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Genetic Diversity and Azole Resistance Among Natural Aspergillus fumigatus Populations in Yunnan, China
The emergence and spread of azole resistance alleles in clinical and environmental isolates of Aspergillus fumigatus is a global human health concern and endangers the “One Health” approach in our fight against antifungal resistance (AFR) in this pathogen. A major challenge to combat AFR in A. fumig...
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Published in: | Microbial ecology 2022-05, Vol.83 (4), p.869-885 |
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creator | Zhou, Duanyong Wang, Ruirui Li, Xiao Peng, Bin Yang, Guangzhu Zhang, Ke-Qin Zhang, Ying Xu, Jianping |
description | The emergence and spread of azole resistance alleles in clinical and environmental isolates of
Aspergillus fumigatus
is a global human health concern and endangers the “One Health” approach in our fight against antifungal resistance (AFR) in this pathogen. A major challenge to combat AFR in
A. fumigatus
is the massive aerial dispersal ability of its asexual spores. Our recent fine-scale survey of greenhouse populations of
A. fumigatus
near Kunming, Yunnan, China, suggested that the use of azole fungicides for plant protection was likely a major driver of the high-frequency azole-resistant
A. fumigatus
(ARAF) in greenhouses. Here, we investigated the potential spread of those ARAF and the structure of geographic populations of
A. fumigatus
by analyzing 452 isolates from 19 geographic locations across Yunnan. We found lower frequencies of ARAF in these outdoor populations than those in greenhouses near Kunming, but there were abundant new alleles and new genotypes, including those associated with azole resistance, consistent with multiple independent origins of ARAF across Yunnan. Interestingly, among the four ecological niches, the sediments of a large lake near Kunming were found to have the highest frequency of ARAF (~ 43%). While most genetic variations were observed within the 19 local populations, statistically significant genetic differentiations were found between many subpopulations within Yunnan. Furthermore, similar to greenhouse populations, these outdoor populations of
A. fumigatus
in Yunnan were significantly different from those in other parts of the world. Our results call for increased attention to local and regional studies of this fungal pathogen to help develop targeted control strategies against ARAF. |
doi_str_mv | 10.1007/s00248-021-01804-w |
format | article |
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Aspergillus fumigatus
is a global human health concern and endangers the “One Health” approach in our fight against antifungal resistance (AFR) in this pathogen. A major challenge to combat AFR in
A. fumigatus
is the massive aerial dispersal ability of its asexual spores. Our recent fine-scale survey of greenhouse populations of
A. fumigatus
near Kunming, Yunnan, China, suggested that the use of azole fungicides for plant protection was likely a major driver of the high-frequency azole-resistant
A. fumigatus
(ARAF) in greenhouses. Here, we investigated the potential spread of those ARAF and the structure of geographic populations of
A. fumigatus
by analyzing 452 isolates from 19 geographic locations across Yunnan. We found lower frequencies of ARAF in these outdoor populations than those in greenhouses near Kunming, but there were abundant new alleles and new genotypes, including those associated with azole resistance, consistent with multiple independent origins of ARAF across Yunnan. Interestingly, among the four ecological niches, the sediments of a large lake near Kunming were found to have the highest frequency of ARAF (~ 43%). While most genetic variations were observed within the 19 local populations, statistically significant genetic differentiations were found between many subpopulations within Yunnan. Furthermore, similar to greenhouse populations, these outdoor populations of
A. fumigatus
in Yunnan were significantly different from those in other parts of the world. Our results call for increased attention to local and regional studies of this fungal pathogen to help develop targeted control strategies against ARAF.</description><identifier>ISSN: 0095-3628</identifier><identifier>EISSN: 1432-184X</identifier><identifier>DOI: 10.1007/s00248-021-01804-w</identifier><identifier>PMID: 34279697</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Alleles ; Antifungal agents ; Antifungal Agents - pharmacology ; Aspergillus fumigatus ; Aspergillus fumigatus - genetics ; Azoles - pharmacology ; Biomedical and Life Sciences ; China ; Ecological distribution ; Ecological niches ; Ecology ; Fungal Microbiology ; Fungicides ; Genetic diversity ; Genetic Variation ; Genotypes ; Geoecology/Natural Processes ; Geographical locations ; Greenhouses ; Humans ; Lakes ; Life Sciences ; Local population ; Microbial Ecology ; Microbiology ; Nature Conservation ; Niches ; Pathogens ; Plant protection ; Population genetics ; Populations ; Regional development ; Sediments ; Spores ; Statistical analysis ; Subpopulations ; Surveying ; Water Quality/Water Pollution</subject><ispartof>Microbial ecology, 2022-05, Vol.83 (4), p.869-885</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021</rights><rights>2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.</rights><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-ab8e9038799325c31d2f67601f60d55d8c8cfcd0bebc6193eb4484bc3eb791d83</citedby><cites>FETCH-LOGICAL-c375t-ab8e9038799325c31d2f67601f60d55d8c8cfcd0bebc6193eb4484bc3eb791d83</cites><orcidid>0000-0003-2915-2780</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34279697$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Duanyong</creatorcontrib><creatorcontrib>Wang, Ruirui</creatorcontrib><creatorcontrib>Li, Xiao</creatorcontrib><creatorcontrib>Peng, Bin</creatorcontrib><creatorcontrib>Yang, Guangzhu</creatorcontrib><creatorcontrib>Zhang, Ke-Qin</creatorcontrib><creatorcontrib>Zhang, Ying</creatorcontrib><creatorcontrib>Xu, Jianping</creatorcontrib><title>Genetic Diversity and Azole Resistance Among Natural Aspergillus fumigatus Populations in Yunnan, China</title><title>Microbial ecology</title><addtitle>Microb Ecol</addtitle><addtitle>Microb Ecol</addtitle><description>The emergence and spread of azole resistance alleles in clinical and environmental isolates of
Aspergillus fumigatus
is a global human health concern and endangers the “One Health” approach in our fight against antifungal resistance (AFR) in this pathogen. A major challenge to combat AFR in
A. fumigatus
is the massive aerial dispersal ability of its asexual spores. Our recent fine-scale survey of greenhouse populations of
A. fumigatus
near Kunming, Yunnan, China, suggested that the use of azole fungicides for plant protection was likely a major driver of the high-frequency azole-resistant
A. fumigatus
(ARAF) in greenhouses. Here, we investigated the potential spread of those ARAF and the structure of geographic populations of
A. fumigatus
by analyzing 452 isolates from 19 geographic locations across Yunnan. We found lower frequencies of ARAF in these outdoor populations than those in greenhouses near Kunming, but there were abundant new alleles and new genotypes, including those associated with azole resistance, consistent with multiple independent origins of ARAF across Yunnan. Interestingly, among the four ecological niches, the sediments of a large lake near Kunming were found to have the highest frequency of ARAF (~ 43%). While most genetic variations were observed within the 19 local populations, statistically significant genetic differentiations were found between many subpopulations within Yunnan. Furthermore, similar to greenhouse populations, these outdoor populations of
A. fumigatus
in Yunnan were significantly different from those in other parts of the world. Our results call for increased attention to local and regional studies of this fungal pathogen to help develop targeted control strategies against ARAF.</description><subject>Alleles</subject><subject>Antifungal agents</subject><subject>Antifungal Agents - pharmacology</subject><subject>Aspergillus fumigatus</subject><subject>Aspergillus fumigatus - genetics</subject><subject>Azoles - pharmacology</subject><subject>Biomedical and Life Sciences</subject><subject>China</subject><subject>Ecological distribution</subject><subject>Ecological niches</subject><subject>Ecology</subject><subject>Fungal Microbiology</subject><subject>Fungicides</subject><subject>Genetic diversity</subject><subject>Genetic Variation</subject><subject>Genotypes</subject><subject>Geoecology/Natural Processes</subject><subject>Geographical locations</subject><subject>Greenhouses</subject><subject>Humans</subject><subject>Lakes</subject><subject>Life Sciences</subject><subject>Local population</subject><subject>Microbial Ecology</subject><subject>Microbiology</subject><subject>Nature Conservation</subject><subject>Niches</subject><subject>Pathogens</subject><subject>Plant protection</subject><subject>Population genetics</subject><subject>Populations</subject><subject>Regional development</subject><subject>Sediments</subject><subject>Spores</subject><subject>Statistical analysis</subject><subject>Subpopulations</subject><subject>Surveying</subject><subject>Water Quality/Water 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Diversity and Azole Resistance Among Natural Aspergillus fumigatus Populations in Yunnan, China</title><author>Zhou, Duanyong ; Wang, Ruirui ; Li, Xiao ; Peng, Bin ; Yang, Guangzhu ; Zhang, Ke-Qin ; Zhang, Ying ; Xu, Jianping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-ab8e9038799325c31d2f67601f60d55d8c8cfcd0bebc6193eb4484bc3eb791d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Alleles</topic><topic>Antifungal agents</topic><topic>Antifungal Agents - pharmacology</topic><topic>Aspergillus fumigatus</topic><topic>Aspergillus fumigatus - genetics</topic><topic>Azoles - pharmacology</topic><topic>Biomedical and Life Sciences</topic><topic>China</topic><topic>Ecological distribution</topic><topic>Ecological niches</topic><topic>Ecology</topic><topic>Fungal Microbiology</topic><topic>Fungicides</topic><topic>Genetic diversity</topic><topic>Genetic Variation</topic><topic>Genotypes</topic><topic>Geoecology/Natural Processes</topic><topic>Geographical locations</topic><topic>Greenhouses</topic><topic>Humans</topic><topic>Lakes</topic><topic>Life Sciences</topic><topic>Local population</topic><topic>Microbial Ecology</topic><topic>Microbiology</topic><topic>Nature Conservation</topic><topic>Niches</topic><topic>Pathogens</topic><topic>Plant protection</topic><topic>Population genetics</topic><topic>Populations</topic><topic>Regional development</topic><topic>Sediments</topic><topic>Spores</topic><topic>Statistical analysis</topic><topic>Subpopulations</topic><topic>Surveying</topic><topic>Water Quality/Water Pollution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Duanyong</creatorcontrib><creatorcontrib>Wang, Ruirui</creatorcontrib><creatorcontrib>Li, Xiao</creatorcontrib><creatorcontrib>Peng, Bin</creatorcontrib><creatorcontrib>Yang, 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Atmospheric & Aquatic Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><jtitle>Microbial ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Duanyong</au><au>Wang, Ruirui</au><au>Li, Xiao</au><au>Peng, Bin</au><au>Yang, Guangzhu</au><au>Zhang, Ke-Qin</au><au>Zhang, Ying</au><au>Xu, Jianping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic Diversity and Azole Resistance Among Natural Aspergillus fumigatus Populations in Yunnan, China</atitle><jtitle>Microbial ecology</jtitle><stitle>Microb Ecol</stitle><addtitle>Microb Ecol</addtitle><date>2022-05-01</date><risdate>2022</risdate><volume>83</volume><issue>4</issue><spage>869</spage><epage>885</epage><pages>869-885</pages><issn>0095-3628</issn><eissn>1432-184X</eissn><abstract>The emergence and spread of azole resistance alleles in clinical and environmental isolates of
Aspergillus fumigatus
is a global human health concern and endangers the “One Health” approach in our fight against antifungal resistance (AFR) in this pathogen. A major challenge to combat AFR in
A. fumigatus
is the massive aerial dispersal ability of its asexual spores. Our recent fine-scale survey of greenhouse populations of
A. fumigatus
near Kunming, Yunnan, China, suggested that the use of azole fungicides for plant protection was likely a major driver of the high-frequency azole-resistant
A. fumigatus
(ARAF) in greenhouses. Here, we investigated the potential spread of those ARAF and the structure of geographic populations of
A. fumigatus
by analyzing 452 isolates from 19 geographic locations across Yunnan. We found lower frequencies of ARAF in these outdoor populations than those in greenhouses near Kunming, but there were abundant new alleles and new genotypes, including those associated with azole resistance, consistent with multiple independent origins of ARAF across Yunnan. Interestingly, among the four ecological niches, the sediments of a large lake near Kunming were found to have the highest frequency of ARAF (~ 43%). While most genetic variations were observed within the 19 local populations, statistically significant genetic differentiations were found between many subpopulations within Yunnan. Furthermore, similar to greenhouse populations, these outdoor populations of
A. fumigatus
in Yunnan were significantly different from those in other parts of the world. Our results call for increased attention to local and regional studies of this fungal pathogen to help develop targeted control strategies against ARAF.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>34279697</pmid><doi>10.1007/s00248-021-01804-w</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0003-2915-2780</orcidid></addata></record> |
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subjects | Alleles Antifungal agents Antifungal Agents - pharmacology Aspergillus fumigatus Aspergillus fumigatus - genetics Azoles - pharmacology Biomedical and Life Sciences China Ecological distribution Ecological niches Ecology Fungal Microbiology Fungicides Genetic diversity Genetic Variation Genotypes Geoecology/Natural Processes Geographical locations Greenhouses Humans Lakes Life Sciences Local population Microbial Ecology Microbiology Nature Conservation Niches Pathogens Plant protection Population genetics Populations Regional development Sediments Spores Statistical analysis Subpopulations Surveying Water Quality/Water Pollution |
title | Genetic Diversity and Azole Resistance Among Natural Aspergillus fumigatus Populations in Yunnan, China |
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