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Tick transmission of Borrelia burgdorferi to the murine host is not influenced by environmentally acquired midgut microbiota
BACKGROUND: Ixodes scapularis is the predominant tick vector of Borrelia burgdorferi, the agent of Lyme disease, in the USA. Molecular interactions between the tick and B. burgdorferi orchestrate the migration of spirochetes from the midgut to the salivary glands—critical steps that precede transmis...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575305/ https://www.ncbi.nlm.nih.gov/pubmed/36253842 http://dx.doi.org/10.1186/s40168-022-01378-w |
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author | Narasimhan, Sukanya Rajeevan, Nallakkandi Graham, Morven Wu, Ming-Jie DePonte, Kathleen Marion, Solenne Masson, Orlanne O’Neal, Anya J. Pedra, Joao H. F. Sonenshine, Daniel E. Fikrig, Erol |
author_facet | Narasimhan, Sukanya Rajeevan, Nallakkandi Graham, Morven Wu, Ming-Jie DePonte, Kathleen Marion, Solenne Masson, Orlanne O’Neal, Anya J. Pedra, Joao H. F. Sonenshine, Daniel E. Fikrig, Erol |
author_sort | Narasimhan, Sukanya |
collection | PubMed |
description | BACKGROUND: Ixodes scapularis is the predominant tick vector of Borrelia burgdorferi, the agent of Lyme disease, in the USA. Molecular interactions between the tick and B. burgdorferi orchestrate the migration of spirochetes from the midgut to the salivary glands—critical steps that precede transmission to the vertebrate host. Over the last decade, research efforts have invoked a potential role for the tick microbiome in modulating tick-pathogen interactions. RESULTS: Using multiple strategies to perturb the microbiome composition of B. burgdorferi-infected nymphal ticks, we observe that changes in the microbiome composition do not significantly influence B. burgdorferi migration from the midgut, invasion of salivary glands, or transmission to the murine host. We also show that within 24 and 48 h of the onset of tick feeding, B. burgdorferi spirochetes are within the peritrophic matrix and epithelial cells of the midgut in preparation for exit from the midgut. CONCLUSIONS: This study highlights two aspects of tick-spirochete interactions: (1) environmental bacteria associated with the tick do not influence spirochete transmission to the mammalian host and (2) the spirochete may utilize an intracellular exit route during migration from the midgut to the salivary glands, a strategy that may allow the spirochete to distance itself from microbiota in the midgut lumen effectively. This may explain in part, the inability of environment-acquired midgut microbiota to significantly influence spirochete transmission. Unraveling a molecular understanding of this exit strategy will be critical to gain new insights into the biology of the spirochete and the tick. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01378-w. |
format | Online Article Text |
id | pubmed-9575305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95753052022-10-18 Tick transmission of Borrelia burgdorferi to the murine host is not influenced by environmentally acquired midgut microbiota Narasimhan, Sukanya Rajeevan, Nallakkandi Graham, Morven Wu, Ming-Jie DePonte, Kathleen Marion, Solenne Masson, Orlanne O’Neal, Anya J. Pedra, Joao H. F. Sonenshine, Daniel E. Fikrig, Erol Microbiome Research BACKGROUND: Ixodes scapularis is the predominant tick vector of Borrelia burgdorferi, the agent of Lyme disease, in the USA. Molecular interactions between the tick and B. burgdorferi orchestrate the migration of spirochetes from the midgut to the salivary glands—critical steps that precede transmission to the vertebrate host. Over the last decade, research efforts have invoked a potential role for the tick microbiome in modulating tick-pathogen interactions. RESULTS: Using multiple strategies to perturb the microbiome composition of B. burgdorferi-infected nymphal ticks, we observe that changes in the microbiome composition do not significantly influence B. burgdorferi migration from the midgut, invasion of salivary glands, or transmission to the murine host. We also show that within 24 and 48 h of the onset of tick feeding, B. burgdorferi spirochetes are within the peritrophic matrix and epithelial cells of the midgut in preparation for exit from the midgut. CONCLUSIONS: This study highlights two aspects of tick-spirochete interactions: (1) environmental bacteria associated with the tick do not influence spirochete transmission to the mammalian host and (2) the spirochete may utilize an intracellular exit route during migration from the midgut to the salivary glands, a strategy that may allow the spirochete to distance itself from microbiota in the midgut lumen effectively. This may explain in part, the inability of environment-acquired midgut microbiota to significantly influence spirochete transmission. Unraveling a molecular understanding of this exit strategy will be critical to gain new insights into the biology of the spirochete and the tick. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01378-w. BioMed Central 2022-10-17 /pmc/articles/PMC9575305/ /pubmed/36253842 http://dx.doi.org/10.1186/s40168-022-01378-w 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 Narasimhan, Sukanya Rajeevan, Nallakkandi Graham, Morven Wu, Ming-Jie DePonte, Kathleen Marion, Solenne Masson, Orlanne O’Neal, Anya J. Pedra, Joao H. F. Sonenshine, Daniel E. Fikrig, Erol Tick transmission of Borrelia burgdorferi to the murine host is not influenced by environmentally acquired midgut microbiota |
title | Tick transmission of Borrelia burgdorferi to the murine host is not influenced by environmentally acquired midgut microbiota |
title_full | Tick transmission of Borrelia burgdorferi to the murine host is not influenced by environmentally acquired midgut microbiota |
title_fullStr | Tick transmission of Borrelia burgdorferi to the murine host is not influenced by environmentally acquired midgut microbiota |
title_full_unstemmed | Tick transmission of Borrelia burgdorferi to the murine host is not influenced by environmentally acquired midgut microbiota |
title_short | Tick transmission of Borrelia burgdorferi to the murine host is not influenced by environmentally acquired midgut microbiota |
title_sort | tick transmission of borrelia burgdorferi to the murine host is not influenced by environmentally acquired midgut microbiota |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575305/ https://www.ncbi.nlm.nih.gov/pubmed/36253842 http://dx.doi.org/10.1186/s40168-022-01378-w |
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