Background: is a common cause of nosocomial infections. Epidemiological typing of enables control of its spread. The objective of this study was to investigate coagulase gene polymorphisms of isolated from patients at Kosti Hospital in Sudan.
Methods: In total, 110 isolates were recovered from 110 patients who were enrolled in the study. strains were isolated on blood agar and MacConkey agar and then identified by conventional tests. Resistance to methicillin was determined by detection of the gene. Polymorphism in the coagulase gene () was investigated using PCR followed by I RFLP analysis.
Results: Methicillin-resistant accounted for 62/110 (56 %) of the isolates. PCR of the gene showed two different amplicons, one of 680 bp detected in 83/110 (75.5 %) of the isolates and one of 790 bp detected in 27/110 (24.5 %). When digested with the I enzyme, the 790 bp amplicon resulted in three restriction fragments of 500, 210 and 80 bp (1). Restriction of the 680 bp amplicon gave two patterns; the first (2) was found in 22/110 (20 %) of the isolates and showed four fragments of 210, 210, 180 and 80 bp, and the second (3) was found in 61/110 (55.5 %) and revealed three fragments of 390, 210 and 80 bp. Most of the 3 isolates (75.4%) were methicillin-resistant.
Conclusion: Three polymorphic genotypes of were identified in patients at Kosti Hospital. The 3 genotype was the predominant one and was mostly detected in methicillin-resistant isolates.
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http://dx.doi.org/10.1099/acmi.0.000026 | DOI Listing |
J Infect Dev Ctries
December 2024
Department of Microbiology & Hygiene, Bangladesh Agricultural University, Mymensingh-2202, Bangladesh.
Introduction: The emergence of livestock-associated methicillin-resistant Staphylococcus aureus (LA-MRSA) is a growing public health concern. The objective of this study was to determine the prevalence and multi-drug resistant (MDR) profiles of MRSA in goats in Bangladesh.
Methodology: A total of 150 samples from goats comprised of rectal swab (n = 50), nasal swab (n = 50), and milk (n = 50) were collected.
Infect Prev Pract
March 2025
San Juan Bautista School of Medicine, Caguas, Puerto Rico.
Background: Mobile phones used by healthcare workers (HCWs) in hospitals are significant reservoirs of drug-resistant bacteria responsible for hospital-acquired infections (HAIs).
Aim: The objective of this study was to assess the level of contamination with such bacteria in outpatient clinics.
Methods: Swabs from 83 HCWs' mobile phones were processed using standard biochemical and enzymatic procedures to identify pathogenic bacteria.
Lab Chip
January 2025
James Watt School of Engineering, University of Glasgow, Glasgow, UK.
Milk is commonly screened both for indicators of animal disease and health, but also for foodborne hazards. Included in these analyses is the detection of , that can produce an enterotoxin, causing staphylococcal food poisoning (SFP), which often leads to sudden onset of significant gastrointestinal symptoms in humans. Epidemiological data on SFP are limited, particularly in low- and middle-income countries.
View Article and Find Full Text PDFMikrobiyol Bul
October 2024
Pamukkale University Faculty of Medicine, Department of Medical Microbiology, Denizli, Türkiye.
The aim of this study was to investigate the frequency of sasX, arginine catabolic mobile element (ACME) genes, biofilm formation and some biofilm related virulence factor genes in causative and contaminant coagulase negative staphylococci (CNS) strains isolated from blood cultures. Of the 150 CNS strains included in the study, 50 were grouped as infectious agents and 100 as contaminants. Biofilm formation of the strains was investigated by microplate method and the presence of sasX, ACME, mecA and biofilm associated virulence factor genes icaA, icaD, aap, bhp and IS256 were investigated by inhouse polymerase chain reaction method.
View Article and Find Full Text PDFFront Cell Infect Microbiol
January 2025
VBIC, INSERM U1047, University of Montpellier, Montpellier, France.
Introduction: This study identifies as a new coagulase-negative staphylococcal species isolated from diabetic foot osteomyelitis (DFOM) and provides an in-depth analysis of its pathogenic and virulence profile, as well as demonstrating its potential to cause infection.
Methods: The NSD001 strain was examined for its planktonic growth, biofilm production, and phagocytosis rates in murine macrophages compared to NSA739. Additionally, persistence and replication within human osteoblasts were investigated, while the zebrafish embryo model was employed to assess virulence.
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