» Articles » PMID: 29442252

Survey of Staphylococcus Aureus in a General Pediatric Population and Focus on Isolates with Three Clinically Relevant Toxin-encoding Genes

Overview
Journal World J Pediatr
Specialty Pediatrics
Date 2018 Feb 15
PMID 29442252
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Background: In children, surveys on Staphylococcus aureus have focused on specific infections, situations or strains but no study has so far given an overview on S. aureus isolation without any selection. Here, we describe the overall bacteriological and clinical characteristics of S. aureus isolation in children, with a special focus on isolates harbouring tst, sea, and/or luk-PV genes, respectively, encoding the three clinically relevant toxins: toxic shock syndrome toxin-1, enterotoxin A and Panton-Valentine leukocidin.

Methods: Data associated with S. aureus isolation were reviewed: isolation site, infection status, tst, sea and luk-PV genes, antimicrobial susceptibility pattern, agr typing.

Results: Three hundred and seventy-seven isolates retrieved from 328 children during S. aureus infection (55.2%) or colonisation (44.8%) were included. tst, sea and luk-PV genes were amplified in 14.3, 9.5 and 5.8% of the isolates, respectively. These isolates were significantly more frequently retrieved during infection (69.1%) than colonisation but differences were observed according to isolation site. Methicillin-resistance was found in 7.2% of the isolates, 78% of which harboured ≥ 1 of the targeted toxin-encoding genes.

Conclusions: This first comprehensive study of S. aureus in children showed S. aureus to be mainly retrieved during infection and a high rate of colonisation, not limited to the nasopharynx. Predominant infections were skin and soft tissue infections where tst was most frequently detected. luk-PV was most commonly detected during bone and joint infections. Isolates harbouring targeted toxin-encoding genes were significantly associated with infections but a quarter of children were asymptomatic carriers representing a reservoir for dissemination of isolates with virulence potency.

Citing Articles

Bifidobacteria shape antimicrobial T-helper cell responses during infancy and adulthood.

Vogel K, Arra A, Lingel H, Bretschneider D, Pratsch F, Schanze D Nat Commun. 2023; 14(1):5943.

PMID: 37741816 PMC: 10517955. DOI: 10.1038/s41467-023-41630-x.


PD-1/PD-L1 Control of Antigen-Specifically Activated CD4 T-Cells of Neonates.

Majer C, Lingel H, Arra A, Heuft H, Bretschneider D, Balk S Int J Mol Sci. 2023; 24(6).

PMID: 36982735 PMC: 10051326. DOI: 10.3390/ijms24065662.

References
1.
Otter J, Kearns A, French G, Ellington M . Panton-Valentine leukocidin-encoding bacteriophage and gene sequence variation in community-associated methicillin-resistant Staphylococcus aureus. Clin Microbiol Infect. 2009; 16(1):68-73. DOI: 10.1111/j.1469-0691.2009.02925.x. View

2.
Filleron A, Lotthe A, Jourdes E, Jeziorski E, Prodhomme O, Didelot M . Atypical pneumonia linked to community-acquired staphylococcus aureus cross-transmission in the nursery. Neonatology. 2013; 104(2):156-60. DOI: 10.1159/000351019. View

3.
Stadhouders R, Pas S, Anber J, Voermans J, Mes T, Schutten M . The effect of primer-template mismatches on the detection and quantification of nucleic acids using the 5' nuclease assay. J Mol Diagn. 2009; 12(1):109-17. PMC: 2797725. DOI: 10.2353/jmoldx.2010.090035. View

4.
Wang X, Li X, Liu W, Huang W, Fu Q, Li M . Molecular Characteristic and Virulence Gene Profiles of Community-Associated Isolates from Pediatric Patients in Shanghai, China. Front Microbiol. 2016; 7:1818. PMC: 5108810. DOI: 10.3389/fmicb.2016.01818. View

5.
Sollid J, Furberg A, Hanssen A, Johannessen M . Staphylococcus aureus: determinants of human carriage. Infect Genet Evol. 2013; 21:531-41. DOI: 10.1016/j.meegid.2013.03.020. View