Detection of Babesia bigemina infection in strains of Rhipicephalus ( Boophilus) microplus collected from outbreaks in South Texas

• Published in: Veterinary parasitology Vol. 145; no. 1; pp. 156 - 163
• Main Authors: Guerrero, F.D., Bendele, K.G., Davey, R.B., George, J.E.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 10.04.2007
• Subjects: Animals; Arachnid Vectors - parasitology; Babesia; Babesia - classification; Babesia - isolation & purification; Babesia bigemina; Babesiosis; Babesiosis - transmission; Boophilus microplus; Cattle; Cattle Diseases - parasitology; Cattle Diseases - transmission; disease detection; disease outbreaks; Disease Outbreaks - veterinary; disease vectors; PCR; polymerase chain reaction; Rhipicephalus ( Boophilus); Rhipicephalus - parasitology; ribosomal DNA; strains; Texas - epidemiology; Tick; ticks; Texas; Babesiosis; Rhipicephalus ( Boophilus); Tick; PCR; Babesia
• ISSN: 0304-4017; 1873-2550
• DOI: 10.1016/j.vetpar.2006.11.014

The sudden death of several cattle infested experimentally with Rhipicephalus ( Boophilus) microplus led to a clinical investigation into the reasons for the unexpected mortality. Microscopic evidence for Babesia bigemina infection was found in blood smears from the affected animals and a PCR assay was designed to detect the presence of B. bigemina and Babesia bovis in all R. microplus strains received and propagated at the laboratory. The assay utilizes a nested PCR approach with the first PCR amplifying a well-conserved segment from the Babesia 18S ribosomal RNA gene followed by a nested PCR with Babesia species-specific primers and annealing temperatures enabling amplification of the 18S ribosomal RNA gene fragment specific to either B. bigemina or B. bovis. DNA from groups of 50 larvae was extracted using a rapid DNA preparation protocol, which consisted of grinding the frozen tick larvae in PCR buffer and boiling the mixture for 5 min. The assay sensitivity allowed for the detection of the equivalent of a single infected tick larva. R. microplus eggs were also analyzed, but yolk protein viscosity created inconsistent results with the crush and boil DNA isolation protocol, necessitating the use of a more extensive proteinase K digestion-based DNA purification method. We detected the presence of B. bigemina in all strains of R. microplus currently reared at the laboratory and 4 of 26 strains collected from infestation outbreaks in Texas by the U.S. Cattle Fever Tick Eradication Program.