4.5 Article

Exploring Prokaryotic and Eukaryotic Microbiomes Helps in Detecting Tick-Borne Infectious Agents in the Blood of Camels

Journal

PATHOGENS
Volume 10, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/pathogens10030351

Keywords

Candidatus Anaplasma camelii; eukaryotes; microbiome; Theileria; Trypanosoma evansi

Categories

Funding

  1. KAKENHI [16H06431, 19H03118, 19F19097, 20K21358, 20KK0151]
  2. Japan Agency for Medical Research and Development (AMED) [20wm0225016j0001]
  3. Grants-in-Aid for Scientific Research [20KK0151, 20K21358, 19F19097] Funding Source: KAKEN

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The study found that the bacteria and eukaryotic microorganisms circulating in the blood of dromedary camels are dominated by Proteobacteria, Bacteroidetes, Firmicutes, Actinobacteria, Fungi, Charophyta, and Apicomplexa. The genera Sediminibacterium, Hydrotalea, Bradyrhizobium, Anaplasma, Theileria, Sarcocystis, Hoplorhynchus, and Stylocephalus were found to be the most abundant. The metagenomic approach successfully detected several pathogens including Anaplasma sp., Theileria ovis, and Trypanosoma evansi type A.
Dromedary camels (Camelus dromedarius) are widely distributed in Africa, the Middle East and northern India. In this study, we aimed to detect tick-borne pathogens through investigating prokaryotic and eukaryotic microorganisms in camel blood based on a metagenomic approach and then to characterize potentially pathogenic organisms using traditional molecular techniques. We showed that the bacteria circulating in the blood of camels is dominated by Proteobacteria, Bacteroidetes, Firmicutes and Actinobacteria. At the genus level, Sediminibacterium, Hydrotalea, Bradyrhizobium and Anaplasma were the most abundant taxa. Eukaryotic profile was dominated by Fungi, Charophyta and Apicomplexa. At the genus level, Theileria was detected in 10 out of 18 samples, while Sarcocystis, Hoplorhynchus and Stylocephalus were detected in one sample each. Our metagenomic approach was successful in the detection of several pathogens or potential pathogens including Anaplasma sp., Theileria ovis, Th. separata, Th. annulate, Th. mutans-like and uncharacterized Theileria sp. For further characterization, we provided the partial sequences of citrate synthase (gltA) and heat-shock protein (groEL) genes of Candidatus Anaplasma camelii. We also detected Trypanosoma evansi type A using polymerase chain reaction (PCR) targeting the internal transcribed spacer 1 (ITS1) region. This combined metagenomic and traditional approach will contribute to a better understanding of the epidemiology of pathogens including tick-borne bacteria and protozoa in animals.

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