Introduction
Methicillin-resistant Staphylococcus aureus (MRSA), or multidrug-resistant S. aureus,
first reported in the early 1960s in the United Kingdom, are strains of S. aureus
that through the process of natural selection developed resistance to all available
penicillins and other β-lactam antimicrobial drugs [1]. Although the evolution of
such resistance does not cause the organism to be more intrinsically virulent, resistance
does make MRSA infections more difficult to treat and thus more dangerous, particularly
in hospitalized patients and those with weakened immune systems [2]. MRSA can be spread
from one person to another through casual contact or through contaminated objects,
and a strain acquired in a hospital or health care setting is called health care–associated
methicillin-resistant S. aureus (HA-MRSA) [2]. In fact, MRSA has become an important
cause of nosocomial infections worldwide and is currently the most commonly identified
antibiotic-resistant pathogen in United States hospitals [3–5].
However, although MRSA has been entrenched in hospital settings for several decades,
it has undergone rapid evolutionary changes and epidemiologic expansion, spreading
beyond the confines of health care facilities, where it is emerging anew as a dominant
pathogen known as community associated-MRSA (CA-MRSA) [6]. The rapid dissemination
of CA-MRSA strains among general populations in diverse communities has resulted in
increasing reports of outbreaks worldwide [1]. In fact, in some regions, CA-MRSA isolates
account for 75% of community-associated S. aureus infections in children, creating
a public health crisis in the US [1,7]. In this article, we will provide a brief overview
of what is known about the epidemiology and pathogenesis of community- associated
MRSA and discuss how they differ from the strains originating in health care settings.
Further, therapeutic and preventative measures available to combat the rising spread
of this revamped pathogen are also discussed.
Methicillin-Resistant Staphylococcus aureus
S. aureus is a major human pathogen that causes a wide variety of diseases, ranging
from superficial skin and soft tissue infections to life-threatening conditions such
as endocarditis, osteomyelitis, toxic shock syndrome (TSS) and infections associated
with indwelling medical devices [4,8]. The asymptomatic carriage of S. aureus by humans
is the primary natural reservoir, with the anterior nasal mucosa being the main ecological
niche [9]. Colonization provides a reservoir from which the bacteria can be introduced
when host defenses are breached, and therefore colonization increases the risk for
subsequent infection [10]. Importantly, in addition to humans and domestic animals,
livestock and fomites may also serve as adjunctive reservoirs, giving this bacterial
pathogen dramatic relevance in veterinary medicine [11,12].
The virulence of S. aureus is multifactorial because of the combined action of an
arsenal of virulence factors that facilitate tissue adhesion, immune evasion, and
host cell injury [10]. These virulence determinants involve both structural factors,
such as surface adhesins that mediate adherence to host tissues, and secreted factors,
such as enzymes, which convert host tissue into nutrients (Fig 1). However, of more
significance is the secretion of a variety of pyrogenic toxins known as superantigens;
most notable are the Panton–Valentine leukocidin (PVL) and toxic shock syndrome toxin-1
(TSST-1) [13,14].
10.1371/journal.ppat.1005837.g001
Fig 1
Staphylococcus aureus cell structure and pathogenic factors.
Staphylococcus aureus has a complex cell wall structure composed of a thick peptidoglycan
layer and polysaccharide capsule. In addition, S. aureus possesses an elaborate arsenal
of structural and secreted virulence factors involved in toxin production, adherence
to and invasion of host tissue, and immune evasion.
Importantly, the success of S. aureus as a pathogen has been attributed to the various
measures it utilizes to protect itself from the host’s immune system. Among these
strategies are production of complement inhibitory molecules, antibody-binding proteins,
cytolytic peptides, pore-forming toxins, and most notably, production of polysaccharide
capsules, which protect against phagocytosis [8,11,15–17]. Further, the species signature
gene spa, which encodes protein A, also contributes to the prevention of opsonization
and subsequent phagocytosis by binding to and neutralizing activity of the Fc region
of immunoglobulin G (IgG). In addition, it also initiates a proinflammatory cascade
in the airway by activating tumor necrosis factor receptor 1 (TNFR1) and B cells in
concert with other ligands. Yet, despite what is known about the expansive armament
available to this important bacterial pathogen, the role of different virulence factors
in the development of staphylococcal infections remains poorly understood.
What Is Community-Associated MRSA?
MRSA strains were once confined largely to hospitals, other health care environments,
and patients frequenting these facilities; these health care–associated strains are
known as hospital-associated MRSA (HA-MRSA) [1]. However, in a recent and dramatic
evolutionary development, since the mid-1990s, there has been an explosion in the
number of MRSA infections reported in the general populations [18]. This increase
was associated with the recognition of new strains, which were named community-associated
MRSA (CA-MRSA).
In 1999, following a report describing four pediatric fatalities in the mid-western
US, CA-MRSA was recognized as a distinct clinical entity. Prior to that time, CA-MRSA
cases were associated with intravenous drug users in Detroit, Michigan, and aboriginal
populations in Western Australia. Beginning in 2000, CA-MRSA lineages were reported
from numerous countries, with some lineages exhibiting restricted geographic ranges
and others characterized by international epidemicity [1,19]. In 2000, the CDC created
a case definition for MRSA infections occurring among healthy people in the community:
any infection diagnosed in patients lacking health care–associated MRSA risk factors
such as hospitalization, hemodialysis, surgery, presence of indwelling catheters,
and other medical devices [1].
Infections with CA-MRSA typically occur in previously healthy individuals who likely
have cuts or wounds and are in close contact with one another; therefore, outbreaks
are characteristically reported in prisons, daycare centers, athletic teams, and schools
[2,9]. In fact, CA-MRSA infections tend to occur in younger patients and are predominantly
associated with skin and soft tissue infections and TSS. However, severe, life-threatening
cases linked to several clinical syndromes, such as necrotizing pneumonia and necrotizing
fasciitis, have been reported [7]. In contrast, HA-MRSA strains have been isolated
largely from people who are exposed to the health care setting, where the patients
are older and have one or more comorbid conditions, and these strains tend to cause
pneumonia, bacteremia, and invasive infections. Although by definition, both CA-MRSA
and HA-MRSA are resistant to all β-lactam antibiotics, important differences exist
in epidemiology, microbiologic characteristics, clinical syndromes, and antimicrobial
susceptibility patterns, indicating that these so-called “community-associated MRSA”
have evolved independently of hospital MRSA [7].
CA-MRSA Is Distinct from HA-MRSA Both Genetically and Phenotypically
CA-MRSA strains are now recognized as distinct clonal entities that differ from the
traditional MRSA strains. In addition to the differences in epidemiological features,
distinct clinical syndromes and antibiotic susceptibilities, the terms CA-MRSA and
HA-MRSA have been used to call attention to genotypic differences [1]. Although the
molecular determinants underlying the pathogenic success of CA-MRSA are not understood,
studies have shown that the epidemic of CA-MRSA is caused by an extraordinarily infectious
strain named USA300 (Fig 2) [9]. This strain, which originated in the community and
is not related to strains from health care settings, is characterized by a phenotype
of high virulence that is clearly distinct from other MRSA strains [18]. However,
while USA300 (ST-8) in Europe was the first clone to be recognized, it is now clear
that other clones with similar pathogenic properties dominate CA-MRSA isolates in
other parts of the world [5,18].
10.1371/journal.ppat.1005837.g002
Fig 2
A false-colored transmission electron micrograph of USA300 strain Staphylococcus aureus
cell.
CA-MRSA infections have mostly been associated with staphylococcal strains bearing
the staphylococcal cassette chromosome mec type IV element and Panton–Valentine leukocidin
genes. Methicillin resistance, signifying resistance to all β-lactam antibiotics,
is mediated by the mecA gene encoding penicillin-binding protein 2a (PBP2a), which
differs from other penicillin-binding proteins in that its active site does not bind
methicillin or other β-lactam antibiotics [2]. Once acquired, the mecA gene is integrated
into S. aureus chromosome and is thereafter contained within a genetic island called
the Staphylococcal Cassette Chromosome mec (SCCmec). Although the presence of the
SCCmec is common to nearly all MRSA strains, specific differences in the genetic island
differentiate CA-MRSA from HA-MRSA. Whereas HA-MRSA strains carry a relatively large
SCCmec, defined as types I–III, and are often resistant to many classes of non–β-lactam
antimicrobials, CA-MRSA isolates carry smaller SCCmec elements, most commonly SCCmec
type IV or type V. Further, CA-MRSA tend to be susceptible to narrow-spectrum non–β-lactams
such as clindamycin, trimethoprim-sulfamethoxazole (TMP-SMX), and tetracyclines [1,20].
Another distinguishing genetic feature of CA-MRSA is that a high percentage of strains
carry genes for Panton–Valentine leukocidin (PVL), which is largely absent from HA-MRSA
strains. This exotoxin functions as a two-component pore-forming protein, encoded
by the lukF-PV and lukS-PV genes, and acts as a leukocidin that can lyse the cell
membranes of human neutrophils [2,7,16]. Therefore, PVL is hypothesized to be responsible
for the enhanced pathogenicity of CA-MRSA strains. The first clinical isolate known
to carry the PVL genes in the CA-MRSA era was reported in 2003, and approximately
60% to 100% of CA-MRSA strains have been shown to carry these genes, which can spread
from strain to strain by bacteriophages [1]. However, although PVL has been closely
linked to infections caused by CA-MRSA strains and shown to be instrumental in producing
necrotic skin lesions and necrotizing pneumonia, it is not known with certainty how
this toxin contributes to their fitness and/or virulence.
Although it has been speculated that determinants such as PVL encoded on mobile genetic
elements (MGEs) have a predominant impact on virulence, recent reports seem to imply
that the contribution of these MGEs to CA-MRSA virulence may be comparatively minor.
In fact, based on genome comparisons and epidemiological data, findings from one study
indicated that high expression of core genome-encoded virulence determinants—such
as the global virulence and quorum-sensing regulator agr—rather than the acquisition
of additional virulence genes, may have a more profound impact on the evolution of
virulence [18]. However, PVL was proposed to have an important role in defining the
virulence gene expression pattern, which results in the increased virulence potential
[18].
Treatment, Prevention, and Future Perspectives
Treatment options for CA-MRSA include incision and drainage, oral or parenteral antibiotics,
and topical therapy. However, there are relatively few antibiotic agents available
to treat MRSA, as the worldwide spread of multidrug-resistant clones during the past
several decades has severely limited treatment options [20]. The glycopeptide antibiotic
vancomycin is one of the few antibiotics that remains effective against MRSA [21].
However, with the antibiotic pressure exerted by the increasing use of vancomycin
to treat MRSA infections, in 2002, the first clinical isolate with high-level vancomycin
resistance, vancomycin-resistant S. aureus (VRSA), was reported in the US [22]. However,
these strains are rare and there is little evidence for increasing frequency. The
VRSA strains carry transposon Tn1546, acquired from vancomycin-resistant Enterococcus
faecalis, which is known to alter cell wall structure and metabolism [21]. Therefore,
clinical reliance on vancomycin may no longer be possible [1]. The emergence of vancomycin-intermediate
Staphylococcus aureus (VISA), which were first identified in 1996 and have since been
detected globally, has further compounded the therapeutic challenges. Although the
resistance mechanism of these strains with reduced susceptibility to vancomycin is
not fully clear, it was predominately associated with cell wall thickening and vancomycin
binding, thereby restricting access of the drug to its site of activity [23,24]. Clindamycin
is an excellent oral option for the treatment of CA-MRSA, as in addition to its efficacy
it also has the benefit of inhibiting toxin production and therefore has a theoretical
benefit in patients with toxic shock or other toxin-mediated complications [20]. The
limitations of the available agents combined with the slow rate of development of
new antibiotic classes have raised the notional possibility of untreatable multidrug-resistant
S. aureus infections [1]. Therefore, continuous efforts should be made to prevent
the spread and the emergence of resistance by early detection of the resistant strains
[25].
Often, outbreaks of CA-MRSA have been in populations in which close contact appears
to be the common characteristic. Although data on the effectiveness of strategies
to prevent new and recurrent CA-MRSA infections are currently limited, hygiene, environmental
cleaning, and proper wound care are essential components to infection control [2].
However, attempts to contain MRSA using current infection control based in health
care facilities are unlikely to succeed without a similar effort to control spread
in the community. Until these studies are conducted, health care practitioners will
need to extrapolate from infection control guidelines for controlling MRSA within
the hospital.
The increasing burden of CA-MRSA underscores the need to find innovative therapeutics
for MRSA disease. Although CA-MRSA isolates are typically susceptible to many non–β-lactam
antibiotics, there is recent emergence of multidrug-resistant CA-MRSA, thus confounding
the current serious public health problem [18]. An effective multicomponent vaccine
may be the only effective long-term solution against the spread of CA-MRSA [16]. The
role of capsules as an important immune evasion mechanism supports the inclusion of
capsular polysaccharides in the formulation of prophylactic vaccines [17]. Further,
secreted products, such as the staphylococcal protein A (SpA), may also be exploited
for the development of vaccines and therapeutics [15]. Thus, comprehensive understanding
of the pathogen’s ability to manipulate the host immune response is crucial for the
development of efficacious vaccines against CA-MRSA [8,11].
CA-MRSA infections have become commonplace, and their worldwide emergence in healthy
individuals represents an ominous threat. Ironically, CA-MRSA strains are now being
introduced from their site of origin in the community into the hospital, reversing
the epidemiologic cycle. In fact, in some hospitals, CA-MRSA are displacing classic
health care–associated strains of S. aureus, supporting the hypothesis that CA-MRSA
may be more fit [26]. Mathematical modeling demonstrates difficulty in the epidemiologic
control of CA-MRSA in the face of its increased prevalence in the community and the
increasingly daunting tasks for infection control programs. There is an acute need
to reduce the global burden of infections, and therefore, as the definitions of a
“community-associated” infection continue to evolve, it is imperative that studies
are directed toward examining effective prevention and outbreak control strategies.
Importantly, increased vigilance in the diagnosis and management of suspected and
confirmed staphylococcal infections is warranted [7].