scholarly journals Distribution of mercury resistance among Staphylococcus aureus isolated from a hospital community

1970 ◽  
Vol 68 (1) ◽  
pp. 111-119 ◽  
Author(s):  
Barbara M. Hall

SummaryResults from clinical isolations confirmed that mercury resistance is common among antibiotic-resistant strains of Staphylococcus aureus present in a large general hospital although the correlation is not as high as that found by Moore (1960).The distribution of mercury-resistant strains among infections and carriers in surgical, medical, obstetric and geriatric patients and staff was studied. Attention was directed to the distribution among carriers since there are fewer extraneous factors operating among them, and a statistical analysis was made on the total number of mercury-resistant strains and the number of non-endemic strains; this latter figure was obtained by subtracting the dominant type 80/81, which is nearly always mercury-resistant and antibiotic-resistant, from the total. Analysis showed the geriatric patients to have a significantly higher proportion of mercury-resistant strains in both cases, and obstetric patients to have a significantly lower proportion when the total number of mercury-resistant strains was considered. Among the surgical, medical and staff categories, no significant difference in proportions could be found although a trend, in that order, of decreasing proportions of mercury-resistant strains present was noted.In those cases infected on admission with tetracycline-resistant strains, although mercury-resistant strains still predominate, mercury-sensitive strains make a sizeable contribution. This is a reflexion of their dominance in the non-hospital environment.

2012 ◽  
Vol 1 (1) ◽  
Author(s):  
Marco Antonio Becerril-Flores ◽  
César Arturo Gómez Durán ◽  
José Anselmo Hernández Ibarra ◽  
Erika Janet Varela-Prado ◽  
Areli Cruz Castañeda ◽  
...  

Infections by Staphylococcus aureus are a great worldwide public health problem due to easiness of transmission, via inhalation or direct contact in hospitals. Among infected individuals there are asymptomatic carriers that cause propagation and transmission of these infections within the hospital population. In Mexico, studies about prevalence of infections in healthy carriers by this bacterium are scarce. We investigated the prevalence of pharyngeal infections by S. aureus in asymptomatic children (3 to 8 years old) resident in Pachuca, Hidalgo. There were previous old clinic inspections as part of the study wherein 138 healthy children were studied. Samples of exudates from children were obtained and seeded in selective and differential media and they were morphologically identified as S. aureus by Gram staining. Antibiotics resistance was determined for each sample of bacteria. Prevalence of S. aureus infection was 20.29%, 12.69% in girls, and 26.66% in boys. Pre-school children showed a higher rate of infection than those in elementary school but there was not a significant difference between them (Χ2=0.92, p>0.05). More than 40% of S. aureus strains were ß-hemolytic, and half of the bacteria isolated from children in preschool is resistant to any of the antibiotics studied and resistant to at least one of the antibiotics assayed. The greatest resistance was to ciprofloxacin and erythromycin. Finding children infected with S. aureus as healthy carriers may be, in fact an epidemiologic risk for the entire population. Furthermore, since there are resistant strains of this microorganism, physicians must be very sensible of resistant patterns when selecting antibiotics.


1970 ◽  
Vol 68 (1) ◽  
pp. 121-128 ◽  
Author(s):  
Barbara M. Hall

SummaryReasons for the accumulation of mercury-resistant strains of Staphylococcus aureus in hospital have been studied. A collection of paired strains, that is staphylococci similar in every respect except sensitivity to mercury salts, was made. Tests were made in an attempt to demonstrate a link between mercury resistance and some other factor which might aid survival, viz. resistance to drying and heat, production of bound coagulase, growth in the presence of sublethal amounts of tetracycline, survival in human blood at 37°C. and uptake by polymorphs at 30°0. and 37°C., development of resistance to antibiotics and competition in mixed cultures. It was not possible to demonstrate any consistent link between mercury resistance and any of these properties. Paper strips impregnated with the mercurial diuretic, Mersalyl, were shown to differentiate between mercury-resistant and -sensitive strains in vitro. Furthermore, development of resistance to mercury by passage in mercuric chloride-broth was demonstrated.It is proposed that mercury resistance has developed as a result of exposure to the mercury ion. Mercurial diuretics have been frequently used in medical and geriatric patients and it is among these that the higher carrier rates of mercury-resistant strains are found even when the local endemic strain is disregarded. In obstetric patients, where mercurials are seldom used, mercury-resistant strains are rare.Nasal carriage of factory workers exposed to mercury products showed that this group is likely to carry resistant or partially resistant strains.


1978 ◽  
Vol 81 (1) ◽  
pp. 125-130 ◽  
Author(s):  
M. L. Burr ◽  
C. H. L. Howells ◽  
P. W. J. Rees

SUMMARYNasal swabs were taken from 492 babies born consecutively to residents of two South Wales towns soon after their discharge from maternity hospitals. Staphylococcus aureus was isolated from 352 babies (72%) and in 79 (22%) of these it was resistant to at least one antibiotic. By the time these babies were a year old the prevalence of both sensitive and resistant strains had fallen, so that only 12% still carried nasal staphylococci, but 64% of these organisms were then resistant to penicillin. Administration of penicillin to the baby seemed to be a more important factor in selecting resistant organisms than other antibiotics given to the baby, any antibiotic treatment to other members of the household, or discharge from hospital.


2005 ◽  
Vol 49 (9) ◽  
pp. 3690-3696 ◽  
Author(s):  
Michelle L. Embleton ◽  
Sean P. Nair ◽  
Wendy Heywood ◽  
Dev C. Menon ◽  
Barry D. Cookson ◽  
...  

ABSTRACT Light-activated antimicrobial agents (photosensitizers) are promising alternatives to antibiotics for the treatment of topical infections. To improve efficacy and avoid possible damage to host tissues, targeting of the photosensitizer to the infecting organism is desirable, and this has previously been achieved using antibodies and chemical modification of the agent. In this study we investigated the possibility of using a bacteriophage to deliver the photosensitizer tin(IV) chlorin e6 (SnCe6) to Staphylococcus aureus. SnCe6 was covalently linked to S. aureus bacteriophage 75, and the ability of the conjugate to kill various strains of S. aureus when exposed to red light was determined. Substantial kills of methicillin- and vancomycin-intermediate strains of S. aureus were achieved using low concentrations of the conjugate (containing 1.5 μg/ml SnCe6) and low light doses (21 J/cm2). Under these conditions, the viability of human epithelial cells (in the absence of bacteria) was largely unaffected. On a molar equivalent basis, the conjugate was a more effective bactericide than the unconjugated SnCe6, and killing was not growth phase dependent. The conjugate was effective against vancomycin-intermediate strains of S. aureus even after growth in vancomycin. The results of this study have demonstrated that a bacteriophage can be used to deliver a photosensitizer to a target organism, resulting in enhanced and selective killing of the organism. Such attributes are desirable in an agent to be used in the photodynamic therapy of infectious diseases.


mSphere ◽  
2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Sara B. Snell ◽  
Ann Lindley Gill ◽  
Constantine G. Haidaris ◽  
Thomas H. Foster ◽  
Timothy M. Baran ◽  
...  

ABSTRACT Staphylococcus aureus is an opportunistic pathogen with a clinical spectrum ranging from asymptomatic skin colonization to invasive infections. While traditional antibiotic therapies can be effective against S. aureus, the increasing prevalence of antibiotic-resistant strains results in treatment failures and high mortality rates. Photodynamic inactivation (PDI) is an innovative and promising alternative to antibiotics. While progress has been made in our understanding of the bacterial response to PDI, major gaps remain in our knowledge of PDI tolerance, the global cellular response, and adaptive genomic mutations acquired as a result of PDI. To address these gaps, S. aureus HG003 and isogenic mutants with mutations in agr, mutS, mutL, and mutY exposed to single or multiple doses of PDI were assessed for survival and tolerance and examined by global transcriptome and genome analyses to identify regulatory and genetic adaptations that contribute to tolerance. Pathways in inorganic ion transport, oxidative response, DNA replication recombination and repair, and cell wall and membrane biogenesis were identified in a global cellular response to PDI. Tolerance to PDI was associated with superoxide dismutase and the S. aureus global methylhydroquinone (MHQ)-quinone transcriptome network. Genome analysis of PDI-tolerant HG003 identified a nonsynonymous mutation in the quinone binding domain of the transcriptional repressor QsrR, which mediates quinone sensing and oxidant response. Acquisition of a heritable QsrR mutation through repeated PDI treatment demonstrates selective adaption of S. aureus to PDI. PDI tolerance of a qsrR gene deletion in HG003 confirmed that QsrR regulates the S. aureus response to PDI. IMPORTANCE Staphylococcus aureus can cause disease at most body sites, with illness ranging from asymptomatic infection to death. The increasing prevalence of antibiotic-resistant strains results in treatment failures and high mortality rates. S. aureus acquires resistance to antibiotics through multiple mechanisms, often by genetic variation that alters antimicrobial targets. Photodynamic inactivation (PDI), which employs a combination of a nontoxic dye and low-intensity visible light, is a promising alternative to antibiotics that effectively eradicates S. aureus in human infections when antibiotics are no longer effective. In this study, we demonstrate that repeated exposure to PDI results in resistance of S. aureus to further PDI treatment and identify the underlying bacterial mechanisms that contribute to resistance. This work supports further analysis of these mechanisms and refinement of this novel technology as an adjunctive treatment for S. aureus infections.


2018 ◽  
Vol 2 (1) ◽  
pp. 30-41 ◽  
Author(s):  
A.G. Salmanov ◽  
O.M. Verner ◽  
N.G. Shelkova ◽  
O.I. Nicolska ◽  
V.M. Blahodatny ◽  
...  

BACKGROUND. Nasal carriage of Staphylococcus aureus among hospital personnel is a common cause of hospital acquired infections. Emergence of drug resistant strains especially methicillin resistant S. aureus (MRSA) is a serious problem in hospital environment. Therefore, the aim of this study was to determine the prevalence of nasal carriage of Staphylococcus aureus its antibiotic susceptibility among healthcare workers (HCWs) in Ukraine. METHODS. This cross-sectional study was conducted from January to December 2017. The study included medical workers from 19 hospitals in different Ukrainian regions. Nasal swabs were taken from 755 randomly selected HCWs. The mean age of participants was 32.41 ± 8.29 years (range 19—74 years) with a male-to- female ratio of 0.47. The isolates were identified as S. aureus based on morphology, Gram stain, catalase test, coagulase test, and mannitol salt agar fermentation. The sensitivity patterns of S. aureus strains were determined by disk diffusion method (Kirby — Bauer). The panel of antibiotics used in sensitivity tests included: penicillin, oxacillin, cefoxitin, amoxicillin/clavulanic acid, gentamicin, tobramicin, ciprofloxacin, levofloxacin, moxifloxacin, mupirocin, nitrofurantoin, vancomycin, teicoplanin, fosfomycin, clindamycin, erythromycin, rifampicin, linezolid, tetracycline, tigecycline, trimethoprim/sulphamethoxazole, and fusidic acid. Interpretative criteria were those suggested by the CLSI (Clinical and Laboratory Standards Institute). MRSA were confirmed by detection of the mecA gene by polymerase chain reaction. RESULTS. Nasal screening identified 31.1 % (235/755) S. aureus carriers. Of the 235 nasal carriers of S. aureus, 4 % (196/755) carried MSSA (methicillin-sensitive S. aureus) and 39/755 (16.6 %) carried MRSA. The frequency of MRSA and MSSA carriage also varied according to the department/ward. The highest prevalence of nasal carriage of MRSA was in the surgical wards. The staff of the general, pediatric, cardiovascular, neuro and orthopedic surgery wards together with the emergency department accounted for 56.4 % of all MRSA carriers. There was no significant difference between the sexes (p = 0.247), age (p = 0.817), and years of healthcare service (p = 0.15) with regard to the nasal carriage of MRSA and MSSA. In univariate analysis we divided the hospital departments into: emergency, internal medicine, pediatrics, ICUs, surgery, and non-medical units and found no significant difference between MSSA and MRSA carriers (p = 0.224). In the multivariate analysis, the occupation «nurse» was independently associated with MRSA carriage (p = 0.012, odds ratio 3.6, 95 % confidence interval 1.3—9.7). All the S. aureus isolates recovered from nasal carriers, were susceptible to linezolid, tigecycline, vancomycin, teicoplanin, and mupirocin. Susceptibility to the other antimicrobials was also on a high level: 98.3 % of strains were found susceptible to trimethoprim/sulphamethoxazole, 96.2 % — to nitrofurantoin, 95.3 % — to fusidic acid, 92.3 % — to fosfomicin, 88.5 % — to amoxicillin/clavulanic acid, 87.2 % — to tobramycin, 86.8 % — to clindamycin. Resistance to oxacyllin came up to 16.6 %. CONCLUSIONS. Nasal carriage of S. aureus appears to play a key role in the epidemiology and pathogenesis of infection. HCWs who are at interface between the hospital and the community may serve as agents of cross contamination of hospital acquired and community acquired MRSA. It is of importance to follow the evolution of resistance to antibiotics in this species, especially to β-lactams.


Viruses ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 337
Author(s):  
Adriana Ene ◽  
Taylor Miller-Ensminger ◽  
Carine R. Mores ◽  
Silvia Giannattasio-Ferraz ◽  
Alan J. Wolfe ◽  
...  

Staphylococcus aureus infections are of growing concern given the increased incidence of antibiotic resistant strains. Egypt, like several other countries, has seen alarming increases in methicillin-resistant S. aureus (MRSA) infections. This species can rapidly acquire genes associated with resistance, as well as virulence factors, through mobile genetic elements, including phages. Recently, we sequenced 56 S. aureus genomes from Alexandria Main University Hospital in Alexandria, Egypt, complementing 17 S. aureus genomes publicly available from other sites in Egypt. In the current study, we found that the majority (73.6%) of these strains contain intact prophages, including Biseptimaviruses, Phietaviruses, and Triaviruses. Further investigation of these prophages revealed evidence of horizontal exchange of the integrase for two of the prophages. These Egyptian S. aureus prophages are predicted to encode numerous virulence factors, including genes associated with immune evasion and toxins, including the Panton–Valentine leukocidin (PVL)-associated genes lukF-PV/lukS-PV. Thus, prophages are likely to be a major contributor to the virulence of S. aureus strains in circulation in Egypt.


Pharmaceutics ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 711
Author(s):  
Olga Urbanek ◽  
Alicja Wysocka ◽  
Paweł Nakielski ◽  
Filippo Pierini ◽  
Elżbieta Jagielska ◽  
...  

The spread of antimicrobial resistance requires the development of novel strategies to combat superbugs. Bacteriolytic enzymes (enzybiotics) that selectively eliminate pathogenic bacteria, including resistant strains and biofilms, are attractive alternatives to antibiotics, also as a component of a new generation of antimicrobial wound dressings. AuresinePlus is a novel, engineered enzybiotic effective against Staphylococcus aureus—one of the most common pathogenic bacteria, found in infected wounds with a very high prevalence of antibiotic resistance. We took advantage of its potent lytic activity, selectivity, and safety to prepare a set of biodegradable PLGA/chitosan fibers generated by electrospinning. Our aim was to produce antimicrobial nonwovens to deliver enzybiotics directly to the infected wound and better control its release and activity. Three different methods of enzyme immobilization were tested: physical adsorption on the previously hydrolyzed surface, and covalent bonding formation using N-hydroxysuccinimide/N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide (NHS/EDC) or glutaraldehyde (GA). The supramolecular structure and functional properties analysis revealed that the selected methods resulted in significant development of nanofibers surface topography resulting in an efficient enzybiotic attachment. Both physically adsorbed and covalently bound enzymes (by NHS/EDC method) exhibited prominent antibacterial activity. Here, we present the extensive comparison between methods for the effective attachment of the enzybiotic to the electrospun nonwovens to generate biomaterials effective against antibiotic-resistant strains. Our intention was to present a comprehensive proof-of-concept study for future antimicrobial wound dressing development.


1970 ◽  
Vol 60 (4) ◽  
Author(s):  
Marta Maroszyńska ◽  
Alina Kunicka-Styczyńska ◽  
Katarzyna Rajkowska ◽  
Iwona Maroszyńska

Candida is a yeast species recognized as the most frequent etiological agent of systemic and invasive thrush in humans. Invasions can affect all tissues, organs and systems of human in various stages of development. In the last 10 years Candida infections have increased 15 times. The purpose of our study was to determine the sensitivity of four antibiotics belonging to three different groups of antifungal agents against clinical and food-borne Candida strains. Our studies showed that of all tested strains, 7% was resistant to nystatin, 32% to fluconazole, 23% to voriconazole, and no strains grew in the presence of caspofungin. Despite the differences in biochemical profiles of clinical and food-borne isolates of Candida, a group of strains showing resistance to antibiotics include both types of isolates. At the same time circulating of antibiotic-resistant strains outside the hospital environment and the yeast infection via food is possible.


2003 ◽  
Vol 58 (1-2) ◽  
pp. 70-75 ◽  
Author(s):  
Girma M. Woldemichael ◽  
Maya P. Singh ◽  
William M. Maiese ◽  
Barbara N. Timmermann

The Argentinean legume Caesalpinia paraguariensis Burk. (Fabaceae) was selected for further fractionation work based on the strong antimicrobial activity of its CH2Cl2-MeOH (1:1 v/v) extract against a host of clinically significant microorganisms, including antibiotic resistant strains. 1D and 2D NMR enabled the identification of the novel benzoxecin derivative caesalpinol along with the known compounds bilobetin, stigma-5-en-3-O-β-6′-stearoyl-glucopyranoside, stigma-5-en-3-β-6′-palmitoylglucopyranoside, stigma-5-en-3-β-glucopyranoside, oleanolic acid, 3-O-(E)-hydroxycinnamoyl oleanolic acid, betulinic acid, 3-O-(E)- hydroxycinnamoyl betulinic acid, and lupeol from the active fractions. Oleanolic acid was found active against Bacillus subtilis and both methicillin-sensitive and -resistant Staphylococcus aureus with MICs of 8 (17.5 μm), 8 and 64 (140 μm) μg/ml, respectively. The rest of the compounds, however, did not show activity


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