| Literature DB >> 30158190 |
Thillaiampalam Sivakumar1,2, Bumduuren Tuvshintulga1, Atambekova Zhyldyz1, Hemal Kothalawala2, Palitha Rohana Yapa3, Ratnam Kanagaratnam4, Singarayar Caniciyas Vimalakumar5, Thuduwege Sanath Abeysekera6, Amitha Sampath Weerasingha7, Junya Yamagishi8,9, Ikuo Igarashi1, Seekkuge Susil Priyantha Silva2, Naoaki Yokoyama10.
Abstract
Bovine babesiosis is a serious threat to the cattle industry. We prepared blood DNA samples from 13 cattle with clinical babesiosis from the Badulla (n = 8), Jaffna (n = 3), and Kilinochchi (n = 2) districts in Sri Lanka. These DNA samples tested positive in PCR assays specific for Babesia bovis (n = 9), Babesia bigemina (n = 9), and Babesia ovata (n = 1). Twelve cattle were positive for B. bovis and/or B. bigemina One cow was negative for the tested Babesia species but was positive for Babesia on microscopic examination; the phylogenetic positions of 18S rRNA and cytochrome oxidase subunit III gene sequences suggested that the cow was infected with Babesia sp. Mymensingh, which was recently reported from a healthy cow in Bangladesh. We then developed a novel Babesia sp. Mymensingh-specific PCR assay and obtained positive results for one other sample. Analysis of gene sequences from the cow with positive B. ovata-specific PCR results demonstrated that the animal was infected not with B. ovata but with Babesia sp. Hue-1, which was recently reported from asymptomatic cattle in Vietnam. The virulence of Babesia sp. Hue-1 is unclear, as the cow was coinfected with B. bovis and B. bigemina However, Babesia sp. Mymensingh probably causes severe clinical babesiosis, as it was the sole Babesia species detected in a clinical case. The present study revealed the presence of two bovine Babesia species not previously reported in Sri Lanka, plus the first case of severe bovine babesiosis caused by a Babesia species other than B. bovis, B. bigemina, and Babesia divergens.Entities:
Keywords: Babesia; Sri Lanka; cattle; clinical babesiosis
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Year: 2018 PMID: 30158190 PMCID: PMC6204690 DOI: 10.1128/JCM.00895-18
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948