Detection and quantification of Staphylococcus in chronic rhinosinusitis.

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dc.contributor.author Wagner Mackenzie, Brett
dc.contributor.author Baker, Jesse
dc.contributor.author Douglas, Richard G
dc.contributor.author Taylor, Michael W
dc.contributor.author Biswas, Kristi
dc.coverage.spatial United States
dc.date.accessioned 2024-06-10T00:44:34Z
dc.date.available 2024-06-10T00:44:34Z
dc.date.issued 2019-12
dc.identifier.citation (2019). International Forum of Allergy and Rhinology, 9(12), 1462-1469.
dc.identifier.issn 2042-6976
dc.identifier.uri https://hdl.handle.net/2292/68735
dc.description.abstract <h4>Background</h4>The sinonasal microbiota has been implicated in chronic rhinosinusitis (CRS) pathogenesis, particularly related to the presence of Staphylococcus aureus. Staphylococcus epidermidis is also prevalent within the sinonasal microbiota and may inhibit S. aureus colonization. We investigated polymerase chain reaction (PCR) primer pairs for measuring absolute abundances of S. aureus and S. epidermidis, then compared bacterial community composition and absolute abundances of these species between CRS patients and controls.<h4>Methods</h4>Six candidate Staphylococcus species-specific primer pairs were tested in silico and in vitro against pure bacterial isolates. Quantitative PCR (qPCR) for absolute quantification of S. aureus, S. epidermidis, and overall bacterial load were assessed in 40 CRS (CRS without nasal polyposis [CRSsNP] = 22, CRS with nasal polyposis [CRSwNP] = 18) patients and 14 controls. Amplicon sequencing of the V3-V4 hypervariable regions of the 16S ribosomal RNA (rRNA) bacterial gene were conducted to investigate community composition.<h4>Results</h4>Primer pairs targeting the gmk gene of S. aureus and nrd gene from S. epidermidis were the most specific and sensitive primers. S. aureus (CRSsNP = 81.8% occurrence, CRSwNP = 83%, control = 92.9%) and S. epidermidis (CRSsNP = 95.5%, CRSwNP = 100%, control = 92.9%) were very prevalent, as indicated by qPCR results. Both CRSsNP and CRSwNP had significantly (p < 0.05) higher bacterial load when compared with controls (p < 0.05 for both). No significant correlation was observed between S. aureus and S. epidermidis abundances (p > 0.05).<h4>Conclusion</h4>Bacterial community sequencing detected Staphylococcus-assigned sequences in nearly all patients; however, it could not differentiate between S. aureus and S. epidermidis. Here, we present primer pairs that can distinguish between these species. We report a very high prevalence of S. aureus in both CRS patients and controls.
dc.format.medium Print-Electronic
dc.language eng
dc.publisher Wiley
dc.relation.ispartofseries International forum of allergy & rhinology
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher.
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm
dc.subject Paranasal Sinuses
dc.subject Humans
dc.subject Staphylococcus aureus
dc.subject Staphylococcus epidermidis
dc.subject Sinusitis
dc.subject Rhinitis
dc.subject Chronic Disease
dc.subject RNA, Bacterial
dc.subject RNA, Ribosomal, 16S
dc.subject Genes, Bacterial
dc.subject Adult
dc.subject Aged
dc.subject Middle Aged
dc.subject Female
dc.subject Male
dc.subject Staphylococcus spp
dc.subject bacteriology
dc.subject chronic rhinosinusitis
dc.subject qPCR
dc.subject statistics
dc.subject 32 Biomedical and Clinical Sciences
dc.subject 3202 Clinical Sciences
dc.subject Genetics
dc.subject Emerging Infectious Diseases
dc.subject Infectious Diseases
dc.subject Infection
dc.subject Science & Technology
dc.subject Life Sciences & Biomedicine
dc.subject Otorhinolaryngology
dc.subject 1103 Clinical Sciences
dc.subject 1107 Immunology
dc.subject 3204 Immunology
dc.title Detection and quantification of Staphylococcus in chronic rhinosinusitis.
dc.type Journal Article
dc.identifier.doi 10.1002/alr.22425
pubs.issue 12
pubs.begin-page 1462
pubs.volume 9
dc.date.updated 2024-05-02T21:18:29Z
dc.rights.holder Copyright: The authors en
dc.identifier.pmid 31483577 (pubmed)
pubs.author-url https://www.ncbi.nlm.nih.gov/pubmed/31483577
pubs.end-page 1469
pubs.publication-status Published
dc.rights.accessrights http://purl.org/eprint/accessRights/RetrictedAccess en
pubs.subtype Research Support, Non-U.S. Gov't
pubs.subtype Journal Article
pubs.elements-id 782655
pubs.org-id Engineering
pubs.org-id Medical and Health Sciences
pubs.org-id Science
pubs.org-id Biological Sciences
pubs.org-id School of Medicine
pubs.org-id Surgery Department
pubs.org-id Chemical and Materials Eng
dc.identifier.eissn 2042-6984
pubs.record-created-at-source-date 2024-05-03
pubs.online-publication-date 2019-09-04


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