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Prevalence of resistance and toxin genes in community-acquired and hospital-acquired methicillin-resistant Staphylococcus aureus clinical isolates

Methicillin-resistant (MRSA) is one of the major health hazards and became of greater public health concern since the emergence of community-acquired MRSA. This work aimed to study the prevalence of , , , -PV, -PV (PVL), I, and II genes among community-acquired (CA) hospital-acquired (HA) MRSA to in...

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Published in:Iranian journal of basic medical sciences 2020-10, Vol.23 (10), p.1251-1260
Main Authors: El-Baghdady, Khaled Z, El-Borhamy, Mervat I, Abd El-Ghafar, Hisham A
Format: Article
Language:English
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Summary:Methicillin-resistant (MRSA) is one of the major health hazards and became of greater public health concern since the emergence of community-acquired MRSA. This work aimed to study the prevalence of , , , -PV, -PV (PVL), I, and II genes among community-acquired (CA) hospital-acquired (HA) MRSA to increase vigilance in the diagnosis and management of suspected infections. isolates recovered from clinical samples were classified into community or hospital-acquired and tested for their antibiotic susceptibility against 19 antibiotics. All isolates were screened for , , -PV, -PV, I, and II genes. Statistical correlations were carried out. Out of 338 isolates, only 105 were MRSA and classified as 77 CA-MRSA and 28 HA-MRSA. and genes were present in all HA-MRSA and CA-MRSA isolates. was found in all HA-MRSA and 93.5% of CA-MRSA isolates. PVL genes were detected in 28.6% HA-MRSA isolates and 92.2% CA-MRSA. I gene was recovered from 60.7% HA-MRSA isolates and 37.7% CA-MRSA isolates while the II gene recovered from only 10.7% HA-MRSA isolates and 6.5% CA-MRSA. The high prevalence of MRSA colonizing the groin, axilla, and nose may play a significant role in endogenous infection, re-infection, and also acts as a route for MRSA transmission. and genes could be used as a sole and fast step for identification of MRSA, while PVL genes cannot be used as a sole stable marker for CA-MRSA identification.
ISSN:2008-3866
2008-3874
DOI:10.22038/ijbms.2020.40260.9534