In vitro investigation of the effects of Lactobacillus delbrueckii ssp. bulgaricus OLL1073R-1 exopolysaccharides on tight junction damage caused by influenza virus infection.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-04-08 DOI:10.1093/lambio/ovae029
Hiroki Ishikawa, Yoshihiro Kuno, Takehiro Yokoo, Ryuichi Nagashima, Takashi Takaki, Hiraku Sasaki, Chikara Kohda, Masayuki Iyoda
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Abstract

It is a problem that influenza virus infection increases susceptibility to secondary bacterial infection in lungs leading to lethal pneumonia. We previously reported that exopolysaccharides (EPS) derived from Lactobacillus delbrueckii ssp. bulgaricus OLL1073R-1 (OLL1073R-1) could prevent against influenza virus infection followed by secondary bacterial infection in vitro. Therefore, the present study assessed whether EPS derived OLL1073R-1 protects the alveolar epithelial barrier disfunction caused by influenza virus infection. After A549 cells treated with EPS or without EPS were infected influenza virus A/Puerto Rico/8/34 (IFV) for 12 h, the levels of tight junction genes expression and inflammatory genes expression were measured by reverse transcription polymerase chain reaction. As results, EPS treatment could protect against low-titer IFV infection, but not high-titer IFV infection, followed by suppression of the increased expression of inflammatory cytokine gene levels and recovery of the decrease in the expression level of ZO-1 gene that was caused by low-titer IFV infection, leading to an improvement trend in the barrier function. Our findings showed that EPS derived from OLL1073R-1 could inhibit low-titer IFV infection leading to maintenance of the epithelial barrier function through the suppression of inflammatory cytokine genes expression.

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体外研究保加利亚乳杆菌OLL1073R-1外多糖对流感病毒感染引起的紧密连接损伤的影响。
有一个问题是,流感病毒感染会增加肺部继发性细菌感染的易感性,从而导致致命性肺炎。我们以前曾报道,从保加利亚乳杆菌 OLL1073R-1 (OLL1073R-1)中提取的外多糖(EPS)可在体外防止流感病毒感染后继发细菌感染。因此,本研究评估了 EPS 衍生的 OLL1073R-1 是否能保护流感病毒感染引起的肺泡上皮屏障功能障碍。用 EPS 或不使用 EPS 的 A549 细胞感染流感病毒 A/Puerto Rico/8/34 (IFV)12 小时后,通过 RT-PCR 检测紧密连接基因表达水平和炎症基因表达水平。结果表明,EPS 处理可防止低滴度 IFV 感染,但不能防止高滴度 IFV 感染,并可抑制炎性细胞因子基因水平的表达增加,恢复因低滴度 IFV 感染导致的 ZO-1 基因表达水平的下降,从而使屏障功能呈改善趋势。我们的研究结果表明,OLL1073R-1提取的EPS可抑制低滴度IFV感染,从而通过抑制炎性细胞因子基因的表达维持上皮屏障功能。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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