This in-vitro study aimed to assess in 120 [40 community-acquired (CA-MRSA) & 80 hospital-acquired (HA-MRSA)] isolates from cancer patients whether the transmissible staphylococcal cassette chromosome (SCC) typing, and the Panton-Valentine leukocidin (PVL) virulence genes detection could be employed as tools for molecular diagnostic purposes to distinguish both methicillin-resistant Staphylococcus aureus (MRSA) categories in radiotherapy treated cancer patients. SCC typing was determined by the combination of the type of the cassette chromosome recombinase genes () gene complex and the class of the methicillin resistance () gene complex. Besides, a rapid slide latex agglutination test (LAT) and antibiotic resistance spectrum determination before and after irradiation were performed. In the strict sense, with the effect of irradiation; the presence of SCC subtypes IVa (22.5% vs. 10.0%), b (47.5% vs. 25.0%), & d (7.5 vs. 2.5%) or type V (15.0% vs. 7.5%) genetic elements and PVL genes ( < .001) were not proved as a signature for CA-MRSA. While, the larger SCC types II, and III elements were not detected in 14, and 19 from the 38, and 36 typed HA-MRSA isolates ( < .001), respectively. Remarkable effects on class A & class B gene complex and type2, type 3 & type 5 gene complex and an increase in agglutination reaction strength in response to gamma irradiation external stimulus were observed. Different heterogeneous genetic composition with upregulation gene expression was detected after irradiation in the HA- MRSA studied population. CA-MRSA showed remarkable ability to acquire multi-antibiotic resistance after irradiation and propose a novel paradigm for future chemotherapy against the multi-resistant pathogens whose proliferation especially among immunocompromised cancer patients is on the increase.
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http://dx.doi.org/10.1080/09553002.2019.1664785 | DOI Listing |
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