All tests produced highly reliable results. However, the Candida ID agar misidentified Candida dubliniensis as C. albicans. Determination of filamentous colony morphology allowed 100% reliable identification of C. albicans, but took 48 h. FISH allowed identification of clinical C. albicans isolates within 3 h with a sensitivity and specificity of 100%. FISH was additionally applied to 48 blood cultures showing yeasts in the Gram stain and correctly identified all 33 cases of C. albicans. “
“Mucormycosis has emerged as a relatively common severe mycosis in patients with haematological GDC-0449 clinical trial and allogeneic stem cell transplantation.

Source of transmission is from unidentified sources in the environment. Early diagnosis of infection and its source of contamination

are paramount for rapid and appropriate therapy. In this study, rolling circle amplification (RCA) is introduced as a sensitive, specific and reproducible isothermal DNA amplification technique for rapid molecular identification of six of the most virulent species (Rhizopus microsporus, R. arrhizus var. arrhizus, R. arrhizus var. delemar, Mucor irregularis, Mucor circinelloides, Lichtheimia ramosa, Lichtheimia corymbifera). DNAs of target species were successfully amplified, with no cross reactivity between species. RCA can be considered as a rapid detection method with high specificity and sensitivity, suitable for large screening. Most members of AZD2014 ic50 Mucorales are fast-growing saprotrophic fungi that are found Sclareol as first colonisers of organic materials in soil, dung and dead plant material. Several species are used for the fermentation of soya-based foodstuffs such as ragi, tempe or peka because of their production of hydrolytic enzymes.[1-3] The same or similar species are prevalent as aetiologic agents of infections in patients with severe immune or metabolic impairments.[1] Patients with diabetic ketoacidosis, haematologic malignancies, stem cell or solid organ transplantation, neutropenia, increased serum levels of available

iron or birth prematurity are at risk. Clinically the infection presents as rhinocerebral, pulmonary, gastrointestinal, renal or disseminated disease, and is life threatening in susceptible patient populations. Usually extended necrosis is observed within days because of significant angio-invasion. Rhizopus arrhizus is the most common infectious agent, being responsible for 70% of all cases of mucormycosis and 90% of all rhinocerebral cases.[3-6] Incidence of R. arrhizus is followed by that of Mucor and Lichtheimia species (formerly known as Absidia), and Rhizopus microsporus.[7] In another study, the dominant species were R. arrhizus (85% of rhinocerebral forms, and 32% of all mucormycoses), followed by Lichtheimia (approximately 29% of all mucormycoses) and R. microsporus.