Prevalence of Adhesion and Regulation of Biofilm-Related Genes in Different Clones ofStaphylococcus aureus

Author:

Atshan Salman Sahab12,Nor Shamsudin Mariana13,Sekawi Zamberi1,Lung Leslie Than Thian1,Hamat Rukman Awang1,Karunanidhi Arunkumar1,Mateg Ali Alreshidi1,Ghaznavi-Rad Ehsanollah4,Ghasemzadeh-Moghaddam Hamed1,Chong Seng Johnson Shueh1,Nathan Jayakayatri Jeevajothi1,Pei Pei Chong5

Affiliation:

1. Laboratory of Medical Microbiology and Parasitology, Faculty of Medicine and Health Science, Universiti Putra Malaysia, Selangor 43400 Serdang, Malaysia

2. Department of Medical Microbiology, Basrah University, Basrah, Iraq

3. Laboratory of Marine Science and Aquaculture, Institute of Bioscience, Universiti Putra Malaysia, Selangor 43400 Serdang, Malaysia

4. Department of Microbiology and Immunology, Arak University of Medical Sciences, Arak, Iran

5. Department of Obstetrics and Gynaecology, Faculty of Medicine and Health Science, Universiti Putra Malaysia, Putra Malaysia, Selangor 43400 Serdang, Malaysia

Abstract

Clinical information about genotypically different clones of biofilm-producingStaphylococcus aureusis largely unknown. We examined whether different clones of methicillin-sensitive and methicillin-resistantS. aureus(MSSA and MRSA) differ with respect to staphylococcal microbial surface components recognizing adhesive matrix molecules (MSCRAMMs) in biofilm formation. The study used 60 different types ofspaand determined the phenotypes, the prevalence of the 13 MSCRAMM, and biofilm genes for each clone. The current investigation was carried out using a modified Congo red agar (MCRA), a microtiter plate assay (MPA), polymerase chain reaction (PCR), and reverse transcriptase polymerase chain reaction (RT-PCR). Clones belonging to the samespatype were found to have similar properties in adheringto thepolystyrene microtiter plate surface. However, their ability to produce slime on MCRA medium was different. PCR experiments showed that 60 clones of MSSA and MRSA were positive for 5 genes (out of 9 MSCRAMM genes).icaADBCgenes were found to be present in all the 60 clones tested indicating a high prevalence, and these genes were equally distributed among the clones associated with MSSA and those with MRSA. The prevalence of other MSCRAMM genes among MSSA and MRSA clones was found to be variable. MRSA and MSSA gene expression (MSCRAMM andicaADBC) was confirmed by RT-PCR.

Funder

Ministry of Science, Technology and Innovation Malaysia

Publisher

Hindawi Limited

Subject

Health, Toxicology and Mutagenesis,Genetics,Molecular Biology,Molecular Medicine,General Medicine,Biotechnology

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