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A detailed macroscopic and histological description is given of tuberculous-like lesions in mandibular lymph nodes obtained from wild boar (Sus scrofa) collected in Italy during the 1995/1996 hunting season, as well as a correlation with results obtained from a Mycobacterium tuberculosis complex target amplified test system. According to macroscopic appearance, lesions were largely represented by caseous-necrotic-calcified granulomata (n = 272/285; 95.4%), while histological investigations showed mainly necrotic-calcified (n = 82/218; 37.6%) and fibronecrotic-calcified (n = 81/218; 37.2%) lesions. When tested with a target rRNA amplification/hybridization technique to detect M. tuberculosis complex, 112 (43.6%) samples out of 275 tested gave positive results.

Abstract. The current study describes the development of a set of 5 multiplex polymerase chain reaction (mPCR) assays for the simultaneous detection of abortive infection agents in bovine fetal tissues, including Brucella spp., Leptospira spp., and Campylobacter fetus (mPCR1); Hammondia heydorni, Neospora caninum, and Toxoplasma gondii (mPCR2); Coxiella burnetii and Chlamydophila psittaci (mPCR3); Mycoplasma bovis, Mycoplasma bovigenitalium, and Ureaplasma diversum (mPCR4); and Bovine viral diarrhea virus (BVDV) and Bovine herpesvirus-1 (BoHV-1; mPCR5). The protocol was tested on different tissue samples collected from 50 aborted bovine fetuses, and it showed that out of the 50 fetuses, 7 (14%, mPCR2) were PCR-positive for N. caninum, 4 (8%, mPCR5) were PCR-positive for BVDV, and 2 (4%, mPCR4) were PCR-positive for U. diversum. The results obtained by using each multiplex PCR were 100% concordant with those obtained by using the respective PCR assays targeting single genes on the same specimens. Moreover, all multiplex PCR assays on clinical samples were compared with reference methods, obtaining a perfect accordance in all samples and confirming the validity of the set of multiplex PCR assays. The proposed set of multiplex PCR assays is, therefore, suitable for the simultaneous detection of the main infectious agents responsible for bovine abortion.

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