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Biology subjects

Wu, K.-Y.

Publications and source records attributed to Wu, K.-Y..

2 recordsLinked to original sources

Establishment and comparison of three kinds of chronic bacterial cystitis models in mice

Cystitis is a common urinary system disease in women. However, there are currently no effective treatment options except antibiotics. Therefore, establishing an effective and stable animal model is helpful for further study of cystitis. In this study, we established three chronic cystitis models from C57BL/6 female mice inoculated with urinary tract pathogenic Escherichia UTI89 through urethral perfusion: CPP co-infection group, seven days interval repeated infection group, and two consecutive days repeated infection group. The three models were successfully constructed, and the survival rates of the three models were 66%, 75%, 100%, respectively. The bladder infection rates of the surviving mice were 100%, 100%, 50%, respectively. H&E staining showed that the inflammation and damage were the most severe in seven days interval repeated infection group. Sirius red staining showed that the degree of fibrosis was the highest in CPP co-infection group. Immunofluorescence staining of bladder inflammatory cells showed that inflammatory cells and macrophages in the CPP co-infection group and the seven days interval repeated infection group expressed more. Basal layer epithelial cell staining showed that the epithelial cells of the three infection models had different degrees of proliferation. The three strategies can all prepare mouse chronic cystitis models with their own characteristics, and these models can be used for experimental studies related to different levels of bladder infection and fibrosis, laying a foundation for further research on the mechanism of chronic cystitis.

microbiology↗

An atypical F-actin capping protein modulates cytoskeleton behaviors crucial to colonization of Trichomonas vaginalis

Cytoadherence and consequential migration are crucial for pathogens to establish colonization in the host. In contrast to the nonadherent isolate of Trichomonas vaginalis, the adherent one expresses more actin-related machinery proteins with more active flagellate-amoeboid morphogenesis, amoeba migration, and cytoadherence, activities that were abrogated by an actin assembly blocker. By immunoprecipitation coupled with label-free quantitative proteomics, an F-actin capping protein (TvFACP) was identified from the actin-centric interactome, with an atypically greater binding preference to G-actin than F-actin. TvFACP partially colocalized with F-actin at the parasite pseudopodia protrusion and formed the protein complexes with -actin through its c-terminal domain. Meanwhile, TvFACP overexpression suppresses F-actin polymerization, amoeboid morphogenesis, and cytoadherence in this parasite. Ser2 phosphorylation of TvFACP enriched in the amoeboid stage of adhered trophozoites was reduced by a CKII inhibitor. The site-directed mutagenesis and CKII inhibitor treatment revealed that Ser2 phosphorylation acts as a switching signal to alter TvFACP actin-binding activity and consequent actin cytoskeleton behaviors. Through CKII signaling, TvFACP also controls the conversion of adherent trophozoite from amoeboid migration to flagellate form with axonemal motility. Together, CKII-dependent Ser2 phosphorylation regulates TvFACP binding actin to fine-tune cytoskeleton dynamics and drive crucial behaviors underlying host colonization of T. vaginalis.

microbiology↗