4.4 Article

Molecular identification and genetic characterization of tick-borne pathogens in sheep and goats at two farms in the central and southern regions of Malawi

Journal

TICKS AND TICK-BORNE DISEASES
Volume 12, Issue 2, Pages -

Publisher

ELSEVIER GMBH
DOI: 10.1016/j.ttbdis.2020.101629

Keywords

Tick-borne pathogens; Goats; Sheep; Malawi; Molecular identification; Genetic characterization

Funding

  1. JSPS KAKENHI [15H05633, 16H06429, 16K21723, 16H06431, 19H03118]
  2. International Collaborative Research Programme for Tackling Neglected Tropical Disease (NTD) Challenges in African countries [JP18jm0510001]
  3. Japan Agency for Medical Research and Development (AMED)
  4. Grants-in-Aid for Scientific Research [15H05633] Funding Source: KAKEN

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Tick-borne diseases caused by Anaplasma, Ehrlichia, Babesia and Theileria are widespread in small ruminants in tropical and sub-tropical countries. The study in Malawi found that 76.6% of sheep and goats tested positive for at least one tick-borne pathogen, with 45% exhibiting co-infections with multiple pathogens. This research represents a significant milestone in understanding and controlling tick-borne pathogens in small ruminants in Malawi.
Tick-borne diseases (TBDs) caused by pathogens belonging to the genera Anaplasma, Ehrlichia, Babesia and Theileria in small ruminants are widespread in the tropical and sub-tropical countries. The epidemiology of tick borne pathogens (TBPs) in small ruminants is less understood compared to those infecting cattle in general. This study was carried out to investigate and characterize TBPs in sheep and goats using molecular tools. A total of 107 blood samples from sheep (n = 8) and goats (n = 99) were collected from animals that were apparently healthy from two farms in the central and the southern regions of Malawi. The V4 hypervariable region of the 18S ribosomal RNA gene (rDNA) and the V1 hypervariable region of the 16S rDNA polymerase chain reaction (PCR) assays were used for detection of tick-borne piroplasms and Anaplasmataceae, respectively. Almost the full-length 18S rDNA and the heat shock protein (groEL) gene sequences were used for genetic characterization of the piroplasms and Anaplasmataceae, respectively. The results showed that 76.6 % of the examined animals (n = 107) were positive for at least one TBP. The overall co-infection with at least two TBPs was observed in fortyeight animals (45 %). The detected TBPs were Anaplasma ovis (65 %), Ehrlichia ruminantium (4%), Ehrlichia canis (2%), Babesia strain closely related to Babesia gibsoni (1%), Theileria ovis (52 %), Theileria mutans (3%), Theileria separata (2%), Anaplasma sp. (1%) and Theileria sp. strain MSD-like (17 %). To the authors knowledge this is the first molecular study of TBPs in sheep and goats in Malawi. These results have therefore provided a significant milestone in the knowledge of occurrence of TBPs in sheep and goats in Malawi, which is prerequisite to proper diagnosis and control.

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