Author/Authors :
Ghasemian, Abdolmajid Department of Bacteriology - Faculty of Medical Sciences - Tarbiat Modares University - Tehran, Iran , Najar Peerayeh, Shahin Department of Bacteriology - Faculty of Medical Sciences - Tarbiat Modares University - Tehran, Iran , Bakhshi, Bita Department of Bacteriology - Faculty of Medical Sciences - Tarbiat Modares University - Tehran, Iran , Mirzaee, Mohsen Department of Laboratory Sciences - Borujerd Branch - Islamic Azad University - Borujerd, Iran
Abstract :
The aim of this study was to compare the biofilm formation and the prevalence of biofilm-associated
genes between the isolates of methicillin-resistant (MRSA) and methicillin-susceptible (MSSA) Staphylococcus
aureus. Methods: In total, 209 S. aureus isolates were collected. The antibiotic susceptibility test was conducted
using nine antibiotics according to the guidelines of Clinical and Laboratory Standards Institute. Phenotypic
biofilm formation was performed with microtiter plate assay. The polymerase chain reaction was employed to
detect icaA, icaD, icaB, icaC, clfA, clfB, fnbA, fnbB, fib, cna, eno, ebps, bbp, mecA, and SCCmec types as well as agr
group genes with specific primers. Results: Sixty-four (30.62%) isolates were resistant to methicillin, and 54 (83%)
MRSA harbored SCCmec III. Furthermore, 122 (58.3%) isolates belonged to agr group I. Twenty-six (36.1%) MRSA
and 42 (28.9%) MSSA isolates were strong biofilm producers (no significant difference). The prevalence of icaA,
icaD, icaB, and icaC genes in MSSA isolates was 71, 41, 76, and 72%, respectively. The frequency of clfA, clfB, fnbA,
fnbB, fib, cna, eno, ebps, and bbp in MSSA was 100, 100, 56, 46, 74, 54, 78, 11, and 1%, respectively. However, in
MRSA isolates, the frequency was 97, 97, 64, 51, 76, 56, 79, and 12% with no track of bbp, respectively.
Conclusion: Statistical difference between MSSA and MRSA regarding biofilm formation and the frequency of all
biofilm-encoding genes was not significant. The majority of the S. aureus isolates harbored clfA, clfB, eno, fib,
icaA, and icaD genes.