Farnesol is an extracellular quorum-sensing molecule produced by Candida albicans. Farnesol is also a sesquiterpene alcohol existing in many herbal products and has various activity against fungal cells. We aimed to investigate the efficacy of farnesol alone and the contribution of farnesol on the activity of voriconazole and amphotericin B against Aspergillus clinical isolates in vitro. A total of 45 Aspergillus clinical isolates were used in this study. The MIC values of voriconazole, amphotericin B, and farnesol were determined using reference broth microdilution method. The interactions of farnesol with voriconazole and amphotericin B were investigated by the checkerboard method and evaluated based on the fractional inhibitor concentration index (FICI). The MIC ranges of farnesol, voriconazole, and amphotericin B were 1,500-6,000 µM, 0.125-1 µg/mL, and 0.125-0.5 µg/mL against Aspergillus fumigatus isolates, 3,000-12,000 µM, 0.125-0.5 µg/mL, and 0.25-2 µg/mL against Aspergillus flavus isolates, respectively. The most common interaction in combination tests was "no interaction," and synergistic interaction was not detected. The combinations of farnesol with voriconazole and amphotericin B had antagonistic activity against 38% and 27% of all isolates, respectively. We concluded that the responses of different fungal species against farnesol are variable, and different interactions may be observed when it is combined with different antifungals. Therefore, it should be noted that farnesol may have an adverse effect on some fungi or interact negatively with antifungals used in combination.

Introduction. Polymicrobial infections including yeasts and bacteria are not rare and patients with polymicrobial bloodstream infection have higher early and overall case fatality rates. The diagnosis of invasive fungal and bacterial infections is mainly based on blood culture. Aim. The aim was to reveal the effect of concomitant bacteraemia on the detection of fungi from blood cultures in the presence of polymicrobial bloodstream infections involving Candida and non-Candida fungi and to show the superiority of blood culture bottles including selective fungal media in such situations. Methodology. Twenty-four polymicrobial bloodstream infection models – involving one fungus and one bacterium – were constituted by using clinical blood culture isolates ( Escherichia coli , Staphylococcus aureus , Pseudomonas aeruginosa , Candida albicans, Candida glabrata, Fusarium solani and Trichosporon asahii). The Plus Aerobic/F (PAF) and Mycosis IC/F (MICF) culture bottles were used with the BACTEC 9240 device. After a bottle signalled positive, direct microscopic examination and subcultures on agar plates were performed. Results. All of fungi that were inoculated alone and in combination were detected by both direct microscopic examination and subcultures on agar plates from MICF bottles, whereas direct microscopic examination only revealed the bacterial agents from PAF bottles including combinations. Furthermore, fungal growth was hidden by bacterial growth on blood agar subcultures from PAF bottles including combinations of F. solani, C. glabrata or T. asahii with bacteria. Conclusion. Blood culture bottles including selective fungal media that can allow selective growth of fungi and earlier detection of some species should be preferred in addition to non-selective blood culture bottles, especially in specific patient populations. Further, the use of selective agar plates such as inhibitory mould agar may contribute to the solution of this problem in clinical laboratories.

Sistemik dolaşımda anti-nükleer antikorların (ANA) varlığının tespiti birçok otoimmün hastalığın tanısı için anahtar rol oynamaktadır. Ancak indirekt immünofloresan (IIF) tarama testlerinde sıkça karşılaşılan ve anti-DFS70 antikorlarının varlığı ile ilişkilendirilebilen yoğun ince benekli (dense fine spekled, DFS) ANA paterninin hastalıklar ile ilişkili olup olmadığı henüz netleşmemiştir. Bu çalışmada, DFS paterninde ANA varlığı ile hastaların klinik tanıları ya da semptomları arasındaki ilişkisinin araştırılması amaçlanmıştır. Gereç ve Yöntem: ANA-IIF tarama testinde DFS paterni varlığı belirlenen 200 hasta çalışmaya dâhil edilmiştir. Hastaların klinik bilgilerinin elde edilmesi amacıyla hastaların hekimleri tarafından belirlenen International Statistical Classification of Diseases and Related Health Problems (ICD) kodları retrospektif olarak incelenmiştir. Bulgular: DFS paterninde ANA varlığı tespit edilen hastaların 158'i (%79.0) kadın, 42'si (%21.0) erkektir. Bu antikorlar en sık 1-10 yaş (58 hasta, %29.0), en az 71-80 yaş aralığında (bir hasta, %0.5) olan hastalarda tespit edilmiş, yaş ilerledikçe görülme sıklığının azaldığı belirlenmiştir. Hastaların 26'sında (%13.0) sistemik otoimmün romatizmal hastalık (SORH), sekizinde (%4.0) organa spesifik otoimmün hastalık, dokuzunda (%4.5) malignensi tanısı konduğu, 127 hastanın (%63.5) ise çeşitli sistemlere ait farklı hastalıklar, semptomlar ya da tanımlamalar içeren ICD kodları ile takip edildiği görülmüştür. Hastaların 30'unda (%15.0) ICD kodu belirtilmemiştir. Sonuç: Bu çalışmada DFS paternindeki ANA pozitifliğinin kadın hastalarda ve erken çocukluk evrelerinde daha sık görüldüğü tespit edilmiştir. Spesifik bir hastalık ile ilişkilendirilemese de bu paternin SORH'da da pozitif olabileceği, bu nedenle DFS paterninde ANA varlığı tespit edilen hastaların klinik bulgular eşliğinde değerlendirilmesi gerektiği sonucuna ulaşılmıştır.

Summary The sexual cycle of Candida glabrata is not known; however, genomic evidence is indicative of recombination among subpopulations and the genome harbours genes necessary for undergoing mating and meiosis, which may increase fitness. The relationship between specific mating type‐like (MTL) loci and antifungal susceptibility is not well understood in C. glabrata. We investigated different combinations of clinical C. glabrata isolate mating types and their antifungal susceptibility profiles. Allele profiles of the mating genes of 103 clinical C. glabrata isolates were identified, and their antifungal susceptibility to azoles, echinocandins and amphotericin B were compared. The majority (88.3%) of screened isolates harboured the a allele in the locus. The MTL1, MTL2 and MTL3 loci harboured a (88.3%), a (95.1%), and α (71.8%) alleles, respectively. The C. glabrata isolates were susceptible to echinocandins but displayed high minimal inhibitory concentrations (MICs) for azoles. The MIC ranges and MIC90 values of all isolates were 1.0 to ≥64 and 8.0 μg mL−1 for fluconazole, 0.06 to ≥16.0 and 0.5 μg mL−1 for voriconazole, 0.06 to ≥16.0 and 1.0 μg mL−1 for posaconazole, ≤0.015 to 0.06, and 0.03 μg mL−1 for caspofungin, ≤0.015 to 0.06 and 0.015 μg mL−1 for anidulafungin and 0.5‐2 and 2.0 μg mL−1 for amphotericin B, respectively. The mating gene alleles of the clinical C. glabrata isolates were not associated with differences in the MICs of the tested antifungals, except for the MTL3 α‐allele and echinocandins. The mating genotypes of the clinical C. glabrata isolates had no recognisable common effect on antifungal susceptibility.