Molecular characterization of methicillin-resistant Staphylococcus aureus (MRSA)isolated from bovine wounds
Author:
Khan Muhammad1, Nadeem Asif2, Javed Maryam1, Shehzad Wasim1, Ali Asad1
Affiliation:
1. University of Veterinary and Animal Sciences, Lahore, Pakistan 2. University of Veterinary and Animal Sciences, Lahore, Pakistan + Department of Biotechnology, Virtual University of Pakistan, Lahore, Pakistan
Abstract
Staphylococcus aureus (S. aureus) is a Gram-positive coccus with
golden-colored colonies 0.5-1.5 ?m in diameter. It is an opportunistic
pathogen and colonizes as healthy flora. When the host defense system is
breached it provides a source for the introduction of (Methicillin-resistant
S. aureus) MRSA. The incorporation of the mecA gene shift S. aureus into
MRSA, mecA is a primary gene for the confirmation of MRSA, so, it is used as
a useful marker to determine Methicillin resistance in S. aureus. In this
study, we investigated the molecular characterization of mecA,
Panton-Valentine Leukocidin (PVL), and 16S rRNA genes in MRSA to determine
diversity, phylogenetic analysis, and multidrug resistance (MDR) of MRSA
isolated from chronic bovine wounds. A total of 8 antibiotics were used for
MDR profiling and the results obtained are as follows: 100% of MRSA isolates
were resistant to Augmentin and Cefipime, 81.8% to Vancomycin and
Tetracyclin, 36.4% to Streptomycin and Ciprofloxacin, Azithromycin 54.5 and
0% to Chloramphenicol which warrants that it?s the best antibiotic according
to this study. Multiplex PCRs were performed for the confirmation of
targeted genes and diversity analysis. The diversity of MRSA in the bovine
population was 22% (11/50) on the microbiological scale that considered high
as compared to reported data. When the PCR of MRSA isolates was performed,
there was a unique phenomenon observed i.e., no mecA gene was present in 2
isolates 18.18% (2/11) which connotes the importance of molecular
methods/PCR for the identification of microbes. The prevalence of the PVL
gene was 18.18%, comparatively high as compared to previous studies
conducted on bovine chronic wounds. When the Sanger sequencing of 16S rRNA
of MRSA isolates was performed there was a change of one nucleotide
identified (C>T) at position 1031. After performing phylogenetic analysis
with S. aureus of different countries distinct and separate dendrogram was
obtained which differentiates the Pakistani S. aureus isolates from other
countries.
Publisher
National Library of Serbia
Subject
Plant Science,Genetics
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