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Staphylococcal infection

Staphylococcal infections are a diverse group of illnesses caused by bacteria from the genus Staphylococcus, predominantly Staphylococcus aureus, which are gram-positive, cocci-shaped microorganisms often found as part of the normal human flora on the skin and in the nasal passages of about 30% of healthy individuals.^[1]^[2] These bacteria are typically commensal and harmless but can become opportunistic pathogens, leading to a spectrum of infections from mild, localized skin conditions such as boils and impetigo to severe, life-threatening systemic diseases including bacteremia, endocarditis, pneumonia, and osteomyelitis.^[3]^[1] Transmission of Staphylococcus primarily occurs through direct person-to-person contact or indirect contact with contaminated surfaces, objects, or fomites such as towels, razors, or medical equipment.^[2] In healthcare settings, the bacteria can spread via invasive devices like catheters or surgical wounds, contributing to both community-acquired and nosocomial infections.^[1] Foodborne staphylococcal illness, a distinct form, results from ingestion of preformed toxins produced by the bacteria in contaminated food, often due to improper storage or handling.^[3] Epidemiologically, S. aureus colonization rates can reach up to 50% in adults, with persistent nasal carriage in about 15% and higher prevalence among healthcare workers, intravenous drug users, and immunocompromised patients.^[1] S. aureus is a leading global cause of bacterial deaths, associated with approximately 196,000 attributable deaths in 2021, with antimicrobial resistance projected to cause over 39 million deaths worldwide from 2025 to 2050.^[4] Risk factors for developing symptomatic infections include skin breaches from cuts, burns, or surgical procedures; underlying conditions such as diabetes, HIV, or chronic illnesses that impair immunity; and close-contact environments like sports teams or prisons.^[3] A notable challenge is the emergence of methicillin-resistant S. aureus (MRSA), which carries resistance genes like mecA and complicates treatment, accounting for significant morbidity in both community and hospital settings.^[1] The pathogenicity of Staphylococcus stems from virulence factors such as protein A, which evades host immune responses; toxins like toxic shock syndrome toxin-1 (TSST-1); and the ability to form biofilms on prosthetic devices, enabling persistent infections.^[1] Common symptoms vary by infection site but often include redness, swelling, pain, and fever for skin and soft tissue involvement, while invasive cases may present with sepsis, organ failure, or rapid progression to shock.^[3] Untreated complications can be fatal, underscoring the importance of prompt diagnosis and antibiotic therapy, though resistance patterns necessitate tailored approaches.^[2]

Overview and Microbiology

Definition and Classification

Staphylococcal infections are caused by bacteria belonging to the genus Staphylococcus, a group of Gram-positive, spherical cocci that characteristically arrange in grape-like clusters due to cell division in multiple planes.^[5] These facultative anaerobes are ubiquitous in the environment and commonly colonize human skin and mucous membranes without causing harm, but they can lead to a spectrum of diseases ranging from superficial skin and soft tissue infections to invasive systemic conditions when host defenses are compromised or bacteria enter deeper tissues.^[6] The genus includes over 40 species, though only a subset are significant human pathogens, thriving as opportunistic invaders in both community and healthcare settings.^[5] Classification of staphylococci is primarily based on the production of coagulase, an extracellular enzyme that promotes blood clotting by activating prothrombin to form staphylothrombin, which converts fibrinogen to insoluble fibrin.^[5] Coagulase-positive staphylococci (CoPS), exemplified by Staphylococcus aureus, are generally more virulent and associated with acute, aggressive infections due to their enhanced ability to evade host immunity and form abscesses.^[6] In contrast, coagulase-negative staphylococci (CoNS), such as Staphylococcus epidermidis and Staphylococcus saprophyticus, are typically less pathogenic, often causing opportunistic infections in immunocompromised individuals or those with indwelling medical devices, though some species like S. lugdunensis exhibit heightened virulence.^[6] This coagulase-based dichotomy guides clinical identification and underscores differences in pathogenicity, with CoPS responsible for the majority of severe staphylococcal diseases.^[5] Staphylococci were first recognized as opportunistic pathogens over a century ago, with S. aureus identified in the late 19th century as a cause of boils, abscesses, and wound infections despite its frequent presence as a commensal in healthy individuals.^[7] Their ubiquity in human flora is evident from carriage rates, where approximately 20-30% of healthy adults harbor S. aureus in the anterior nares and on the skin, facilitating transmission and predisposing certain populations—such as healthcare workers or those with skin breaches—to infection.^[6]^[2] This dual role as commensals and pathogens highlights their evolutionary adaptation to human hosts, contributing to recurrent epidemics and the emergence of antibiotic-resistant strains throughout the 20th century.^[7]

Key Pathogenic Species

Staphylococcus aureus is the most significant pathogenic species within the genus, recognized as a Gram-positive, catalase-positive, facultative anaerobe that commonly colonizes the human skin and nares.^[8] It produces a characteristic golden-yellow pigment due to the accumulation of staphyloxanthin, which contributes to its visibility on culture media and aids in its identification.^[9] As the primary cause of acute bacterial infections in humans, S. aureus is responsible for a broad spectrum of diseases ranging from localized skin abscesses to life-threatening conditions like bacteremia and pneumonia.^[1] Notably, methicillin-resistant S. aureus (MRSA) strains have emerged as a major public health concern, exhibiting resistance to multiple antibiotics and complicating treatment in both community and hospital settings.^[1] Coagulase-negative staphylococci (CoNS) represent a diverse group of species that are typically commensal on human skin but can act as opportunistic pathogens under specific conditions.^[10] Among these, Staphylococcus epidermidis is the most prevalent, serving as a normal skin flora member that frequently causes infections associated with indwelling medical devices, such as catheters and prosthetic joints, due to its ability to adhere to synthetic surfaces.^[11] Another key species, Staphylococcus saprophyticus, is a common cause of urinary tract infections, particularly in sexually active young women, where it accounts for 5-20% of community-acquired cases in this demographic.^[12] In terms of pathogenicity, S. aureus stands out as an aggressive invader capable of causing severe, invasive infections even in healthy individuals, in contrast to most CoNS, which primarily opportunistically infect immunocompromised hosts or those with foreign body implants.^[10] This distinction aligns with the traditional classification of staphylococci based on coagulase production, where S. aureus is coagulase-positive and CoNS are negative.^[10] However, certain CoNS like Staphylococcus lugdunensis exhibit heightened virulence resembling that of S. aureus, notably in causing aggressive native valve endocarditis with high rates of complications and mortality.^[13]

Pathogenesis

Virulence Factors

Staphylococci, particularly Staphylococcus aureus, possess an arsenal of virulence factors that contribute to their pathogenicity through immune evasion, adhesion, and host cell damage at the molecular level. These factors include surface-anchored proteins, secreted enzymes, and toxins, many of which are encoded by genes in the bacterial chromosome or mobile genetic elements. Regulation of these factors often occurs via global regulators like the accessory gene regulator (Agr) system, which coordinates expression based on environmental cues such as quorum sensing.^[14] Protein A (SpA), a key surface protein in S. aureus, is covalently anchored to the cell wall peptidoglycan and binds the Fc region of immunoglobulin G (IgG) molecules, forming a molecular shield that inhibits opsonization and subsequent phagocytosis by neutrophils and macrophages. This interaction exploits the host's own antibodies, preventing effective antibody-dependent cellular cytotoxicity. Seminal structural studies have revealed that SpA's five tandem Ig-binding domains adopt a helical conformation to facilitate multivalent binding.^[15] Coagulase (Coa), another cell wall-associated enzyme unique to S. aureus, activates prothrombin to generate staphylothrombin, which converts fibrinogen to fibrin, leading to the formation of dense fibrin networks that encapsulate bacteria and block immune cell access. This process is enhanced by von Willebrand factor-binding protein (vWbp), forming a complementary system for clot protection.^[16] Hemolysins represent a class of secreted pore-forming toxins that disrupt host cell membranes. Alpha-hemolysin (Hla), encoded by the hla gene in nearly all S. aureus strains, is a 33-kDa beta-barrel toxin that oligomerizes into heptameric pores on target cells, particularly via binding to the ADAM10 metalloprotease receptor, causing ion imbalance and cytolysis of erythrocytes and epithelial cells. Other hemolysins, such as beta-hemolysin, contribute to sphingomyelin hydrolysis, amplifying membrane damage. Superantigenic toxins further enhance virulence by non-specifically bridging major histocompatibility complex class II molecules on antigen-presenting cells and T-cell receptors, bypassing normal antigen processing. Staphylococcal enterotoxins (SEs), a family of over 20 related proteins (e.g., SEA-SEE), are heat-stable exotoxins encoded on prophages or plasmids, with low-affinity binding to MHC II via zinc coordination sites that trigger excessive T-cell proliferation. Toxic shock syndrome toxin-1 (TSST-1), structurally similar to SEs and encoded by a chromosomal gene, exhibits even higher superantigenic potency through its unique disulfide loop, facilitating strong MHC II interactions. Exfoliative toxins (ETs), such as ETA and ETB, are serine proteases secreted by specific S. aureus strains; ETA is chromosomally encoded while ETB resides on plasmids, and both selectively cleave the desmoglein-1 adhesion protein in desmosomes via a catalytic triad, disrupting intercellular junctions at the biochemical level.^[17]^[18] Biofilm formation, critical for persistent infections, involves polysaccharide intercellular adhesin (PIA) in Staphylococcus epidermidis and some S. aureus strains. PIA, a polycationic homoglycan of β-1,6-linked N-acetylglucosamine residues synthesized by the icaADBC operon, promotes bacterial aggregation by electrostatic interactions with negatively charged cell surfaces and extracellular matrix, while also resisting cationic antimicrobial peptides through charge shielding. In S. aureus, biofilm matrix components include poly-β-1,6-N-acetylglucosamine (PNAG), a deacetylated PIA variant, aiding device-associated adherence. Panton-Valentine leukocidin (PVL), a bicomponent pore-forming leukocidin prevalent in community-associated methicillin-resistant S. aureus (CA-MRSA), consists of LukS-PV and LukF-PV subunits that assemble into octameric beta-barrel pores on leukocyte plasma membranes, selectively lysing phagocytes by targeting the plasma membrane after receptor binding to CXCR1/2. PVL genes are carried on bacteriophages and are present in less than 5% of S. aureus strains.^[19]^[20]

Mechanisms of Infection Establishment

Staphylococcal infections, primarily caused by Staphylococcus aureus, begin with the bacterium's adhesion to host tissues or medical devices, a critical step in establishing colonization. The process is mediated by microbial surface components recognizing adhesive matrix molecules (MSCRAMMs), such as fibronectin-binding proteins A and B (FnBPA and FnBPB), which bind to fibronectin in the extracellular matrix, enabling initial attachment to damaged skin, mucosal surfaces, or implanted devices like catheters.^[14] This adhesion is often facilitated by a dock-lock-latch (DLL) mechanism, where the proteins first dock to host ligands and then zipper-like interactions strengthen the bond, promoting bacterial aggregation and biofilm formation for persistent colonization.^[21] Once attached, S. aureus exploits host factors like fibrinogen or cytokeratins to further secure its position, particularly in the nasal cavity or skin, setting the stage for potential invasion if host barriers are breached.^[22] Following adhesion, S. aureus employs sophisticated immune evasion strategies to avoid clearance by the host's innate defenses, allowing the infection to persist. The bacterial capsule, predominantly serotypes 5 and 8, forms a protective polysaccharide layer that inhibits phagocytosis by neutrophils and macrophages by masking surface antigens and reducing opsonization.^[23] Complementing this, surface protein A (SpA) binds the Fc region of immunoglobulin G (IgG), preventing antibody-mediated recognition and redirecting B-cell responses toward non-protective antibodies.^[14] Superantigens, such as toxic shock syndrome toxin-1 (TSST-1) and staphylococcal enterotoxins, further disrupt immunity by non-specifically activating T cells, leading to massive cytokine release—including interleukin-2 and tumor necrosis factor-α—that induces a cytokine storm, systemic inflammation, and immune exhaustion.^[22] These mechanisms collectively shield the bacteria during early colonization, minimizing immune detection for hours to days. Tissue invasion and dissemination occur as S. aureus produces enzymes and toxins to breach host barriers and spread systemically, often culminating in abscess formation. Secreted enzymes like hyaluronidase hydrolyze hyaluronic acid in connective tissues, creating pathways for bacterial migration, while proteases and lipases degrade surrounding proteins and lipids to facilitate deeper penetration.^[23] Coagulases (Coa and vWbp) promote fibrin clot formation around bacterial aggregates, trapping neutrophils and forming a fibrous capsule that limits immune access and fosters anaerobic niches for persistence.^[14] Toxins such as α-hemolysin and Panton-Valentine leukocidin (PVL) lyse host cells, including endothelial barriers, enabling dissemination via bloodstream or lymphatics, with abscesses serving as protected reservoirs that can seed distant infections like osteomyelitis or endocarditis.^[22] This coordinated process ensures the bacterium transitions from localized colonization to potentially life-threatening invasive disease.

Causes and Transmission

Routes of Entry

Staphylococcus aureus, the primary pathogenic species causing staphylococcal infections, typically enters the human body through breaches in natural barriers. Common portals of entry include breaks in the skin such as cuts, abrasions, and surgical sites, where the bacterium can invade underlying tissues. Mucous membranes, particularly in the nasal passages and respiratory tract, serve as another key entry point, often following initial colonization. Indwelling medical devices like catheters, prosthetics, and intravenous lines provide additional access routes, as biofilms formed by S. aureus on these surfaces facilitate persistent invasion.^[1]^[24] Transmission occurs predominantly through direct contact with infected individuals or colonized carriers, as well as indirect contact with contaminated fomites such as towels, clothing, or medical equipment. In healthcare settings, this mode is amplified by unwashed hands of personnel. Airborne transmission, though less common, can occur via respiratory droplets or aerosols, particularly in post-surgical environments where bacterial dispersal from skin shedding contributes to wound contamination. Foodborne transmission is relevant for toxin-mediated illnesses, where S. aureus contaminates food through handlers' skin or nasal secretions, leading to ingestion of preformed toxins.^[25]^[24]^[26] Environmental sources further enable entry, including contaminated water bodies like recreational beaches or swimming pools, where S. aureus persists and can infect through skin contact or ingestion. Zoonotic transmission holds potential in veterinary settings, with livestock, pets, and wildlife acting as reservoirs; direct animal contact or exposure to contaminated animal products can introduce the bacterium via skin abrasions or mucous membranes. Healthcare environments, rife with high bacterial loads on surfaces and air, represent a concentrated source for device-related and surgical entries.^[27]^[28]^[1]

Risk Factors

Individuals with compromised immune systems, such as those with HIV, undergoing chemotherapy, or suffering from other immunosuppressive conditions, face heightened susceptibility to staphylococcal infections due to impaired defense mechanisms against bacterial invasion.^[1] Diabetes mellitus significantly increases risk through factors like impaired wound healing and frequent skin breaches from needle use, leading to higher colonization rates of up to 50% in affected individuals.^[1] Chronic skin conditions, including eczema and other dermatoses, provide entry points for Staphylococcus aureus by disrupting the skin barrier, with studies showing elevated infection odds ratios of approximately 2.7 in children with such disorders.^[29] Age extremes also contribute to vulnerability; infants and the elderly often exhibit weakened immunity or thinner skin, making them more prone to severe manifestations, particularly in healthcare settings.^[30] Behavioral and environmental factors further elevate infection risk. Poor personal hygiene facilitates bacterial transmission and colonization, while participation in close-contact sports increases direct skin-to-skin exposure, though specific data on sports-related risks emphasize general contact precautions.^[1] Intravenous drug use is a prominent risk, with colonization rates of approximately 40% among users due to shared needles and injection-site trauma.^[1]^[31]^[32] Overcrowding in communal living situations or households promotes transmission through shared items like towels and razors, with household contact associated with an odds ratio of 3.3 for skin infections.^[2]^[29] Iatrogenic factors are particularly relevant in clinical contexts. Recent surgery heightens risk via surgical wounds and tissue disruption, often compounded by device-related complications.^[2] Hemodialysis patients experience increased susceptibility from repeated vascular access and underlying renal disease, contributing to higher infection rates in this group.^[30] Prosthetic implants and indwelling devices, such as catheters or artificial joints, provide surfaces for biofilm formation, substantially raising the likelihood of device-associated staphylococcal infections.^[1]^[30]

Clinical Manifestations

Skin and Soft Tissue Infections

Skin and soft tissue infections (SSTIs) caused by Staphylococcus aureus represent a significant portion of community-acquired bacterial infections, primarily affecting the epidermis, dermis, and subcutaneous tissues through direct bacterial invasion. These infections are characterized by localized inflammation, often presenting with erythema, edema, warmth, tenderness, and purulent discharge, reflecting the bacterium's ability to form abscesses and evade host immune responses. S. aureus is the predominant pathogen in purulent SSTIs, accounting for up to 59% of cases presenting in emergency departments, with methicillin-resistant strains (MRSA) frequently implicated in community settings.^[33]^[34] Common manifestations include folliculitis, which involves superficial inflammation of hair follicles and appears as small red papules or pustules less than 5 mm in diameter, typically resolving without scarring but potentially progressing in deeper variants. Furuncles, or boils, develop as tender, erythematous nodules with a central pustule, forming localized abscesses often in areas prone to friction such as the axillae or buttocks. Carbuncles arise from coalescing furuncles, presenting as larger, indurated lesions with multiple draining sinuses, accompanied by more intense pain and systemic symptoms like fever. Impetigo manifests as superficial, contagious lesions with honey-colored crusts, vesicles, or bullae, commonly affecting children and spreading via direct contact. Cellulitis involves deeper dermal and subcutaneous extension, featuring poorly demarcated erythema, swelling, and pain that may impair limb function.^[33]^[34]^[35] If untreated, these infections can progress from localized abscess formation to spreading cellulitis, where bacterial proliferation leads to lymphatic dissemination and broader tissue involvement, potentially increasing morbidity through tissue necrosis or secondary bacteremia. S. aureus strains, particularly those producing virulence factors like Panton-Valentine leukocidin, facilitate this progression by promoting neutrophil lysis and persistent inflammation. Entry often occurs through minor skin breaks, such as abrasions or insect bites, allowing colonization to escalate into infection.^[34]^[35] Special cases highlight heightened vulnerability in certain populations. Surgical site infections, frequently caused by S. aureus, complicate postoperative recovery by forming abscesses at incision sites, contributing to prolonged hospital stays and increased healthcare costs. Diabetic foot ulcers serve as hotspots for staphylococcal SSTIs due to impaired wound healing and neuropathy, with S. aureus often colonizing chronic ulcers and leading to recurrent or severe infections that necessitate multidisciplinary management.^[33]^[34]

Systemic and Invasive Infections

Systemic and invasive staphylococcal infections arise when Staphylococcus aureus disseminates hematogenously from primary foci, such as skin lesions or indwelling devices, to internal organs and tissues, resulting in life-threatening conditions including bacteremia, endocarditis, osteomyelitis, and pneumonia. These infections are characterized by rapid progression, systemic inflammatory responses, and frequent complications like sepsis, with S. aureus being a leading cause of hospital-acquired bloodstream infections worldwide.^[36]^[1] Bacteremia, defined as the presence of viable S. aureus in the blood, serves as a critical entry point for dissemination and is often healthcare-associated, linked to intravascular catheters or surgical sites. Clinical features include high fever, chills, hypotension, and leukocytosis, which may evolve into septic shock if untreated. The 30-day mortality rate for S. aureus bacteremia approximates 20%, with higher rates in cases involving persistent bacteremia or metastatic foci.^[37]^[38] Infective endocarditis occurs when S. aureus adheres to damaged heart valves or prosthetic materials, predominantly affecting left-sided valves like the mitral or aortic, though right-sided involvement is common in intravenous drug users. Patients exhibit persistent fever, new or changing heart murmurs, embolic events such as stroke, and signs of congestive heart failure, with S. aureus responsible for 16-40% of all endocarditis cases. Mortality rates range from 22% to 66%, elevated in healthcare-associated or prosthetic valve infections.^[36]^[1] Osteomyelitis involves bacterial invasion of bone tissue, typically via hematogenous seeding in children (affecting long bones) or contiguous spread in adults (often vertebral), leading to bone necrosis and abscess formation. Manifestations include localized bone pain, swelling, fever, and elevated inflammatory markers, with S. aureus implicated in 30-60% of cases; vertebral osteomyelitis presents with back pain in 85-100% of patients. These infections carry significant morbidity due to chronicity and risk of recurrence.^[36]^[39] Staphylococcal pneumonia, particularly the necrotizing form, develops through aspiration or hematogenous spread, often superimposed on influenza or in ventilated patients, causing cavitary lung lesions and pleural effusions. Symptoms encompass acute respiratory distress, high fever, hemoptysis, and multilobar infiltrates on imaging, with hospital-acquired strains predominating. Ventilator-associated pneumonia is frequently caused by methicillin-resistant S. aureus (MRSA), accounting for up to 28% of cases and associated with mortality exceeding 30%.^[36]^[39] Septic arthritis, a form of osteoarticular invasion, targets synovial joints and presents with acute monoarticular pain, swelling, erythema, and restricted movement, often involving the knee or hip, alongside systemic fever and chills. S. aureus drives 40-50% of adult cases, emphasizing the need for prompt recognition to prevent joint destruction.^[36] Immunosuppression, such as in patients with cancer or diabetes, heightens susceptibility to these disseminated infections by impairing host defenses.^[36]

Toxin-Mediated Diseases

Toxin-mediated diseases caused by Staphylococcus aureus arise from the action of bacterial exotoxins, particularly superantigens and exfoliative toxins, which disseminate systemically without requiring direct bacterial invasion of tissues. These illnesses manifest with abrupt onset of symptoms, often lacking signs of localized infection, due to the toxins' ability to trigger massive immune responses or disrupt cellular structures remotely. Key examples include staphylococcal food poisoning, toxic shock syndrome, and staphylococcal scalded skin syndrome, each linked to specific toxin profiles that induce rapid, characteristic clinical features.^[40] Staphylococcal food poisoning results from ingestion of preformed staphylococcal enterotoxins (SEs), such as SEA, SEB, SEC, SED, and SEE, produced by S. aureus contaminating food. These heat-stable superantigens stimulate the vagus nerve and provoke excessive cytokine release, leading to emetic responses without bacterial replication in the host. Symptoms typically emerge abruptly 1–6 hours after consumption, featuring intense vomiting, abdominal cramps, and sometimes diarrhea, resolving within 24–48 hours without treatment.^[41] Toxic shock syndrome (TSS) is mediated primarily by toxic shock syndrome toxin-1 (TSST-1), a superantigen that hyperactivates T cells, causing a cytokine storm and capillary leak syndrome. This leads to acute multi-organ dysfunction without evidence of bacteremia in many cases. Clinical features include sudden high fever (often >38.9°C), diffuse erythematous rash resembling sunburn, hypotension, and involvement of at least three organ systems, such as gastrointestinal (vomiting/diarrhea), mucous membrane hyperemia, and renal or hepatic impairment; desquamation follows 1–2 weeks later. At-risk groups include menstruating individuals using high-absorbency tampons, which promote toxin production in the vaginal environment, as well as postoperative patients or those with skin barrier disruptions.^[42] Staphylococcal scalded skin syndrome (SSSS) stems from exfoliative toxins (ETs), notably ETA and ETB, which act as serine proteases to cleave desmoglein-1 in the superficial epidermis, disrupting cell adhesion and causing intraepidermal cleavage. The toxins circulate hematogenously from a distant staphylococcal focus, producing widespread skin manifestations without mucosal involvement or deep tissue damage. Onset is rapid, with initial irritability, fever, and tender erythema progressing to large, flaccid bullae and painless sheet-like desquamation, often resembling a scald burn and covering extensive body areas. This condition predominantly affects children under 5 years, particularly neonates, due to their susceptibility to toxin effects and immature renal clearance; adults are rarely impacted unless immunocompromised.^[18]

Diagnosis

Clinical Assessment

The clinical assessment of suspected staphylococcal infections begins with a detailed history taking to identify potential sources and risk factors. Clinicians inquire about recent wounds, cuts, or surgical procedures that could serve as entry points for the bacteria, as well as exposures such as contact with infected individuals or contaminated environments.^[43] Risk factors including recent hospitalizations, use of medical devices like catheters or artificial joints, participation in contact sports, or underlying conditions such as diabetes or immunosuppression are elicited, as these increase susceptibility to infection.^[44] The symptom timeline is explored, noting the onset of localized pain, swelling, or systemic symptoms like fever, which often develop acutely over hours to days.^[1] Physical examination focuses on identifying local and systemic signs indicative of staphylococcal involvement. Inspection reveals characteristic lesions such as abscesses, furuncles, or boils—tender, erythematous, fluctuant nodules often centered around hair follicles—along with surrounding erythema and warmth.^[45] Palpation assesses for lymphadenopathy, particularly regional nodes draining the affected area, and tenderness suggesting deeper extension. Vital signs are evaluated for sepsis indicators, including tachycardia (heart rate >100 bpm), hypotension (systolic blood pressure <90 mmHg), and fever (>38°C), which signal potential systemic spread.^[1] In severe cases, patients may exhibit altered mental status or rigors, prompting urgent evaluation.^[44] Differential diagnosis relies on lesion characteristics to distinguish staphylococcal infections from similar presentations. Staphylococcal lesions typically form discrete, pus-filled abscesses or pustules with well-defined borders and central fluctuance, unlike streptococcal infections, which often present as diffuse cellulitis with ill-defined, rapidly spreading erythema and lymphatic streaking but fewer abscesses.^[45] Fungal infections, such as tinea or candidiasis, are differentiated by scaly, annular patches with central clearing and minimal pus, often in moist areas, contrasting the acute, inflammatory nodules of staphylococcal disease. These features, combined with history, guide initial suspicion while awaiting confirmatory tests.^[1]

Laboratory Identification

Laboratory identification of staphylococcal infections begins with the collection of appropriate clinical specimens, such as pus from abscesses, blood, or tissue samples, guided by presenting symptoms to maximize yield.^[46] Initial microbiological confirmation relies on culture-based methods that isolate and characterize Staphylococcus species. Gram staining of clinical specimens or cultured isolates typically reveals Gram-positive cocci arranged in clusters, a hallmark morphology distinguishing staphylococci from other bacteria.^[1] This preliminary observation prompts further selective culturing. Selective media like mannitol salt agar (MSA) are employed to isolate staphylococci from mixed flora, as the high salt concentration (7.5% NaCl) inhibits most non-halotolerant organisms while permitting staphylococcal growth.^[47] On MSA, Staphylococcus aureus typically produces yellow colonies due to mannitol fermentation and acid production, turning the phenol red indicator yellow, whereas coagulase-negative staphylococci (CoNS) yield red or pink colonies without fermentation.^[48] This differential property aids presumptive identification, though confirmatory tests are essential, as some CoNS may also ferment mannitol.^[49] The coagulase test serves as a cornerstone for definitive identification of S. aureus, detecting the enzyme coagulase that clots plasma via fibrin formation. The tube coagulase test (TCT), involving incubation of bacterial suspension with rabbit plasma at 37°C for 4-24 hours, is the gold standard, with positivity indicated by clot formation; the slide coagulase test (SCT) provides rapid bound coagulase detection via agglutination but requires TCT confirmation for accuracy.^[50] Approximately 97-99% of S. aureus strains are coagulase-positive, distinguishing them from CoNS like S. epidermidis.^[51] Molecular techniques enhance specificity and speed, particularly for detecting methicillin-resistant S. aureus (MRSA). Polymerase chain reaction (PCR) targeting the mecA gene, which encodes penicillin-binding protein 2a (PBP2a) responsible for beta-lactam resistance, is a widely used method for MRSA confirmation, with multiplex real-time PCR assays enabling simultaneous detection of mecA, S. aureus-specific markers like nuclease (nuc), and CoNS in under 1 hour from clinical samples.^[52] Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) provides rapid species-level identification by generating protein mass spectra matched against databases, achieving over 95% accuracy for staphylococci within minutes from a single colony.^[53] For staphylococci, it reliably differentiates S. aureus from CoNS and detects resistance biomarkers like PSM-mec in MRSA spectra, with detection limits as low as 10^3 CFU/mL in some protocols.^[54] This technology has revolutionized routine labs, reducing identification time from days to hours.^[55] Antimicrobial susceptibility testing (AST) follows identification to guide therapy, focusing on resistance patterns in staphylococci. Disk diffusion, per Clinical and Laboratory Standards Institute (CLSI) guidelines, involves placing antibiotic-impregnated disks on Mueller-Hinton agar inoculated with bacterial suspension; zone diameters are measured after 16-18 hours incubation to categorize isolates as susceptible, intermediate, or resistant, with cefoxitin disks preferred for MRSA screening due to superior sensitivity over oxacillin.^[56] Broth microdilution determines minimum inhibitory concentrations (MICs) by serial dilutions in 96-well plates, essential for detecting heterogeneous resistance in staphylococci like vancomycin-intermediate S. aureus (VISA), with MIC breakpoints for vancomycin at ≤2 μg/mL for susceptibility per CLSI.^[57] These methods, validated against reference strains, ensure reliable detection of multidrug-resistant strains, informing targeted treatment.^[58]

Treatment

Antimicrobial Therapy

Antimicrobial therapy for staphylococcal infections primarily targets Staphylococcus aureus, distinguishing between methicillin-susceptible S. aureus (MSSA) and methicillin-resistant S. aureus (MRSA) based on susceptibility testing to guide drug selection.^[59] For MSSA infections, first-line agents are beta-lactam antibiotics such as oxacillin, nafcillin, or cefazolin, which exhibit high efficacy due to their bactericidal activity against susceptible strains.^[60] In contrast, MRSA infections require non-beta-lactam alternatives, with intravenous vancomycin or daptomycin as primary options, dosed at 15-20 mg/kg every 8-12 hours for vancomycin, with therapeutic drug monitoring targeting an AUC/MIC ratio of 400–600 mg·h/L (trough levels of 11–20 mcg/mL may approximate this if AUC monitoring is unavailable), or 6-10 mg/kg daily for daptomycin, adjusted for renal function and infection severity.^[61]^[62] Treatment durations vary by infection site and severity, often starting with intravenous administration followed by an oral switch once clinical improvement is evident, such as resolution of fever and declining inflammatory markers. For uncomplicated skin and soft tissue infections, a course of 5-10 days is recommended, with oral agents like clindamycin, trimethoprim-sulfamethoxazole, or doxycycline for outpatient MRSA cases after initial incision and drainage if needed.^[63] More invasive infections, such as osteomyelitis, typically require 4-6 weeks of therapy, extending to 8 weeks or longer for complicated cases involving prosthetic material or poor response, using IV agents initially and transitioning to highly bioavailable oral options like linezolid or clindamycin if susceptibility permits.^[64] Emerging therapeutic options address limitations of standard agents, particularly in complicated MRSA infections with resistance concerns. Linezolid, an oxazolidinone with 100% oral bioavailability, is effective for skin and soft tissue infections and pneumonia, administered at 600 mg twice daily for 10-14 days, offering an alternative to vancomycin in patients with renal impairment.^[65] Ceftaroline, a fifth-generation cephalosporin active against MRSA, is indicated for complicated skin infections and community-acquired pneumonia at 600 mg every 12 hours intravenously, providing beta-lactam-like activity in select cases. Recent additions include ceftobiprole, approved by the FDA in 2024 for methicillin-susceptible and resistant S. aureus bacteremia, administered as 667 mg IV every 6 hours for days 1–8, then every 8 hours up to 42 days.^[66] Additionally, a 2025 study demonstrated that dalbavancin, dosed as 1,500 mg IV on days 1 and 8, is noninferior to standard therapy for complicated S. aureus bacteremia.^[67] Therapy selection must incorporate local resistance patterns from laboratory identification to optimize outcomes and minimize toxicity.^[59]

Surgical and Supportive Interventions

Surgical interventions play a critical role in managing staphylococcal infections by addressing localized collections of pus or necrotic tissue, particularly in skin and soft tissue infections such as abscesses. Incision and drainage (I&D) is the primary treatment for cutaneous abscesses caused by Staphylococcus aureus, allowing for the removal of purulent material and promoting resolution without routine need for antimicrobials in uncomplicated cases among immunocompetent hosts. This procedure is recommended for inflamed epidermoid cysts, carbuncles, and large furuncles, with evidence indicating high efficacy when performed promptly (strong recommendation, high-quality evidence). For more severe presentations like pyomyositis, early I&D of abscesses is essential, often requiring imaging to identify undrained foci if bacteremia persists. In necrotizing staphylococcal infections, such as fasciitis or myonecrosis, surgical debridement is imperative to excise all necrotic tissue and halt disease progression, especially in patients exhibiting systemic toxicity like fever or hemodynamic instability. Guidelines emphasize urgent surgical consultation, with repeat debridement every 24–36 hours until healthy tissue margins are achieved (strong recommendation, moderate-quality evidence). This approach is particularly vital for community-acquired methicillin-resistant S. aureus (MRSA) cases, where delayed intervention can lead to rapid deterioration. Management of staphylococcal infections involving indwelling devices focuses on prompt removal to eradicate biofilms, which shield bacteria from host defenses and impair clearance. For catheter-related bloodstream infections (CRBSI) due to S. aureus, complete catheter removal is recommended, as retention increases the risk of persistent bacteremia and complications like endocarditis (strong recommendation, moderate-quality evidence). ^[68] Similarly, in infections of cardiovascular implantable electronic devices (CIEDs), such as pacemakers or defibrillators, total hardware extraction is advised for definite staphylococcal involvement, given the 60–80% prevalence of staphylococci in these cases and the inefficacy of antimicrobials against biofilms. ^[69] For prosthetic joint infections, debridement and implant removal are standard when retention is not feasible, prioritizing source control to prevent chronic osteomyelitis. ^[70] Supportive care complements surgical measures by stabilizing patients and facilitating recovery from staphylococcal infections, particularly in systemic cases like sepsis. Intravenous (IV) fluid resuscitation is a cornerstone for managing hypovolemia and shock in staphylococcal sepsis, with guidelines recommending 30 mL/kg crystalloid within the first 3 hours to restore perfusion (strong recommendation, moderate-quality evidence). Pain management involves multimodal analgesia, including non-opioid agents like acetaminophen or NSAIDs for post-procedural discomfort, tailored to avoid exacerbating infection-related inflammation. ^[43] For wound care following drainage or debridement, sterile dressings, elevation to reduce edema, and regular monitoring prevent secondary complications, with evidence supporting moist wound healing environments to accelerate tissue repair.

Prevention

Personal and Community Measures

Personal hygiene plays a crucial role in preventing staphylococcal infections, as Staphylococcus aureus is commonly found on the skin and can be transmitted through direct contact. Regular handwashing with soap and water for at least 20 seconds, particularly after touching potentially contaminated surfaces or before handling food, significantly reduces the risk of transmission. ^[71] Covering any cuts, scrapes, or wounds with clean, dry bandages is essential to prevent bacteria from entering the body and to avoid spreading the infection to others. ^[72] Individuals should also avoid sharing personal items such as towels, razors, washcloths, or athletic gear, as these can harbor bacteria and facilitate transmission between people. ^[72] ^[73] Community education efforts are vital for broader prevention, focusing on awareness of staphylococcal carriage and toxin-mediated risks. Public campaigns often promote nasal decolonization using mupirocin ointment for known carriers, which has been shown to effectively reduce Staphylococcus aureus colonization in the nares and lower subsequent infection risks, particularly in high-risk groups like athletes or household contacts. ^[74] ^[75] Education on safe food handling is equally important to prevent staphylococcal enterotoxin poisoning, emphasizing practices such as refrigerating perishable foods promptly, avoiding room-temperature storage of prepared items like meats or dairy, and ensuring thorough cooking to kill bacteria, though preformed enterotoxins are heat-stable and not inactivated by heat. ^[76] ^[77] These initiatives, often led by health organizations, encourage communities to recognize symptoms early and adopt these habits to curb outbreaks. ^[78] Lifestyle adjustments can further minimize exposure, especially in settings prone to skin-to-skin contact. For athletes, showering immediately after practices or games with soap and water helps remove sweat and bacteria from the skin, while using personal towels and avoiding shared equipment reduces contamination risks. ^[71] ^[79] During community outbreaks, maintaining distance from infected individuals and practicing good ventilation in shared spaces can limit close-contact transmission. ^[72] These measures, when integrated into daily routines, promote skin integrity and collective immunity against staphylococcal spread.

Healthcare-Associated Prevention

Healthcare-associated prevention of staphylococcal infections, particularly those caused by methicillin-resistant Staphylococcus aureus (MRSA), relies on multifaceted protocols implemented in medical facilities to interrupt transmission and reduce infection rates. These strategies emphasize institutional measures tailored to high-risk environments like hospitals and surgical units, where staphylococcal pathogens can spread via healthcare workers, contaminated surfaces, or invasive devices. Evidence-based guidelines from organizations such as the Centers for Disease Control and Prevention (CDC) and the Society for Healthcare Epidemiology of America (SHEA) underscore the effectiveness of bundled interventions, which have demonstrated reductions in hospital-onset MRSA bacteremia by up to 16% through consistent application.^[80] Infection control bundles form the cornerstone of these efforts, integrating hand hygiene, contact precautions, and environmental cleaning to minimize cross-contamination. Hand hygiene compliance, achieved through soap and water or alcohol-based hand sanitizers before and after patient contact, is a fundamental practice that nine studies have linked to decreased multidrug-resistant organism (MDRO) transmission, including MRSA.^[81] For patients colonized or infected with MRSA, contact precautions—such as donning gloves and gowns for all interactions—are recommended in acute care settings, with evidence from a Veterans Affairs study showing a 47% reduction in transmission and a cluster-randomized trial reporting a 40.2% decrease in acquisition rates.^[80]^[82] Environmental cleaning targets high-touch surfaces like bedrails and medical equipment using EPA-registered disinfectants, with improved adherence associated with lower vancomycin-resistant Enterococcus acquisition and similar benefits for staphylococcal control in resource-limited settings.^[81]^[83] These bundled approaches, when implemented comprehensively, have sustained reductions in central line-associated bloodstream infections and ventilator-associated pneumonia, thereby limiting opportunities for staphylococcal spread.^[81] Screening and isolation protocols further enhance prevention by identifying and segregating at-risk individuals early. Nasal screening upon admission, typically via swab of the anterior nares, detects MRSA colonization with sensitivities ranging from 48% to 93%, and is recommended for high-risk groups such as intensive care unit (ICU) admissions or preoperative patients to guide targeted interventions.^[82] Active surveillance cultures, followed by isolation in single-patient rooms or cohorting of colonized patients, reduce patient-to-patient transmission; for instance, the REDUCE MRSA Trial demonstrated a 37% decrease in clinical MRSA isolates through universal screening and decolonization in ICUs.^[81]^[82] Cohorting involves grouping MRSA-positive patients together under dedicated nursing staff when single rooms are unavailable, a strategy that has controlled outbreaks in neonatal ICUs and burn units by preventing co-colonization with other MDROs.^[82] These measures are most effective when combined with empiric contact precautions until screening results confirm negative status, particularly in high-prevalence settings.^[82] Device-related protocols address staphylococcal risks associated with invasive procedures, focusing on preoperative preparation and prophylaxis for high-risk surgeries. Chlorhexidine gluconate (CHG) baths or showers, administered at least twice before surgery (e.g., the night before and morning of), serve as skin antisepsis to reduce bacterial load, with guidelines recommending 4% CHG soap for home use in orthopedic and cardiac procedures to prevent surgical site infections (SSIs).^[84] Although meta-analyses show mixed results on CHG versus plain soap in reducing SSIs overall, it is endorsed alongside nasal decolonization for procedures where Staphylococcus aureus is a primary pathogen, such as joint replacements.^[85]^[86] Antibiotic prophylaxis, typically a single intravenous dose of cefazolin administered within 60 minutes of incision, is standard for high-risk procedures like cardiac surgery, hip arthroplasty, and hysterectomies to target staphylococcal contamination; vancomycin is substituted for known MRSA colonization, with evidence supporting ≤24-hour durations to avoid resistance promotion.^[87]^[86] These protocols, when adhered to, have reduced SSIs by up to 15% per month in screened surgical populations.^[82] Research into vaccines against S. aureus is ongoing, with candidates like LBT-SA7 receiving FDA fast-track status in 2024 and entering phase 1 trials as of 2025, though no licensed vaccine is available yet.^[88]

Epidemiology

Incidence and Prevalence

Staphylococcal infections, predominantly caused by Staphylococcus aureus, represent a significant global health burden, with S. aureus accounting for the majority of cases among staphylococcal species. Globally, the incidence of S. aureus bacteremia is estimated at 10-30 cases per 100,000 person-years in industrialized countries, though data from low- and middle-income regions remain limited due to underreporting.^[89]^[90] In the United States, invasive S. aureus infections, including bloodstream infections, occur at a rate of approximately 40 cases per 100,000 population annually, encompassing both methicillin-susceptible and resistant strains.^[91] Skin and soft tissue infections (SSTIs) constitute the most common manifestation of staphylococcal disease, with S. aureus identified as the primary pathogen in a substantial proportion of cases. In the US, the incidence of S. aureus-associated SSTIs is estimated at around 393 cases per 100,000 population yearly, combining methicillin-susceptible S. aureus (MSSA) at 270 per 100,000 and methicillin-resistant S. aureus (MRSA) at 122 per 100,000. These infections contribute to hundreds of thousands of outpatient visits and hospitalizations, underscoring their scale in high-resource settings.^[92]^[93] Regional variations highlight disparities in incidence, with higher rates observed in low-resource settings. In parts of Africa, the prevalence of MRSA among S. aureus infections exceeds 50% in some SSTI cases, driven by factors such as overcrowding and limited healthcare access, leading to elevated overall staphylococcal disease burden compared to high-income areas.^[94] In contrast, high-income countries like the US report invasive disease rates of 38-45 per 100,000 person-years, reflecting better surveillance but persistent community and healthcare-associated transmission.^[91] Demographic factors influence incidence, with higher rates among males, neonates, and the elderly. Males experience elevated risk across age groups, potentially due to behavioral and occupational exposures, while neonates face particularly high vulnerability in neonatal intensive care units, and the elderly show increased susceptibility linked to comorbidities and immune senescence.^[95]^[96]^[97]

Resistance Trends and Outbreaks

Methicillin-resistant Staphylococcus aureus (MRSA) represents a significant portion of staphylococcal infections worldwide, with the proportion of S. aureus bloodstream infections attributable to MRSA ranging from 7% to over 60% globally based on 2024 data, varying by region and healthcare setting.^[98] In Asia and the Middle East, community-acquired MRSA (CA-MRSA) has shown a notable rise, driven by expanding lineages such as CC1153 in areas like the United Arab Emirates, where CA-MRSA now dominates over hospital-acquired strains.^[99] This shift reflects increased transmission in community settings, including among healthy individuals without traditional risk factors.^[100] In the United States, hospital-onset MRSA bloodstream infections decreased by approximately 16% from 2020 to 2024, according to Centers for Disease Control and Prevention (CDC) surveillance, attributed to enhanced infection control measures post-COVID-19.^[101] Conversely, methicillin-susceptible S. aureus (MSSA) infections exhibited a slight increase during the same period, with hospital-onset MSSA incidence rising modestly since 2017 and overall MSSA bacteremia rates climbing from 2.43 to 2.87 per 1,000 admissions between 2015 and 2020, a trend that persisted into the early 2020s.^[102]^[103] Outbreaks and prevalence fluctuations of MRSA have been documented globally from 2022 to 2024, with notable variability in high-burden regions. In Saudi Arabia, MRSA prevalence among S. aureus isolates reached 52.7% overall from 2013 to 2024, with a significant upward trend and higher rates observed among patients with COVID-19 or diabetes.^[100] Certain clonal complexes, such as CC5, have been associated with severe outcomes, exhibiting the highest mortality rate of 50.75% among MRSA strains in meta-analyses of bloodstream infections.^[104] Emerging concerns include the detection of vancomycin-intermediate S. aureus (VISA) strains, which, though rare (prevalence around 1-4% post-2010), pose risks due to reduced treatment efficacy and associations with prolonged vancomycin exposure in vulnerable patients.^[105] Zoonotic transmission of MRSA from livestock and companion animals to humans has also gained attention, with evidence of host-switching events facilitating spread in farm and household settings.^[106] According to 2025 World Health Organization updates, MRSA accounts for 20-50% of S. aureus bloodstream infections in select regions, underscoring ongoing challenges in antimicrobial stewardship.^[98] These resistance patterns complicate antimicrobial therapy, often necessitating alternative agents like daptomycin for persistent cases.^[107]

History and Etymology

Discovery and Early Research

In 1880, Scottish surgeon Alexander Ogston identified clusters of pus-forming cocci in abscesses during his investigations into surgical infections, establishing their role as primary pathogens in suppurative processes and linking them to conditions like blood poisoning.^[108] Ogston's observations, presented at the Surgical Congress in Berlin, highlighted the bacteria's grape-like arrangement under the microscope, which he termed "micrococci," and emphasized their prevalence in acute abscesses, fundamentally advancing the understanding of wound infections in the post-Listerian era.^[109] Building on Ogston's work, German physician Friedrich Julius Rosenbach formally classified the organism in 1884, naming it Staphylococcus to reflect its clustered morphology and distinguishing Staphylococcus aureus based on its golden-yellow colonies from the white Staphylococcus albus (later renamed S. epidermidis).^[110] Rosenbach's classification, derived from studies of purulent infections, provided the taxonomic foundation for recognizing S. aureus—the primary staphylococcal pathogen—as a distinct species capable of causing a spectrum of human diseases, from skin abscesses to systemic infections.^[110] The mid-20th century marked significant advancements in understanding staphylococcal resistance, with penicillin resistance first systematically identified in S. aureus strains by the late 1940s, prompting the development of methicillin in 1959 as a treatment for these resistant infections.^[111] Just two years later, in 1961, British bacteriologist Patricia Jevons reported the first cases of methicillin-resistant S. aureus (MRSA) in UK hospitals, isolated from patients with severe infections, signaling the rapid evolution of antibiotic resistance and the need for ongoing surveillance.^[112] In the 1990s, community-associated MRSA (CA-MRSA) emerged, causing skin and soft tissue infections in healthy individuals outside healthcare settings, particularly in communities with close contact.^[113] Research in the 1980s shifted focus to staphylococcal toxins, spurred by outbreaks of toxic shock syndrome (TSS) linked to superabsorbent tampon use, with over 800 menstrual-related cases reported in the US by 1980, predominantly caused by toxin-producing S. aureus strains.^[114] These investigations identified the pyrogenic exotoxin TSST-1 as the key virulence factor in TSS pathogenesis, leading to regulatory changes in tampon manufacturing and heightened awareness of toxin-mediated diseases.^[115]

Naming Conventions

The genus name Staphylococcus originates from the Ancient Greek words staphýlē (σταφυλή), meaning "bunch of grapes," and kókkos (κόκκος), meaning "berry" or "grain," reflecting the clustered, grape-like arrangement of the bacteria observed under a microscope.^[110]^[116] Scottish surgeon Alexander Ogston first described these bacteria in 1880, and German physician Friedrich Julius Rosenbach formally named the genus in 1884.^[110]^[117] Species names within the genus follow conventions that highlight distinctive morphological or ecological traits. Staphylococcus aureus derives its epithet from the Latin aureus, meaning "golden," due to the characteristic yellow-golden pigmentation of its colonies on agar media.^[118] Similarly, Staphylococcus epidermidis is named from the Greek epidermis (επιδερμίς), referring to its primary habitat on the skin's epidermal layer, emphasizing its commensal role on human and animal epithelia.^[119] The term "coagulase," used to classify certain species like coagulase-positive staphylococci (e.g., S. aureus), stems from the Latin coagulāre, meaning "to curdle" or "clot," alluding to the enzyme's ability to coagulate plasma.^[5] The adjective "staphylococcal" denotes infections or conditions caused by members of the Staphylococcus genus, as in "staphylococcal infection," a term that emerged alongside the genus description in the late 19th century.^[110] Historically, these bacteria were initially grouped under the genus Micrococcus due to their spherical shape and Gram-positive staining, but by the mid-20th century, they were reclassified into the distinct genus Staphylococcus based on physiological tests such as glucose fermentation and novobiocin resistance.^[120] This taxonomic shift, formalized in classifications like that of Baird-Parker in 1963, better reflected their pathogenic potential and biochemical diversity.^[120]

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Burdens of Invasive Methicillin-Susceptible and Methicillin-Resistant ...
Nov 27, 2018 · Incidence for invasive MSSA (27.1 cases/100,000 population) was more than twice that for invasive MRSA (13.1 cases/100,000 population) (p<0.001) ...
[88]
Estimating the Burden of Clinically Significant Staphylococcus ...
Overall MRSA and MSSA infections had respective incidence of 122.27 (SE, 5.59) and 270.43 (SE, 6.73) per 100 000 people. Most common sites included BSI, SSTI, ...
[89]
Clinical Impact of Staphylococcus aureus Skin and Soft Tissue ...
The pathogenic bacterium Staphylococcus aureus is the most common pathogen isolated in skin-and-soft-tissue infections (SSTIs) in the United States.
[90]
Temporal trends of skin and soft tissue infections caused by ...
Jun 25, 2024 · It is estimated that the prevalence of MRSA-associated SSTI in Africa may exceed 50% [11,12,13]. In developing countries, such as Gabon, ...
[91]
Age-Dependent Increase in Incidence of Staphylococcus aureus ...
Demographics of the study population are provided in Table 1. In brief, the median age was 68 years (IQR 56–79 years); 62% of patients were male and 38% female.
[92]
Staphylococcus aureus Bacteremia Among Elderly vs Younger Adult ...
Jun 14, 1999 · Staphylococcus aureus bacteremia among the elderly is associated with high mortality. Both total mortality and mortality directly attributable to SAB are more ...
[93]
Staphylococcus aureus Bacteremia in Children of Rural Areas of ...
Feb 28, 2019 · The incidence was high, particularly among neonates (3.5 cases/1,000 live births), but did not increase with time (Figure 3). The CFR (14.1%) ...
[94]
Proportion of bloodstream infection due to methicillin-resistant ...
Proportion of bloodstream infection due to methicillin-resistant Staphylococcus aureus among patients seeking care and whose blood sample is taken and tested.
[95]
The Shifting Landscape in the United Arab Emirates - MDPI
Jan 2, 2025 · Community-acquired MRSA lineages were dominant, with only one healthcare-associated MRSA lineage isolate identified. Upward trends of CC1153 ...
[96]
Epidemiological dynamics and rising trends of MRSA in Saudi Arabia
The overall MRSA prevalence in this study (52.7%) surpasses earlier estimates from Saudi Arabia, where a systematic review reported MRSA rates ranging from 35.6 ...Missing: outbreaks | Show results with:outbreaks
[97]
CDC report shows decreases in certain health care-associated ...
Nov 6, 2024 · There was a 16% decrease in hospital-onset methicillin-resistant Staphylococcus aureus, or MRSA; a 15% decrease in central line-associated ...
[98]
Invasive Staphylococcus aureus Infection Surveillance | HAIs - CDC
Jun 25, 2025 · The invasive S. aureus infection surveillance program is an active population- and laboratory-based surveillance system.
[99]
Trends and outcomes in community-onset and hospital-onset ...
Sep 16, 2024 · This study revealed an increase in the incidence of MSSA and MRSA bacteremia between 2015 and 2020 across 267 acute-care hospitals in the United ...
[100]
a hospital-based surveillance study from 2022 to 2024 - IJID Regions
MRSA rates fluctuated: 48.9% in 2022, 42.3% in 2023, and 48.5% in 2024, with a temporary decline in 2023 and a rebound in 2024.
[101]
A Systematic Review and Meta-Analysis of the Risk of Mortality ...
Sep 2, 2025 · Among MRSA clonal complexes, the highest mortality was observed among CC5 (50.75%), followed by CC8 (37.56%).
[102]
Global prevalence and distribution of vancomycin resistant ... - Nature
Jul 29, 2020 · The overall prevalence of VRSA, VISA, and hVISA before 2010 was 1.2%, 1.2%, and 4%, respectively, while their prevalence after this year has reached 2.4%, 4.3% ...
[103]
Zoonotic transmission of asymptomatic carriage Staphylococcus ...
Dec 4, 2024 · The spread of S. aureus to humans from livestock is a well-documented zoonotic event with host switching being recorded among wild animals, ...
[104]
Antimicrobial Resistance Threats in the United States, 2021-2022
In 2022, rates for all but one of these pathogens (MRSA) remained above pre-pandemic levels. In addition, the number of reported clinical cases of C. auris—a ...
[105]
Staphylococcus aureus in the antibiotic era - JCI
Oct 1, 2024 · Sir Alexander Ogston first recognized it in 1880 as the most frequent cause of acute abscesses and capable of producing “blood poisoning ...
[106]
Staphylococcus aureus: an introduction - PMC - PubMed Central - NIH
Staphylococcal infection presents most commonly in the skin and soft tissues. These infections cause over ten million outpatient visits and nearly a half- ...Missing: overview | Show results with:overview<|control11|><|separator|>
[107]
Etymologia: Staphylococcus - Emerging Infectious Diseases journal
” In 1884, German physician Friedrich Julius Rosenbach differentiated the bacteria by the color of their colonies: S. aureus (from the Latin aurum, gold) ...
[108]
The evolutionary history of methicillin-resistant Staphylococcus ...
Methicillin was introduced in 1959 to treat infections caused by penicillin-resistant Staphylococcus aureus. In 1961 there were reports from the United ...
[109]
Surveillance and epidemiology of MRSA bacteraemia in the UK
The isolate of MRSA reported in 1961 was the only one found among about 5000 ... First report of the Department of Health's mandatory MRSA bacteraemia ...Introduction · Surveillance programmes for... · The emergence and spread of...
[110]
Toxic shock syndrome surveillance in the United States, 1980 to 1981
The case/fatality ratio for menstrual toxic shock syndrome was 3.1% for cases with onset in 1981. The distribution of reported cases by date of onset showed ...
[111]
Toxic shock syndrome: An update - ScienceDirect
Since late 1979 to early 1980, when toxic shock syndrome achieved notoriety, a substantial body of data has demonstrated that vaginal Staphylococcus aureus ...
[112]
Staphylococcus - Etymology, Origin & Meaning
Originating from Modern Latin in 1882 by Alexander Ogston, staphylococcus means "grape-like cluster," derived from Greek staphylē, referring to its shape.
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Staphylococcus - an overview | ScienceDirect Topics
History. The name 'staphylococcus' (derived from the Greek σταϕυλη, a bunch of grapes) was introduced by Alexander Ogston, a Scottish surgeon who in 1881 ...
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Etymologia: Staphylococcus - PMC - NIH
aureus (from the Latin aurum, gold) and S. albus (Latin for white). S. albus was later renamed S. epidermidis because of its ubiquity on human skin. Footnotes.
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https://www.sciencedirect.com/science/article/pii/S0002937812907346
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A Classification of Micrococci and Staphylococci Based on ...
The genera Staphylococcus, Micrococcus and Sarcina were recognized. Staphylococci were distinguished by their ability to form acid from glucose ...