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Establishment of a novel tick-Babesia experimental infection model
Ticks are potent vectors of many deadly human and animal pathogens. Tick-borne babesiosis is a well-recognized malaria-like disease that occurs worldwide and recently has attracted increased attention as an emerging zoonosis. Although the proliferation of Babesia organisms is essential in the vector...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5107930/ https://www.ncbi.nlm.nih.gov/pubmed/27841321 http://dx.doi.org/10.1038/srep37039 |
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author | Maeda, Hiroki Hatta, Takeshi Alim, M Abdul Tsubokawa, Daigo Mikami, Fusako Matsubayashi, Makoto Miyoshi, Takeharu Umemiya-Shirafuji, Rika Kawazu, Shin-ichiro Igarashi, Ikuo Mochizuki, Masami Tsuji, Naotoshi Tanaka, Tetsuya |
author_facet | Maeda, Hiroki Hatta, Takeshi Alim, M Abdul Tsubokawa, Daigo Mikami, Fusako Matsubayashi, Makoto Miyoshi, Takeharu Umemiya-Shirafuji, Rika Kawazu, Shin-ichiro Igarashi, Ikuo Mochizuki, Masami Tsuji, Naotoshi Tanaka, Tetsuya |
author_sort | Maeda, Hiroki |
collection | PubMed |
description | Ticks are potent vectors of many deadly human and animal pathogens. Tick-borne babesiosis is a well-recognized malaria-like disease that occurs worldwide and recently has attracted increased attention as an emerging zoonosis. Although the proliferation of Babesia organisms is essential in the vectors, their detailed lifecycle with time information for migration in ticks remains unknown. A novel study model for the elucidation of the migration speed of Babesia parasites in their vector tick, Haemaphysalis longicornis, has been developed using an artificial feeding system with quantitative PCR method. The detectable DNA of Babesia parasites gradually disappeared in the tick midgut at 1 day post engorgement (DPE), and in contrary increased in other organs. The results indicated that the Babesia parasite passed the H. longicornis midgut within 24 hours post engorgement, migrated to the hemolymph, and then proliferated in the organs except the midgut. This time point may be an important curfew for Babesia parasites to migrate in the tick lumen. We also visualized the Babesia parasites in the experimentally infected ticks and in their eggs using IFAT for detecting their cytoskeletal structure, which suggested the successful tick infection and transovarial transmission of the parasite. This model will shed light on the further understanding of tick-Babesia interactions. |
format | Online Article Text |
id | pubmed-5107930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51079302016-11-22 Establishment of a novel tick-Babesia experimental infection model Maeda, Hiroki Hatta, Takeshi Alim, M Abdul Tsubokawa, Daigo Mikami, Fusako Matsubayashi, Makoto Miyoshi, Takeharu Umemiya-Shirafuji, Rika Kawazu, Shin-ichiro Igarashi, Ikuo Mochizuki, Masami Tsuji, Naotoshi Tanaka, Tetsuya Sci Rep Article Ticks are potent vectors of many deadly human and animal pathogens. Tick-borne babesiosis is a well-recognized malaria-like disease that occurs worldwide and recently has attracted increased attention as an emerging zoonosis. Although the proliferation of Babesia organisms is essential in the vectors, their detailed lifecycle with time information for migration in ticks remains unknown. A novel study model for the elucidation of the migration speed of Babesia parasites in their vector tick, Haemaphysalis longicornis, has been developed using an artificial feeding system with quantitative PCR method. The detectable DNA of Babesia parasites gradually disappeared in the tick midgut at 1 day post engorgement (DPE), and in contrary increased in other organs. The results indicated that the Babesia parasite passed the H. longicornis midgut within 24 hours post engorgement, migrated to the hemolymph, and then proliferated in the organs except the midgut. This time point may be an important curfew for Babesia parasites to migrate in the tick lumen. We also visualized the Babesia parasites in the experimentally infected ticks and in their eggs using IFAT for detecting their cytoskeletal structure, which suggested the successful tick infection and transovarial transmission of the parasite. This model will shed light on the further understanding of tick-Babesia interactions. Nature Publishing Group 2016-11-14 /pmc/articles/PMC5107930/ /pubmed/27841321 http://dx.doi.org/10.1038/srep37039 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Maeda, Hiroki Hatta, Takeshi Alim, M Abdul Tsubokawa, Daigo Mikami, Fusako Matsubayashi, Makoto Miyoshi, Takeharu Umemiya-Shirafuji, Rika Kawazu, Shin-ichiro Igarashi, Ikuo Mochizuki, Masami Tsuji, Naotoshi Tanaka, Tetsuya Establishment of a novel tick-Babesia experimental infection model |
title | Establishment of a novel tick-Babesia experimental infection model |
title_full | Establishment of a novel tick-Babesia experimental infection model |
title_fullStr | Establishment of a novel tick-Babesia experimental infection model |
title_full_unstemmed | Establishment of a novel tick-Babesia experimental infection model |
title_short | Establishment of a novel tick-Babesia experimental infection model |
title_sort | establishment of a novel tick-babesia experimental infection model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5107930/ https://www.ncbi.nlm.nih.gov/pubmed/27841321 http://dx.doi.org/10.1038/srep37039 |
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