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Tetrahymenosis has resulted in significant economic losses for the ornamental fish farming industry in Harbin. While previous studies have investigated the outbreaks and histopathology of Tetrahymena pyriformis in fish, there is still a lack of study on the use of the application of fish drugs for prevention and treatment. This experiment aims to evaluate the efficacy of three fish drugs (copper, Nitrofural, Methylene Blue) in combating tetrahymenosis in goldfish. We utilized eDNA-based 16 s rDNA gene amplifiers sequencing and qPCR technologies to extract environmental samples and conducted high-throughput sequencing to assess the interaction between the diversity of T. pyriformis and other microorganisms in aquaculture water following the introduction of various fish medications. Our findings revealed that among the three fish drugs test, Nitrofural displayed the most promising effects, followed by Methylene Blue, while copper sulfate proved to be the least effective. Consequently, our study provides a treatment plan for addressing tetrahymenosis in goldfish and offers insights into the pathological changes in goldfish tissues following the onset of the disease., Competing Interests: Declaration of Competing interest The authors declare that there is no conflict of interest., (Copyright © 2024 Elsevier B.V. All rights reserved.)

The major challenge of chemotherapy is the disease resistance for many lung cancer patients. Integrated microfluidic systems offer many desirable characteristics and can be used in cellular biological analysis. This work aimed to study the correlation between the expression of Glucose Regulated Protein-78 (GRP78) and the resistance to anticancer drug VP-16 in human lung squamous carcinoma cell line SK-MES-1 using an integrated microfluidic gradient chip device. We used A23187, a GRP78 inducer, with a gradient concentration in the upstream network of the device to induce the expression of GRP78 in the cells cultured in the downstream before the addition of VP-16. The expression of GRP78 was detected by immunofluorescence, the apoptosis for the cells treated by VP-16 was assessed morphologically by 4',6-diamidino-2-phenylindole (DAPI) staining. The results indicated that the expressions of GRP78 increased greatly for the cells under the induction of A23187 with a dose-depended manner, while the percentage of apoptotic cells decreased significantly after being treated by VP-16. Our results from this study confirmed the role of GRP78 played in the chemotherapy resistance to VP-16 in SK-MES-1 cell line, suggesting that the integrated microfluidic systems may be an unique approach for characterizing the cellular responses.