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Utility of ultra-rapid real-time PCR for detection and prevalence of Rickettsia spp. in ticks

BACKGROUND: Rickettsia spp. are important tick-borne pathogens that cause various human and animal diseases worldwide. A tool for rapid and accurate detection of the pathogens from its vectors is necessary for prevention of Rickettsioses propagation in humans and animals, which are infested by ticks...

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Autores principales: Truong, A-Tai, Yun, Bo-Ram, Yoo, Mi-Sun, Lim, Jiyeon, Min, Subin, Yoon, Soon-Seek, Yun, Young-Min, Kim, Jong-Taek, Cho, Yun Sang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9137179/
https://www.ncbi.nlm.nih.gov/pubmed/35624477
http://dx.doi.org/10.1186/s12917-022-03311-7
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author Truong, A-Tai
Yun, Bo-Ram
Yoo, Mi-Sun
Lim, Jiyeon
Min, Subin
Yoon, Soon-Seek
Yun, Young-Min
Kim, Jong-Taek
Cho, Yun Sang
author_facet Truong, A-Tai
Yun, Bo-Ram
Yoo, Mi-Sun
Lim, Jiyeon
Min, Subin
Yoon, Soon-Seek
Yun, Young-Min
Kim, Jong-Taek
Cho, Yun Sang
author_sort Truong, A-Tai
collection PubMed
description BACKGROUND: Rickettsia spp. are important tick-borne pathogens that cause various human and animal diseases worldwide. A tool for rapid and accurate detection of the pathogens from its vectors is necessary for prevention of Rickettsioses propagation in humans and animals, which are infested by ticks. Therefore, this study was conducted to evaluate a molecular tool, ultra-rapid real-time PCR (UR-qPCR), for rapid and accurate detection of Rickettsia spp. from 5644 ticks in 408 pools collected from livestock and their surrounding environments in Gangwon and Jeju province in South Korea. RESULTS: The UR-qPCR of Rickettsia DNA showed a limit of detection of 2.72 × 10(1) copies of Rickettsia DNA and no cross reaction with other tick-borne pathogens, namely Anaplasma phagocytophilum, Ehrlichia chaffeensis, E. canis, Toxoplasma gondii, and Borrelia burgdorferi. In addition, the PCR assay also showed possibility of various Rickettsia species detection including R. monacensis, “Candidatus R. longicornii”, R. japonica, R. roultii, and R. tamurae. The collected ticks were identified with major species belonged to Haemaphysalis longicornis (81.62%), followed by H. flava (15.19%), and Ixodes nipponensis (3.19%). Rickettsia detection from tick samples using the UR-qPCR showed that the minimum infection rate (MIR) of Rickettsia in collected ticks was 1.24‰ and that all positive pools contained H. longicornis, equal to the MIR of 1.39‰ of this species. Additionally, MIR of Rickettsia spp. detected in ticks collected in Gangwon and Jeju was 1.53‰ and 0.84‰, respectively. Furthermore, the sequencing results of the 17 kDa protein antigen gene and ompA gene showed that Rickettsia spp. sequences from all pools were related to “Candidatus R. longicornii” and “Candidatus R. jingxinensis”. CONCLUSIONS: The UR-qPCR system was demonstrated to be useful tool for accurate and rapid detection of Rickettsia from its vector, ixodid ticks, within 20 min. The data on Rickettsia spp. in ticks detected in this study provide useful information on the distribution of Rickettsia in previously unstudied Korean provinces, which are important for the prevention and control of the spread of rickettsioses in both animals and humans in the country.
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spelling pubmed-91371792022-05-28 Utility of ultra-rapid real-time PCR for detection and prevalence of Rickettsia spp. in ticks Truong, A-Tai Yun, Bo-Ram Yoo, Mi-Sun Lim, Jiyeon Min, Subin Yoon, Soon-Seek Yun, Young-Min Kim, Jong-Taek Cho, Yun Sang BMC Vet Res Research BACKGROUND: Rickettsia spp. are important tick-borne pathogens that cause various human and animal diseases worldwide. A tool for rapid and accurate detection of the pathogens from its vectors is necessary for prevention of Rickettsioses propagation in humans and animals, which are infested by ticks. Therefore, this study was conducted to evaluate a molecular tool, ultra-rapid real-time PCR (UR-qPCR), for rapid and accurate detection of Rickettsia spp. from 5644 ticks in 408 pools collected from livestock and their surrounding environments in Gangwon and Jeju province in South Korea. RESULTS: The UR-qPCR of Rickettsia DNA showed a limit of detection of 2.72 × 10(1) copies of Rickettsia DNA and no cross reaction with other tick-borne pathogens, namely Anaplasma phagocytophilum, Ehrlichia chaffeensis, E. canis, Toxoplasma gondii, and Borrelia burgdorferi. In addition, the PCR assay also showed possibility of various Rickettsia species detection including R. monacensis, “Candidatus R. longicornii”, R. japonica, R. roultii, and R. tamurae. The collected ticks were identified with major species belonged to Haemaphysalis longicornis (81.62%), followed by H. flava (15.19%), and Ixodes nipponensis (3.19%). Rickettsia detection from tick samples using the UR-qPCR showed that the minimum infection rate (MIR) of Rickettsia in collected ticks was 1.24‰ and that all positive pools contained H. longicornis, equal to the MIR of 1.39‰ of this species. Additionally, MIR of Rickettsia spp. detected in ticks collected in Gangwon and Jeju was 1.53‰ and 0.84‰, respectively. Furthermore, the sequencing results of the 17 kDa protein antigen gene and ompA gene showed that Rickettsia spp. sequences from all pools were related to “Candidatus R. longicornii” and “Candidatus R. jingxinensis”. CONCLUSIONS: The UR-qPCR system was demonstrated to be useful tool for accurate and rapid detection of Rickettsia from its vector, ixodid ticks, within 20 min. The data on Rickettsia spp. in ticks detected in this study provide useful information on the distribution of Rickettsia in previously unstudied Korean provinces, which are important for the prevention and control of the spread of rickettsioses in both animals and humans in the country. BioMed Central 2022-05-27 /pmc/articles/PMC9137179/ /pubmed/35624477 http://dx.doi.org/10.1186/s12917-022-03311-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Truong, A-Tai
Yun, Bo-Ram
Yoo, Mi-Sun
Lim, Jiyeon
Min, Subin
Yoon, Soon-Seek
Yun, Young-Min
Kim, Jong-Taek
Cho, Yun Sang
Utility of ultra-rapid real-time PCR for detection and prevalence of Rickettsia spp. in ticks
title Utility of ultra-rapid real-time PCR for detection and prevalence of Rickettsia spp. in ticks
title_full Utility of ultra-rapid real-time PCR for detection and prevalence of Rickettsia spp. in ticks
title_fullStr Utility of ultra-rapid real-time PCR for detection and prevalence of Rickettsia spp. in ticks
title_full_unstemmed Utility of ultra-rapid real-time PCR for detection and prevalence of Rickettsia spp. in ticks
title_short Utility of ultra-rapid real-time PCR for detection and prevalence of Rickettsia spp. in ticks
title_sort utility of ultra-rapid real-time pcr for detection and prevalence of rickettsia spp. in ticks
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9137179/
https://www.ncbi.nlm.nih.gov/pubmed/35624477
http://dx.doi.org/10.1186/s12917-022-03311-7
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