» Articles » PMID: 24850346

Whole-genome Sequencing for High-resolution Investigation of Methicillin-resistant Staphylococcus Aureus Epidemiology and Genome Plasticity

Overview
Specialty Microbiology
Date 2014 May 23
PMID 24850346
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) infections pose a major challenge in health care, yet the limited heterogeneity within this group hinders molecular investigations of related outbreaks. Pulsed-field gel electrophoresis (PFGE) has been the gold standard approach but is impractical for many clinical laboratories and is often replaced with PCR-based methods. Regardless, both approaches can prove problematic for identifying subclonal outbreaks. Here, we explore the use of whole-genome sequencing for clinical laboratory investigations of MRSA molecular epidemiology. We examine the relationships of 44 MRSA isolates collected over a period of 3 years by using whole-genome sequencing and two PCR-based methods, multilocus variable-number tandem-repeat analysis (MLVA) and spa typing. We find that MLVA offers higher resolution than spa typing, as it resolved 17 versus 12 discrete isolate groups, respectively. In contrast, whole-genome sequencing reproducibly cataloged genomic variants (131,424 different single nucleotide polymorphisms and indels across the strain collection) that uniquely identified each MRSA clone, recapitulating those groups but enabling higher-resolution phylogenetic inferences of the epidemiological relationships. Importantly, whole-genome sequencing detected a significant number of variants, thereby distinguishing between groups that were considered identical by both spa typing (minimum, 1,124 polymorphisms) and MLVA (minimum, 193 polymorphisms); this suggests that these more conventional approaches can lead to false-positive identification of outbreaks due to inappropriate grouping of genetically distinct strains. An analysis of the distribution of variants across the MRSA genome reveals 47 mutational hot spots (comprising ∼ 2.5% of the genome) that account for 23.5% of the observed polymorphisms, and the use of this selected data set successfully recapitulates most epidemiological relationships in this pathogen group.

Citing Articles

Bacterial discrimination by Fourier transform infrared spectroscopy, MALDI-mass spectrometry and whole-genome sequencing.

McGalliard R, Muhamadali H, AlMasoud N, Haldenby S, Romero-Soriano V, Allman E Future Microbiol. 2024; 19(9):795-810.

PMID: 38652264 PMC: 11290759. DOI: 10.2217/fmb-2024-0043.


Prospective Genomic Surveillance Reveals Cryptic MRSA Outbreaks with Local to International Origins among NICU Patients.

Worley J, Crothers J, Wolfgang W, Gubbala Venkata S, Hoffmann M, Jayeola V J Clin Microbiol. 2023; 61(5):e0001423.

PMID: 37022157 PMC: 10204624. DOI: 10.1128/jcm.00014-23.


Sensitive Identification of Bacterial DNA in Clinical Specimens by Broad-Range 16S rRNA Gene Enrichment.

Rassoulian Barrett S, Hoffman N, Rosenthal C, Bryan A, Marshall D, Lieberman J J Clin Microbiol. 2020; 58(12).

PMID: 33028602 PMC: 7685877. DOI: 10.1128/JCM.01605-20.


Contaminant DNA in bacterial sequencing experiments is a major source of false genetic variability.

Goig G, Blanco S, Garcia-Basteiro A, Comas I BMC Biol. 2020; 18(1):24.

PMID: 32122347 PMC: 7053099. DOI: 10.1186/s12915-020-0748-z.


Genomic diversity and antimicrobial susceptibility profiling of nasal carriage isolated from pediatric ward in Western Iran.

Poormohammadi S, Farahani A, Mohajeri P Saudi J Biol Sci. 2019; 26(1):1-7.

PMID: 30622401 PMC: 6319195. DOI: 10.1016/j.sjbs.2016.10.001.


References
1.
Saulnier P, Bourneix C, Prevost G, Andremont A . Random amplified polymorphic DNA assay is less discriminant than pulsed-field gel electrophoresis for typing strains of methicillin-resistant Staphylococcus aureus. J Clin Microbiol. 1993; 31(4):982-5. PMC: 263599. DOI: 10.1128/jcm.31.4.982-985.1993. View

2.
Kaida S, Miyata T, Yoshizawa Y, Kawabata S, Morita T, Igarashi H . Nucleotide sequence of the staphylocoagulase gene: its unique COOH-terminal 8 tandem repeats. J Biochem. 1987; 102(5):1177-86. DOI: 10.1093/oxfordjournals.jbchem.a122156. View

3.
Seringhaus M, Kumar A, Hartigan J, Snyder M, Gerstein M . Genomic analysis of insertion behavior and target specificity of mini-Tn7 and Tn3 transposons in Saccharomyces cerevisiae. Nucleic Acids Res. 2006; 34(8):e57. PMC: 1450332. DOI: 10.1093/nar/gkl184. View

4.
Francois P, Huyghe A, Charbonnier Y, Bento M, Herzig S, Topolski I . Use of an automated multiple-locus, variable-number tandem repeat-based method for rapid and high-throughput genotyping of Staphylococcus aureus isolates. J Clin Microbiol. 2005; 43(7):3346-55. PMC: 1169139. DOI: 10.1128/JCM.43.7.3346-3355.2005. View

5.
Perez-Roth E, Lorenzo-Diaz F, Batista N, Moreno A, Mendez-Alvarez S . Tracking methicillin-resistant Staphylococcus aureus clones during a 5-year period (1998 to 2002) in a Spanish hospital. J Clin Microbiol. 2004; 42(10):4649-56. PMC: 522291. DOI: 10.1128/JCM.42.10.4649-4656.2004. View