» Articles » PMID: 33746929

The Surge of Hypervirulent ST398 MRSA Lineage With Higher Biofilm-Forming Ability Is a Critical Threat to Clinics

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2021 Mar 22
PMID 33746929
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

The global increase of community-associated (CA) infections with methicillin-resistant (MRSA) is a major healthcare problem. Although sequence type (ST) 398 MRSA was first described as a livestock-associated (LA) lineage, human-adapted MRSA (HO-MRSA) ST398 without livestock contact has subsequently been reported from China in our previous study and other later research. The proportion of ST398 HO-MRSA has also remarkably increased in recent years in China. Based on 3878 isolates that were collected in a general hospital between 2008 and 2018, we identified 56 ST398 HO-MRSA isolates. The four early appearing isolates of them have been sequenced by whole-genome sequencing (WGS) in our previous study. Here, by usage of WGS on the later-appearing 52 isolates and analyzing the phylogenetic dynamics of the linage, we found that 50 isolates clustered together with the former 4 isolates, making it a main clade out of MSSA clones and other MRSA clones, although ST398 HO-MRSA evolved with multiple origins. Drug resistance and virulence gene analysis based on the WGS data demonstrated that ST398 HO-MRSA main clade exhibited a similar pattern in both parts. Furthermore, they all carried a conserved variant of prophage 3 to guarantee virulence and a short SCC type V element of class D to maintain considerable lower methicillin resistance. Further phenotypical research verified that the epidemic HO-MRSA ST398 displayed enhanced biofilm formation ability when keeping high virulence. The dual advantages of virulence and biofilm formation in the HO-MRSA ST398 subtype promote their fitness in the community and even in the healthcare environment, which poses a serious threat in clinical infections. Therefore, further surveillance is required to prevent and control the problematic public health impact of HO-MRSA ST398 in the future.

Citing Articles

Molecular characteristics, risk factors, and clinical outcomes of methicillin-resistant infections among critically ill pediatric patients in Shanghai, 2016-2021.

Dai C, Ji W, Zhang Y, Huang W, Wang H, Wang X Front Pediatr. 2024; 12:1457645.

PMID: 39483528 PMC: 11524809. DOI: 10.3389/fped.2024.1457645.


Small regulatory RNA RSaX28 promotes virulence by reinforcing the stability of RNAIII in community-associated ST398 clonotype .

Jian Y, Chen T, Yang Z, Xiang G, Xu K, Wang Y Emerg Microbes Infect. 2024; 13(1):2341972.

PMID: 38597192 PMC: 11034457. DOI: 10.1080/22221751.2024.2341972.


Postoperative Staphylococcus aureus Infections in Patients With and Without Preoperative Colonization.

Troeman D, Hazard D, Timbermont L, Malhotra-Kumar S, van Werkhoven C, Wolkewitz M JAMA Netw Open. 2023; 6(10):e2339793.

PMID: 37906196 PMC: 10618839. DOI: 10.1001/jamanetworkopen.2023.39793.


Multi-Host Pathogen -Epidemiology, Drug Resistance and Occurrence in Humans and Animals in Poland.

Troscianczyk A, Nowakiewicz A, Kasela M, Malm A, Tracz A, Hahaj-Siembida A Antibiotics (Basel). 2023; 12(7).

PMID: 37508233 PMC: 10376275. DOI: 10.3390/antibiotics12071137.


Panton-Valentine Leukocidin-Positive CC398 MRSA in Urban Clinical Settings, the Netherlands.

Gooskens J, Konstantinovski M, Kraakman M, Kalpoe J, van Burgel N, Claas E Emerg Infect Dis. 2023; 29(5):1055-1057.

PMID: 36913919 PMC: 10124631. DOI: 10.3201/eid2905.221717.


References
1.
Maiden M, Bygraves J, Feil E, Morelli G, Russell J, Urwin R . Multilocus sequence typing: a portable approach to the identification of clones within populations of pathogenic microorganisms. Proc Natl Acad Sci U S A. 1998; 95(6):3140-5. PMC: 19708. DOI: 10.1073/pnas.95.6.3140. View

2.
Zhao C, Liu Y, Zhao M, Liu Y, Yu Y, Chen H . Characterization of community acquired Staphylococcus aureus associated with skin and soft tissue infection in Beijing: high prevalence of PVL+ ST398. PLoS One. 2012; 7(6):e38577. PMC: 3368899. DOI: 10.1371/journal.pone.0038577. View

3.
Sun L, Chen Y, Wang D, Wang H, Wu D, Shi K . Surgical Site Infections Caused by Highly Virulent Methicillin-Resistant Staphylococcus aureus Sequence Type 398, China. Emerg Infect Dis. 2018; 25(1):157-160. PMC: 6302609. DOI: 10.3201/eid2501.171862. View

4.
Letunic I, Bork P . Interactive Tree Of Life (iTOL) v4: recent updates and new developments. Nucleic Acids Res. 2019; 47(W1):W256-W259. PMC: 6602468. DOI: 10.1093/nar/gkz239. View

5.
Postma B, Kleibeuker W, Poppelier M, Boonstra M, van Kessel K, van Strijp J . Residues 10-18 within the C5a receptor N terminus compose a binding domain for chemotaxis inhibitory protein of Staphylococcus aureus. J Biol Chem. 2004; 280(3):2020-7. DOI: 10.1074/jbc.M412230200. View