The gene expression of the most important structural genes ica A and D of biofilm, sarA, and sigB regulatory genes of some methicillin-resistant Staphylococcus aureus (MRSA) isolates were examined using the real-time polymerase chain reaction after 24 hours of growth. The results revealed that the isolates with strong biofilm production had the highest gene expression of the structural icaA and D genes. Whereas the isolates that showed moderate and weak biofilm production, recorded the lowest gene expression. The results of the regulatory genes sarA, and sigB fluctuated among all MRSA isolates. Isolate No. 64 recorded the highest gene expression, while isolate 50 recorded the lowest gene expression. The purpose of this study was to determine the gene expression of structural genes ica A and D, and regulator genes sigB and sarA in some MRSA isolates with different abilities of biofilm formation where the sarA and sigB play important role in positive regulation of biofilm formation.
This study investigates in vitro biofilm production. Presence of ica A and D genes in methicillin-resistant Staphylococcus aureus was evaluated for biofilm production by the microtiter plate method. Between December 2020 and October 2021, out of 215 clinical specimens were collected from patients with pulmonary fibrosis, pneumonia, bacteremia, chronic burns, deep wounds, urinary tract infection and catheterized patients. Out of which 45 MRSA isolates were identified by the susceptibility test utilizing cefoxitin and the occurrence of mecA gene for resistance for this antibiotic verified by polymerase chain reaction technique. A sensitivity test was conducted for five other antibiotics. All MRSA isolates were producers of biofilms but the formation of robust biofilms by 42% of MRSA isolates, 20% of isolates was intermediate and 38% of isolates weak. Formerly ica A and D genes, responsible for polysaccharide intracellular adhesin dependent biofilm formation were investigated in all MRSA isolates using the polymerase chain reaction technique. ica A were detect in 33 (73.3%) of the isolates and was lacking in 12 (26.6%) of the isolates. ica D gene was present in 38 (84.4%) isolates and was lacking in 7 (15.5%). However, the total number of isolates that contained icaA and D genes was 10 (22.2%). The most noteworthy finding was that the five weak isolates lacked any genes. Thus indicating that these isolates are capable of producing biofilm without the need for ica in order to make polysaccharide intracellular adhesin that means the isolates have an ability to form biofilm in ica independent biofilm mechanisms.
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