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A longitudinal transcriptomic analysis from unfed to post-engorgement midguts of adult female Ixodes scapularis
The hematophagy behavior has evolved independently several times within the Arthropoda phylum. Interestingly, the process of acquiring a blood meal in ticks is considerably distinct from that observed in other blood-feeding arthropods. Instead of taking seconds to minutes to complete a blood meal, a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10345007/ https://www.ncbi.nlm.nih.gov/pubmed/37443274 http://dx.doi.org/10.1038/s41598-023-38207-5 |
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author | Lu, Stephen Martins, Larissa A. Kotál, Jan Ribeiro, José M. C. Tirloni, Lucas |
author_facet | Lu, Stephen Martins, Larissa A. Kotál, Jan Ribeiro, José M. C. Tirloni, Lucas |
author_sort | Lu, Stephen |
collection | PubMed |
description | The hematophagy behavior has evolved independently several times within the Arthropoda phylum. Interestingly, the process of acquiring a blood meal in ticks is considerably distinct from that observed in other blood-feeding arthropods. Instead of taking seconds to minutes to complete a blood meal, an adult female Ixodes scapularis tick can remain attached to its host for numerous days. During this extended feeding period, the tick undergoes drastic morphological changes. It is well established that the tick midgut plays a pivotal role not only in blood meal digestion but also in pathogen acquisition and transmission. However, our understanding of the underlying molecular mechanisms involved in these events remains limited. To expedite tick research, we conducted a comprehensive longitudinal RNA-sequencing of the tick midgut before, during, and after feeding. By collecting ticks in different feeding stages (unfed, slow feeding, rapid feeding, and early post-detached), we obtained a comprehensive overview of the transcripts present in each stage and the dynamic transcriptional changes that occur between them. This provides valuable insights into tick physiology. Additionally, through unsupervised clustering, we identified transcripts with similar patterns and stage-specific sequences. These findings serve as a foundation for selecting targets in the development of anti-tick control strategies and facilitate a better understanding of how blood feeding and pathogen infection impact tick physiology. |
format | Online Article Text |
id | pubmed-10345007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103450072023-07-15 A longitudinal transcriptomic analysis from unfed to post-engorgement midguts of adult female Ixodes scapularis Lu, Stephen Martins, Larissa A. Kotál, Jan Ribeiro, José M. C. Tirloni, Lucas Sci Rep Article The hematophagy behavior has evolved independently several times within the Arthropoda phylum. Interestingly, the process of acquiring a blood meal in ticks is considerably distinct from that observed in other blood-feeding arthropods. Instead of taking seconds to minutes to complete a blood meal, an adult female Ixodes scapularis tick can remain attached to its host for numerous days. During this extended feeding period, the tick undergoes drastic morphological changes. It is well established that the tick midgut plays a pivotal role not only in blood meal digestion but also in pathogen acquisition and transmission. However, our understanding of the underlying molecular mechanisms involved in these events remains limited. To expedite tick research, we conducted a comprehensive longitudinal RNA-sequencing of the tick midgut before, during, and after feeding. By collecting ticks in different feeding stages (unfed, slow feeding, rapid feeding, and early post-detached), we obtained a comprehensive overview of the transcripts present in each stage and the dynamic transcriptional changes that occur between them. This provides valuable insights into tick physiology. Additionally, through unsupervised clustering, we identified transcripts with similar patterns and stage-specific sequences. These findings serve as a foundation for selecting targets in the development of anti-tick control strategies and facilitate a better understanding of how blood feeding and pathogen infection impact tick physiology. Nature Publishing Group UK 2023-07-13 /pmc/articles/PMC10345007/ /pubmed/37443274 http://dx.doi.org/10.1038/s41598-023-38207-5 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . |
spellingShingle | Article Lu, Stephen Martins, Larissa A. Kotál, Jan Ribeiro, José M. C. Tirloni, Lucas A longitudinal transcriptomic analysis from unfed to post-engorgement midguts of adult female Ixodes scapularis |
title | A longitudinal transcriptomic analysis from unfed to post-engorgement midguts of adult female Ixodes scapularis |
title_full | A longitudinal transcriptomic analysis from unfed to post-engorgement midguts of adult female Ixodes scapularis |
title_fullStr | A longitudinal transcriptomic analysis from unfed to post-engorgement midguts of adult female Ixodes scapularis |
title_full_unstemmed | A longitudinal transcriptomic analysis from unfed to post-engorgement midguts of adult female Ixodes scapularis |
title_short | A longitudinal transcriptomic analysis from unfed to post-engorgement midguts of adult female Ixodes scapularis |
title_sort | longitudinal transcriptomic analysis from unfed to post-engorgement midguts of adult female ixodes scapularis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10345007/ https://www.ncbi.nlm.nih.gov/pubmed/37443274 http://dx.doi.org/10.1038/s41598-023-38207-5 |
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