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. 2021 Oct 19;9:209. doi: 10.1186/s40168-021-01158-y

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 1 — Fungal quantity from qPCR of the CA dust embedded in carpet A samples and drywall taken from qPCR of the CA inoculated drywall samples. A Fungal growth in CA carpet A with dust revealed an inflection point between 75% to 80% ERH. B Fungal growth in CA painted drywall A revealed an inflection point between 85% to 95% ERH. *New samples of dust and carpet were incubated at 95% ERH for 4 weeks continuously at a later date to determine accurate quantities of fungal growth. Original samples were inconclusive at 95% ERH as the carpet was too wet to collect adequate dust.