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A Shift Pattern of Bacterial Communities Across the Life Stages of the Citrus Red Mite, Panonychus citri
As one of the most detrimental citrus pests worldwide, the citrus red mite, Panonychus citri (McGregor), shows extraordinary fecundity, polyphagia, and acaricide resistance, which may be influenced by microbes as other arthropod pests. However, the community structure and physiological function of m...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366552/ https://www.ncbi.nlm.nih.gov/pubmed/32754145 http://dx.doi.org/10.3389/fmicb.2020.01620 |
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author | Zhang, Zhen-yu Ali, Muhammad Waqar Saqib, Hafiz Sohaib Ahmed Liu, Sheng-xuan Yang, Xin Li, Qin Zhang, Hongyu |
author_facet | Zhang, Zhen-yu Ali, Muhammad Waqar Saqib, Hafiz Sohaib Ahmed Liu, Sheng-xuan Yang, Xin Li, Qin Zhang, Hongyu |
author_sort | Zhang, Zhen-yu |
collection | PubMed |
description | As one of the most detrimental citrus pests worldwide, the citrus red mite, Panonychus citri (McGregor), shows extraordinary fecundity, polyphagia, and acaricide resistance, which may be influenced by microbes as other arthropod pests. However, the community structure and physiological function of microbes in P. citri are still largely unknown. Here, the high-throughput sequencing of 16S rDNA amplicons was employed to identify and compare the profile of bacterial communities across the larva, protonymph, deutonymph, and adult stages of P. citri. We observed a dominance of phylums Proteobacteria and Firmicutes, and classes α-, γ-, β-Proteobacteria and Bacilli in the bacterial communities across the host lifespan. Based on the dynamic analysis of the bacterial community structure, a significant shift pattern between the immature (larva, protonymph, and deutonymph) and adult stages was observed. Accordingly, among the major families (and corresponding genera), although the relative abundances of Pseudomonadaceae (Pseudomonas), Moraxellaceae (Acinetobacter), and Sphingobacteriaceae (Sphingobacterium) were consistent in larva to deutonymph stages, they were significantly increased to 30.18 ± 8.76% (30.16 ± 8.75%), 20.78 ± 10.86% (18.80 ± 10.84%), and 11.71 ± 5.49% (11.68 ± 5.48%), respectively, in adult stage, which implied the important function of these bacteria on the adults’ physiology. Actually, the functional prediction of bacterial communities and Spearman correlation analysis further confirm that these bacteria had positively correlations with the pathway of “lipid metabolism” (including eight sublevel pathways) and “metabolism of cofactors and vitamins” (including five sublevel pathways), which all only increased in adult stages. In addition, the bacterial communities were eliminated by using broad-spectrum antibiotics, streptomycin, which significantly suppressed the survival and oviposition of P. citri. Overall, we not only confirmed the physiological effects of bacteria community on the vitality and fecundity of adult hosts, but also revealed the shift pattern of bacterial community structures across the life stages and demonstrated the co-enhancements of specific bacterial groups and bacterial functions in nutritional metabolism in P. citri. This study sheds light on basic information about the mutualism between spider mites and bacteria, which may be useful in shaping the next generation of control strategies for spider mite pests, especially P. citri. |
format | Online Article Text |
id | pubmed-7366552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73665522020-08-03 A Shift Pattern of Bacterial Communities Across the Life Stages of the Citrus Red Mite, Panonychus citri Zhang, Zhen-yu Ali, Muhammad Waqar Saqib, Hafiz Sohaib Ahmed Liu, Sheng-xuan Yang, Xin Li, Qin Zhang, Hongyu Front Microbiol Microbiology As one of the most detrimental citrus pests worldwide, the citrus red mite, Panonychus citri (McGregor), shows extraordinary fecundity, polyphagia, and acaricide resistance, which may be influenced by microbes as other arthropod pests. However, the community structure and physiological function of microbes in P. citri are still largely unknown. Here, the high-throughput sequencing of 16S rDNA amplicons was employed to identify and compare the profile of bacterial communities across the larva, protonymph, deutonymph, and adult stages of P. citri. We observed a dominance of phylums Proteobacteria and Firmicutes, and classes α-, γ-, β-Proteobacteria and Bacilli in the bacterial communities across the host lifespan. Based on the dynamic analysis of the bacterial community structure, a significant shift pattern between the immature (larva, protonymph, and deutonymph) and adult stages was observed. Accordingly, among the major families (and corresponding genera), although the relative abundances of Pseudomonadaceae (Pseudomonas), Moraxellaceae (Acinetobacter), and Sphingobacteriaceae (Sphingobacterium) were consistent in larva to deutonymph stages, they were significantly increased to 30.18 ± 8.76% (30.16 ± 8.75%), 20.78 ± 10.86% (18.80 ± 10.84%), and 11.71 ± 5.49% (11.68 ± 5.48%), respectively, in adult stage, which implied the important function of these bacteria on the adults’ physiology. Actually, the functional prediction of bacterial communities and Spearman correlation analysis further confirm that these bacteria had positively correlations with the pathway of “lipid metabolism” (including eight sublevel pathways) and “metabolism of cofactors and vitamins” (including five sublevel pathways), which all only increased in adult stages. In addition, the bacterial communities were eliminated by using broad-spectrum antibiotics, streptomycin, which significantly suppressed the survival and oviposition of P. citri. Overall, we not only confirmed the physiological effects of bacteria community on the vitality and fecundity of adult hosts, but also revealed the shift pattern of bacterial community structures across the life stages and demonstrated the co-enhancements of specific bacterial groups and bacterial functions in nutritional metabolism in P. citri. This study sheds light on basic information about the mutualism between spider mites and bacteria, which may be useful in shaping the next generation of control strategies for spider mite pests, especially P. citri. Frontiers Media S.A. 2020-07-10 /pmc/articles/PMC7366552/ /pubmed/32754145 http://dx.doi.org/10.3389/fmicb.2020.01620 Text en Copyright © 2020 Zhang, Ali, Saqib, Liu, Yang, Li and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Zhang, Zhen-yu Ali, Muhammad Waqar Saqib, Hafiz Sohaib Ahmed Liu, Sheng-xuan Yang, Xin Li, Qin Zhang, Hongyu A Shift Pattern of Bacterial Communities Across the Life Stages of the Citrus Red Mite, Panonychus citri |
title | A Shift Pattern of Bacterial Communities Across the Life Stages of the Citrus Red Mite, Panonychus citri |
title_full | A Shift Pattern of Bacterial Communities Across the Life Stages of the Citrus Red Mite, Panonychus citri |
title_fullStr | A Shift Pattern of Bacterial Communities Across the Life Stages of the Citrus Red Mite, Panonychus citri |
title_full_unstemmed | A Shift Pattern of Bacterial Communities Across the Life Stages of the Citrus Red Mite, Panonychus citri |
title_short | A Shift Pattern of Bacterial Communities Across the Life Stages of the Citrus Red Mite, Panonychus citri |
title_sort | shift pattern of bacterial communities across the life stages of the citrus red mite, panonychus citri |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366552/ https://www.ncbi.nlm.nih.gov/pubmed/32754145 http://dx.doi.org/10.3389/fmicb.2020.01620 |
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