, Edinburgh EH26 0PZ, Midlothian, Scotland
关键词
Coxiella burnetii; Chlamydiales; Leptospira spp; Bovine abortion; Zoonosis; COXIELLA-BURNETII INFECTIONS; INTERROGANS SEROVAR HARDJO; REAL-TIME PCR; DOMESTIC RUMINANTS; CHLAMYDIA-PSITTACI; NEOSPORA-CANINUM; BOVINE ABORTION; LEPTOSPIRA; PARACHLAMYDIA; DISEASE;
D O I
10.1186/s12917-017-1294-y
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Background: Coxiella burnetii, Chlamydia abortus and Leptospira spp. are difficult to grow bacteria that play a role in bovine abortion, but their diagnosis is hampered by their obligate intracellular lifestyle (C. burnetii, C. abortus) or their lability (Leptospira spp.). Their importance is based on the contagious spread in food-producing animals, but also as zoonotic agents. In Switzerland, first-line routine bacteriological diagnostics in cattle abortions is regulated by national law and includes only basic screening by staining for C. burnetii due to the high costs associated with extended spectrum analysis. The aim of this study was to assess the true occurrence of these zoonotic pathogens in 249 cases of bovine abortion in Switzerland by serology (ELISA for anti-C. burnetii and C. abortus antibodies and microscopic agglutination test for anti-Leptospira spp. antibodies), molecular methods (real-time PCR and sequencing of PCR products of Chlamydiales-positive cases), Stamp's modification of the Ziehl-Neelsen (mod-ZN) stain and, upon availability of material, by histology and immunohistochemistry (IHC). Results: After seroanalysis the prevalence was 15.9% for C. burnetii, 38.5% for C. abortus and 21.4% for Leptospira spp. By real-time PCR 12.1% and 16.9% of the cases were positive for C. burnetii and Chlamydiales, respectively, but only 2.4% were positive for C. burnetii or Chlamydiales by mod-ZN stain. Sequencing of PCR products of Chlamydiales-positive cases revealed C. abortus in 10% of cases and the presence of a mix of Chlamydiales-related bacteria in 5.2% of cases. Pathogenic Leptospira spp. were detected in 5.6% of cases. Inflammatory lesions were present histologically in all available samples which were real-time PCR-positive for Chlamydiales and Leptospira spp. One of 12 real-time PCR-positive cases for C. burnetii was devoid of histological lesions. None of the pathogens could be detected by IHC. Conclusion: Molecular detection by real-time PCR complemented by histopathological analysis is recommended to improve definitive diagnosis of bovine abortion cases and determine a more accurate prevalence of these zoonotic pathogens.
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