The present study was undertaken to investigate the presence of Salmonella spp. in the faeces of client-owned cats in urban areas and to evaluate the risk that is posed to public health. Fresh faecal samples were collected directly from the rectums from 53 diarrhoeic and 32 non-diarrhoeic cats. The samples were individually screened for the presence of Salmonella spp. using standard methods and, in the case of positive findings, the resulting typical colonies were then biochemically confirmed using the VITEK®2 automated system. Subsequently, all of the Salmonella spp. isolates were molecularly tested for the presence of the invA gene. All of the isolates were serotyped using the slide agglutination technique according to the White–Kauffmann–Le Minor scheme. The phenotypic antimicrobial susceptibility profile of the isolated strains was obtained from the VITEK®2 system using specific cards from the Gram-negative bacteria. A total of 16 of the samples (18.82%) tested positive for Salmonella spp. according to conventional and molecular testing methods. Serotyping of the Salmonella isolates showed the presence of three serotypes, namely S. enteritidis (n = 9; 56.3%), S. typhimurium (n = 4; 25%), and S. kentucky (n = 3; 18.8%). All of the tested strains showed strong resistance towards cefazolin, cefepime, ceftazidime, and ceftriaxone. Additionally, resistance (listed in descending order of strength) was observed to trimethoprim/sulfamethoxazole (11/16; 68.8%), ampicillin (10/16; 62.5%), ampicillin/sulbactam (9/16; 56.3%), gentamicin (9/16; 56.3%), nitrofurantoin (8/16; 50.0%), and amikacin (5/16; 31.3%). No resistance was expressed against ciprofloxacin, ertapenem, imipenem, levofloxacin, piperacillin/tazobactam, and tobramycin. The results of this study highlight a substantial public health issue and medical concern, especially in vulnerable people, such as children, the elderly, and immunocompromised individuals.

No abstract

The aim of this study was to assess the presence and antimicrobial susceptibility profile of the molecularly serogrouped Listeria monocytogenes isolates in different animal origin food products, collected from a county situated in the historical region of Transylvania, Central Romania. A total of 7.7% (17/221) of the screened samples were positive for L. monocytogenes , with an isolation frequency of 6.2% (8/130) in the ready-to-eat products (i.e., sausages, ham and smoked specialties), 12.8% (6/47) in raw meat (i.e., minced pork, pork organs and snails), and 6.8% (3/44) in dairy (i.e., assortment of cheeses) samples. The identified L. monocytogenes serogroups were: 1/2a-3a (47.1%), 4b-4d-4e (29.4%), 1/2c-3c (11.8%), and 4a-4c (11.8%), respectively. All isolates were resistant to benzylpenicillin and fusidic acid. Resistance was also detected towards oxacillin (88.2%), fosfomycin (82.4%), clindamycin (76.5%), imipenem (52.9%), ciprofloxacin (41.2%), rifampicin (41.2%), trimethoprim – sulfamethoxazole (29.4%) and tetracycline (29.4%). On the other hand, all isolates proved susceptible to gentamicin, moxifloxacin, teicoplanin, vancomycin, tigecycline, erythromycin and linezolid. All tested strains exhibited multidrug resistance, resulting in the expression of a total of 12 resistance profiles. These findings extend the understanding about the spread of an important pathogen in Romanian food products, highlighting a substantial public health issue and medical concern, especially for consumers with a compromised health status.

The aim of this study was to assess the microbiological and chemical air quality in a municipal solid waste landfill and its inhabited surroundings, in a particular context in which Romania struggles with the incapacity to comply with its environmental commitments. The research was conducted on a landfill near the capital Bucharest between November 2018 and September 2019. To evaluate the chemical (oxygen, carbon dioxide, methane, hydrogen sulfide, ammonia and carbon monoxide–MX6 iBrid™ Détector multigas) and microbiological (airborne bacteria and fungi–aspiration method) parameters, eight sampling points were established, located both on the perimeter of the landfill and within its surroundings. CO and CH4 were not detected in any of the sampling points, during the study period; O2 was in normal values 20.09–21.05%; CO2 had a maximum average concentration of 620 ± 215; H2S had values between 0.1 and 5.0 ppm only in the sampling points inside the landfill; NH3 was present only once in a single sampling point with values between 1.0 and 3.0 ppm. The microbiological results provide an overview of the total plate count and total fungal count, with no significant differences between the level of contamination inside the landfill and within its surroundings (p > 0.05). Ten bacterial species and fungi from six genera have been identified. It was also found that the number of microorganisms in the air was significantly lower during the winter, spring and early summer months compared with the late summer and autumn months (p < 0.05).

Keywords: chromogen, methicillin, MRSA, resistanceIntroduction: Currently, both in staphylococci isolated from animals with different diseases, as well as in humans, the MRSA strains (Methicillin Resistant S. aureus) are monitored, as the methicillin resistance is associated with the resistance to other antibiotic groups.Methicillin resistance is encoded by mec staphylococcal chromosomal cassettes (SCCmec), which are islands of resistance. These strains can be identified by molecular biology tests and tests that reveal several phenotypic characteristics.The research was made in order to characterize and identify phenotypically the MRSA staphylococci strains isolated from animals.Materials and Methods: Researches were made on 240 coagulase positive and coagulase negative strains of staphylococci. Mannitol fermentation was tested on Champan medium, free coagulase was revealed on Baird-Parker medium and to identify S. aureus subsp. aureus was used the chromogenic medium Chromatic Staph.Methicillin-resistant strains were detected by disc diffusion method, using biodiscs with methicillin, oxacillin and cefoxitin. Also, to identify the MRSA strains, was used the chromogenic medium Chromatic MRSA.Results: The isolates were positive to mannitol and produced complete haemolysis or were unhaemolytic. A total of 44 strains produced free coagulase on Baird-Parker medium, considered coagulase positive strains, while 196 were coagulase negative strains.The isolates conducted differently to methicillin: 22,08% of strains were resistant, 51,25% of strains were susceptible and 26,66% had intermediate resistance, while the resistant strains to oxacillin were 42,91%.The increased frequency of methicillin-resistant strains of staphylococci and, particularly, MRSA strains, determined using the cefoxitin disk diffusion test, which is more reliable than methicillin and oxacillin.On the MRSA chromogenic medium, the methicillin-resistant strains of staphylococci formed colonies with pigment from mauve to orange mauve.Conclusion: The obtained results by disk diffusion test on resistance patterns to 3 beta-lactams, resistant to penicillinase, indicated a different frequency of the resistant strains to these antibiotics.Cefoxitin disk diffusion test revealed a frequency of 2,51% of resistant strains, that can be considered MRSA strains.

Cellulose acetate (CA) is one of the most important esters of cellulose and it was analyzed by means of Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and EDX spectra. The FT-IR spectrum presented both the C=O and C�O stretching bands for acetyl groups. The EDX spectrum confirms the presence of C and O elements. The SEM image presented a spongy structure that is important for many applications. The antimicrobial properties of cellulose acetate solutions in acetic acid were determined in tests on two gram-negative species (Pseudomonas aeruginosa - ATCC 27853 and Escherichia coli - ATCC 25822), two gram-positive species (Staphylococus aureus - ATCC 29213 and Streptococcus pyogenes - ATCC 19615) and yeast species (Candida albicans - ATCC 10231). We have shown that samples of cellulose acetate solutions in acetic acid can be used to fight microbial and fungal infections. Of the gram-positive species tested, the strongest antimicrobial effect was observed against S. aureus. The diameter of inhibition zones of cellulose acetate solutions in acetic acid (P1 and P2) for S. aureus far exceeded inhibition zone both of reference substance (gentamicin) and of acetic acid solutions (M1 and M2), given values between 3.15 cm (P1) and 3.55 cm (P2). Also, the results suggested that the studied solutions (P1 and P2) had an antimicrobial effect pronounced for gram-negative species as P. aeruginosa, in which the P1 sample gave an inhibition zone of 2.95 cm, and the P2 sample achieved an inhibition of 3.15 cm. So, the antimicrobial activity of cellulose acetate solutions tested in vitro had a good antimicrobial effect, proportional to the concentration of the active substance.