Phenotypic and Genotypic Characterization with MALDI-TOF-MS Based Identification of Staphylococcus spp. Isolated from Mobile Phones with their Antibiotic Susceptibility, Biofilm Formation, and Adhesion Properties (original) (raw)
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ABCS Health Sciences, 2022
Introduction: Contamination of cell phones can contribute to the dissemination of pathogens in the community and/or hospital environment. Objective: To characterize Staphylococcus aureus strains isolated from cell phones of university students. Methods: Samples were collected from 100 cell phones. Detection of genes associated with virulence factors such as biofilm formation (icaA and icaD), enterotoxins production (SEA, SEB, SEC, and SED), and resistance to methicillin (mecA and mecC) was performed in S. aureus isolates by PCR. Typing mecA gene performed by multiplex PCR. Susceptibility to antimicrobials and biofilm formation rate also evaluated by using disk diffusion test and crystal violet staining. Results: S. aureus was present in 40% of the total samples and about 70% of them belonged to Nursing students. Of the isolates, 85% presented resistance to penicillin and 50% were classified as moderate biofilm producers. In addition, 92.5% of isolates contained the gene icaA and 60%...
Biocontrol science, 2016
From May 2014 to February 2015, 319 university students (male, n=173; female n=146) of 18 to 24 years of age who carried mobile phones or computer tablets were selected as subjects. Staphylococcus spp. were detected in 101 of 319 samples (31.7%). In the present study, 11 strains of S. aureus were isolated and identified, not all of which were methicillin-resistant Staphylococcus aureus (MRSA). Overall, 14 species were identified, with 11 strains (10.9%) of S. xylosus being isolated at the highest frequency. Following this were eight strains (7.9%) of S. cohnii and seven strains (6.9%) each of S. capitis and S. haemolyticus. Staphylococcus spp. isolation was performed with bacterial samples obtained from the mobile phones of 22 specific subjects (males, n=12; females, n=10). Staphylococcus spp. isolation was performed on days -1, 7 and 30 of the experiment. Staphylococcus spp. were positively detected one or more times in 12 subjects (54.5%). In one subject (8.3%), all three tests we...
BMC Research Notes
Objectives The aim of this research was to determine drug sensitivity profiles of Staphylococcus species isolated from mobile phones of students in Microbiology and Biomedical Laboratory Sciences from UZIMA University, Kisumu (Kenya) and the University Colleges Leuven-Limburg, Leuven (Belgium), respectively. Results All mobile phones (16/16, 100%) had gram-positive bacteria. 3/8 (37.5%) mobile devices had Staphylococcus aureus. 2/3 (67%) Staphylococcus aureus strains were resistant to ampicillin, oxacillin, ceftazidime, vancomycin and amoxicillin. Guidelines for disinfection of mobile phones need to be developed urgently to stop transmission of resistant bacteria.
International Journal of Pharmacy and Pharmaceutical Sciences
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Pathogens, 2020
Staphylococcus aureus is an opportunistic bacterium causing a wide variety of diseases. Biofilm formation of Staphylococcus aureus is of primary public and animal health concern. The purposes of the present study were to investigate the ability of Staphylococcus aureus isolated from animals, humans, and food samples to form biofilms and to screen for the presence of biofilm-associated and regulatory genes. In total, 55 Staphylococcus aureus isolated from sheep mastitis cases (n = 28), humans (n = 19), and from food matrices (n = 8) were identified using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). The ability of Staphylococcus aureus for slime production and biofilm formation was determined quantitatively. A DNA microarray examination was performed to detect adhesion genes (icaACD and biofilm-associated protein gene (bap)), genes encoding microbial surface components recognizing adhesive matrix molecules (MSCRAMMs), regulatory genes (accessory gene regulator (agr) and staphylococcal accessory regulator (sarA)), and the staphylococcal cassette chromosome mec elements (SCCmec). Out of 55 Staphylococcus aureus isolates, 39 (71.0%) and 23 (41.8%) were producing slime and biofilm, respectively. All Staphylococcus aureus strains isolated from food showed biofilm formation ability. 52.6% of the Staphylococcus aureus strains isolated from sheep with mastitis, and 17.9% of isolates from humans, were able to form a biofilm. Microarray analysis typed the Staphylococcus aureus into 15 clonal complexes. Among all Staphylococcus aureus isolates, four of the human isolates (21.1%) harbored the mecA gene (SCCmec type IV) typed into 2 clonal complexes (CC22-MRSA-IV and CC80-MRSA-IV) and were considered as methicillin-resistant, while two of them were slime-producing. None of the isolates from sheep with mastitis harbored the cna gene which is associated with biofilm production. The fnbB gene was found in 100%, 60% and 40% of biofilm-producing Staphylococcus aureus isolated from food, humans, and sheep with mastitis, respectively. Three agr groups were present and agr group III was predominant with 43.6%, followed by agr group I (38.2%), and agr group II (18.2%). This study revealed the capacity of Staphylococcus aureus isolates to form biofilms and highlighted the genetic background displayed by Staphylococcus aureus isolates from different sources in Algeria.
International Journal of Microbiology
Staphylococcus spp. is most often implicated in nosocomial infections. The objective of this study is to evaluate the susceptibility to antibiotics and the biofilm formation capacity of staphylococci species isolated from surfaces and medicotechnical materials at the university hospital center of Abomey-Calavi/Sô-Ava in Benin. Samples were collected according to ISO/DIS14698-1 standard from the surfaces and medicotechnical materials by the dry swab method. The isolation of Staphylococcus strains was performed on Chapman agar, and their identification was performed using microscopic and biochemical methods. The susceptibility of Staphylococcus isolates to antibiotics was evaluated by the disc diffusion method according to EUCAST and CLSI recommendations. The biofilm formation was qualitatively assessed using microplates. Of the 128 surfaces and medicotechnical material samples analyzed, 77% were contaminated with Staphylococcus spp. Thirteen species of Staphylococcus were isolated in...
ANTIBIOTIC SUSCEPTIBILITY PROFILING OF BACTERIA RECOVERED FROM CELL PHONES
JIRMEPS, 2018
This study was conducted to establish bacterial contamination of cell phones and microbial contamination of mobile phones and isolate the significant bacterial species associated with these cell phones in reference to give necessary remedial measure. A total of 80 samples were collected to isolate microbial population associated with cell phones. Sterile swabs were firmly rubbed on the surface of the handset, the key buttons and on the screens of cell phones. The swabs were then inoculated into different media viz. Nutrient agar, MacConkey agar, Mannitol Salt agar and Eosin Methelyne Blue agar. A total of 143 different bacterial isolates recovered from these sample and were classified as: Staphylococcus spp. Corynebacterium spp., Streptococcus spp., Pseudomonas spp., Micrococcus spp., Proteus spp., Bacillus spp., and Enterobacter spp. at the ratio of 52, 17, 14, 7, 4, 3, 2 and 1% respectively. The isolates …
Journal of Bacteriology Research, 2014
The burden of disease caused by Staphylococcus aureus continues to grow; this organism has the ability to form biofilm and it is also a frequent cause of medical device and implant-related infections. The objective of this study was to evaluate the biofilm-forming ability of a collection of clinical isolates of S. aureus. In a total of 240 Staphylococcus spp. isolated from catheters, retrieved at five services (neonatology, internal medicine, pneumology, pediatric and neurology), only 50 (20.83%) strains were identified by conventional microbiological methods as S. aureus species; these strains were screened by microtiter plate assay for detection of biofilm formation. Of the 50 clinical isolates, 16 (32%) were non adherent, 20(40%) weakly, 10 (20%) moderately and 4(8%) strongly adherent. The quantitative method of microtiter plate can be involved as a simple, rapid, inexpensive and reproducible assay to assess biofilm formation which is further an important feature of pathogenecity of S. aureus in the clinical setting.
BioMed Research International, 2013
This study evaluated whether genotypically different clinical isolates of S. aureus have similar susceptibilities to individual antibiotics. It further aims to check the impact of biofilm on the in vitro activity of vancomycin, daptomycin, linezolid, and tigecycline against S. aureus clones. The study used a total of 60 different clinical MSSA and MRSA isolates. Susceptibilities were performed in planktonic cultures by macrobroth dilution and epsilon-test (E test) system. Biofilm production was determined using an adherent plate assay. The efficacy of antimicrobial activities against biofilms formation was checked using confocal laser scanning microscopy (CLSM). The study found that similar and different spa, MLST, and SCCmec types displayed high variation in their susceptibilities to antibiotics with tigecycline and daptomycin being the most effective. The biofilms were found resistant to high concentrations of most antibiotics tested with daptomycin being the most effective drug used in adhesive biofilms. A considerable difference exists among similar and various clone types against antibiotics tested. This variation could have contributed to the degree of virulence even within the same clonal genotype and enhanced heterogeneity in the infection potential. Thus, the development of a rapid and precise identification profile for each clone in human infections is important.
IP Innovative Publication Pvt. Ltd., 2019
Introduction: Smart phones have become omnipresent in Clinical and Non clinical environment. They have been implicated as a source of bacterial contamination. Drug resistant pathogens such as methicillin resistant staphylococcus aureus (MRSA), Gram negative bacteria. Aims and Objectives: To evaluate the role of mobile phones in relation to transmission of bacteria from mobile phone to health care workers and their pathogenicity. Inclusion Criteria: Medical faculty present on the days of data collection. Exclusion Criteria: Who ever don’t give consent. Materials and Methods: In total, 200 mobile phones were sampled. Two senior medical students were trained by a senior microbiologist to obtain the swabs in a standardized manner. The sides, screen and back of mobile phones were swabbed using a sterile cotton swab. The swabs were taken to the laboratory without delay and are incubated in brain heart infusion broth and incubated at 37 degrees for 24-48 hrs. Positive samples were further sub cultured on different growth media; mannitolsaltagar to isolate Staphylococci, MacConkey-agar to isolate Gram negative bacteria and Entero coccosel-agar to isolate fecal Enterococci. Results: Out of 200 cell phones sampled, 66 were found contaminated with varied number of bacteria. The most commonly isolated organism was aerobic spore bacilli 33(16.5%) followed by Pseudomonas 13(6.5%), Proteus 11(5.5%), Escherichia coli 7(3.5%), Klebsiella 1(0.5%), Staphylococcus aureus 1(0.5%). Keywords: Nosocomial infections, Drug resistance, Sterile swab, MRSA, Antibiotic susceptibility testing.