4.6 Review

Clinical Infections, Antibiotic Resistance, and Pathogenesis of Staphylococcus haemolyticus

Journal

MICROORGANISMS
Volume 10, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/microorganisms10061130

Keywords

S; haemolyticus; pathogenesis; antibiotic resistance; biofilm; virulence factors; clinical infections

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Staphylococcus haemolyticus is a common microbe on human skin and an emerging microbe causing nosocomial infections. It is resistant to antibiotics and can transfer resistance genes to other Staphylococcus species. Severe infections, especially in immunocompromised patients, are associated with S. haemolyticus. It forms biofilms and secretes factors for bacterial invasion.
Staphylococcus haemolyticus (S. haemolyticus) constitutes the main part of the human skin microbiota. It is widespread in hospitals and among medical staff, resulting in being an emerging microbe causing nosocomial infections. S. haemolyticus, especially strains that cause nosocomial infections, are more resistant to antibiotics than other coagulase-negative Staphylococci. There is clear evidence that the resistance genes can be acquired by other Staphylococcus species through S. haemolyticus. Severe infections are recorded with S. haemolyticus such as meningitis, endocarditis, prosthetic joint infections, bacteremia, septicemia, peritonitis, and otitis, especially in immunocompromised patients. In addition, S. haemolyticus species were detected in dogs, breed kennels, and food animals. The main feature of pathogenic S. haemolyticus isolates is the formation of a biofilm which is involved in catheter-associated infections and other nosocomial infections. Besides the biofilm formation, S. haemolyticus secretes other factors for bacterial adherence and invasion such as enterotoxins, hemolysins, and fibronectin-binding proteins. In this review, we give updates on the clinical infections associated with S. haemolyticus, highlighting the antibiotic resistance patterns of these isolates, and the virulence factors associated with the disease development.

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