Brilhante Raimunda Sâmia Nogueira, Costa Anderson da Cunha, Mesquita Jacó Ricarte Lima de, Dos Santos Araújo Gessica, Freire Rosemeyre Souza, Nunes João Victor Serra, Nobre Augusto Feynman Dias, Fernandes Mirele Rodrigues, Rocha Marcos Fábio Gadelha, Pereira Neto Waldemiro de Aquino, Crouzier Thomas, Schimpf Ulrike, Viera Rodrigo Silveira
Department of Pathology and Legal Medicine, School of Medicine, Specialized Medical Mycology Center, Postgraduate Program in Medical Sciences, Federal University of Ceará, Rua Barão de Canindé, 210, Montese, Fortaleza 60425-540, CE, Brazil.
São José Hospital, Fortaleza 60455-610, CE, Brazil.
J Fungi (Basel). 2023 Dec 15;9(12):1201. doi: 10.3390/jof9121201.
Histoplasmosis is a respiratory disease caused by , a dimorphic fungus, with high mortality and morbidity rates, especially in immunocompromised patients. Considering the small existing therapeutic arsenal, new treatment approaches are still required. Chitosan, a linear polysaccharide obtained from partial chitin deacetylation, has anti-inflammatory, antimicrobial, biocompatibility, biodegradability, and non-toxicity properties. Chitosan with different deacetylation degrees and molecular weights has been explored as a potential agent against fungal pathogens. In this study, the chitosan antifungal activity against was evaluated using the broth microdilution assay, obtaining minimum inhibitory concentrations (MIC) ranging from 32 to 128 µg/mL in the filamentous phase and 8 to 64 µg/mL in the yeast phase. Chitosan combined with classical antifungal drugs showed a synergic effect, reducing chitosan's MICs by 32 times, demonstrating that there were no antagonistic interactions relating to any of the strains tested. A synergism between chitosan and amphotericin B or itraconazole was detected in the yeast-like form for all strains tested. For biofilms, chitosan reduced biomass and metabolic activity by about 40% at 512 µg/mL. In conclusion, studying chitosan as a therapeutic strategy against is promising, mainly considering its numerous possible applications, including its combination with other compounds.
组织胞浆菌病是一种由双相真菌引起的呼吸道疾病,死亡率和发病率都很高,尤其是在免疫功能低下的患者中。考虑到现有的治疗手段有限,仍需要新的治疗方法。壳聚糖是一种通过部分几丁质脱乙酰化获得的线性多糖,具有抗炎、抗菌、生物相容性、生物降解性和无毒性等特性。不同脱乙酰度和分子量的壳聚糖已被探索作为对抗真菌病原体的潜在药物。在本研究中,使用肉汤微量稀释法评估了壳聚糖对[具体真菌名称缺失]的抗真菌活性,在丝状相获得的最低抑菌浓度(MIC)范围为32至128 µg/mL,在酵母相为8至64 µg/mL。壳聚糖与经典抗真菌药物联合使用显示出协同作用,使壳聚糖的MIC降低了32倍,表明与所测试的任何菌株均无拮抗相互作用。在所有测试菌株的酵母样形态中,均检测到壳聚糖与两性霉素B或伊曲康唑之间存在协同作用。对于[具体真菌名称缺失]生物膜,在512 µg/mL时,壳聚糖使生物量和代谢活性降低了约40%。总之,将壳聚糖作为对抗[具体真菌名称缺失]的治疗策略进行研究很有前景,主要考虑到其众多可能的应用,包括与其他化合物联合使用。