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Staphylococcus saprophyticus is a bacterium that is part of the normal flora, colonizing areas such as the genital tract, rectum, and gastrointestinal tract in both humans and animals.
S. saprophyticus is characterized by its ability to adhere to human urothelium, making it a frequent cause of urinary tract infections, especially in young sexually active women.
The urinary test strips may yield a falsely negative result in the case of S. saprophyticus infection (due to the absence of nitrite formation), and treatment with fosfomycin is often ineffective.
The treatment for Staphylococcus saprophyticus infection involves culturing a given sample, identifying the bacteria, and conducting an antibiogram to determine the most effective antibiotic.
Staphylococcus saprophyticus on culture media (1- chromogenic, 2- blood agar).
The name Staphylococcus saprophyticus was first proposed by Shaw et al. in 1951, based on the isolation of this bacterium from human urine samples.
The classification of different species within the genus Staphylococci is based on a variety of factors, including morphology, chemical properties, amino acid sequences, biochemical characteristics, and nucleotide sequences.
Staphylococcus saprophyticus is one of the main causes of uncomplicated urinary infections in sexually active young women and more rarely in young men or the elderly.
S. saprophyticus has been associated with cases of peritonitis during peritoneal dialysis, endocarditis on native valves, and nosocomial pneumonia.
S. saprophyticus can be identified by its cultural, biochemical, and molecular characteristics. The two main features aiding in its identification are, firstly, that it belongs to coagulase-negative Staphylococci, and secondly, it exhibits inherent resistance to novobiocin.
Some of the methods used for identification include:
Staphylococcus saprophyticus is a Gram-positive cocci, non-motile, non-sporulating, usually non-capsulated with an average diameter of 0.8 to 1.2 µm. It can appear as small, round, and isolated cells or in diplococci, or in irregular clusters.
Like all Staphylococci, the culture of Staphylococcus saprophyticus generally poses no problem, as it has no specific nutritional requirements. It can be cultivated in a facultative aerobic-anaerobic atmosphere, on simple, enriched, chromogenic media, or on selective agar for staphylococci.
The appearance of colonies can vary from one culture media to another; typically, colonies appear round, convex, opaque, white, and somewhat creamy after 18 hours at 37°C, with a diameter of 2 to 3 mm.
The genus Staphylococcus comprises Gram-positive cocci bacteria that are catalase-positive and oxidase-negative, and non-demanding. These characteristics allow differentiation from bacteria of the genera Streptococcus, Enterococcus, and Micrococcus.
Identifying the species Staphylococcus saprophyticus and differentiating it from other species is essential, especially in cases of urinary tract infections.
Staphylococcus saprophyticus belongs to the group of coagulase-negative Staphylococcus. That's why the initial test to perform is aimed at eliminating Staphylococcus aureus, such as the coagulase test, DNase test, or agglutination test.
For more complete biochemical identification, biochemical galleries such as Api 20 staph or bacteriological identification automates (MicroScan WalkAway plus System, ALFRED 60/AST.. ) can be used.
S. saprophyticus has intrinsic resistance to novobiocin and fosfomycin, which can help detect it from other species.
PCR (Polymerase Chain Reaction)
PCR can be used to identify S. saprophyticus by targeting its 16S rRNA gene. This gene has a unique sequence that can be distinguished from other staphylococci through the use of specific primers.
RFLP (Restriction Fragment Length Polymorphism)
RFLP can be employed to identify S. saprophyticus by utilizing a restriction enzyme that cuts the S. saprophyticus DNA into a distinctive pattern of fragments. These fragments can be separated through gel electrophoresis and compared to those of other staphylococci.
Staphylococcus saprophyticus is naturally resistant to nalidixic acid, fosfomycin, novobiocin due to a mutation in the GyrB subunit of DNA gyrase, and to fusidic acid due to the presence of the chromosomal gene fusD, encoding a protein that protects the elongation factor G.
In conclusion, Staphylococcus saprophyticus poses a significant health concern, especially for young women with urinary tract infections. By enhancing our understanding of this bacterium and implementing preventive measures, we can strive to reduce the burden of Staphylococcus saprophyticus infections and improve patient outcomes.