» Articles » PMID: 39343893

Genome-wide Comparative Analysis of CC1 Staphylococcus Aureus Between Colonization and Infection

Overview
Journal Eur J Med Res
Publisher Biomed Central
Specialty General Medicine
Date 2024 Sep 29
PMID 39343893
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Staphylococcus aureus is one of the most important bacteria in human colonization and infection. Clonal complex1 (CC1) is one of the largest and most important S. aureus CCs, and it is a predominant clone in S. aureus colonization and can cause a series of S. aureus infections including bloodstream infections. No studies on the relationship of CC1 S. aureus between colonization and infection have been published.

Methods: To figure out if there are some significant factors in CC1 S. aureus help its colonization or infection, 15 CC1 S. aureus isolates including ten from colonization and five from bloodstream infections were enrolled in this study. Whole-genome sequencing and bioinformatics analysis were performed.

Results: Virulence factor regulators XdrA, YSIRK signal peptide, CPBP family and OmpR family specifically found in infection isolates can promote virulence factors and enhance the pathogenicity of S. aureus. In addition, some significant differences in metabolism and human diseases were discovered between colonization and infection. Fst family of type I toxin-antitoxin system that mainly maintains stable inheritance was specifically found in CC1 S. aureus colonization isolates and might help S. aureus survive for colonization. No significant differences in genomic evolutionary relationship were found among CC1 S. aureus isolates between colonization and infection.

Conclusions: Virulence factor regulators and metabolic state can promote CC1 S. aureus pathogenic process compared with colonization, and it seems that the strains of colonization origin cannot have pathogenic potential. Experimental confirmation and a bigger number of CC1 S. aureus strains are necessary for further study about the details and mechanism between colonization and infection.

References
1.
Kwiecinski J, Horswill A . Staphylococcus aureus bloodstream infections: pathogenesis and regulatory mechanisms. Curr Opin Microbiol. 2020; 53:51-60. PMC: 7244392. DOI: 10.1016/j.mib.2020.02.005. View

2.
Liang X, Yu C, Sun J, Liu H, Landwehr C, Holmes D . Inactivation of a two-component signal transduction system, SaeRS, eliminates adherence and attenuates virulence of Staphylococcus aureus. Infect Immun. 2006; 74(8):4655-65. PMC: 1539584. DOI: 10.1128/IAI.00322-06. View

3.
Vidal C, Moulin F, Nassif X, Galmiche L, Borgel D, Charbit A . Fulminant arterial vasculitis as an unusual complication of disseminated staphylococcal disease due to the emerging CC1 methicillin-susceptible Staphylococcus aureus clone: a case report. BMC Infect Dis. 2019; 19(1):302. PMC: 6446405. DOI: 10.1186/s12879-019-3933-3. View

4.
Earls M, Steinig E, Monecke S, Samaniego Castruita J, Simbeck A, Schneider-Brachert W . Exploring the evolution and epidemiology of European CC1-MRSA-IV: tracking a multidrug-resistant community-associated meticillin-resistant clone. Microb Genom. 2021; 7(7). PMC: 8477393. DOI: 10.1099/mgen.0.000601. View

5.
Oscarsson J, Harlos C, Arvidson S . Regulatory role of proteins binding to the spa (protein A) and sarS (staphylococcal accessory regulator) promoter regions in Staphylococcus aureus NTCC 8325-4. Int J Med Microbiol. 2005; 295(4):253-66. DOI: 10.1016/j.ijmm.2005.05.003. View