Amblyomma ticks
publication ID |
https://doi.org/ 10.1016/j.ijppaw.2021.09.005 |
persistent identifier |
https://treatment.plazi.org/id/03AE0242-FFCD-FFC9-FFCE-48F1FEEEFCA1 |
treatment provided by |
Felipe |
scientific name |
Amblyomma ticks |
status |
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3.2. Molecular analysis of Amblyomma ticks and their Hepatozoon spp .
The PCR analysis of the DNA isolates indicates amplification of 460bp for the 16S rRNA gene and ~700bp for the CO1 gene. BLASTn results for both mtDNA genes matched with the expected species, although notable divergence levels were observed in both cases ( Fig. 1 View Fig ). The CO1 gene was not able to amplify the A. latum . Based on the 16S rRNA phylogenetic analysis, the A. marmoreum from the current study constitutes a monophyletic clade (99% bootstrap value) closely affiliated to the same lineage group of A. marmoreum , while A. latum from this study formed a monophyletic clade with A. latum with 99% bootstrap value. Both A. marmoreum and A. latum formed a monophyletic group with other Amblyomma species of reptiles, clearly distinct from other Amblyomma species of mammals with a> 70% bootstrap value ( Fig. 2 View Fig ).
The overall prevalence of Hepatozoon was 10/100 (10%). It was detected from 1/4 (25%) A. marmoreum parasitizing Varanus albigularis and 9/94 (10%) A. marmoreum parasitizing tortoises. No Hepatozoon was detected from A. latum . The BLASTn analysis for the 430bp 18S rRNA of the Hepatozoon sequences had a 99% similarity with H. fitzsimonsi (KR069084.1) from South African tortoise Kinixys zombensis , and clustered in a single clade with H. fitzsimonsi from another South African tortoise, a tortoise collected from Nigeria and a tick collected from a tortoise in Kenya ( Fig. 2 View Fig ).
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