Comparison of diagnostic methods to detect piroplasms in asymptomatic cattle

• Published in: Veterinary parasitology 2012-02, Vol.183 (3-4), p.364-368
• Main Authors: Galuppi, R., Bonoli, C., Aureli, S., Cassini, R., Marcer, F., Foley, J.E., Tampieri, M.P.
• Format: Article
• Language: English
• Subjects: Animals; Asymptomatic Infections; Babesia - classification; Babesia - genetics; Babesia - isolation & purification; Babesia spp; Babesiosis - diagnosis; Babesiosis - epidemiology; Babesiosis - veterinary; Blood cultures; Blood smear; Cattle; Cattle Diseases - diagnosis; Cattle Diseases - epidemiology; Cattle Diseases - parasitology; Coinfection - diagnosis; Coinfection - epidemiology; Coinfection - parasitology; Coinfection - veterinary; DNA, Protozoan - blood; Female; Fluorescent Antibody Technique - veterinary; Italy - epidemiology; Male; Microscopy - veterinary; Molecular Sequence Data; Parasitology - methods; PCR; Polymerase Chain Reaction - veterinary; Prevalence; RNA, Protozoan - analysis; RNA, Ribosomal, 18S - analysis; Sensitivity and Specificity; Sequence Analysis, DNA; Serology; Sheep; Theileria - classification; Theileria - genetics; Theileria - isolation & purification; Theileria spp; Theileriasis - diagnosis; Theileriasis - epidemiology
• ISSN: 0304-4017; 1873-2550
• DOI: 10.1016/j.vetpar.2011.07.037

This study was carried out to compare different diagnostic techniques to reveal the presence of piroplasms in asymptomatic cattle kept at pasture. Nineteen blood samples were collected from animals of two different areas of Emilia Romagna Region of Italy and processed for microscopic observation, PCR, serological test (IFAT) for Babesia bovis and Babesia bigemina antibodies and in vitro cultivation. The cultures were performed on both bovine and ovine erythrocytes. Seventeen blood smears (89%) were positive for piroplasms, while PCR was positive on 18 samples (95%). DNA sequencing of 18S rRNA identified the piroplasms as Theileria spp. In vitro cultures were successful for 6 samples (32%) cultured on bovine blood and subsequent identified these as Babesia major by PCR. On IFAT analyses of 16 samples, 36.8% resulted positive for B. bovis and 31.6% positive for B. bigemina. These results show, in the same animals, the co-infection with Babesia spp. and Theileria spp.; the detection of B. major was possible only using the in vitro cultures.