High prevalence of pharyngeal bacterial pathogens among healthy adolescents and young adultsShow others and affiliations
2021 (English)In: Acta Pathologica, Microbiologica et Immunologica Scandinavica (APMIS), ISSN 0903-4641, E-ISSN 1600-0463, Vol. 129, no 12, p. 711-716Article in journal (Refereed) Published
Abstract [en]
The pharyngeal mucosa can be colonized with bacteria that have potential to cause pharyngotonsillitis. By the use of culturing techniques and PCR, we aimed to assess the prevalence of bacterial pharyngeal pathogens among healthy adolescents and young adults. We performed a cross-sectional study in a community-based cohort of 217 healthy individuals between 16 and 25 years of age. Samples were analyzed for Group A streptococci (GAS), Group C/G streptococci (SDSE), Fusobacterium necrophorum, and Arcanobacterium haemolyticum. Compared to culturing, the PCR method resulted in more frequent detection, albeit in most cases with low levels of DNA, of GAS (20/217 vs. 5/217; p < 0.01) and F. necrophorum (20/217 vs. 8/217; p < 0.01). Culturing and PCR yielded similar rates of SDSE detection (14/217 vs. 12/217; p = 0.73). Arcanobacterium haemolyticum was rarely detected (3/217), and only by PCR. Overall, in 25.3% (55/217) of these healthy adolescents and young adults at least one of these pathogens was detected, a rate that is higher than previously described. Further studies are needed before clinical adoption of PCR-based detection methods for pharyngeal bacterial pathogens, as our findings suggest a high incidence of asymptomatic carriage among adolescents and young adults without throat infections.
Place, publisher, year, edition, pages
John Wiley & Sons, 2021. Vol. 129, no 12, p. 711-716
Keywords [en]
Adolescence, carriage, Fusobacterium necrophorum, pharyngeal bacteria, Streptococcus dysgalactiae subspecies equisimilis, Streptococcus pyogenes, young adulthood
National Category
Infectious Medicine Microbiology in the medical area
Research subject
Microbiology
Identifiers
URN: urn:nbn:se:umu:diva-189129DOI: 10.1111/apm.13179ISI: 000711821300001PubMedID: 34580908Scopus ID: 2-s2.0-85117912479OAI: oai:DiVA.org:umu-189129DiVA, id: diva2:1609788
2021-11-092021-11-092023-04-17Bibliographically approved