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. 2015 Mar 10;6(2):e00054.
doi: 10.1128/mBio.00054-15.

Transmission and microevolution of USA300 MRSA in U.S. households: evidence from whole-genome sequencing

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Transmission and microevolution of USA300 MRSA in U.S. households: evidence from whole-genome sequencing

Md Tauqeer Alam et al. mBio. .

Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) USA300 is a successful S. aureus clone in the United States and a common cause of skin and soft tissue infections (SSTIs). We performed whole-genome sequencing (WGS) of 146 USA300 MRSA isolates from SSTIs and colonization cultures obtained from an investigation conducted from 2008 to 2010 in Chicago and Los Angeles households that included an index case with an S. aureus SSTI. Identifying unique single nucleotide polymorphisms (SNPs) and analyzing whole-genome phylogeny, we characterized isolates to understand transmission dynamics, genetic relatedness, and microevolution of USA300 MRSA within the households. We also compared the 146 USA300 MRSA isolates from our study with the previously published genome sequences of the USA300 MRSA isolates from San Diego (n = 35) and New York City (n = 277). We found little genetic variation within the USA300 MRSA household isolates from Los Angeles (mean number of SNPs ± standard deviation, 17.6 ± 35; π nucleotide diversity, 3.1 × 10(-5)) or from Chicago (mean number of SNPs ± standard deviation, 12 ± 19; π nucleotide diversity, 3.1 × 10(-5)). The isolates within a household clustered into closely related monophyletic groups, suggesting the introduction into and transmission within each household of a single common USA300 ancestral strain. From a Bayesian evolutionary reconstruction, we inferred that USA300 persisted within households for 2.33 to 8.35 years prior to sampling. We also noted that fluoroquinolone-resistant USA300 clones emerged around 1995 and were more widespread in Los Angeles and New York City than in Chicago. Our findings strongly suggest that unique USA300 MRSA isolates are transmitted within households that contain an individual with an SSTI. Decolonization of household members may be a critical component of prevention programs to control USA300 MRSA spread in the United States.

Importance: USA300, a virulent and easily transmissible strain of methicillin-resistant Staphylococcus aureus (MRSA), is the predominant community-associated MRSA clone in the United States. It most commonly causes skin infections but also causes necrotizing pneumonia and endocarditis. Strategies to limit the spread of MRSA in the community can only be effective if we understand the most common sources of transmission and the microevolutionary processes that provide a fitness advantage to MRSA. We performed a whole-genome sequence comparison of 146 USA300 MRSA isolates from Chicago and Los Angeles. We show that households represent a frequent site of transmission and a long-term reservoir of USA300 strains; individuals within households transmit the same USA300 strain among themselves. Our study also reveals that a large proportion of the USA300 isolates sequenced are resistant to fluoroquinolone antibiotics. The significance of this study is that if households serve as long-term reservoirs of USA300, household MRSA eradication programs may result in a uniquely effective control method.

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Figures

FIG 1
FIG 1
Maximum clade credibility tree resulting from BEAST analysis of the core genome alignment of 146 USA300 isolates from Los Angeles and Chicago. Bayesian analysis was run under a strict molecular clock and with an HKY model of nucleotide substitution assuming a Bayesian skyline demographic model. Blue branches are isolates from Chicago households, and black ones are from Los Angeles households. The green and red branches, respectively, are the USA300 TCH1516 and FPR3757 reference strains. The fluoroquinolone-susceptible (with grlA 84S and gyrA 80S) and -resistant (with grlA 84Yand gyrA 80L) clades are indicated by vertical green and red bars, respectively. The arrow indicates a single strain with the grlA 84F gyrA 80L genotype.
FIG 2
FIG 2
BLAST map showing ACME deletion in the USA300 isolates from Chicago household 9033. The map was generated by the CCT, which uses all-versus-all BLAST and arranges the genomes compared according to their homology with reference genomes (the reference genome here is TCH1516, which is shown in the outermost two rings). Each ring is a genome (isolate), as indicated. As shown, one isolate in household 9033 (the outermost blue ring) was ACME positive, while the remaining isolates had this element deleted. Strain Newman also lacks ACME (shown as the green ring). FPR3757 was included here as another ACME-positive USA300 reference strain.
FIG 3
FIG 3
Minimum spanning tree showing genetic relationships among all household USA300 isolates. Each circle represents an individual genotype based on a 1,335,849-bp core gene alignment, and each color represents a different household. The size of the circle is proportional to the number of isolates with the genotype indicated. The household numbers are prefixed with CH (for Chicago) or LA (for Los Angeles). The index infection isolate in the household is indicated by an asterisk. The clades of USA300 strains with and without the grlA 80Y and gyrA 84L mutations are labeled clades I and II, respectively. As shown, the isolates from Los Angeles household 8203 split into two clusters but still remained in larger clade II. The isolates from Chicago household 9141 separated into two different clades with the presence or absence of grlA and gyrA mutations.
FIG 4
FIG 4
Weir and Cockerham FST at 1,595 SNP positions identified in 146 USA300 MRSA isolates analyzed in this study. Each dot represents an SNP, and those with elevated FST values are indicated (FST across all SNPs, 0.15). Numbers in parentheses are genomic coordinates corresponding to the TCH1516 reference genome.
FIG 5
FIG 5
ML tree of 460 USA300 MRSA isolates along with two non-USA300 strains (Newman and COL) included as outgroups. The ML tree was constructed with the 2,104,213-bp core sequence alignment of these isolate genomes in REALPHY. The fluoroquinolone-susceptible isolates (i.e., with no mutations in the grlA and gyrA genes) are indicated by green branch tips, whereas fluoroquinolone-resistant strains (i.e., with the grlA 80Y and gyrA 84L mutations) are indicated by red branch tips. Five fluoroquinolone-resistant isolates had a different set of mutations (grlA 80F and gyrA 84L) and are indicated by orange branch tips. Three isolates indicated by purple tips had only one mutation in the grlA gene (80F). The two non-USA300 strains, Newman (grlA 80S and gyrA 84S) and COL (grlA 80S and gyrA 84S), and two USA300 reference strains, TCH1516 (grlA 80S and gyrA 84S) and FPR3757 (grlA 80Y and gyrA 84L), are indicated by open circles to the right of the tree. USA300 strains TCH1516 and FPR3757 segregated with their fluoroquinolone-susceptible and -resistant clades, respectively. Isolates from San Diego (SD), Los Angeles (LA), Chicago (CH), and New York (NY) are indicated by the bars on the right.

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References

    1. Lowy FD. 1998. Staphylococcus aureus infections. N Engl J Med 339:520–532. doi:10.1056/NEJM199808203390806. - DOI - PubMed
    1. Jevons MP. 1961. Celbenin-resistant staphylococci. BMJ 1:124–125.
    1. Herold BC, Immergluck LC, Maranan MC, Lauderdale DS, Gaskin RE, Boyle-Vavra S, Leitch CD, Daum RS. 1998. Community-acquired methicillin-resistant Staphylococcus aureus in children with no identified predisposing risk. JAMA 279:593–598. doi:10.1001/jama.279.8.593. - DOI - PubMed
    1. Talan DA, Krishnadasan A, Gorwitz RJ, Fosheim GE, Limbago B, Albrecht V, Moran GJ, EMERGEncy ID Net Study Group . 2011. Comparison of Staphylococcus aureus from skin and soft-tissue infections in US emergency department patients, 2004 and 2008. Clin Infect Dis 53:144–149. doi:10.1093/cid/cir308. - DOI - PubMed
    1. Pan ES, Diep BA, Carleton HA, Charlebois ED, Sensabaugh GF, Haller BL, Perdreau-Remington F. 2003. Increasing prevalence of methicillin-resistant Staphylococcus aureus infection in California jails. Clin Infect Dis 37:1384–1388. doi:10.1086/379019. - DOI - PubMed

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