Bhattacharyya Sayan, Gupta Prashant, Banerjee Gopa, Jain Amita, Singh Mastan
Department of Microbiology, AIIMS, Phulwari Sharif, Patna, Bihar, India.
Department of Microbiology, KGMU, Lucknow, Uttar Pradesh, India.
Int J Appl Basic Med Res. 2014 Sep;4(Suppl 1):S27-30. doi: 10.4103/2229-516X.140721.
Candida spp. are fourth most common cause of bloodstream infection in developed countries and emerging agents of fungemia in developing countries, with considerable attributable mortality. Candidemia is associated with the formation of complex, structured microbial communities called biofilms. Biofilm formation makes treatment difficult due to improper drug penetration and factors like high cost and adverse effects of antifungal drugs available. Hence, low-cost alternatives are urgently required to treat device-associated invasive candidiasis.
To study the effect of culture filtrate of Staphylococcus epidermidis on biofilm formation and lipase expression of Candida albicans in vitro.
Yeast cells isolated from clinical samples were suspended to a turbidity of 10(6) in (a) Yeast extract-peptone-dextrose (YPD) broth and (b) culture filtrate, and 100 μl of each were dispensed in separate wells of microtiter plate. After repeated washing and reloading with respective liquid media, readings were taken spectrophotometrically. To check for lipase inhibition, yeasts were incubated overnight in YPD and filtrate and subcultured on media containing Tween-80 and CaCl2. Positive lipase activity was denoted by haziness around colonies.
Mean reading of C. albicans in YPD broth was 0.579 while the same when yeasts were suspended in S. epidermidis culture filtrate was 0.281 (P < 0.05 by Z-test of significance). Lipase of C. albicans was inhibited by culture filtrate. Filtrate was found to be nontoxic to human cell line.
Culture filtrate of S. epidermidis can hence pave the way for development of new strategies to inhibit biofilm formation in device-associated candidemia.
念珠菌属是发达国家血流感染的第四大常见病因,在发展中国家是真菌血症的新兴病原体,具有相当高的归因死亡率。念珠菌血症与称为生物膜的复杂结构化微生物群落的形成有关。生物膜的形成使治疗变得困难,原因包括药物渗透不当以及现有抗真菌药物的高成本和副作用等因素。因此,迫切需要低成本的替代方法来治疗与装置相关的侵袭性念珠菌病。
研究表皮葡萄球菌培养滤液对白色念珠菌体外生物膜形成和脂肪酶表达的影响。
从临床样本中分离的酵母细胞在(a)酵母提取物 - 蛋白胨 - 葡萄糖(YPD)肉汤和(b)培养滤液中悬浮至浊度为10(6),并将每种100μl分别分配到微量滴定板的单独孔中。在用各自的液体培养基反复洗涤和重新加载后,通过分光光度法进行读数。为了检查脂肪酶抑制作用,将酵母在YPD和滤液中孵育过夜,并在含有吐温 - 80和氯化钙的培养基上进行传代培养。菌落周围的模糊表示阳性脂肪酶活性。
白色念珠菌在YPD肉汤中的平均读数为0.579,而当酵母悬浮在表皮葡萄球菌培养滤液中时,平均读数为0.281(通过Z检验显著性,P < 0.05)。白色念珠菌的脂肪酶被培养滤液抑制。发现滤液对人细胞系无毒。
因此,表皮葡萄球菌培养滤液可为开发抑制与装置相关的念珠菌血症中生物膜形成的新策略铺平道路。