{"title":"DNA metabarcoding analysis of fungal community on surface of four root herbs","authors":"Yujie Dao, Jingsheng Yu, Meihua Yang, Jianping Han, Chune Fan, Xiaohui Pang","doi":"10.1016/j.chmed.2023.01.003","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p><em>Angelicae Sinensis Radix</em> (ASR, Danggui in Chinese), <em>Cistanches Herba</em> (CH, Roucongrong in Chinese), <em>Ginseng Radix</em> et <em>Rhizoma</em> (PG, Renshen in Chinese), and <em>Panacis Quinquefolii Radix</em> (PQ, Xiyangshen in Chinese), widely used as medicine and dietary supplement around the world, are susceptible to fungal and mycotoxin contamination. In this study, we aim to analyze their fungal community by DNA metabarcoding.</p></div><div><h3>Methods</h3><p>A total of 12 root samples were collected from three main production areas in China. The samples were divided into four groups based on herb species, including ASR, CH, PG, and PQ groups. The fungal community on the surface of four root groups was investigated through DNA metabarcoding via targeting the internal transcribed spacer 2 region (ITS2).</p></div><div><h3>Results</h3><p>All the 12 samples were detected with fungal contamination. <em>Rhizopus</em> (13.04%−74.03%), <em>Aspergillus</em> (1.76%−23.92%), and <em>Fusarium</em> (0.26%−15.27%) were the predominant genera. Ten important fungi were identified at the species level, including two potential toxigenic fungi (<em>Penicillium citrinum</em> and <em>P</em>. <em>oxalicum</em>) and eight human pathogenic fungi (<em>Alternaria infectoria</em>, <em>Candida sake</em>, <em>Hyphopichia burtonii</em>, <em>Malassezia globosa</em>, <em>M</em>. <em>restricta</em>, <em>Rhizopus arrhizus</em>, <em>Rhodotorula mucilaginosa</em>, and <em>Ochroconis tshawytschae</em>). Fungal community in ASR and CH groups was significantly different from other groups, while fungal community in PG and PQ groups was relatively similar.</p></div><div><h3>Conclusion</h3><p>DNA metabarcoding revealed the fungal community in four important root herbs. This study provided an important reference for preventing root herbs against fungal and mycotoxin contamination.</p></div>","PeriodicalId":9916,"journal":{"name":"Chinese Herbal Medicines","volume":null,"pages":null},"PeriodicalIF":4.7000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1674638423000461/pdfft?md5=a057dc5cad3ba0b1c38dea69ba691bd5&pid=1-s2.0-S1674638423000461-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Herbal Medicines","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1674638423000461","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
Abstract
Objective
Angelicae Sinensis Radix (ASR, Danggui in Chinese), Cistanches Herba (CH, Roucongrong in Chinese), Ginseng Radix et Rhizoma (PG, Renshen in Chinese), and Panacis Quinquefolii Radix (PQ, Xiyangshen in Chinese), widely used as medicine and dietary supplement around the world, are susceptible to fungal and mycotoxin contamination. In this study, we aim to analyze their fungal community by DNA metabarcoding.
Methods
A total of 12 root samples were collected from three main production areas in China. The samples were divided into four groups based on herb species, including ASR, CH, PG, and PQ groups. The fungal community on the surface of four root groups was investigated through DNA metabarcoding via targeting the internal transcribed spacer 2 region (ITS2).
Results
All the 12 samples were detected with fungal contamination. Rhizopus (13.04%−74.03%), Aspergillus (1.76%−23.92%), and Fusarium (0.26%−15.27%) were the predominant genera. Ten important fungi were identified at the species level, including two potential toxigenic fungi (Penicillium citrinum and P. oxalicum) and eight human pathogenic fungi (Alternaria infectoria, Candida sake, Hyphopichia burtonii, Malassezia globosa, M. restricta, Rhizopus arrhizus, Rhodotorula mucilaginosa, and Ochroconis tshawytschae). Fungal community in ASR and CH groups was significantly different from other groups, while fungal community in PG and PQ groups was relatively similar.
Conclusion
DNA metabarcoding revealed the fungal community in four important root herbs. This study provided an important reference for preventing root herbs against fungal and mycotoxin contamination.