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Molecular epidemiology and antifungal susceptibilities of Cryptococcus species isolates from HIV and non-HIV patients in Southwest China
To investigated the molecular epidemiology and in vitro antifungal susceptibility of Cryptococcus isolates from West China Hospital from HIV and non-HIV patients between 2009 and 2015. A total of 132 C. neoformans and C. gattii were subjected to antifungal susceptibility testing by E -test method. A...
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Published in: | European journal of clinical microbiology & infectious diseases 2021-02, Vol.40 (2), p.287-295 |
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creator | Wu, Si-Ying Kang, Mei Liu, Ya Chen, Zhi-Xing Xiao, Yu-Ling He, Chao Ma, Ying |
description | To investigated the molecular epidemiology and in vitro antifungal susceptibility of
Cryptococcus
isolates from West China Hospital from HIV and non-HIV patients between 2009 and 2015. A total of 132
C. neoformans
and
C. gattii
were subjected to antifungal susceptibility testing by
E
-test method. Among the 132 isolates, 42
C. neoformans
and
C. gattii
were analyzed by mating type and
URA5
-RFLP. A total of 113
C. neoformans
and
C. gattii
were subjected to multi-locus sequence typing (MLST). MLST results revealed that ST5 was the major molecular type. The wild-type (WT) phenotype was seen in 91.5–100% of
C. neoformans
isolates for amphotericin B, 5-flucytosine, fluconazole, and voriconazole. However, 72.3% (94/130) of
C. neoformans
isolates were non-wild-type (non-WT) to itraconazole by
E
-test method. In the sixth study year, the geometric mean, MIC
50
and MIC
90
of fluconazole were the highest (
P
|
doi_str_mv | 10.1007/s10096-020-04013-4 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2440904828</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2440904828</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2904-4647ed19e7e8df01d93060939374d23142e2c48902abb89dd0992ade0452a1223</originalsourceid><addsrcrecordid>eNp9kc9uVCEUxomxsdPqC7gwJG7coPy7w2VpJmqb1Lho65YwwJ3S3AtXuMTMG_jYnunUmrhwAZzA73wfJx9Crxl9zyhVHyrsek0op4RKygSRz9CKSdERKZR4jlZUC0m04uIUndV6T6GpV-oFOhW8153quhX69TWPwbXRFhzm6MMU85h3e2yTh7XEoaWdHXFt1YV5ids4xiWGivOAN2U_L9ll51rFdQ7ucB9rHu0CxVDyhC8uvz8opZzIoZ4tNKcFsISvc1vufoa64M1dTPYlOhnsWMOrx_Mc3X7-dLO5IFffvlxuPl4RxzWVRK6lCp7poELvB8q8FnQNc2qhpOeCSR64k72m3G63vfaeas2tD1R23DLOxTl6d9SdS_7RwN5MEWYbR5tCbtVwKSkY9bwH9O0_6H1uJcHvgFKag7FkQPEj5UqutYTBzCVOtuwNo-aQkznmZCAn85CTkdD05lG6bafgn1r-BAOAOAIVntIulL_e_5H9DTkcnjg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2479206041</pqid></control><display><type>article</type><title>Molecular epidemiology and antifungal susceptibilities of Cryptococcus species isolates from HIV and non-HIV patients in Southwest China</title><source>Springer Nature</source><creator>Wu, Si-Ying ; Kang, Mei ; Liu, Ya ; Chen, Zhi-Xing ; Xiao, Yu-Ling ; He, Chao ; Ma, Ying</creator><creatorcontrib>Wu, Si-Ying ; Kang, Mei ; Liu, Ya ; Chen, Zhi-Xing ; Xiao, Yu-Ling ; He, Chao ; Ma, Ying</creatorcontrib><description>To investigated the molecular epidemiology and in vitro antifungal susceptibility of
Cryptococcus
isolates from West China Hospital from HIV and non-HIV patients between 2009 and 2015. A total of 132
C. neoformans
and
C. gattii
were subjected to antifungal susceptibility testing by
E
-test method. Among the 132 isolates, 42
C. neoformans
and
C. gattii
were analyzed by mating type and
URA5
-RFLP. A total of 113
C. neoformans
and
C. gattii
were subjected to multi-locus sequence typing (MLST). MLST results revealed that ST5 was the major molecular type. The wild-type (WT) phenotype was seen in 91.5–100% of
C. neoformans
isolates for amphotericin B, 5-flucytosine, fluconazole, and voriconazole. However, 72.3% (94/130) of
C. neoformans
isolates were non-wild-type (non-WT) to itraconazole by
E
-test method. In the sixth study year, the geometric mean, MIC
50
and MIC
90
of fluconazole were the highest (
P
< 0.001). Among 132 patients. 52 were coinfected with HIV and 80 were HIV-negative. Isolates from HIV and non-HIV patients showed no differences in susceptibility to amphotericin B (
P
= 0.544), 5-flucytosine (
P
= 0.063), fluconazole (
P
= 0.570), voriconazole (
P
= 0.542), and itraconazole (
P
= 0.787). Our study showed that
Cryptococcus
in southwest China showed a low degree of genetic diversity. The increased MIC values of fluconazole are noted.
Cryptococcus
isolates from HIV and non-HIV patients have shown no differences in susceptibility to five antifungal agents.</description><identifier>ISSN: 0934-9723</identifier><identifier>EISSN: 1435-4373</identifier><identifier>DOI: 10.1007/s10096-020-04013-4</identifier><identifier>PMID: 32895755</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Amphotericin B ; Antifungal agents ; Biomedical and Life Sciences ; Biomedicine ; Cryptococcus ; Cryptococcus neoformans ; Epidemiology ; Fluconazole ; Flucytosine ; Fungal infections ; Fungi ; Fungicides ; Genetic diversity ; HIV ; Human immunodeficiency virus ; Internal Medicine ; Itraconazole ; Medical Microbiology ; Minimum inhibitory concentration ; Multilocus sequence typing ; Original Article ; Phenotypes ; Susceptibility ; Test methods ; Voriconazole</subject><ispartof>European journal of clinical microbiology & infectious diseases, 2021-02, Vol.40 (2), p.287-295</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2904-4647ed19e7e8df01d93060939374d23142e2c48902abb89dd0992ade0452a1223</citedby><cites>FETCH-LOGICAL-c2904-4647ed19e7e8df01d93060939374d23142e2c48902abb89dd0992ade0452a1223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32895755$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Si-Ying</creatorcontrib><creatorcontrib>Kang, Mei</creatorcontrib><creatorcontrib>Liu, Ya</creatorcontrib><creatorcontrib>Chen, Zhi-Xing</creatorcontrib><creatorcontrib>Xiao, Yu-Ling</creatorcontrib><creatorcontrib>He, Chao</creatorcontrib><creatorcontrib>Ma, Ying</creatorcontrib><title>Molecular epidemiology and antifungal susceptibilities of Cryptococcus species isolates from HIV and non-HIV patients in Southwest China</title><title>European journal of clinical microbiology & infectious diseases</title><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><description>To investigated the molecular epidemiology and in vitro antifungal susceptibility of
Cryptococcus
isolates from West China Hospital from HIV and non-HIV patients between 2009 and 2015. A total of 132
C. neoformans
and
C. gattii
were subjected to antifungal susceptibility testing by
E
-test method. Among the 132 isolates, 42
C. neoformans
and
C. gattii
were analyzed by mating type and
URA5
-RFLP. A total of 113
C. neoformans
and
C. gattii
were subjected to multi-locus sequence typing (MLST). MLST results revealed that ST5 was the major molecular type. The wild-type (WT) phenotype was seen in 91.5–100% of
C. neoformans
isolates for amphotericin B, 5-flucytosine, fluconazole, and voriconazole. However, 72.3% (94/130) of
C. neoformans
isolates were non-wild-type (non-WT) to itraconazole by
E
-test method. In the sixth study year, the geometric mean, MIC
50
and MIC
90
of fluconazole were the highest (
P
< 0.001). Among 132 patients. 52 were coinfected with HIV and 80 were HIV-negative. Isolates from HIV and non-HIV patients showed no differences in susceptibility to amphotericin B (
P
= 0.544), 5-flucytosine (
P
= 0.063), fluconazole (
P
= 0.570), voriconazole (
P
= 0.542), and itraconazole (
P
= 0.787). Our study showed that
Cryptococcus
in southwest China showed a low degree of genetic diversity. The increased MIC values of fluconazole are noted.
Cryptococcus
isolates from HIV and non-HIV patients have shown no differences in susceptibility to five antifungal agents.</description><subject>Amphotericin B</subject><subject>Antifungal agents</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cryptococcus</subject><subject>Cryptococcus neoformans</subject><subject>Epidemiology</subject><subject>Fluconazole</subject><subject>Flucytosine</subject><subject>Fungal infections</subject><subject>Fungi</subject><subject>Fungicides</subject><subject>Genetic diversity</subject><subject>HIV</subject><subject>Human immunodeficiency virus</subject><subject>Internal Medicine</subject><subject>Itraconazole</subject><subject>Medical Microbiology</subject><subject>Minimum inhibitory concentration</subject><subject>Multilocus sequence typing</subject><subject>Original Article</subject><subject>Phenotypes</subject><subject>Susceptibility</subject><subject>Test methods</subject><subject>Voriconazole</subject><issn>0934-9723</issn><issn>1435-4373</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kc9uVCEUxomxsdPqC7gwJG7coPy7w2VpJmqb1Lho65YwwJ3S3AtXuMTMG_jYnunUmrhwAZzA73wfJx9Crxl9zyhVHyrsek0op4RKygSRz9CKSdERKZR4jlZUC0m04uIUndV6T6GpV-oFOhW8153quhX69TWPwbXRFhzm6MMU85h3e2yTh7XEoaWdHXFt1YV5ids4xiWGivOAN2U_L9ll51rFdQ7ucB9rHu0CxVDyhC8uvz8opZzIoZ4tNKcFsISvc1vufoa64M1dTPYlOhnsWMOrx_Mc3X7-dLO5IFffvlxuPl4RxzWVRK6lCp7poELvB8q8FnQNc2qhpOeCSR64k72m3G63vfaeas2tD1R23DLOxTl6d9SdS_7RwN5MEWYbR5tCbtVwKSkY9bwH9O0_6H1uJcHvgFKag7FkQPEj5UqutYTBzCVOtuwNo-aQkznmZCAn85CTkdD05lG6bafgn1r-BAOAOAIVntIulL_e_5H9DTkcnjg</recordid><startdate>20210201</startdate><enddate>20210201</enddate><creator>Wu, Si-Ying</creator><creator>Kang, Mei</creator><creator>Liu, Ya</creator><creator>Chen, Zhi-Xing</creator><creator>Xiao, Yu-Ling</creator><creator>He, Chao</creator><creator>Ma, Ying</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20210201</creationdate><title>Molecular epidemiology and antifungal susceptibilities of Cryptococcus species isolates from HIV and non-HIV patients in Southwest China</title><author>Wu, Si-Ying ; Kang, Mei ; Liu, Ya ; Chen, Zhi-Xing ; Xiao, Yu-Ling ; He, Chao ; Ma, Ying</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2904-4647ed19e7e8df01d93060939374d23142e2c48902abb89dd0992ade0452a1223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Amphotericin B</topic><topic>Antifungal agents</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cryptococcus</topic><topic>Cryptococcus neoformans</topic><topic>Epidemiology</topic><topic>Fluconazole</topic><topic>Flucytosine</topic><topic>Fungal infections</topic><topic>Fungi</topic><topic>Fungicides</topic><topic>Genetic diversity</topic><topic>HIV</topic><topic>Human immunodeficiency virus</topic><topic>Internal Medicine</topic><topic>Itraconazole</topic><topic>Medical Microbiology</topic><topic>Minimum inhibitory concentration</topic><topic>Multilocus sequence typing</topic><topic>Original Article</topic><topic>Phenotypes</topic><topic>Susceptibility</topic><topic>Test methods</topic><topic>Voriconazole</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Si-Ying</creatorcontrib><creatorcontrib>Kang, Mei</creatorcontrib><creatorcontrib>Liu, Ya</creatorcontrib><creatorcontrib>Chen, Zhi-Xing</creatorcontrib><creatorcontrib>Xiao, Yu-Ling</creatorcontrib><creatorcontrib>He, Chao</creatorcontrib><creatorcontrib>Ma, Ying</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of clinical microbiology & infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Si-Ying</au><au>Kang, Mei</au><au>Liu, Ya</au><au>Chen, Zhi-Xing</au><au>Xiao, Yu-Ling</au><au>He, Chao</au><au>Ma, Ying</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular epidemiology and antifungal susceptibilities of Cryptococcus species isolates from HIV and non-HIV patients in Southwest China</atitle><jtitle>European journal of clinical microbiology & infectious diseases</jtitle><stitle>Eur J Clin Microbiol Infect Dis</stitle><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><date>2021-02-01</date><risdate>2021</risdate><volume>40</volume><issue>2</issue><spage>287</spage><epage>295</epage><pages>287-295</pages><issn>0934-9723</issn><eissn>1435-4373</eissn><abstract>To investigated the molecular epidemiology and in vitro antifungal susceptibility of
Cryptococcus
isolates from West China Hospital from HIV and non-HIV patients between 2009 and 2015. A total of 132
C. neoformans
and
C. gattii
were subjected to antifungal susceptibility testing by
E
-test method. Among the 132 isolates, 42
C. neoformans
and
C. gattii
were analyzed by mating type and
URA5
-RFLP. A total of 113
C. neoformans
and
C. gattii
were subjected to multi-locus sequence typing (MLST). MLST results revealed that ST5 was the major molecular type. The wild-type (WT) phenotype was seen in 91.5–100% of
C. neoformans
isolates for amphotericin B, 5-flucytosine, fluconazole, and voriconazole. However, 72.3% (94/130) of
C. neoformans
isolates were non-wild-type (non-WT) to itraconazole by
E
-test method. In the sixth study year, the geometric mean, MIC
50
and MIC
90
of fluconazole were the highest (
P
< 0.001). Among 132 patients. 52 were coinfected with HIV and 80 were HIV-negative. Isolates from HIV and non-HIV patients showed no differences in susceptibility to amphotericin B (
P
= 0.544), 5-flucytosine (
P
= 0.063), fluconazole (
P
= 0.570), voriconazole (
P
= 0.542), and itraconazole (
P
= 0.787). Our study showed that
Cryptococcus
in southwest China showed a low degree of genetic diversity. The increased MIC values of fluconazole are noted.
Cryptococcus
isolates from HIV and non-HIV patients have shown no differences in susceptibility to five antifungal agents.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>32895755</pmid><doi>10.1007/s10096-020-04013-4</doi><tpages>9</tpages></addata></record> |
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language | eng |
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source | Springer Nature |
subjects | Amphotericin B Antifungal agents Biomedical and Life Sciences Biomedicine Cryptococcus Cryptococcus neoformans Epidemiology Fluconazole Flucytosine Fungal infections Fungi Fungicides Genetic diversity HIV Human immunodeficiency virus Internal Medicine Itraconazole Medical Microbiology Minimum inhibitory concentration Multilocus sequence typing Original Article Phenotypes Susceptibility Test methods Voriconazole |
title | Molecular epidemiology and antifungal susceptibilities of Cryptococcus species isolates from HIV and non-HIV patients in Southwest China |
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