While the original published version presented the methods of polymicrobial biofilm formation in the Results section, more detailed methods are presented here as requested by a reader. For the dual-species biofilm formation of C. albicans and S. aureus, C. albicans cells (23 ± 3 × 10⁵ CFU) cells and S. aureus cells (59 ± 4 × 10⁷ CFU) were inoculated at the same time in a mixture of 50% potato dextrose broth and 50% LB medium and incubated in 96-well polystyrene plates (total 300 μL/well, SPL Life Sciences, Korea) at 37 °C for 24 h without agitation. For the dual-species biofilm formation of the C. albicans and A. baumannii models, C. albicans cells (23 ± 3 × 10⁵ CFU) and A. baumannii cells (87 ± 13 × 10⁷ CFU) were inoculated at the same time in a mixture of 50% potato dextrose broth and 50% trypticase soy broth and incubated in 96-well polystyrene plates (total 300 μL/well) at 37 °C for 24 h without agitation. This article has not yet been cited by other publications.

中文翻译：

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纠正由Nepodin通过菌丝生长抑制对白色念珠菌和微生物微生物的生物膜形成的抑制作用。

原始出版版本在“结果”部分介绍了微生物生物膜形成的方法，但此处应读者要求提供了更详细的方法。为了形成白色念珠菌和金黄色葡萄球菌的双物种生物膜，同时接种白色念珠菌细胞（23±3×10 ⁵ CFU）细胞和金黄色葡萄球菌细胞（59±4×10 ⁷ CFU）。加入50％马铃薯葡萄糖肉汤和50％LB培养基的混合物中，并在96孔聚苯乙烯平板（总量300μL/孔，SPL Life Sciences，韩国）中于37°C孵育24 h，无需搅拌。对于白色念珠菌和鲍曼不动杆菌模型的双物种生物膜形成，将白色念珠菌细胞（23±3×10 ⁵ CFU）和鲍曼不动杆菌细胞（87±13×10 ⁷ CFU）同时接种在50％马铃薯葡萄糖肉汤和50％胰蛋白酶酶大豆肉汤的混合物中并孵育于96孔聚苯乙烯平板中（总共300μL/孔）在37°C下搅拌24小时。本文尚未被其他出版物引用。