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The nose is the best niche for detection of experimental pneumococcal colonisation in adults of all ages, using nasal wash.

Nikolaou, E; German, EL; Blizard, A; Howard, A; Hitchins, L; Chen, T; Chadwick, J; Pojar, S; Mitsi, E; Solórzano, C; et al. Nikolaou, E; German, EL; Blizard, A; Howard, A; Hitchins, L; Chen, T; Chadwick, J; Pojar, S; Mitsi, E; Solórzano, C; Sunny, S; Dunne, F; Gritzfeld, JF; Adler, H; Hinds, J; Gould, KA; Rylance, J; Collins, AM; Gordon, SB; Ferreira, DM (2021) The nose is the best niche for detection of experimental pneumococcal colonisation in adults of all ages, using nasal wash. Sci Rep, 11 (1). p. 18279. ISSN 2045-2322 https://doi.org/10.1038/s41598-021-97807-1
SGUL Authors: Gould, Katherine Ann

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Abstract

Previous studies have suggested that the pneumococcal niche changes from the nasopharynx to the oral cavity with age. We use an Experimental Human Pneumococcal Challenge model to investigate pneumococcal colonisation in different anatomical niches with age. Healthy adults (n = 112) were intranasally inoculated with Streptococcus pneumoniae serotype 6B (Spn6B) and were categorised as young 18-55 years (n = 57) or older > 55 years (n = 55). Colonisation status (frequency and density) was determined by multiplex qPCR targeting the lytA and cpsA-6A/B genes in both raw and culture-enriched nasal wash and oropharyngeal swab samples collected at 2-, 7- and 14-days post-exposure. For older adults, raw and culture-enriched saliva samples were also assessed. 64% of NW samples and 54% of OPS samples were positive for Spn6B in young adults, compared to 35% of NW samples, 24% of OPS samples and 6% of saliva samples in older adults. Many colonisation events were only detected in culture-enriched samples. Experimental colonisation was detected in 72% of young adults by NW and 63% by OPS. In older adults, this was 51% by NW, 36% by OPS and 9% by saliva. The nose, as assessed by nasal wash, is the best niche for detection of experimental pneumococcal colonisation in both young and older adults.

Item Type: Article
Additional Information: Open Access This 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 Author(s) 2021
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Sci Rep
ISSN: 2045-2322
Language: eng
Dates:
DateEvent
14 September 2021Published
10 August 2021Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
MR/M011569/1Medical Research Council/FAPESPUNSPECIFIED
OPP1117728Bill & Melinda Gates FoundationUNSPECIFIED
PubMed ID: 34521967
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/113669
Publisher's version: https://doi.org/10.1038/s41598-021-97807-1

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