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Tick-Borne Pathogens Shape the Native Microbiome Within Tick Vectors
Ticks are blood-feeding arthropods and transmit a variety of medically important viral, bacterial, protozoan pathogens to animals and humans. Ticks also harbor a diverse community of microbes linked to their biological processes, such as hematophagy, and hence affect vector competence. The interacti...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563471/ https://www.ncbi.nlm.nih.gov/pubmed/32854447 http://dx.doi.org/10.3390/microorganisms8091299 |
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author | Adegoke, Abdulsalam Kumar, Deepak Bobo, Cailyn Rashid, Muhammad Imran Durrani, Aneela Zameer Sajid, Muhammad Sohail Karim, Shahid |
author_facet | Adegoke, Abdulsalam Kumar, Deepak Bobo, Cailyn Rashid, Muhammad Imran Durrani, Aneela Zameer Sajid, Muhammad Sohail Karim, Shahid |
author_sort | Adegoke, Abdulsalam |
collection | PubMed |
description | Ticks are blood-feeding arthropods and transmit a variety of medically important viral, bacterial, protozoan pathogens to animals and humans. Ticks also harbor a diverse community of microbes linked to their biological processes, such as hematophagy, and hence affect vector competence. The interactions between bacterial and/or protozoan pathogens and the tick microbiome is a black-box, and therefore we tested the hypothesis that the presence of a protozoan or bacterial pathogen will alter the microbial composition within a tick. Hence, this study was designed to define the microbial composition of two tick species, Hyalomma (H.) anatolicum and Rhipicephalus (R.) microplus. We used a combination of PCR based pathogen (Anaplasma marginale and Theileria species) and symbiont (Wolbachia species) identification followed by metagenomic sequencing and comparison of the microbial communities in PCR positive and negative ticks. A total of 1786 operational taxonomic units was identified representing 25 phyla, 50 classes, and 342 genera. The phylum Proteobacteria, Firmicutes, Actinobacteriota, and Bacteroidota were the most represented bacteria group. Alpha and beta diversity were not significantly affected in the presence or absence of Theileria sp. and A. marginale as see with H. anatolicum ticks. Interestingly, bacterial communities were significantly reduced in Theileria sp. infected R. microplus ticks, while also exhibiting a significant reduction in microbial richness and evenness. Putting these observations together, we referred to the effect the presence of Theileria sp. has on R. microplus a “pathogen-induced dysbiosis”. We also identify the presence of Plasmodium falciparum, the causative agent of human malaria from the microbiome of both H. anatolicum and R. microplus ticks. These findings support the presence of a “pathogen-induced dysbiosis” within the tick and further validation experiments are required to investigate how they are important in the vector competence of ticks. Understanding the mechanism of “pathogen-induced dysbiosis” on tick microbial composition may aid the discovery of intervention strategies for the control of emerging tick-borne infections. |
format | Online Article Text |
id | pubmed-7563471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75634712020-10-27 Tick-Borne Pathogens Shape the Native Microbiome Within Tick Vectors Adegoke, Abdulsalam Kumar, Deepak Bobo, Cailyn Rashid, Muhammad Imran Durrani, Aneela Zameer Sajid, Muhammad Sohail Karim, Shahid Microorganisms Article Ticks are blood-feeding arthropods and transmit a variety of medically important viral, bacterial, protozoan pathogens to animals and humans. Ticks also harbor a diverse community of microbes linked to their biological processes, such as hematophagy, and hence affect vector competence. The interactions between bacterial and/or protozoan pathogens and the tick microbiome is a black-box, and therefore we tested the hypothesis that the presence of a protozoan or bacterial pathogen will alter the microbial composition within a tick. Hence, this study was designed to define the microbial composition of two tick species, Hyalomma (H.) anatolicum and Rhipicephalus (R.) microplus. We used a combination of PCR based pathogen (Anaplasma marginale and Theileria species) and symbiont (Wolbachia species) identification followed by metagenomic sequencing and comparison of the microbial communities in PCR positive and negative ticks. A total of 1786 operational taxonomic units was identified representing 25 phyla, 50 classes, and 342 genera. The phylum Proteobacteria, Firmicutes, Actinobacteriota, and Bacteroidota were the most represented bacteria group. Alpha and beta diversity were not significantly affected in the presence or absence of Theileria sp. and A. marginale as see with H. anatolicum ticks. Interestingly, bacterial communities were significantly reduced in Theileria sp. infected R. microplus ticks, while also exhibiting a significant reduction in microbial richness and evenness. Putting these observations together, we referred to the effect the presence of Theileria sp. has on R. microplus a “pathogen-induced dysbiosis”. We also identify the presence of Plasmodium falciparum, the causative agent of human malaria from the microbiome of both H. anatolicum and R. microplus ticks. These findings support the presence of a “pathogen-induced dysbiosis” within the tick and further validation experiments are required to investigate how they are important in the vector competence of ticks. Understanding the mechanism of “pathogen-induced dysbiosis” on tick microbial composition may aid the discovery of intervention strategies for the control of emerging tick-borne infections. MDPI 2020-08-25 /pmc/articles/PMC7563471/ /pubmed/32854447 http://dx.doi.org/10.3390/microorganisms8091299 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Adegoke, Abdulsalam Kumar, Deepak Bobo, Cailyn Rashid, Muhammad Imran Durrani, Aneela Zameer Sajid, Muhammad Sohail Karim, Shahid Tick-Borne Pathogens Shape the Native Microbiome Within Tick Vectors |
title | Tick-Borne Pathogens Shape the Native Microbiome Within Tick Vectors |
title_full | Tick-Borne Pathogens Shape the Native Microbiome Within Tick Vectors |
title_fullStr | Tick-Borne Pathogens Shape the Native Microbiome Within Tick Vectors |
title_full_unstemmed | Tick-Borne Pathogens Shape the Native Microbiome Within Tick Vectors |
title_short | Tick-Borne Pathogens Shape the Native Microbiome Within Tick Vectors |
title_sort | tick-borne pathogens shape the native microbiome within tick vectors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563471/ https://www.ncbi.nlm.nih.gov/pubmed/32854447 http://dx.doi.org/10.3390/microorganisms8091299 |
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