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无细胞培养对从囊性纤维化患者中分离出的细菌病原体的影响:及研究。

Effect of cell-free culture on bacterial pathogens isolated from cystic fibrosis patients: and studies.

作者信息

Abán Carla Luciana, Orosco Silvia, Argañaraz Aybar Julio Nicolás, Albarracín Leonardo, Venecia Analía, Perret Liliana, Ortiz Mayor Sonia, Nishiyama Keita, Valdéz Juan Carlos, Kitazawa Haruki, Villena Julio, Gobbato Nadia

机构信息

National Council of Scientific and Technological Research (CONICET)-CCT (Salta-Jujuy), Salta, Argentina.

Pneumonology Department, Niño Jesus Children Hospital, SIPROSA, Tucuman, Argentina.

出版信息

Front Microbiol. 2024 Sep 16;15:1440090. doi: 10.3389/fmicb.2024.1440090. eCollection 2024.

DOI:10.3389/fmicb.2024.1440090
PMID:39351305
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11439784/
Abstract

This study aimed to investigate the effects of the cell-free supernatant of ATCC 10241 on the biofilm-forming capacity of strains isolated from cystic fibrosis (CF) patients. In addition, the study evaluated the potential of the cell-free supernatant to modulate inflammation and reduce lung damage in mice infected with strains or co-challenged with and the group (SMG). The results showed that CF-derived strains can infect the respiratory tract of adult mice, inducing local inflammation and lung damage. The severity of these infections was exacerbated when was co-administered with SMG. Notably, nebulization with the cell-free supernatant of produced beneficial effects, reducing respiratory infection severity and inflammatory responses induced by , both alone or in combination with SMG. Reduced bacterial loads and lung damage were observed in supernatant-treated mice compared to controls. Although further mechanistic studies are necessary, the results show that the cell-free supernatant of ATCC 10241 is an interesting adjuvant alternative to treat respiratory infections and superinfections in CF patients.

摘要

本研究旨在调查ATCC 10241的无细胞上清液对从囊性纤维化(CF)患者分离出的菌株生物膜形成能力的影响。此外,该研究评估了无细胞上清液调节炎症以及减轻感染该菌株或与该菌株和SMG组共同攻击的小鼠肺部损伤的潜力。结果表明,源自CF的菌株可感染成年小鼠的呼吸道,引发局部炎症和肺部损伤。当与SMG共同给药时,这些感染的严重程度会加剧。值得注意的是,用ATCC 10241的无细胞上清液进行雾化产生了有益效果,降低了单独或与SMG联合使用时由该菌株引起的呼吸道感染严重程度和炎症反应。与对照组相比,在上清液处理的小鼠中观察到细菌载量和肺部损伤减少。尽管需要进一步的机制研究,但结果表明,ATCC 10241的无细胞上清液是治疗CF患者呼吸道感染和重叠感染的一种有趣的辅助替代品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/9b9ee6a6d6b7/fmicb-15-1440090-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/9dbe53e22387/fmicb-15-1440090-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/c2431a9f7554/fmicb-15-1440090-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/12b571b28d2b/fmicb-15-1440090-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/2fe382b02ce0/fmicb-15-1440090-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/41a1a0f8cea4/fmicb-15-1440090-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/bfb24e3a2bb2/fmicb-15-1440090-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/89c77df86c2d/fmicb-15-1440090-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/75f0b0dcf414/fmicb-15-1440090-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/9b9ee6a6d6b7/fmicb-15-1440090-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/9dbe53e22387/fmicb-15-1440090-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/c2431a9f7554/fmicb-15-1440090-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/12b571b28d2b/fmicb-15-1440090-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/2fe382b02ce0/fmicb-15-1440090-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/41a1a0f8cea4/fmicb-15-1440090-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/bfb24e3a2bb2/fmicb-15-1440090-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/89c77df86c2d/fmicb-15-1440090-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/75f0b0dcf414/fmicb-15-1440090-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff83/11439784/9b9ee6a6d6b7/fmicb-15-1440090-g0009.jpg

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Microbes Infect. 2024 May-Jun;26(4):105301. doi: 10.1016/j.micinf.2024.105301. Epub 2024 Jan 17.
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Immunobiotic FFIG58 Confers Long-Term Protection against .免疫生物制剂 FFIG58 提供针对. 的长期保护。
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Post-immunobiotics increase resistance to primary respiratory syncytial virus infection and secondary pneumococcal pneumonia.免疫后生物活性物质可增强对原发性呼吸道合胞病毒感染和继发性肺炎球菌肺炎的抵抗力。
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