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酸处理的金黄色葡萄球菌诱导家蚕血液黑化。

Acid-treated Staphylococcus aureus induces acute silkworm hemolymph melanization.

机构信息

Department of Microbiology, Meiji Pharmaceutical University, Tokyo, Japan.

出版信息

PLoS One. 2024 May 30;19(5):e0298502. doi: 10.1371/journal.pone.0298502. eCollection 2024.

Abstract

The skin microbiome maintains healthy human skin, and disruption of the microbiome balance leads to inflammatory skin diseases such as folliculitis and atopic dermatitis. Staphylococcus aureus and Cutibacterium acnes are pathogenic bacteria that simultaneously inhabit the skin and cause inflammatory diseases of the skin through the activation of innate immune responses. Silkworms are useful invertebrate animal models for evaluating innate immune responses. In silkworms, phenoloxidase generates melanin as an indicator of innate immune activation upon the recognition of bacterial or fungal components. We hypothesized that S. aureus and C. acnes interact to increase the innate immunity-activating properties of S. aureus. In the present study, we showed that acidification is involved in the activation of silkworm hemolymph melanization by S. aureus. Autoclaved-killed S. aureus (S. aureus [AC]) alone does not greatly activate silkworm hemolymph melanization. On the other hand, applying S. aureus [AC] treated with C. acnes culture supernatant increased the silkworm hemolymph melanization. Adding C. acnes culture supernatant to the medium decreased the pH. S. aureus [AC] treated with propionic acid, acetic acid, or lactic acid induced higher silkworm hemolymph melanization activity than untreated S. aureus [AC]. S. aureus [AC] treated with hydrochloric acid also induced silkworm hemolymph melanization. The silkworm hemolymph melanization activity of S. aureus [AC] treated with hydrochloric acid was inhibited by protease treatment of S. aureus [AC]. These results suggest that acid treatment of S. aureus induces innate immune activation in silkworms and that S. aureus proteins are involved in the induction of innate immunity in silkworms.

摘要

皮肤微生物组维持着健康的人类皮肤,而微生物组平衡的破坏会导致炎症性皮肤病,如毛囊炎和特应性皮炎。金黄色葡萄球菌和痤疮丙酸杆菌是同时栖息在皮肤上的致病菌,通过激活先天免疫反应引起皮肤炎症性疾病。家蚕是评估先天免疫反应的有用的无脊椎动物模型。在家蚕中,酚氧化酶在识别细菌或真菌成分后产生黑色素作为先天免疫激活的指标。我们假设金黄色葡萄球菌和痤疮丙酸杆菌相互作用,增加金黄色葡萄球菌激活先天免疫的特性。在本研究中,我们表明金黄色葡萄球菌通过酸化参与家蚕血液黑化的激活。单独的巴氏杀菌杀死的金黄色葡萄球菌(金黄色葡萄球菌 [AC])不会大大激活家蚕血液黑化。另一方面,应用经痤疮丙酸杆菌培养上清液处理的金黄色葡萄球菌 [AC] 增加了家蚕血液黑化。向培养基中添加痤疮丙酸杆菌培养上清液会降低 pH 值。经丙酸、乙酸或乳酸处理的金黄色葡萄球菌 [AC] 诱导的家蚕血液黑化活性高于未经处理的金黄色葡萄球菌 [AC]。经盐酸处理的金黄色葡萄球菌 [AC] 也诱导家蚕血液黑化。经盐酸处理的金黄色葡萄球菌 [AC] 的家蚕血液黑化活性被金黄色葡萄球菌 [AC] 的蛋白酶处理所抑制。这些结果表明,金黄色葡萄球菌的酸化处理在家蚕中诱导先天免疫激活,并且金黄色葡萄球菌蛋白参与家蚕先天免疫的诱导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/11139275/53013ba64b55/pone.0298502.g001.jpg

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