Screening of pathogenic molecular markers of Staphylococcus aureus in children based on whole genome sequencing technology.
10.7499/j.issn.1008-8830.2304128
- Author:
Jian-Yu CHEN
1
;
Xu-Lin WANG
1
;
Wen-Yu LI
1
;
Min-Qi CHEN
1
;
Jun-Li ZHOU
1
;
Zhen-Jiang YAO
1
;
Jin-Jian FU
;
Xiao-Hua YE
1
Author Information
1. School of Public Health, Guangdong Pharmaceutical University, Guangzhou 510310, China.
- Publication Type:Journal Article
- Keywords:
Child;
Genome wide sequencing;
Molecular characteristic;
Random forest;
Staphylococcus aureus
- MeSH:
Child;
Humans;
Staphylococcus aureus/genetics*;
Cross-Sectional Studies;
Enterotoxins/genetics*;
Staphylococcal Infections;
Whole Genome Sequencing
- From:
Chinese Journal of Contemporary Pediatrics
2023;25(11):1161-1169
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVES:To explore the molecular characteristics of Staphylococcus aureus (S. aureus) in children, and to compare the molecular characteristics of different types of strains (infection and colonization strains) so as to reveal pathogenic molecular markers of S. aureus.
METHODS:A cross-sectional study design was used to conduct nasopharyngeal swab sampling from healthy children in the community and clinical samples from infected children in the hospital. Whole genome sequencing was used to detect antibiotic resistance genes and virulence genes. A random forest method to used to screen pathogenic markers.
RESULTS:A total of 512 S. aureus strains were detected, including 272 infection strains and 240 colonization strains. For virulence genes, the carrying rates of enterotoxin genes (seb and sep), extracellular enzyme coding genes (splA, splB, splE and edinC), leukocytotoxin genes (lukD, lukE, lukF-PV and lukS-PV) and epidermal exfoliating genes (eta and etb) in infection strains were higher than those in colonization strains. But the carrying rates of enterotoxin genes (sec, sec3, seg, seh, sei, sel, sem, sen, seo and seu) were lower in infection strains than in colonization strains (P<0.05). For antibiotic resistance genes, the carrying rates of lnuA, lnuG, aadD, tetK and dfrG were significantly higher in infection strains than in colonization strains (P<0.05). The accuracy of cross-validation of the random forest model for screening pathogenic markers of S. aureus before and after screening was 69% and 68%, respectively, and the area under the curve was 0.75 and 0.70, respectively. The random forest model finally screened out 16 pathogenic markers (sem, etb, splE, sep, ser, mecA, lnuA, sea, blaZ, cat(pC233), blaTEm-1A, aph(3')-III, ermB, ermA, ant(9)-Ia and ant(6)-Ia). The top five variables in the variable importance ranking were sem (OR=0.40), etb (OR=3.95), splE (OR=1.68), sep (OR=3.97), and ser (OR=1.68).
CONCLUSIONS:The random forest model can screen out pathogenic markers of S. aureus and exhibits a superior predictive performance, providing genetic evidence for tracing highly pathogenic S. aureus and conducting precise targeted interventions.
