Evidence map›Paper›PMID 39437562›Full record

ArticleInternational journal of medical microbiology : IJMM2024

Desiccation tolerance and reduced antibiotic resistance: Key drivers in ST239-III to ST22-IV MRSA clonal replacement at a Malaysian teaching hospital.

Nurul Amirah Mohamad Farook, Silvia Argimón, Muttaqillah Najihan Abdul Samat, Sharifah Azura Salleh, Sunita Sulaiman, Toh Leong Tan, Petrick Periyasamy, Chee Lan Lau, Nor Azila Muhammad Azami, Raja Mohd Fadhil Raja Abd Rahman and 2 more

Abstract read
In one paragraph

Article in International journal of medical microbiology : IJMM, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Nurul Amirah Mohamad FarookUKM Medical Molecular Biology Institute (UMBI), Universiti Kebangsaan Malaysia, Malaysia.
Silvia ArgimónCentre for Genomic Pathogen Surveillance, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Old Road Campus, Oxford, United Kingdom.
Muttaqillah Najihan Abdul SamatDepartment of Medical Microbiology and Immunology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Malaysia.
Sharifah Azura SallehInfection Control Unit, Hospital Canselor Tuanku Muhriz, Universiti Kebangsaan Malaysia, Malaysia.
Sunita SulaimanInfection Control Unit, Hospital Canselor Tuanku Muhriz, Universiti Kebangsaan Malaysia, Malaysia.
Toh Leong TanDepartment of Emergency Medicine, Faculty of Medicine, Universiti Kebangsaan Malaysia, Malaysia.
Petrick PeriyasamyDepartment of Medicine, Faculty of Medicine, Universiti Kebangsaan Malaysia, Malaysia.
Chee Lan LauDepartment of Pharmacy, Hospital Canselor Tuanku Muhriz, Universiti Kebangsaan Malaysia, Malaysia.
Nor Azila Muhammad AzamiUKM Medical Molecular Biology Institute (UMBI), Universiti Kebangsaan Malaysia, Malaysia.
Raja Mohd Fadhil Raja Abd RahmanUKM Medical Molecular Biology Institute (UMBI), Universiti Kebangsaan Malaysia, Malaysia.
Mia Yang AngDepartment of Diagnostics & Allied Health Science, Faculty of Health & Life Sciences, Management & Science University, Malaysia.
Hui-Min NeohUKM Medical Molecular Biology Institute (UMBI), Universiti Kebangsaan Malaysia, Malaysia. Electronic address: hui-min@ppukm.ukm.edu.my.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular surveillance of methicillin-resistant Staphylococcus aureus (MRSA) isolated from Hospital Canselor Tuanku Muhriz (HCTM), a Malaysian teaching hospital revealed clonal replacement events of SCCmec type III-SCCmercury to SCCmec type IV strains before the year 2017; however, the reasons behind this phenomenon are still unclear. This study aimed to identify factors associated with the clonal replacement using genomic sequencing and phenotypic investigations (antibiogram profiling, growth rate and desiccation tolerance determination, survival in vancomycin sub-minimum inhibitory concentration (MIC) determination) of representative HCTM MRSA strains isolated in four-year intervals from 2005 - 2017 (n = 16). HCTM Antimicrobial Stewardship (AMS) and Infection Prevention and Control (IPC) policies were also reviewed. Phylogenetic analyses revealed the presence of 3 major MRSA lineages: ST239-III, ST22-IV and ST6-IV; MRSAs with the same STs shared similar core and accessory genomes. Majority of the ST239-III strains isolated in earlier years of the surveillance (2005, 2009 and 2013) were resistant to many antibiotics and harboured multiple AMR and virulence genes compared to ST22-IV and ST6-IV strains (isolated in 2013 and 2017). Interestingly, ST22-IV and ST6-IV MRSAs grew significantly faster and were more resistant to desiccation than ST239-III (p < 0.05), even though the later clone survived better post-vancomycin exposure. Intriguingly, ST22-IV was outcompeted by ST239-III in broth co-cultures; though it survived better when desiccated together with ST239-III. Higher desiccation tolerance and fewer carriage of AMR genes by ST22-IV, together with reduction of antibiotic selection pressure in HCTM (due to AMS and IPC policies) during 2005 - 2017 may have provided the clone a competitive edge in replacing the previously dominant ST239-III in HCTM. This study highlights the importance of MRSA surveillance for a clearer picture of circulating clones and clonal changes. To our knowledge, this is the first genomic epidemiology study of MRSA in Malaysia, which will serve as baseline genomic data for future surveillance.

Indexed as

Anti-Bacterial AgentsHospitals, TeachingMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsPhylogenyStaphylococcal InfectionsAntimicrobial StewardshipDesiccationGenome, BacterialHumansMalaysiaVancomycinVirulence FactorsAnti-Bacterial AgentsVancomycinVirulence FactorsAntimicrobial resistanceBacterial FitnessClonal replacementGenomics surveillanceMRSA

Identifiers

PMID39437562
PMCPMC11646208

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.