2D nanomaterial sensing array using machine learning for differential profiling of pathogenic microbial taxonomic identification

dc.contributor.authorLi Zhijun
dc.contributor.authorJiang Yizhou
dc.contributor.authorTang Shihuan
dc.contributor.authorZou Haixia
dc.contributor.authorWang Wentao
dc.contributor.authorQi Guangpei
dc.contributor.authorZhang Hongbo
dc.contributor.authorJin Kun
dc.contributor.authorWang Yuhe
dc.contributor.authorChen Hong
dc.contributor.authorZhang Liyuan
dc.contributor.authorQu Xiangmeng
dc.contributor.organizationfi=Turun biotiedekeskus|en=Turku Bioscience Centre|
dc.contributor.organization-code1.2.246.10.2458963.20.18586209670
dc.converis.publication-id175913092
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/175913092
dc.date.accessioned2022-10-28T13:24:41Z
dc.date.available2022-10-28T13:24:41Z
dc.description.abstractAn integrated custom cross-response sensing array has been developed combining the algorithm module's visible machine learning approach for rapid and accurate pathogenic microbial taxonomic identification. The diversified cross-response sensing array consists of two-dimensional nanomaterial (2D-n) with fluorescently labeled single-stranded DNA (ssDNA) as sensing elements to extract a set of differential response profiles for each pathogenic microorganism. By altering the 2D-n and different ssDNA with different sequences, we can form multiple sensing elements. While interacting with microorganisms, the competition between ssDNA and 2D-n leads to the release of ssDNA from 2D-n. The signals are generated from binding force driven by the exfoliation of either ssDNA or 2D-n from the microorganisms. Thus, the signal is distinguished from different ssDNA and 2D-n combinations, differentiating the extracted information and visualizing the recognition process. Fluorescent signals collected from each sensing element at the wavelength around 520 nm are applied to generate a fingerprint. As a proof of concept, we demonstrate that a six-sensing array enables rapid and accurate pathogenic microbial taxonomic identification, including the drug-resistant microorganisms, under a data size of n=288. We precisely identify microbial with an overall accuracy of 97.9%, which overcomes the big data dependence for identifying recurrent patterns in conventional methods. For each microorganism, the detection concentration is 10(5) similar to 10(8) CFU/mL for Escherichia coli, 10(2) similar to 10(7) CFU/mL for E. coli beta, 10(3) similar to 10(8) CFU/mL for Staphylococcus aureus, 10(3) similar to 10(7) CFU/mL for MRSA, 10(2) similar to 10(8) CFU/ mL for Pseudomonas aeruginosa, 10(3) similar to 10(8) CFU/mL for Enterococcus faecalis, 10(2) similar to 10(8) CFU/mL for Klebsiella pneumoniae, and 10(3) similar to 10(8) CFU/mL for Candida albicans. Combining the visible machine learning approach, this sensing array provides strategies for precision pathogenic microbial taxonomic identification.
dc.identifier.eissn1436-5073
dc.identifier.jour-issn0026-3672
dc.identifier.olddbid181897
dc.identifier.oldhandle10024/164991
dc.identifier.urihttps://www.utupub.fi/handle/11111/38982
dc.identifier.urlhttps://link.springer.com/article/10.1007/s00604-022-05368-5
dc.identifier.urnURN:NBN:fi-fe2022091258618
dc.language.isoen
dc.okm.affiliatedauthorZhang, Hongbo
dc.okm.discipline318 Medical biotechnologyen_GB
dc.okm.discipline318 Lääketieteen bioteknologiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherSPRINGER WIEN
dc.publisher.countryAustriaen_GB
dc.publisher.countryItävaltafi_FI
dc.publisher.country-codeAT
dc.relation.articlenumber273
dc.relation.doi10.1007/s00604-022-05368-5
dc.relation.ispartofjournalMicrochimica Acta
dc.relation.issue8
dc.relation.volume189
dc.source.identifierhttps://www.utupub.fi/handle/10024/164991
dc.title2D nanomaterial sensing array using machine learning for differential profiling of pathogenic microbial taxonomic identification
dc.year.issued2022

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