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回顾P30黏附蛋白的研究进展为未来的诊断和治疗提供了思路。

Reviewing advancement in P30 adhesin protein provides insights for future diagnosis and treatment.

作者信息

Zuo Yingying, Zhang Ru, Li Shuihong

机构信息

Hengyang Medical School, University of South China, Hengyang, China.

The Seventh Affiliated Hospital of University of South China, Changsha, China.

出版信息

Front Microbiol. 2024 Dec 13;15:1515291. doi: 10.3389/fmicb.2024.1515291. eCollection 2024.

DOI:10.3389/fmicb.2024.1515291
PMID:39735188
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11671514/
Abstract

is a major pathogen that causes upper and lower respiratory tract infections in children, adolescents, and elderly individuals and can lead to pneumonia, intrapulmonary and extrapulmonary complications, and respiratory sequelae. must adhere to respiratory epithelial cells of a host for infection. The P1 and P30 proteins, as two adhesin proteins of , have attracted extensive attention from many researchers. In this paper, we present the latest research progress on the P30 protein in terms of structure and mutation typing, physiological function, clinical serological diagnosis and vaccine development in a literature review. This study deepens our knowledge on the pathogenesis of and is useful for diagnosing and preventing infection.

摘要

是一种主要病原体,可导致儿童、青少年和老年人的上呼吸道和下呼吸道感染,并可引发肺炎、肺内和肺外并发症以及呼吸后遗症。 必须粘附于宿主的呼吸道上皮细胞才能进行感染。P1和P30蛋白作为 的两种粘附蛋白,已引起众多研究人员的广泛关注。在本文中,我们通过文献综述介绍了P30蛋白在结构和突变分型、生理功能、临床血清学诊断及疫苗研发方面的最新研究进展。本研究加深了我们对 发病机制的认识,有助于 感染的诊断和预防。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8075/11671514/f4e01d3a247a/fmicb-15-1515291-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8075/11671514/dcab086ded66/fmicb-15-1515291-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8075/11671514/acb5218a00a6/fmicb-15-1515291-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8075/11671514/d094d1d8d87b/fmicb-15-1515291-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8075/11671514/65749dd061a4/fmicb-15-1515291-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8075/11671514/198eee768067/fmicb-15-1515291-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8075/11671514/f4e01d3a247a/fmicb-15-1515291-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8075/11671514/dcab086ded66/fmicb-15-1515291-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8075/11671514/acb5218a00a6/fmicb-15-1515291-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8075/11671514/d094d1d8d87b/fmicb-15-1515291-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8075/11671514/65749dd061a4/fmicb-15-1515291-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8075/11671514/198eee768067/fmicb-15-1515291-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8075/11671514/f4e01d3a247a/fmicb-15-1515291-g006.jpg

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Chained Structure of Dimeric F-like ATPase in Mycoplasma mobile Gliding Machinery.二聚 F 型 ATP 酶在黏体支原体滑行机制中的链式结构。
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Immunodominant proteins P1 and P40/P90 from human pathogen Mycoplasma pneumoniae.来自人类病原体肺炎支原体的免疫优势蛋白 P1 和 P40/P90。
Nat Commun. 2020 Oct 14;11(1):5188. doi: 10.1038/s41467-020-18777-y.
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Distinct Mycoplasma pneumoniae Interactions with Sulfated and Sialylated Receptors.肺炎支原体与硫酸化和唾液酸化受体的独特相互作用。
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