Direct PCR-RFLP based detection and differentiation of Anaplasma species in naturally infected goats of eastern Haryana, India


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Authors

  • BISWA RANJAN MAHARANA Scientist, Lala Lajpat Rai University of Veterinary and Animal Sciences, Karnal, Haryana 132 001 India
  • ANITA GANGULY Senior Scientist, Lala Lajpat Rai University of Veterinary and Animal Sciences, Karnal, Haryana 132 001 India
  • RANBIR SINGH BISLA Regional Director-cum-Principal Scientist, Lala Lajpat Rai University of Veterinary and Animal Sciences, Karnal, Haryana 132 001 India
  • DEVAN ARORA Scientist, Lala Lajpat Rai University of Veterinary and Animal Sciences, Karnal, Haryana 132 001 India
  • ANKIT KUMAR Scientist, Lala Lajpat Rai University of Veterinary and Animal Sciences, Karnal, Haryana 132 001 India
  • SANDEEP POTLIYA Scientist, Lala Lajpat Rai University of Veterinary and Animal Sciences, Karnal, Haryana 132 001 India
  • CHINMOY MISHRA Assistant Professor, Department of Animal Genetics and Breeding, Odisha University of Agriculture and Technology, Bhubaneswar, Odisha.
  • INDRAJIT GANGULY Principal Scientist, Department of Animal Genetics and Breeding, ICAR-National Bureau of Animal Genetic Resources, Karnal, Haryana

https://doi.org/10.56093/ijans.v89i4.89098

Keywords:

Anaplasma marginale, Anaplasma ovis, Goat, msp5, PCR-RFLP

Abstract

The present investigation was designed to develop a novel, rapid and cost effective direct PCR-RFLP assay, as a specific diagnostic tool for detection and differentiation of two Anaplasma species (A. ovis and A. marginale). Blood samples were collected randomly from 83 goats. A direct blood polymerase chain reaction (DT-PCR) for amplifying a fragment of the major surface protein 5 (msp5) gene of A. ovis/A. marginale from whole blood was developed and standardized. Blood smear examination revealed 24 samples (28.91%) positive for Anaplasma inclusion bodies. While, 39 (47%) samples were positive by DT-PCR. The results revealed that DT- PCR was 100% sensitive and 74.57% specific compared to microscopy based detection (k =0.62). Additionally DT-PCR showed 94.44% sensitivity and 100% specificity compared to conventional PCR results with suspected blood samples (k=0.94). All DT-PCR positive samples were confirmed to be A. ovis by restriction fragments length polymorphism (RFLP) analysis. The phylogenetic tree and sequence analysis revealed msp5 gene of Anaplasma species Indian isolate had maximum distance from A. phagocytophilum followed by A. centrale and A. marginale and 100% sequence identity with A. ovis isolates of Chinese origin which further confirmed the sequence identified in native goats to be of A. ovis. The simplified DT-PCR assay as a viable alternative to conventional PCR could be helpful for fast and accurate diagnosis of Anaplasma species and suitable for screening a large number of samples. Furthermore, results revealed that DT-PCR-RFLP of the msp5 gene might be a useful method for simultaneous detection and differentiation of A. ovis and A. marginale in goats.

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2019-04-22

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2019-04-23

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How to Cite

MAHARANA, B. R., GANGULY, A., BISLA, R. S., ARORA, D., KUMAR, A., POTLIYA, S., MISHRA, C., & GANGULY, I. (2019). Direct PCR-RFLP based detection and differentiation of Anaplasma species in naturally infected goats of eastern Haryana, India. The Indian Journal of Animal Sciences, 89(4), 385–389. https://doi.org/10.56093/ijans.v89i4.89098
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