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Utilizing pyrosequencing and quantitative PCR to characterize fungal populations among house dust samples

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JOURNAL OF ENVIRONMENTAL MONITORING
卷 14, 期 8, 页码 2038-2043

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c2em30229b

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资金

  1. National Institutes of Health, Eunice Kennedy Shriver National institute of Child Health and Human Development
  2. US EPA [RD-83273301, 2W-2296-NATA]
  3. NIEHS [RD-83170901, ES-09601]
  4. National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services [HHSN267200700023C]

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Molecular techniques are an alternative to culturing and counting methods in quantifying indoor fungal contamination. Pyrosequencing offers the possibility of identifying unexpected indoor fungi. In this study, 50 house dust samples were collected from homes in the Yakima Valley, WA. Each sample was analyzed by quantitative PCR (QPCR) for 36 common fungi and by fungal tag-encoded flexible (FLX) amplicon pyrosequencing (fTEFAP) for these and additional fungi. Only 24 of the samples yielded amplified results using fTEFAP but QPCR successfully amplified all 50 samples. Over 450 fungal species were detected by fTEFAP but most were rare. Twenty-two fungi were found by fTEFAP to occur with at least an average of >= 0.5% relative occurrence. Many of these fungi seem to be associated with plants, soil or human skin. Combining fTEFAP and QPCR can enhance studies of fungal contamination in homes.

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