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The molecular and functional characterization of ferritins in the hard tick Hyalomma rufipes

BACKGROUND: The protein ferritin, which plays an important role in the maintenance of iron homeostasis, is indispensable for iron detoxification, resistance to oxidative stress and innate immunity. Ticks, which are obligate blood-sucking ectoparasites, have to deal with a large amount of iron when t...

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Autores principales: Gao, Zhihua, Zheng, Peijing, Wang, Kuang, Ji, Xin, Shi, Yanqing, Song, Xuecheng, Liu, Jingze, Yu, Zhijun, Yang, Xiaolong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563847/
https://www.ncbi.nlm.nih.gov/pubmed/36242057
http://dx.doi.org/10.1186/s13071-022-05515-0
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author Gao, Zhihua
Zheng, Peijing
Wang, Kuang
Ji, Xin
Shi, Yanqing
Song, Xuecheng
Liu, Jingze
Yu, Zhijun
Yang, Xiaolong
author_facet Gao, Zhihua
Zheng, Peijing
Wang, Kuang
Ji, Xin
Shi, Yanqing
Song, Xuecheng
Liu, Jingze
Yu, Zhijun
Yang, Xiaolong
author_sort Gao, Zhihua
collection PubMed
description BACKGROUND: The protein ferritin, which plays an important role in the maintenance of iron homeostasis, is indispensable for iron detoxification, resistance to oxidative stress and innate immunity. Ticks, which are obligate blood-sucking ectoparasites, have to deal with a large amount of iron when they take a blood meal. METHODS: Sequence analysis was undertaken using bioinformatics. A recombinant (r) expression vector, rferritin, was constructed for a prokaryotic expression system. A quantitative polymerase chain reaction platform was used to detect the spatial and temporal expression patterns of target genes and their responses to a low temperature environment. Knockdown of the ferritin genes through RNA interference was used to analyze their effects on physiological parameters of ticks. RESULTS: Two ferritin genes, HrFer1 and HrFer2, were cloned from the tick Hyalomma rufipes. Their open reading frames are 519 base pairs (bp) and 573 bp in length, and number of coding amino acids 170 and 190, respectively. The phylogenetic tree showed that HrFer1 and HrFer2 have a close evolutionary relationship with the H subunit of ferritin. In vitro experiments showed that rHrFer1 and rHrFer2 had concentration-dependent iron chelating activity. The relative expression of the two ferritin genes was higher in the ovary and midgut of H. rufipes. RNA interference results demonstrated that HrFer1 and HrFer2 expression had a significant effect on engorged body weight, number of eggs laid, and mortality of H. rufipes, and that HrFer2 also had a significant effect on feeding duration. Furthermore, the relative expression of ferritin decreased significantly in a low temperature environment, suggesting that HrFer1 and HrFer2 play a regulatory role in the cold stress response of H. rufipes. CONCLUSIONS: The results of the present study improve our understanding of the involvement of ferritins in tick blood-feeding. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-95638472022-10-15 The molecular and functional characterization of ferritins in the hard tick Hyalomma rufipes Gao, Zhihua Zheng, Peijing Wang, Kuang Ji, Xin Shi, Yanqing Song, Xuecheng Liu, Jingze Yu, Zhijun Yang, Xiaolong Parasit Vectors Research BACKGROUND: The protein ferritin, which plays an important role in the maintenance of iron homeostasis, is indispensable for iron detoxification, resistance to oxidative stress and innate immunity. Ticks, which are obligate blood-sucking ectoparasites, have to deal with a large amount of iron when they take a blood meal. METHODS: Sequence analysis was undertaken using bioinformatics. A recombinant (r) expression vector, rferritin, was constructed for a prokaryotic expression system. A quantitative polymerase chain reaction platform was used to detect the spatial and temporal expression patterns of target genes and their responses to a low temperature environment. Knockdown of the ferritin genes through RNA interference was used to analyze their effects on physiological parameters of ticks. RESULTS: Two ferritin genes, HrFer1 and HrFer2, were cloned from the tick Hyalomma rufipes. Their open reading frames are 519 base pairs (bp) and 573 bp in length, and number of coding amino acids 170 and 190, respectively. The phylogenetic tree showed that HrFer1 and HrFer2 have a close evolutionary relationship with the H subunit of ferritin. In vitro experiments showed that rHrFer1 and rHrFer2 had concentration-dependent iron chelating activity. The relative expression of the two ferritin genes was higher in the ovary and midgut of H. rufipes. RNA interference results demonstrated that HrFer1 and HrFer2 expression had a significant effect on engorged body weight, number of eggs laid, and mortality of H. rufipes, and that HrFer2 also had a significant effect on feeding duration. Furthermore, the relative expression of ferritin decreased significantly in a low temperature environment, suggesting that HrFer1 and HrFer2 play a regulatory role in the cold stress response of H. rufipes. CONCLUSIONS: The results of the present study improve our understanding of the involvement of ferritins in tick blood-feeding. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2022-10-14 /pmc/articles/PMC9563847/ /pubmed/36242057 http://dx.doi.org/10.1186/s13071-022-05515-0 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
Gao, Zhihua
Zheng, Peijing
Wang, Kuang
Ji, Xin
Shi, Yanqing
Song, Xuecheng
Liu, Jingze
Yu, Zhijun
Yang, Xiaolong
The molecular and functional characterization of ferritins in the hard tick Hyalomma rufipes
title The molecular and functional characterization of ferritins in the hard tick Hyalomma rufipes
title_full The molecular and functional characterization of ferritins in the hard tick Hyalomma rufipes
title_fullStr The molecular and functional characterization of ferritins in the hard tick Hyalomma rufipes
title_full_unstemmed The molecular and functional characterization of ferritins in the hard tick Hyalomma rufipes
title_short The molecular and functional characterization of ferritins in the hard tick Hyalomma rufipes
title_sort molecular and functional characterization of ferritins in the hard tick hyalomma rufipes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563847/
https://www.ncbi.nlm.nih.gov/pubmed/36242057
http://dx.doi.org/10.1186/s13071-022-05515-0
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