Genetic characterization and phylogenetic relationships based on 18S rRNA and ITS1 region of small form of canine Babesia spp. from India.

Autor: Mandal M; Division of Parasitology, Indian Veterinary Research Institute, Izatnagar 243 122, Uttar Pradesh, India., Banerjee PS; Division of Parasitology, Indian Veterinary Research Institute, Izatnagar 243 122, Uttar Pradesh, India. Electronic address: banerjeeparth62@gmail.com., Garg R; Division of Parasitology, Indian Veterinary Research Institute, Izatnagar 243 122, Uttar Pradesh, India., Ram H; Division of Parasitology, Indian Veterinary Research Institute, Izatnagar 243 122, Uttar Pradesh, India., Kundu K; Division of Parasitology, Indian Veterinary Research Institute, Izatnagar 243 122, Uttar Pradesh, India., Kumar S; Division of Parasitology, Indian Veterinary Research Institute, Izatnagar 243 122, Uttar Pradesh, India., Kumar GV; Division of Veterinary Biotechnology, Indian Veterinary Research Institute, Izatnagar 243 122, Uttar Pradesh, India.
Jazyk: angličtina
Zdroj: Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases [Infect Genet Evol] 2014 Oct; Vol. 27, pp. 325-31. Date of Electronic Publication: 2014 Aug 10.
DOI: 10.1016/j.meegid.2014.07.033
Abstrakt: Canine babesiosis is a vector borne disease caused by intra-erythrocytic apicomplexan parasites Babesia canis (large form) and Babesia gibsoni (small form), throughout the globe. Apart from few sporadic reports on the occurrence of B. gibsoni infection in dogs, no attempt has been made to characterize Babesia spp. of dogs in India. Fifteen canine blood samples, positive for small form of Babesia, collected from northern to eastern parts of India, were used for amplification of 18S rRNA gene (∼1665bp) of Babesia sp. and partial ITS1 region (∼254bp) of B. gibsoni Asian genotype. Cloning and sequencing of the amplified products of each sample was performed separately. Based on sequences and phylogenetic analysis of 18S rRNA and ITS1 sequences, 13 were considered to be B. gibsoni. These thirteen isolates shared high sequence identity with each other and with B. gibsoni Asian genotype. The other two isolates could not be assigned to any particular species because of the difference(s) in 18S rRNA sequence with B. gibsoni and closer identity with Babesiaoccultans and Babesiaorientalis. In the phylogenetic tree, all the isolates of B. gibsoni Asian genotype formed a separate major clade named as Babesia spp. sensu stricto clade with high bootstrap support. The two unnamed Babesia sp. (Malbazar and Ludhiana isolates) clustered close together with B. orientalis, Babesia sp. (Kashi 1 isolate) and B. occultans of bovines. It can be inferred from this study that 18S rRNA gene and ITS1 region are highly conserved among 13 B. gibsoni isolates from India. It is the maiden attempt of genetic characterization by sequencing of 18S rRNA gene and ITS1 region of B. gibsoni from India and is also the first record on the occurrence of an unknown Babesia sp. of dogs from south and south-east Asia.
(Copyright © 2014 Elsevier B.V. All rights reserved.)
Databáze: MEDLINE
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