Please use this identifier to cite or link to this item: https://doi.org/10.3389/fmicb.2021.709562
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dc.titleCirculating Antibodies to Skin Bacteria Detected by Serological Lateral Flow Immunoassays Differentially Correlated With Bacterial Abundance
dc.contributor.authorHuang, Ryan Yuki
dc.contributor.authorLee, Chuen Neng
dc.contributor.authorMoochhala, Shabbir
dc.date.accessioned2022-10-12T07:59:36Z
dc.date.available2022-10-12T07:59:36Z
dc.date.issued2021-11-10
dc.identifier.citationHuang, Ryan Yuki, Lee, Chuen Neng, Moochhala, Shabbir (2021-11-10). Circulating Antibodies to Skin Bacteria Detected by Serological Lateral Flow Immunoassays Differentially Correlated With Bacterial Abundance. Frontiers in Microbiology 12 : 709562. ScholarBank@NUS Repository. https://doi.org/10.3389/fmicb.2021.709562
dc.identifier.issn1664-302X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/232369
dc.description.abstractThe serological lateral flow immunoassay (LFIA) was used to detect circulating antibodies to skin bacteria. Next-generation sequencing analysis of the skin microbiome revealed a high relative abundance of Cutibacterium acnes but low abundance of Staphylococcus aureus and Corynebacterium aurimucosum on human facial samples. Yet, results from both LFIA and antibody titer quantification in 96-well microplates illustrated antibody titers that were not correspondent, and instead negatively correlated, to their respective abundance with human blood containing higher concentrations of antibodies to both S. aureus and C. aurimucosum than C. acnes. Acne vulgaris develops several unique microbial and cellular features, but its correlation with circulating antibodies to bacteria in the pilosebaceous unit remains unknown. Results here revealed that antibodies to C. acnes and S. aureus were approximately 3-fold higher and 1.5-fold lower, respectively, in acne patients than in healthy subjects. Although the results can be further validated by larger sample sizes, the proof-of-concept study demonstrates a newfound discrepancy between the abundance of skin bacteria and amounts of their corresponding antibodies. And in light of acne-correlated amplified titers of specific anticommensal antibodies, we highlight that profiling these antibodies in the pilosebaceous unit by LFIAs may provide a unique signature for monitoring acne vulgaris. Copyright © 2021 Huang, Lee and Moochhala.
dc.publisherFrontiers Media S.A.
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2021
dc.subjectacne vulgaris
dc.subjectantibody
dc.subjectC. acnes
dc.subjectC. aurimucosum
dc.subjectlateral flow immunoassays
dc.subjectS. aureus
dc.typeArticle
dc.contributor.departmentSURGERY
dc.contributor.departmentPHARMACOLOGY
dc.description.doi10.3389/fmicb.2021.709562
dc.description.sourcetitleFrontiers in Microbiology
dc.description.volume12
dc.description.page709562
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