Cargando…
Development and field evaluation of PCR assays based on minimum length Bm86 cDNA fragments required for Rhipicephalus and Hyalomma tick species delineation
INTRODUCTION: Hyalomma and Rhipicephalus ticks are important genera that can transmit diseases to both animals and humans, including Crimean-Congo hemorrhagic fever, tick-borne encephalitis, and several types of spotted fever. The accurate identification of tick species is essential for the effectiv...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10340088/ https://www.ncbi.nlm.nih.gov/pubmed/37456966 http://dx.doi.org/10.3389/fvets.2023.1209210 |
_version_ | 1785071995961999360 |
---|---|
author | Zamiti, Sayed Mhadhbi, Moez Dhibi, Mokhtar Darghouth, Mohamed Aziz Ben Said, Mourad |
author_facet | Zamiti, Sayed Mhadhbi, Moez Dhibi, Mokhtar Darghouth, Mohamed Aziz Ben Said, Mourad |
author_sort | Zamiti, Sayed |
collection | PubMed |
description | INTRODUCTION: Hyalomma and Rhipicephalus ticks are important genera that can transmit diseases to both animals and humans, including Crimean-Congo hemorrhagic fever, tick-borne encephalitis, and several types of spotted fever. The accurate identification of tick species is essential for the effective control and prevention of tick-borne diseases. However, traditional identification methods based on morphology can be challenging and subjective, leading to errors. The development of DNA markers has provided more precise and efficient methods for tick species identification, but the currently available markers have limitations in their discriminatory power and sensitivity. To address this need for more sensitive and specific markers, this study aimed to identify two minimum sequence fragments required for tick Hyalomma and Rhipicephalus species identification using the Bm86 cDNA marker, which has previously been shown to be in perfect agreement with the current taxonomy of hard ticks based on its complete sequence. METHODS: Based on our in silico determination that a minimum sequence of 398 bp for Rhipicephalus spp. (from 1487 to 1884) and 559 bp for Hyalomma species (from 539 to 1097) was necessary for species delineation, two distinct PCR assays were developed to apply these sequences in practice. RESULTS AND DISCUSSION: Discrimination between species within each genus was achieved through sequence homology and phylogenetic analysis following the sequencing of the two PCR products. Subsequently, their performance was evaluated by testing them on the field-collected ticks of the Hyalomma and Rhipicephalus genera obtained from various host animals in different geographic regions of Tunisia. The use of shorter partial sequences specific to the tick genera Rhipicephalus and Hyalomma, which target the tick's RNA banks, could represent a significant advance in the field of tick species identification, providing a sensitive and discriminatory tool for interspecific and intraspecific diversity analysis. |
format | Online Article Text |
id | pubmed-10340088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103400882023-07-14 Development and field evaluation of PCR assays based on minimum length Bm86 cDNA fragments required for Rhipicephalus and Hyalomma tick species delineation Zamiti, Sayed Mhadhbi, Moez Dhibi, Mokhtar Darghouth, Mohamed Aziz Ben Said, Mourad Front Vet Sci Veterinary Science INTRODUCTION: Hyalomma and Rhipicephalus ticks are important genera that can transmit diseases to both animals and humans, including Crimean-Congo hemorrhagic fever, tick-borne encephalitis, and several types of spotted fever. The accurate identification of tick species is essential for the effective control and prevention of tick-borne diseases. However, traditional identification methods based on morphology can be challenging and subjective, leading to errors. The development of DNA markers has provided more precise and efficient methods for tick species identification, but the currently available markers have limitations in their discriminatory power and sensitivity. To address this need for more sensitive and specific markers, this study aimed to identify two minimum sequence fragments required for tick Hyalomma and Rhipicephalus species identification using the Bm86 cDNA marker, which has previously been shown to be in perfect agreement with the current taxonomy of hard ticks based on its complete sequence. METHODS: Based on our in silico determination that a minimum sequence of 398 bp for Rhipicephalus spp. (from 1487 to 1884) and 559 bp for Hyalomma species (from 539 to 1097) was necessary for species delineation, two distinct PCR assays were developed to apply these sequences in practice. RESULTS AND DISCUSSION: Discrimination between species within each genus was achieved through sequence homology and phylogenetic analysis following the sequencing of the two PCR products. Subsequently, their performance was evaluated by testing them on the field-collected ticks of the Hyalomma and Rhipicephalus genera obtained from various host animals in different geographic regions of Tunisia. The use of shorter partial sequences specific to the tick genera Rhipicephalus and Hyalomma, which target the tick's RNA banks, could represent a significant advance in the field of tick species identification, providing a sensitive and discriminatory tool for interspecific and intraspecific diversity analysis. Frontiers Media S.A. 2023-06-29 /pmc/articles/PMC10340088/ /pubmed/37456966 http://dx.doi.org/10.3389/fvets.2023.1209210 Text en Copyright © 2023 Zamiti, Mhadhbi, Dhibi, Darghouth and Ben Said. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Veterinary Science Zamiti, Sayed Mhadhbi, Moez Dhibi, Mokhtar Darghouth, Mohamed Aziz Ben Said, Mourad Development and field evaluation of PCR assays based on minimum length Bm86 cDNA fragments required for Rhipicephalus and Hyalomma tick species delineation |
title | Development and field evaluation of PCR assays based on minimum length Bm86 cDNA fragments required for Rhipicephalus and Hyalomma tick species delineation |
title_full | Development and field evaluation of PCR assays based on minimum length Bm86 cDNA fragments required for Rhipicephalus and Hyalomma tick species delineation |
title_fullStr | Development and field evaluation of PCR assays based on minimum length Bm86 cDNA fragments required for Rhipicephalus and Hyalomma tick species delineation |
title_full_unstemmed | Development and field evaluation of PCR assays based on minimum length Bm86 cDNA fragments required for Rhipicephalus and Hyalomma tick species delineation |
title_short | Development and field evaluation of PCR assays based on minimum length Bm86 cDNA fragments required for Rhipicephalus and Hyalomma tick species delineation |
title_sort | development and field evaluation of pcr assays based on minimum length bm86 cdna fragments required for rhipicephalus and hyalomma tick species delineation |
topic | Veterinary Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10340088/ https://www.ncbi.nlm.nih.gov/pubmed/37456966 http://dx.doi.org/10.3389/fvets.2023.1209210 |
work_keys_str_mv | AT zamitisayed developmentandfieldevaluationofpcrassaysbasedonminimumlengthbm86cdnafragmentsrequiredforrhipicephalusandhyalommatickspeciesdelineation AT mhadhbimoez developmentandfieldevaluationofpcrassaysbasedonminimumlengthbm86cdnafragmentsrequiredforrhipicephalusandhyalommatickspeciesdelineation AT dhibimokhtar developmentandfieldevaluationofpcrassaysbasedonminimumlengthbm86cdnafragmentsrequiredforrhipicephalusandhyalommatickspeciesdelineation AT darghouthmohamedaziz developmentandfieldevaluationofpcrassaysbasedonminimumlengthbm86cdnafragmentsrequiredforrhipicephalusandhyalommatickspeciesdelineation AT bensaidmourad developmentandfieldevaluationofpcrassaysbasedonminimumlengthbm86cdnafragmentsrequiredforrhipicephalusandhyalommatickspeciesdelineation |