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Staphylococcus saprophyticus

Staphylococcus saprophyticus is a Gram-positive, coagulase-negative, non-hemolytic coccus that belongs to the genus Staphylococcus and is recognized as a significant uropathogen, particularly causing uncomplicated urinary tract infections (UTIs) in young, sexually active women.^[1] It is distinguished from other staphylococci by its resistance to novobiocin and ability to produce urease, while lacking nitrate reduction capabilities.^[1] As an opportunistic pathogen, it colonizes the skin, perineum, and genitourinary tract as part of the normal human microbiota but can ascend to the bladder via adhesins and virulence factors, leading to infections that account for 5–20% of community-acquired UTIs.^[1]^[2] Microbiologically, S. saprophyticus forms clusters of spherical cells, typically 0.7–1.3 μm in diameter, and exhibits aerobic or facultatively anaerobic growth, thriving at temperatures between 10–45°C with an optimal pH of 7.0–7.5.^[1] Its genome, as sequenced in strains like ATCC 15305, reveals adaptations for survival in urine, including genes for urease production that alkalinize urine and promote stone formation, as well as surface proteins like Aas (ammonia-binding adhesin) and UafA (uroadherence factor A) that facilitate binding to uroepithelial cells.^[3] These adhesins, along with biofilm-forming capabilities present in up to 70% of clinical isolates, enhance persistence in the urinary tract and contribute to antibiotic resistance, such as increased tolerance to vancomycin.^[3] Additionally, proteomic analyses highlight strain-specific variations, with some expressing D-serine deaminase (DsdA) for nutrient utilization in urine and thioredoxin for oxidative stress resistance, underscoring its pathogenic flexibility.^[3] Epidemiologically, S. saprophyticus is the second most common cause of UTIs after Escherichia coli, accounting for 5–20% of cases, particularly in young women, with higher incidence during warmer months possibly linked to increased sexual activity or environmental exposure.^[1] Genomic studies of over 300 global isolates identify two major lineages: lineage G (74%), associated with foodborne transmission from meat production chains like pork (contaminating 35% of slaughterhouse samples) and spreading across 11 countries; and lineage S (26%), more adapted to human hosts via hormone-responsive genes and found in 6 countries.^[2] It also inhabits the gastrointestinal tract, skin of animals like cows and pigs, and food products, facilitating zoonotic and environmental reservoirs that contribute to human colonization.^[1]^[2] While primarily causing cystitis with symptoms like dysuria, frequency, and urgency, it can progress to pyelonephritis, prostatitis, or rarely bacteremia in immunocompromised individuals, and is associated with high rates of recurrence.^[1] Diagnosis relies on urine culture showing >10^5 colony-forming units/mL, as it does not reduce nitrates and may yield false negatives on dipstick tests; identification confirms novobiocin resistance.^[1] Treatment for uncomplicated cases typically involves short courses of nitrofurantoin (100 mg twice daily for 5–7 days) or trimethoprim-sulfamethoxazole (for 3 days), given its general susceptibility to these agents despite intrinsic resistance to beta-lactams like ampicillin and cephalosporins.^[1] However, biofilm producers and certain lineages may carry resistance plasmids, emphasizing the need for targeted antimicrobial stewardship to combat emerging resistance.^[3]

Taxonomy and Description

Classification and Etymology

Staphylococcus saprophyticus is a Gram-positive bacterium classified within the domain Bacteria, phylum Bacillota, class Bacilli, order Bacillales, family Staphylococcaceae, genus Staphylococcus, and species saprophyticus. This taxonomic placement reflects its phylogenetic position among low-GC-content Gram-positive bacteria, distinguished by its spherical morphology and clustering arrangement. The species includes two subspecies: S. saprophyticus subsp. saprophyticus and S. saprophyticus subsp. bovis, with the former being the primary human-associated variant.^[4]^[5] The genus name Staphylococcus derives from the Greek words staphýlē (meaning "bunch of grapes") and kókkos (meaning "berry" or "grain"), referring to the characteristic grape-like clusters observed in microscopic preparations of these cocci. The specific epithet saprophyticus originates from the Greek sapros (meaning "rotten" or "putrid") and phýton (meaning "plant"), combined with the Latin suffix -icus, indicating a saprophytic lifestyle, originally described as growth on decaying vegetable matter. This etymology underscores the bacterium's early recognition as an environmental saprophyte before its pathogenic potential was established.^[5]^[6] S. saprophyticus is distinguished as a coagulase-negative staphylococcus (CoNS), lacking the coagulase enzyme that defines Staphylococcus aureus and contributes to its virulence. Unlike coagulase-positive species, CoNS like S. saprophyticus are generally opportunistic pathogens with lower pathogenicity in healthy hosts. Historically, S. saprophyticus was misclassified within the genus Micrococcus as subgroup 3 due to its slow anaerobic glucose fermentation, but in 1975, it was formally reclassified into the genus Staphylococcus based on comprehensive phenotypic traits, including cell wall composition, biochemical reactions, and physiological characteristics. This reclassification clarified its distinction from micrococci and solidified its position among staphylococci.^[7]

Morphology and Physiology

Staphylococcus saprophyticus is a Gram-positive coccus measuring 0.6-1.4 μm in diameter, typically arranged in irregular clusters resembling grapes.^[7] The bacterium is non-motile and non-spore-forming, lacking flagella or other structures for movement.^[7] As a facultative anaerobe, S. saprophyticus grows under both aerobic and anaerobic conditions, with optimal growth occurring at 37°C, the human body temperature.^[8] It thrives in a neutral pH range of approximately 7.0-7.5 and forms non-hemolytic, white to creamy colonies, 2-4 mm in diameter, on blood agar after 24-48 hours of incubation.^[9]^[10] Key biochemical characteristics distinguish S. saprophyticus from other staphylococci: it is catalase-positive, producing bubbles in the presence of hydrogen peroxide; coagulase-negative, failing to clot plasma; urease-positive, hydrolyzing urea to ammonia and carbon dioxide; novobiocin-resistant with a minimum inhibitory concentration (MIC) greater than 1.6 μg/mL; and nitrate-negative, unable to reduce nitrate to nitrite.^[7]^[1]^[11] Metabolically, S. saprophyticus ferments glucose to produce acid under anaerobic conditions and can utilize sucrose and lactose, though lactose fermentation may vary by strain.^[10] It produces lipase, enabling the hydrolysis of lipids, but does not produce hemolysins, consistent with its non-hemolytic growth on blood agar.^[12]^[1] Adherence properties of S. saprophyticus involve surface proteins such as the autolysin adhesin (Aas), which binds to fibronectin on host cells.^[13]

History

Discovery

Staphylococcus saprophyticus was first proposed as a distinct species in 1940 by R. W. Fairbrother, who named it based on isolates exhibiting a saprophytic lifestyle, consistent with recovery from soil and decaying plant material, distinguishing it from pathogenic coagulase-positive staphylococci.^[5] In 1951, C. Shaw, J. M. Stitt, and S. T. Cowan provided the first valid taxonomic description of the species, drawing on isolates from environmental sources and human skin, where it was classified as a commensal organism without recognized pathogenic potential.^[14] Throughout the early to mid-20th century, including studies from the 1920s to 1950s, S. saprophyticus was frequently noted as part of the normal human skin flora, but when recovered from urine cultures, it was typically regarded as a laboratory contaminant rather than a true pathogen.^[15] A pivotal shift occurred in the 1970s through Swedish research, such as studies by B. Hovelius and colleagues in the late 1970s, which utilized the organism's unique resistance to novobiocin for reliable identification and established its frequent association with urinary tract infections, moving beyond prior dismissals of its clinical relevance. Novobiocin resistance also aided differentiation in mid-1970s studies.^[16]^[17]

Recognition as a Pathogen

The recognition of Staphylococcus saprophyticus as a human pathogen emerged in the early 1970s, when clinical studies began linking novobiocin-resistant, coagulase-negative staphylococci to urinary tract infections (UTIs) in young women. In 1974, R. Maskell reported a series of cases in the UK where these organisms were isolated from symptomatic patients with acute cystitis, demonstrating significant pyuria and bacteriuria comparable to Escherichia coli infections, thus challenging the prior dismissal of such staphylococci as contaminants.^[18] This work highlighted the organism's role in community-acquired UTIs, particularly among sexually active females, and emphasized its resistance to novobiocin as a key identifying feature. By 1975, taxonomic revisions solidified its status, with W. E. Kloos and K. H. Schleifer providing amended descriptions that reclassified Micrococcus subgroup 3 isolates from clinical sources as S. saprophyticus, distinguishing it from saprophytic skin flora based on physiological and biochemical traits like urease activity and novobiocin resistance.^[19] The species was formally validated in the Approved Lists of Bacterial Names in 1980.^[5] During the 1980s, global epidemiological studies confirmed its prevalence, accounting for 10-20% of community-acquired UTIs in young women across the USA and Europe, often associated with sexual activity and termed "honeymoon cystitis" due to its link with mechanical introduction during intercourse.^[20]^[1] In the 1990s, further molecular characterization reinforced its pathogenicity, including the identification of key virulence adhesins, such as the Aas protein enabling uropathogenic adhesion to uroepithelial cells, which helped explain its tropism for the urinary tract. In 1996, the subspecies S. saprophyticus subsp. bovis was described from bovine sources by V. Hajek and colleagues, suggesting broader ecological reservoirs.^[21]^[22] Into the 2010s, research demonstrated the organism's capacity for biofilm formation contributing to persistent or recurrent infections and antibiotic tolerance in the urinary tract.^[23] Recent studies from 2023 to 2025 have highlighted the zoonotic potential of S. saprophyticus, with genomic analyses of strains from companion animals and humans revealing shared virulence genes and antimicrobial resistance profiles that indicate possible animal-to-human transmission, particularly in close-contact settings.^[24]

Ecology and Epidemiology

Habitat and Reservoirs

Staphylococcus saprophyticus primarily inhabits the human skin and mucosal surfaces, particularly the perineal and genital regions of healthy individuals, where it serves as a commensal bacterium. It is detected in the gastrointestinal and genitourinary tracts of 5 to 10% of healthy women, with the rectum being the most common colonization site, followed by the urethra and cervix.^[7] The gastrointestinal tract acts as a major reservoir, facilitating potential translocation to adjacent urogenital sites.^[10] Beyond human hosts, S. saprophyticus is isolated from various environmental reservoirs, including soil, sewage, and food products such as meat and dairy. It has been recovered from soil samples in industrial settings and wastewater, highlighting its adaptability to nutrient-rich, organic environments.^[25]^[26] Contamination occurs frequently in raw beef, pork, and cheese, with prevalence rates up to 34% in certain meat samples.^[27] The bacterium is also found in animals, including livestock such as cattle and pigs, as well as companion animals like dogs and cats. Recent studies from 2023 to 2025 have isolated S. saprophyticus from companion animals with urinary tract symptoms, noting its presence in approximately 2.9% of such cases.^[28] In livestock, it colonizes the gut and rectal flora, contributing to food chain contamination.^[2] Zoonotic links are evident through genomic analyses showing identical strains between farm animals and human urinary tract infections, supporting environmental dispersal via One Health pathways. A 2024 study on integrated farms identified S. saprophyticus in environmental samples, underscoring potential transmission risks from animal reservoirs to humans through contaminated food or direct contact.^[29] Phylogenetic evidence indicates that major clonal lineages causing human infections originate from meat-production chains involving pigs and cattle.^[2] In non-human settings, S. saprophyticus demonstrates persistence in moist environments, aided by its ability to form biofilms on surfaces. Biofilm production, dependent on polysaccharide intercellular adhesin, enhances colonization and survival in wet, organic matrices like sewage or food processing areas.^[7]^[23] This saprophytic lifestyle allows it to thrive in decaying matter and contaminated water sources.^[30]

Prevalence and Risk Factors

Staphylococcus saprophyticus is a significant cause of uncomplicated urinary tract infections (UTIs), accounting for 5-20% of cases among young women, making it the second most common pathogen after Escherichia coli.^[1] This prevalence is particularly notable in women aged 16-35 years, where rates can reach up to 42% in certain cohorts of sexually active individuals.^[15] Infections are rare in men and children, with the bacterium primarily affecting females due to its association with community-acquired rather than nosocomial settings.^[2] Demographic patterns highlight the highest incidence among sexually active young women, where S. saprophyticus represents a leading uropathogen in outpatient settings. Overall, it contributes to 1-2% of all reported UTIs across populations, though this rises substantially in targeted groups. Asymptomatic carriage occurs in up to 40% of sexually active young women in the genitourinary tract, facilitating potential opportunistic infections.^[31] Key risk factors include recent sexual intercourse, which promotes bacterial ascension into the urinary tract, and the use of spermicide-coated condoms or diaphragms, associated with odds ratios of 6-10 for S. saprophyticus-specific UTIs.^[32]^[33] Recent genomic analyses (2021) indicate a foodborne origin with global spread, suggesting potential links to animal and environmental exposure, though direct rural risk factors require further confirmation.^[2] Geographically, higher prevalence is observed in Europe and North America, with consistent reports of 10-20% in young women, while cases are emerging in urban Asian settings amid increasing community surveillance.^[2] Worldwide distribution underscores its role as a cosmopolitan pathogen, with variations tied to lifestyle and diagnostic practices.^[34]

Pathogenesis

Virulence Factors

Staphylococcus saprophyticus possesses several key virulence factors that facilitate its adherence to host tissues, persistence in the urinary tract, and evasion of immune responses. These include surface adhesins, biofilm-forming components, and enzymatic activities that contribute to colonization and infection. Unlike some other staphylococci, its virulence is primarily driven by chromosomal genes rather than plasmid-encoded elements. Adhesins play a central role in the initial attachment of S. saprophyticus to uroepithelial cells and extracellular matrix proteins. The Aas protein, a bifunctional autolysin-adhesin, binds to fibronectin and fibrinogen, promoting bacterial adhesion and hemagglutination in the urinary tract. Similarly, the UafA protein mediates adherence to uroepithelial cells and contributes to hemagglutination activity, enhancing colonization of the bladder epithelium. These adhesins are conserved across clinical and environmental isolates, underscoring their importance in pathogenesis. Biofilm production allows S. saprophyticus to persist in the urinary tract by forming protective matrices on uroepithelial surfaces. While polysaccharide intercellular adhesin (PIA), encoded by the ica locus, is present in a minority of strains and contributes to biofilm structure in those cases, most biofilms rely on proteinaceous components and extracellular DNA (eDNA). eDNA, released from lysed cells, stabilizes the biofilm matrix and promotes bacterial aggregation. Recent studies indicate that 91% of analyzed isolates (including clinical and environmental) form biofilms, with protein and eDNA being predominant in infection-associated strains, thereby enhancing persistence and antibiotic tolerance.^[35] Enzymatic factors further support tissue invasion and environmental adaptation. Urease hydrolyzes urea in urine to ammonia and carbon dioxide, alkalinizing the environment and facilitating ascension to the upper urinary tract; this enzyme is a hallmark of S. saprophyticus and aids in its identification. The surface-associated lipase Ssp enables degradation of host lipids, promoting tissue invasion and nutrient acquisition during infection. Lipoteichoic acid (LTA), a cell wall component, contributes to immune evasion by modulating host inflammatory responses and inhibiting phagocyte function. Recent research highlights the role of stress response genes, such as mgrA and those involved in cell envelope integrity, in enabling survival under urinary tract conditions like osmotic stress and nutrient limitation; alternative sigma factors like SigB regulate these responses. A 2023 study highlighted correlations between stress response genes, such as mgrA, and bacteriophages in developing antibiotic resistance, enhancing survival in uropathogenic lineages.^[36] The genetic basis of these virulence factors resides primarily on the chromosome. Genes encoding Aas (aas) and UafA (uafA) are chromosomally located and highly conserved, present in nearly all strains regardless of origin. S. saprophyticus typically lacks plasmids carrying virulence determinants, with its two small native plasmids encoding non-pathogenic traits like restriction-modification systems.

Mechanisms of Infection

Staphylococcus saprophyticus primarily colonizes the urinary tract through an ascending route, originating from its reservoir in the perineal and genital areas. As a component of the normal flora in the perineum, rectum, urethra, cervix, and gastrointestinal tract, the bacterium ascends to the bladder via adhesins that bind to the uroepithelial cells, facilitating initial attachment and persistent colonization.^[1] Specific adhesins, such as Aas, enable this adherence to the bladder epithelium, allowing the pathogen to establish a foothold despite the flushing action of urine flow.^[37] Once attached, invasion proceeds through mechanisms that disrupt the mucosal barrier and promote bacterial survival. The production of urease hydrolyzes urea in urine to ammonia and carbon dioxide, elevating the local pH and creating an alkaline environment that damages the bladder mucosa, leading to inflammation and tissue injury.^[38] Concurrently, S. saprophyticus forms biofilms on the uroepithelium, which shield the bacteria from mechanical clearance by urine and initial host immune responses, enhancing persistence within the bladder.^[39] Immune evasion is further supported by biofilm architecture and surface components that hinder phagocytosis and modulate host responses. While biofilms provide a physical barrier against immune cells, the activation of toll-like receptors by bacterial components triggers an inflammatory cascade, including neutrophil and macrophage recruitment, which paradoxically aids in the development of cystitis by promoting epithelial shedding.^[40] Recent studies have highlighted the role of quorum sensing in biofilm maturation, where the agr system regulates gene expression to coordinate community behavior and virulence factor production during infection.^[41] Infection can progress upward if unchecked, with S. saprophyticus ascending from the bladder to the kidneys, potentially causing pyelonephritis, as demonstrated in animal models where transurethral inoculation led to renal involvement.^[37] Host factors significantly influence susceptibility; in females, estrogen enhances the expression of receptors on uroepithelial cells, thereby aiding bacterial adherence and increasing the risk of infection, particularly in young, sexually active individuals.^[42]

Clinical Features

Urinary Tract Infections

Staphylococcus saprophyticus is a leading cause of uncomplicated urinary tract infections (UTIs), particularly acute cystitis, in young, sexually active women, accounting for 10-20% of community-acquired cases in this demographic.^[1] The infection often follows sexual intercourse, earning the colloquial term "honeymoon cystitis" for recurrent post-coital episodes.^[1] Symptoms of acute cystitis typically include dysuria, urinary frequency, urgency, suprapubic pain, and hematuria.^[1]^[7] These uncomplicated infections generally resolve within 3 days with appropriate management, though symptomatic relief is key in the interim.^[7] The infection can rarely ascend to the upper urinary tract, resulting in pyelonephritis characterized by flank pain, high fever, nausea, and vomiting.^[1]^[43] This progression is more common in individuals with predisposing factors but remains relatively infrequent given the pathogen's tropism for the lower tract.^[43] Recurrence occurs in up to 60% of cases within one year, potentially due to biofilm formation, which enhances bacterial persistence, particularly in the presence of urinary catheters.^[1] Potential zoonotic reservoirs in animals like pigs and cows may contribute to human colonization.^[7] Clinically, S. saprophyticus UTIs mimic those caused by Escherichia coli, the most common etiologic agent, but can be differentiated by the bacterium's characteristic resistance to novobiocin.^[1]

Other Manifestations

Staphylococcus saprophyticus primarily causes urinary tract infections, but rare cases of extraurogenital infections have been documented, including bacteremia, endocarditis, prostatitis, osteomyelitis, and pneumonia. These manifestations typically occur in vulnerable populations such as immunocompromised individuals or those with indwelling devices, and they represent a small fraction of infections attributed to coagulase-negative staphylococci (CoNS).^[1] Bacteremia due to S. saprophyticus is uncommon and often originates from urinary tract sources, though isolated cases have been reported in patients without evident urogenital involvement, particularly among the immunocompromised or those with urinary catheters. It represents a small fraction of CoNS-associated bloodstream infections. For instance, a retrospective analysis identified S. saprophyticus among CoNS isolates in bacteremia cases, with higher proportions in specific cohorts like diabetic patients with neurogenic bladders. These infections can lead to complications such as native valve endocarditis, as seen in case reports of elderly patients with comorbidities like diabetes and mitral valve prolapse.^[1]^[44]^[45] Skin and wound infections by S. saprophyticus are exceedingly rare, given its occasional presence as part of the normal skin flora, but have been linked to post-surgical sites or chronic wounds in patients with diabetes, where skin carriage facilitates opportunistic invasion. These cases are often polymicrobial and occur in the context of disrupted skin barriers.^[1] Respiratory tract involvement is exceptional, with pneumonia reported primarily in nosocomial settings among elderly or ventilated patients. A documented case involved a postoperative patient developing ventilator-associated pneumonia confirmed by bronchoalveolar lavage culture positive for S. saprophyticus. Such presentations remain anecdotal, with no large-scale series available as of 2023.^[46] Emerging reports highlight S. saprophyticus in prostatitis among men, an unusual site given its typical association with female uropathology. Acute bacterial prostatitis cases have been described in otherwise healthy middle-aged men, presenting with fever, pelvic pain, and urinary symptoms, often requiring prolonged antibiotic therapy. Additionally, osteomyelitis has been noted rarely, potentially linked to bacteremic spread, though specific risk factors like animal exposure remain understudied; recent genomic analyses suggest environmental reservoirs, including animal sources, may contribute to such zoonotic-like transmissions in handlers. These non-urinary infections collectively comprise less than 5% of S. saprophyticus cases and frequently involve polymicrobial co-infections.^[47]^[48]^[1]^[28]

Diagnosis

Clinical Assessment

The clinical assessment of suspected Staphylococcus saprophyticus infection begins with a detailed history, emphasizing symptoms such as dysuria, urinary frequency, and urgency, which are hallmark features of lower urinary tract involvement.^[1] Clinicians should inquire about recent sexual activity, as it is a primary risk factor for acquisition in young women, and use of contraception, particularly spermicide-containing methods, which can disrupt vaginal flora and increase susceptibility.^[49] Additionally, the history must screen for factors suggesting sexually transmitted infections (e.g., vaginal discharge or partner symptoms) or complicating conditions such as pregnancy, diabetes mellitus, or immunosuppression to differentiate uncomplicated cases.^[50] Physical examination in uncomplicated S. saprophyticus infections typically reveals suprapubic tenderness upon palpation in 10% to 20% of cases, with possible mild pelvic discomfort, but lacks systemic signs like fever or chills.^[1] Costovertebral angle tenderness may indicate upper tract extension, though it is uncommon in initial presentations of cystitis caused by this pathogen.^[51] The exam should also assess for abdominal or flank pain to rule out pyelonephritis, while noting the absence of significant findings in most community-acquired cases among healthy individuals.^[52] Initial urinalysis plays a key role in supporting the clinical suspicion, demonstrating pyuria (defined as >10 white blood cells per high-power field) and bacteriuria, often with hematuria, but typically negative for nitrites due to S. saprophyticus being a non-Enterobacteriaceae organism incapable of reducing nitrates.^[53] These findings, combined with symptoms, guide empirical evaluation without immediate culture in low-risk settings.^[54] Risk stratification is essential to classify the infection as uncomplicated or complicated. Uncomplicated cases predominate in healthy, premenopausal women aged 18-35 years without structural abnormalities, while complicated infections occur in males, pregnant individuals, those with diabetes, recurrent episodes, or urologic anomalies, necessitating further investigation.^[1] The Infectious Diseases Society of America (IDSA) 2011 guidelines for acute uncomplicated cystitis recommend this empirical clinical assessment for community-onset urinary tract infections in otherwise healthy women, prioritizing symptom-based evaluation to facilitate prompt management.^[55]

Laboratory Identification

Laboratory identification of Staphylococcus saprophyticus primarily involves isolation from clinical specimens, particularly urine, followed by morphological, biochemical, and molecular confirmation to distinguish it from other coagulase-negative staphylococci. The process begins with culturing the sample on non-selective media such as 5% sheep blood agar, where S. saprophyticus typically produces round, raised, opaque colonies measuring 1-2 mm in diameter after 24-48 hours of incubation at 35-37°C. For urinary tract infection (UTI) diagnostics, selective media like cystine-lactose-electrolyte-deficient (CLED) agar is preferred, as S. saprophyticus forms distinct, smooth, opaque yellow colonies larger than 1 mm, aiding differentiation from lactose-fermenting Enterobacteriaceae that produce blue-green colonies.^[10] A significant bacteriuria threshold of greater than 10^5 colony-forming units per milliliter (CFU/mL) in a midstream clean-catch urine sample supports the diagnosis of UTI caused by S. saprophyticus.^[1] Microscopic examination of unspun urine via Gram staining reveals Gram-positive cocci arranged in clusters, often appearing as intracellular bacteria within epithelial cells, providing a preliminary indication of staphylococcal involvement.^[1] Further confirmation relies on biochemical tests: the organism is catalase-positive, producing bubbles upon addition of hydrogen peroxide, and coagulase-negative, failing to clot rabbit plasma.^[9] It is also urease-positive, hydrolyzing urea to produce ammonia and causing a color change in urea broth within 4-24 hours.^[11] The hallmark test is novobiocin susceptibility using a 5 μg disk on Mueller-Hinton agar; S. saprophyticus exhibits resistance with a zone of inhibition less than or equal to 16 mm after 24 hours of incubation.^[56] Molecular methods offer rapid and specific identification, particularly in complex samples. Polymerase chain reaction (PCR) targeting the 16S rRNA gene or the elongation factor Tu-encoding tuf gene enables genus- and species-level detection, with the tuf gene providing higher discriminatory power for coagulase-negative staphylococci.^[57] Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) is widely used for routine laboratory identification, achieving over 99% accuracy in distinguishing S. saprophyticus from closely related species like Staphylococcus epidermidis based on protein spectral profiles.^[58] Recent advances include whole-genome sequencing (WGS) for epidemiological tracing, as demonstrated in 2024 studies analyzing S. saprophyticus genomes from clinical isolates to identify outbreak clusters and virulence determinants.^[59] Antimicrobial susceptibility testing, when performed, follows Clinical and Laboratory Standards Institute (CLSI) guidelines using broth microdilution or disk diffusion methods to assess resistance to agents like trimethoprim-sulfamethoxazole, though routine testing is not always recommended due to predictable susceptibility patterns.^[60]

Treatment and Prevention

Antimicrobial Therapy

Staphylococcus saprophyticus infections, primarily manifesting as uncomplicated urinary tract infections (UTIs), are typically treated with empiric antibiotics targeting common uropathogens, with adjustments based on local susceptibility patterns and patient factors. First-line therapies for uncomplicated cystitis include trimethoprim-sulfamethoxazole (TMP-SMX) at a dose of 160/800 mg orally twice daily for 3 days or nitrofurantoin 100 mg orally twice daily for 5 days, as these agents demonstrate high efficacy against S. saprophyticus and promote short treatment durations to minimize resistance development.^[55] Alternative options are considered when first-line agents are contraindicated or local resistance exceeds 20%, including fluoroquinolones such as ciprofloxacin 250 mg orally twice daily for 3 days (used as second-line per guidelines to avoid due to resistance risks), or beta-lactam antibiotics like amoxicillin-clavulanate 500/125 mg orally twice daily for 3-7 days if susceptibility is confirmed.^[55]^[61] S. saprophyticus often shows resistance to penicillins due to beta-lactamase production; antimicrobial susceptibility testing is essential prior to beta-lactam use. Recent guidelines, including the 2025 IDSA guidance on complicated UTIs, continue to emphasize these short-course regimens and suggest avoiding fluoroquinolones empirically if prior exposure to reduce the selective pressure for antimicrobial resistance in community-acquired UTIs.^[62] For complicated infections or pyelonephritis caused by S. saprophyticus, initial intravenous therapy with ceftriaxone 1-2 g daily is often employed, followed by oral step-down therapy to complete a total duration of 7-14 days (5-7 days for fluoroquinolones or 7 days for non-fluoroquinolones per 2025 IDSA), depending on clinical response and severity.^[55]^[62] Supportive non-antibiotic measures, such as increased fluid intake for hydration and analgesics like phenazopyridine for symptom relief, are recommended adjunctively to alleviate dysuria and urgency without promoting resistance. In pregnant individuals, TMP-SMX should be avoided, particularly in the first and third trimesters, with alternatives like nitrofurantoin (after the first trimester) or beta-lactams preferred for a 5-7 day course to ensure maternal and fetal safety.^[63]^[64]

Resistance Patterns and Prevention

Staphylococcus saprophyticus exhibits emerging patterns of antibiotic resistance, particularly among isolates causing urinary tract infections (UTIs). Resistance to tetracyclines has been reported in 9-18% of isolates in recent studies from Brazil and Iran.^[36] Resistance to methicillin, often mediated by mecA genes resembling MRSA phenotypes, occurs in approximately 9% of strains globally.^[65] Multidrug resistance (MDR), defined as resistance to at least three antibiotic classes, affects approximately 15-20% of strains, including those from animal sources, highlighting a zoonotic reservoir.^[36]^[28] Key resistance mechanisms in S. saprophyticus include efflux pumps, which actively export antibiotics such as tetracyclines and quinolones, and production of beta-lactamases that hydrolyze penicillins and cephalosporins.^[66] Recent research has further linked biofilm formation to enhanced antibiotic tolerance, where embedded cells exhibit reduced susceptibility through limited drug penetration and metabolic dormancy, exacerbating persistence in UTIs.^[39] Surveillance of resistance relies on standardized breakpoints from CLSI and EUCAST guidelines, which categorize isolates as susceptible, intermediate, or resistant based on minimum inhibitory concentrations (MICs); however, routine susceptibility testing is not always recommended for S. saprophyticus due to its general susceptibility profile.^[67] Regional variations show higher resistance in Asia, with quinolone resistance exceeding 30% in some Iranian and Pakistani studies, compared to lower rates in North American isolates.^[68] ^[69] Prevention strategies emphasize behavioral and hygienic interventions to reduce UTI risk. Post-coital voiding and condom use during sexual activity are effective in limiting bacterial ascension in sexually active individuals, while general hygiene practices, such as proper genital cleaning, minimize introduction from skin flora.^[1] For those with animal contact, enhanced hygiene during handling of livestock like pigs and cows—potential reservoirs—helps curb zoonotic transmission.^[1] From a public health perspective, the One Health approach integrates human, animal, and environmental surveillance to address zoonotic spread of resistant S. saprophyticus, promoting antibiotic stewardship to avoid unnecessary use and mitigate MDR emergence.^[24]

Genetic Variants

Subspecies

Staphylococcus saprophyticus is classified into two subspecies: S. saprophyticus subsp. saprophyticus and S. saprophyticus subsp. bovis. The nominal subspecies, S. saprophyticus subsp. saprophyticus, serves as the type strain and is characterized by large colonies exceeding 5 mm in diameter on agar media, resistance to novobiocin, and negativity for nitrate reduction. This subspecies is the predominant cause of urinary tract infections in humans.^[70]^[1] In contrast, S. saprophyticus subsp. bovis produces smaller colonies under 5 mm in diameter (≤4 mm after 3 days), exhibits novobiocin resistance, tests positive for nitrate reductase activity, and is positive for urease and pyrrolidonyl arylamidase (PYR) activity. It is primarily isolated from bovine sources, such as milk associated with mastitis and bovine nostrils.^[70] Differentiation between the subspecies relies on the criteria established in 1996, incorporating biochemical tests such as colony morphology, nitrate reduction, and pyrrolidonyl arylamidase activity, alongside molecular methods like 16S rRNA gene sequencing for confirmation.^[70] Clinically, S. saprophyticus subsp. saprophyticus accounts for nearly all human infections, while subsp. bovis remains rare in human clinical isolates and is mainly associated with veterinary contexts.^[70] Recent studies suggest a potential zoonotic role for S. saprophyticus strains from animal reservoirs, though subsp. bovis involvement in human disease is exceptional.^[7] As of 2025, no additional subspecies have been recognized for S. saprophyticus.

Genomic Diversity

The genome of Staphylococcus saprophyticus typically ranges from 2.5 to 2.8 Mb in size, with a G+C content of approximately 33%, and consists of a single circular chromosome along with a limited number of plasmids.^[71]^[72] For instance, the type strain ATCC 15305 has a chromosome of 2,516,575 bp and harbors two small plasmids. The core genome of S. saprophyticus comprises approximately 1,646 to 2,000 genes shared across strains, while the pan-genome encompasses over 9,500 genes, reflecting significant accessory diversity that includes adhesin islands associated with host interaction.^[36]^[71] This open pan-genome structure indicates ongoing gene acquisition, with adhesin-related elements contributing to strain-specific adaptations. Genetic variations among S. saprophyticus strains include single nucleotide polymorphisms (SNPs) in virulence loci, such as polymorphisms in the aas gene encoding a bifunctional adhesin-autolysin, which show non-synonymous changes linked to host specificity.^[73] Comparative genomics analyses from 2023 have identified distinct clades, with core genome phylogenies separating strains associated with human clinical infections from those in animal or environmental sources, highlighting evolutionary divergence.^[74] Mobile genetic elements in S. saprophyticus genomes include prophages, insertion sequences like IS431, and transposases, with antimicrobial resistance genes predominantly integrated into the chromosome rather than plasmids.^[71]^[36] Approximately 30% of strains carry staphylococcal cassette chromosomes, some bearing resistance determinants such as mecA for methicillin resistance (prevalence ~8%), while prophages are present in over 90% of strains.^[36] Recent research employs multi-locus sequence typing (MLST) based on seven housekeeping genes (aroE, dnaJ, glpF, gmk, hsp60, mutS, pta) to identify sequence types (STs), revealing over 25 STs with predominant types like ST11 and ST7 clustered into clonal groups that partially correlate with isolation sources.^[75] Phylogenomic studies further link environmental and clinical isolates through core genome SNPs, demonstrating shared ancestry and adaptation across niches.^[2]

References

[1]
Staphylococcus saprophyticus Infection - StatPearls - NCBI Bookshelf
Staphylococcus saprophyticus is a Gram-positive bacterium that is a common cause of uncomplicated urinary tract infections, especially in young sexually active ...
[2]
Foodborne Origin and Local and Global Spread of Staphylococcus ...
Feb 9, 2021 · Staphylococcus saprophyticus is a primary cause of community-acquired urinary tract infections (UTIs) in young women. S. saprophyticus colonizes ...Methods · Bacterial Isolates · Results
[3]
Staphylococcus saprophyticus Proteomic Analyses Elucidate ...
Jan 19, 2020 · The Gram-positive and coagulase negative cocci Staphylococcus saprophyticus is the causative agent of urinary tract infections (UTI), being the ...
[4]
https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?id=29385
[5]
Species: Staphylococcus saprophyticus - LPSN
Proposed as: comb. nov. Basonym: "Staphylococcus saprophyticus" Fairbrother 1940. Etymology: sa.pro.phy'ti.cus. Gr. masc. adj.
[6]
Etymologia: Staphylococcus - PMC - NIH
From the Greek staphyle (bunch of grapes) and kokkos (berry), Staphylococcus is a genus of gram-positive spherical bacteria that commonly cause surgical and ...Missing: saprophyticus | Show results with:saprophyticus
[7]
Staphylococcus saprophyticus: Infectious substances pathogen ...
Oct 3, 2024 · Formerly classified as Micrococcus subgroup 3. S. saprophyticus is a member of the coagulase-negative Staphylococcus (CoNS) group.
[8]
Staphylococcus saprophyticus subsp. saprophyticus S-41 - BacDive
Staphylococcus saprophyticus subsp. saprophyticus S-41 is a facultative anaerobe, mesophilic, Gram-positive bacterium that was isolated from urine.Missing: hemolysins | Show results with:hemolysins
[9]
[PDF] ID 7 - Identification of Staphylococcus species, Micrococcus species ...
May 26, 2023 · Staphylococcus saprophyticus They are positive for catalase and urease tests while they are negative for motility, coagulase, nitrate reduction ...
[10]
Staphylococcus saprophyticus- An Overview - Microbe Notes
Jun 30, 2022 · Classification of different species of the genus Staphylococci is based on various factors ranging from morphology, chemical properties, amino ...Missing: taxonomy | Show results with:taxonomy
[11]
Staphylococcus saprophyticus: Characteristics and Diagnosis
Jun 23, 2022 · Biochemical Tests for Staphylococcus saprophyticus ; Mannitol fermentation, Yes ; PYR broth hydrolysis test, Negative ; Urease test, Positive.Missing: physiology | Show results with:physiology
[12]
Biochemical characterization of the surface-associated lipase of ...
Staphylococcus saprophyticus, an important cause of urinary tract infections ... In contrast, Sal1 and SEL3 were active over a broad pH range with an optimum ...<|separator|>
[13]
The Surface-Associated Protein of Staphylococcus saprophyticus Is ...
It produces two major surface proteins, the S. saprophyticus surface-associated protein (Ssp) (6) and an autolysin adhesin (Aas) (7, 9, 21). Ssp was the ...
[14]
https://doi.org/10.1099/00221287-5-5-1010
[15]
Who Are You—Staphylococcus saprophyticus? - Oxford Academic
The organism was found to belong to micrococcus subgroup 3. It was later reclassified as S. saprophyticus. Urease production is another important ...
[16]
https://pubmed.ncbi.nlm.nih.gov/6377440
[17]
Isolation and Characterization of Staphylococci from Human Skin I ...
Jan 1, 1975 · Staphylococci were classified on the basis of cell wall composition, lactic acid configuration, and a variety of morphological and ...
[18]
Staphylococcus saprophyticus as a common cause of urinary tract ...
S. saprophyticus is, after Escherichia coli, the second-most-frequent causative agent of acute UTI. Patients with UTI caused by S. saprophyticus usually ...Missing: 1974 | Show results with:1974
[19]
Whole genome sequence of Staphylococcus saprophyticus reveals ...
Comparative genomic analysis revealed that S. saprophyticus has abundant transporter systems to facilitate adaptation to human urine by paralog expansion, in ...<|control11|><|separator|>
[20]
Staphylococcus saprophyticus From Clinical and Environmental ...
Whole genome sequence of Staphylococcus saprophyticus reveals the pathogenesis of uncomplicated urinary tract infection. PNAS 102 13272–13277. 10.1073/pnas ...
[21]
Characteristics of Staphylococcus saprophyticus Isolated from ... - NIH
Staphylococcus saprophyticus (S. saprophyticus) is an opportunistic coagulase-negative staphylococcus (CoNS) known to cause urinary tract infections in humans ...
[22]
Isolation and Characterization of Staphylococcus saprophyticus from ...
Jul 16, 2024 · Staphylococcus saprophyticus was isolated from soil of a textile plant and selected as the most active dye degrader of 11 isolates.Missing: sewage | Show results with:sewage
[23]
Isolation of lytic bacteriophages and their relationships with the ...
Jul 22, 2024 · In 1961, Torres Pereira isolated a coagulase-negative Staphylococcus carrying 51 antigens from the urine of women with acute UTI. The organism ...<|control11|><|separator|>
[24]
Staphylococcus saprophyticus found to be a common contaminant ...
Staphylococcus saprophyticus was found to contaminate 16.4% of the various food samples with a high prevalence of 34% in raw beef and pork.Missing: soil sewage 2023-2025
[25]
Characteristics of Staphylococcus saprophyticus Isolated from ...
These findings indicate that S. saprophyticus strains from both humans and companion animals possess notable virulence and multidrug resistance.
[26]
Ecological distribution of Staphylococcus in integrated farms within ...
Apr 23, 2024 · Farm animals serve as major reservoirs of many zoonotic pathogens ... Staphylococcus saprophyticus causing human urinary tract infections.
[27]
Staphylococcus Saprophyticus - an overview | ScienceDirect Topics
The Staphylococcus genus is included in the Bacilli class and Bacillales order and contains 45 species. Its cells are spherical and occur in microscopic ...Missing: classification | Show results with:classification
[28]
[PDF] Ukrainian Journal of Nephrology and Dialysis
Jun 25, 2025 · Staphylococcus saprophyticus is detected in up to 40% of sexually active young women as part of the normal genitourinary flora. Maternal ...
[29]
Use of spermicide-coated condoms and other risk factors for urinary ...
Spermicide-coated condoms were associated with an increase risk of UTI caused by S saprophyticus. Because sexual activity and spermicide exposure are important ...
[30]
Spermicide-Coated Condoms and Urinary Tract Infections - AAFP
Aug 1, 1998 · Staphylococcus saprophyticus is responsible for up to 26 percent of urinary tract infections reported in young sexually active women.
[31]
Molecular Epidemiology of Staphylococcus saprophyticus Isolated ...
Compared with other uropathogens, S. saprophyticus differs in seasonal variation and geographic distribution. UTI has been documented mostly in women in the ...Missing: Asia | Show results with:Asia
[32]
Gram-Positive Uropathogens, Polymicrobial Urinary Tract Infection ...
In addition to cell-wall associated proteins, S. saprophyticus encodes urease that is important for efficient colonization of the bladder and kidneys, for ...S. Saprophyticus Uti... · E. Faecalis Uti Virulence... · Vaginal Microbiota...<|separator|>
[33]
Staphylococcus saprophyticus urease - NIH
Our data indicate that urease is a major factor for invasiveness of S. saprophyticus, especially in the tissue of the bladder.Missing: lipase | Show results with:lipase
[34]
Study of biofilm formation, structure and antibiotic resistance in ... - NIH
Some strains of S. saprophyticus can create biofilms, increasing their virulence. Once biofilms have been produced, antibiotic resistance is exacerbated. Hence, ...
[35]
Characterization of a Novel Murine Model of Staphylococcus ... - NIH
saprophyticus induced epithelial cell shedding in the bladder and an inflammatory response characterized by macrophage and neutrophil infiltration in the ...<|control11|><|separator|>
[36]
Baicalin Inhibits Biofilm Formation and the Quorum-Sensing System ...
Dec 9, 2019 · We demonstrate for the first time that baicalin inhibits biofilm formation and the agr quorum-sensing system by inhibiting the efflux pump in S. saprophyticus.Missing: maturation | Show results with:maturation
[37]
Recurrent Urinary Tract Infections - StatPearls - NCBI Bookshelf - NIH
Spermicides and lack of estrogen effect will disrupt the normal vaginal flora, while sexual intercourse tends to introduce vaginal bacteria into the urethra and ...
[38]
UTI Caused by Staphylococcus saprophyticus - IntechOpen
Staphylococcus saprophyticus is a Gram-positive bacterium well known for causing uncomplicated urinary tract infections in young sexually active females.2. Definition Of Uti · Figure 1 · 3. Pathogenicity And...Missing: 1884 | Show results with:1884
[39]
Clinical Impact of Bacteremia Due to Staphylococcus saprophyticus
Here, we report accumulated cases of bacteremia related to S. saprophyticus and retrospectively evaluate the patient's background and the clinical virulence ...
[40]
Staphylococcus saprophyticus native valve endocarditis possibly ...
Feb 11, 2020 · Herein, we report the case of a 77-year-old woman diagnosed with S. saprophyticus native bivalve endocarditis. Interestingly, blood and ...
[41]
Staphylococcus saprophyticus as an Unusual Agent of Nosocomial ...
Staphylococcus saprophyticus as an Unusual Agent of Nosocomial Pneumonia ; Wolfgang Hell · Wolfgang Hell ; Thomas Kern · Thomas Kern ; Mariam Klouche. Mariam Klouche.
[42]
Acute Bacterial Prostatitis Caused by Staphylococcus saprophyticus
Jul 9, 2024 · This case involves a patient who acquired ABP from Staphylococcus saprophyticus. This etiology is quite unusual, as S. saprophyticus is usually ...
[43]
Acute Bacterial Prostatitis Caused by Staphylococcus saprophyticus
Jul 9, 2024 · This case involves a 46-year-old Caucasian male with no previous history of prostate diseases who presented to the clinic with fevers, chills, diarrhea, and ...
[44]
URINARY TRACT INFECTIONS (Urethritis, Cystitis, Pyelonephritis)
Women; recent use of a diaphragm with spermicide, frequent sexual intercourse, and a history of UTI are each risk factors for acute cystitis. Pregnant women ...
[45]
Uncomplicated Urinary Tract Infections - StatPearls - NCBI Bookshelf
Feb 21, 2025 · UTIs occur at least 4 times more frequently in females than males. The following are key statistics regarding UTIs: Approximately 40% of women ...<|separator|>
[46]
Urinary Tract Infection (UTI) and Cystitis (Bladder Infection) in ...
Sep 15, 2025 · Patients may demonstrate some suprapubic tenderness to palpation. Abnormal physical examination findings generally are lacking in women with ...
[47]
Diagnosing Uncomplicated Cystitis in Women - AAFP
Nov 15, 2002 · Other findings that may be helpful include presence of fever, costovertebral angle tenderness, and evaluation of vaginal discharge. The ...<|separator|>
[48]
Interpretation of Urinalysis and Urine Culture for UTI Treatment
Nov 15, 2013 · Pyuria, which is defined as urine WBC >10 or positive leukocyte esterase, indicates the presence of inflammation. However, pyuria does not ...
[49]
High Frequency of Staphylococcus Saprophyticus Urinary Tract ...
Second, due to its retrospective nature, we had little information about the history ... Guidelines for Complicated Urinary Tract Infections in Children: A Review ...Methods · Results · Discussion
[50]
International Clinical Practice Guidelines for the Treatment of Acute ...
The focus of this work is treatment of women with acute uncomplicated cystitis and pyelonephritis, diagnoses limited in these guidelines to premenopausal, non- ...
[51]
Novobiocin Susceptibility Test- Principle, Procedure, Results
Feb 11, 2023 · Zone size of >16 mm = Sensitive to novobiocin; Zone size of ≤16 mm = Resistant to novobiocin. If the test Staphylococcus spp. is isolated ...Requirements · Procedure of Novobiocin... · Result and Interpretation of...
[52]
tuf Gene Sequence Analysis Has Greater Discriminatory Power than ...
We compared and analyzed 16S rRNA and tuf gene sequences for 97 clinical isolates of coagulase-negative staphylococci (CNS) by use of the GenBank, MicroSeq, ...
[53]
Evaluation of matrix-assisted laser desorption ionization-time-of ...
A correct species identification by MALDI-TOF was obtained in 99.3% (447/450), with only three isolates being misidentified. In addition, MALDI-TOF correctly ...
[54]
https://journals.lww.com/pidj/fulltext/2015/09000/high_frequency_of_staphylococcus_saprophyticus.26.aspx
[55]
Antimicrobial resistance and its detection in Staphylococcus ...
The Clinical and Laboratory Standards Institute (CLSI) state that 'Routine testing of urine isolates of Staphylococcus saprophyticus is not advised, because ...
[56]
Urinary Tract Infection (UTI) and Cystitis (Bladder Infection) in ...
Sep 15, 2025 · According to the IDSA guidelines, beta-lactam agents (eg, amoxicillin-clavulanate, cefdinir, cefaclor, cefpodoxime-proxetil) in 3–7-day regimens ...
[57]
Antimicrobial Resistance Patterns of Staphylococcus saprophyticus ...
Mar 12, 2023 · S. saprophyticus isolates showed the highest level of resistance to penicillin (85.7%) and erythromycin (51.4%). A variation was detected among ...
[58]
Recurrent Uncomplicated Urinary Tract Infections in Women: AUA ...
This document seeks to establish guidance for the evaluation and management of patients with rUTIs to prevent inappropriate use of antibiotics.<|separator|>
[59]
Complicated Urinary Tract Infections (cUTI): Clinical Guidelines for ...
Jul 17, 2025 · IDSA has released the first IDSA guidelines on management and treatment of complicated urinary tract infections (cUTIs). These guidelines ...Missing: saprophyticus | Show results with:saprophyticus
[60]
Urinary Tract Infections in Pregnant Individuals
Jul 20, 2023 · Once a diagnosis of acute cystitis is made, treatment of pregnant individuals should be initiated with a 5–7-day course of antibiotics.
[61]
Treatment of Urinary Tract Infections in Pregnancy - The ObG Project
Sep 5, 2023 · Recommendations · Cephalexin: 250 to 500 mgs q6hr po 5 to 7 days · Fosfomycin: 3 g po once · Amoxicillin: 500 mg po q8hr for 5 to 7 days | 875 mg ...
[62]
Trend of distribution and antimicrobial resistance in uropathogens in ...
May 22, 2024 · This study analyzed antimicrobial resistance and distribution trends of uropathogens from 2015 to 2021 using the CHINET system.
[63]
Detection of mecA-mediated methicillin resistance and evaluation of ...
Our study evaluated the antimicrobial resistance profiles of 277 S. saprophyticus isolates from North America and a globally diverse cohort.
[64]
Bacterial profiling and antibiotic resistance patterns in urinary tract ...
Sep 26, 2025 · Imipenem with linezolid could be effective against methicillin-resistant Staphylococcus Aureus (MRSA) and MDR-Staphylococcus saprophyticus. For ...
[65]
Efflux Pump Mediated Antimicrobial Resistance by Staphylococci in ...
One of these resistance mechanisms is the export of antimicrobial agents through the activity of membrane-embedded multidrug efflux pump proteins. The use of ...
[66]
Staphylococcus saprophyticus antibiotic susceptibility testing
Staphylococcus saprophyticus, a common uropathogen, is usually susceptible to urine-concentrating antimicrobials, so routine AST is not recommended by CLSI.
[67]
Antimicrobial Resistance Patterns of Staphylococcus saprophyticus ...
Aug 4, 2025 · The present study aimed to study the drug resistance pattern and phenotypic and genotypic variation of S. saprophyticus isolates from women with UTI in Gorgan, ...
[68]
Genetic Classification and Distinguishing of Staphylococcus ... - NIH
16S rRNA gene sequencing and PCR-restriction fragment length polymorphism (PCR-RFLP) analysis have been described for Staphylococcus species identification ...
[69]
Antimicrobial Resistance Patterns of Staphylococcus saprophyticus ...
The saprophyticus subspecies is the major cause of uncomplicated UTIs, following uropathogenic E.coli (UPEC) (2). Novobiocin resistance is a laboratory trait ...
[70]
Whole genome sequence of Staphylococcus saprophyticus reveals ...
We sequenced the whole genome of S. saprophyticus type strain ATCC 15305, which harbors a circular chromosome of 2,516,575 bp with 2,446 ORFs and two plasmids.
[71]
Genome Sequence of Staphylococcus saprophyticus DPC5671, a ...
The draft genome of S. saprophyticus DPC5671 includes 2,676,318 bp, with an average G+C content of 33.1%. It consists of a single circular chromosome and does ...
[72]
Comparative genomics reveals the correlations of stress response ...
Dec 5, 2023 · Staphylococcus saprophyticus is the leading Gram-positive cause of uncomplicated urinary tract infections. Recent reports of increasing ...<|control11|><|separator|>
[73]
Adaptation in a Fibronectin Binding Autolysin of Staphylococcus ...
Adhesins such as Aas are important in the pathogenesis of S. saprophyticus urinary tract infections, and the gene encoding Aas has been previously implicated as ...
[74]
[PDF] environments shape diversity of Staphylococcus saprophyticus
Aug 18, 2023 · Inner ring around the core genome phylogeny indicates isolates from cases of bovine mastitis as well as isolates from other animal sources.
[75]
Genetic diversity and antibiotic resistance of Staphylococcus ...
Jun 17, 2015 · A multilocus sequence typing (MLST) scheme was developed to evaluate the genetic diversity and background of Staphylococcus saprophyticus ...