Comparison of DNA sequencing and morphological identification techniques to characterize environmental fungal communities

Abstract Culture-independent DNA sequencing of fungal internal transcribed spacer 2 (ITS2) region was compared to a culture-dependent morphological identification technique to characterize house dust-borne fungal communities. The abundant genera were Aspergillus, Wallemia, Cladosporium, and Penicill...

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Autores principales: Naohide Shinohara, Cheolwoon Woo, Naomichi Yamamoto, Kazuhiro Hashimoto, Hiroko Yoshida-Ohuchi, Yuji Kawakami
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/d2d4024f820344429d3ecf2af9b62a40
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spelling oai:doaj.org-article:d2d4024f820344429d3ecf2af9b62a402021-12-02T13:24:25ZComparison of DNA sequencing and morphological identification techniques to characterize environmental fungal communities10.1038/s41598-021-81996-w2045-2322https://doaj.org/article/d2d4024f820344429d3ecf2af9b62a402021-01-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-81996-whttps://doaj.org/toc/2045-2322Abstract Culture-independent DNA sequencing of fungal internal transcribed spacer 2 (ITS2) region was compared to a culture-dependent morphological identification technique to characterize house dust-borne fungal communities. The abundant genera were Aspergillus, Wallemia, Cladosporium, and Penicillium. Statistically significant between-method correlations were observed for Wallemia and Cladosporium (Spearman’s ρ = 0.75 and 0.72, respectively; p < 0.001). Penicillium tended to be detected with much higher (averaged 26-times) relative abundances by the culture-based method than by the DNA-based method, although statistically significant inter-method correlation was observed with Spearman’s ρ = 0.61 (p = 0.002). Large DNA sequencing-based relative abundances observed for Alternaria and Aureobasidium were likely due to multicellularity of their spores with large number of per-spore ITS2 copies. The failure of the culture-based method in detectiing Toxicocladosporium, Verrucocladosporium, and Sterigmatomyces was likely due to their fastidiousness growth on our nutrient medium. Comparing between the two different techniques clarified the causes of biases in identifying environmental fungal communities, which should be amended and/or taken into consideration when the methods are used for future fungal ecological studies.Naohide ShinoharaCheolwoon WooNaomichi YamamotoKazuhiro HashimotoHiroko Yoshida-OhuchiYuji KawakamiNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Naohide Shinohara
Cheolwoon Woo
Naomichi Yamamoto
Kazuhiro Hashimoto
Hiroko Yoshida-Ohuchi
Yuji Kawakami
Comparison of DNA sequencing and morphological identification techniques to characterize environmental fungal communities
description Abstract Culture-independent DNA sequencing of fungal internal transcribed spacer 2 (ITS2) region was compared to a culture-dependent morphological identification technique to characterize house dust-borne fungal communities. The abundant genera were Aspergillus, Wallemia, Cladosporium, and Penicillium. Statistically significant between-method correlations were observed for Wallemia and Cladosporium (Spearman’s ρ = 0.75 and 0.72, respectively; p < 0.001). Penicillium tended to be detected with much higher (averaged 26-times) relative abundances by the culture-based method than by the DNA-based method, although statistically significant inter-method correlation was observed with Spearman’s ρ = 0.61 (p = 0.002). Large DNA sequencing-based relative abundances observed for Alternaria and Aureobasidium were likely due to multicellularity of their spores with large number of per-spore ITS2 copies. The failure of the culture-based method in detectiing Toxicocladosporium, Verrucocladosporium, and Sterigmatomyces was likely due to their fastidiousness growth on our nutrient medium. Comparing between the two different techniques clarified the causes of biases in identifying environmental fungal communities, which should be amended and/or taken into consideration when the methods are used for future fungal ecological studies.
format article
author Naohide Shinohara
Cheolwoon Woo
Naomichi Yamamoto
Kazuhiro Hashimoto
Hiroko Yoshida-Ohuchi
Yuji Kawakami
author_facet Naohide Shinohara
Cheolwoon Woo
Naomichi Yamamoto
Kazuhiro Hashimoto
Hiroko Yoshida-Ohuchi
Yuji Kawakami
author_sort Naohide Shinohara
title Comparison of DNA sequencing and morphological identification techniques to characterize environmental fungal communities
title_short Comparison of DNA sequencing and morphological identification techniques to characterize environmental fungal communities
title_full Comparison of DNA sequencing and morphological identification techniques to characterize environmental fungal communities
title_fullStr Comparison of DNA sequencing and morphological identification techniques to characterize environmental fungal communities
title_full_unstemmed Comparison of DNA sequencing and morphological identification techniques to characterize environmental fungal communities
title_sort comparison of dna sequencing and morphological identification techniques to characterize environmental fungal communities
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/d2d4024f820344429d3ecf2af9b62a40
work_keys_str_mv AT naohideshinohara comparisonofdnasequencingandmorphologicalidentificationtechniquestocharacterizeenvironmentalfungalcommunities
AT cheolwoonwoo comparisonofdnasequencingandmorphologicalidentificationtechniquestocharacterizeenvironmentalfungalcommunities
AT naomichiyamamoto comparisonofdnasequencingandmorphologicalidentificationtechniquestocharacterizeenvironmentalfungalcommunities
AT kazuhirohashimoto comparisonofdnasequencingandmorphologicalidentificationtechniquestocharacterizeenvironmentalfungalcommunities
AT hirokoyoshidaohuchi comparisonofdnasequencingandmorphologicalidentificationtechniquestocharacterizeenvironmentalfungalcommunities
AT yujikawakami comparisonofdnasequencingandmorphologicalidentificationtechniquestocharacterizeenvironmentalfungalcommunities
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