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1.
Braz J Microbiol ; 52(4): 2085-2089, 2021 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-34545554

RESUMEN

Fungal infections are responsible for high morbidity and mortality in neonatal patients, especially in premature newborns. Infections in neonates caused by Cryptococcus spp. are rare, but it has occurred in an immunocompromised population. This study aims to describe the isolation of Cryptococcus liquefaciens from the hands of a health professional in a neonatal intensive care unit, and to evaluate the production of biofilm and virulence factors and susceptibility to antifungals. Antifungal susceptibility tests were performed according to Clinical and Laboratory Standard Institute document M27-A3. Thermotolerance virulence factors and DNase, phospholipase, proteinase, and hemolytic activities were verified through phenotypic tests; biofilm was evaluated by determining the metabolic activity and biomass. The isolate did not produce any of the tested enzymes and was susceptible to all antifungals (amphotericin B, fluconazole, and micafungin). The growth at 37 °C was very weak; however, the isolate showed a strong biomass production and low metabolic activity. This is the first report of C. liquefaciens isolated from the hands of a health professional. The isolate did not express any of the studied virulence factors in vitro, except for the low growth at 37 °C in the first 48 h, and the strong production of biofilm biomass. Cryptococcus liquefaciens can remain in the environment for a long time and is a human pathogen because it tolerates temperature variations. This report draws attention to the circulation of rare species in critical locations, information that may help in a fast and correct diagnosis and, consequently, implementation of an appropriate treatment.


Asunto(s)
Basidiomycota , Unidades de Cuidado Intensivo Neonatal , Antifúngicos/farmacología , Basidiomycota/aislamiento & purificación , Basidiomycota/patogenicidad , Basidiomycota/fisiología , Fluconazol/farmacología , Personal de Salud , Humanos , Recién Nacido , Pruebas de Sensibilidad Microbiana , Factores de Virulencia/genética
2.
Folia Microbiol (Praha) ; 64(2): 133-141, 2019 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-30269301

RESUMEN

When it comes to women's health, treating vaginal infections makes up a high proportion of the gynecological services. Among the forms of vaginitis, vulvovaginal candidiasis (VVC) is considered the second most common. Demand for new treatment alternatives is increasingly relevant, especially for therapies with fewer side effects, better tolerability, and lower cost, while still offering improved quality of life in terms of disease prevention. This study intended to investigate the alternative therapies described for the adjuvant treatment of vulvovaginitis caused by Candida species, including alternative and complementary treatment methods used by women. This literature review is based on articles written in English and Portuguese in the PubMed, Google Scholar, and SciELO databases. This study was conducted for the most part using the Brazilian Government's Capes Periodicals Portal, which directs to Google Scholar and PubMed. Since the 1980s, there has been growing interest in alternative therapies in Brazil, a trend which also began in other Western countries in the second half of the twentieth century. Some alternative treatments include substances with antifungal activity, some substances help restore the balance of the vaginal microbiota, while others have an inhibitory activity on microbial virulence factors. The proper use of therapeutic alternatives can effectively contribute to the treatment of VVC, but it should be remembered that some chemical products, such as boric acid or vinegar, and even natural products such as propolis, garlic, and tea tree may have undesirable side effects, having not been tested by well-designed clinical studies. Even so, alternative therapies in the treatment of VVC do have support in the scientific literature.


Asunto(s)
Antifúngicos/uso terapéutico , Candidiasis Vulvovaginal/terapia , Terapias Complementarias , Antifúngicos/efectos adversos , Antifúngicos/farmacología , Candida/efectos de los fármacos , Femenino , Humanos , Calidad de Vida , Resultado del Tratamiento
3.
Arch Oral Biol ; 66: 61-5, 2016 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-26913969

RESUMEN

The colonization by Candida species is one of the most important factors related to the development of oral candidiasis in HIV-infected individuals. The aim of the study was to evaluate and discuss the phospholipase, proteinase, DNAse and haemolytic activities of Candida albicans isolated from the oral cavity of HIV individuals with high efficiency antiretroviral therapy. Seventy-five isolates of C. albicans obtained from saliva samples of patients with HIV and 41 isolates from HIV-negative individuals were studied. Haemolytic activity was determined in Sabouraud dextrose agar plates containing 3% glucose and 7% sheep red cells. Culture medium containing DNA base-agar, egg yolk, and bovine albumin were used to determine DNase, phospholipase and proteinase activities, respectively. All isolates from the HIV patients group had haemolytic activity, 98% showed phospholipase activity, 92% were positive for proteinase and 32% DNAse activity. Regarding the group of indivídios HIV negative, all 41 isolates presented hemolytic activity, 90.2% showed phospholipase and proteinase activity and 12.2% were positive for DNAse. The phospholipase activity was more intense for the group of HIV positive individuals. DNase production was more frequently observed in the group of HIV-positive individuals. The percentage of isolates having DNAse activity was also significantly different between the groups of patients not using any antiretroviral therapy, those using transcriptase inhibitors and those using transcriptase inhibitor and protease inhibitor in combination.


Asunto(s)
Terapia Antirretroviral Altamente Activa , Candida albicans/aislamiento & purificación , Candida albicans/metabolismo , Candidiasis Bucal/microbiología , Infecciones por VIH/tratamiento farmacológico , Infecciones por VIH/microbiología , Factores de Virulencia/metabolismo , Antirretrovirales/farmacología , Candida albicans/enzimología , Candida albicans/patogenicidad , Candidiasis Bucal/virología , Medios de Cultivo , ARN Polimerasas Dirigidas por ADN , Desoxirribonucleasas/biosíntesis , Activación Enzimática , Infecciones por VIH/virología , Humanos , Boca/microbiología , Péptido Hidrolasas/biosíntesis , Fosfolipasas/biosíntesis , Inhibidores de Proteasas , Saliva/microbiología
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