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金黄色葡萄球菌宿主相互作用和适应。

Staphylococcus aureus host interactions and adaptation.

机构信息

Centre for Pathogen Genomics, The University of Melbourne, Melbourne, Victoria, Australia.

Department of Microbiology and Immunology, The University of Melbourne, The Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia.

出版信息

Nat Rev Microbiol. 2023 Jun;21(6):380-395. doi: 10.1038/s41579-023-00852-y. Epub 2023 Jan 27.


DOI:10.1038/s41579-023-00852-y
PMID:36707725
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9882747/
Abstract

Invasive Staphylococcus aureus infections are common, causing high mortality, compounded by the propensity of the bacterium to develop drug resistance. S. aureus is an excellent case study of the potential for a bacterium to be commensal, colonizing, latent or disease-causing; these states defined by the interplay between S. aureus and host. This interplay is multidimensional and evolving, exemplified by the spread of S. aureus between humans and other animal reservoirs and the lack of success in vaccine development. In this Review, we examine recent advances in understanding the S. aureus-host interactions that lead to infections. We revisit the primary role of neutrophils in controlling infection, summarizing the discovery of new immune evasion molecules and the discovery of new functions ascribed to well-known virulence factors. We explore the intriguing intersection of bacterial and host metabolism, where crosstalk in both directions can influence immune responses and infection outcomes. This Review also assesses the surprising genomic plasticity of S. aureus, its dualism as a multi-mammalian species commensal and opportunistic pathogen and our developing understanding of the roles of other bacteria in shaping S. aureus colonization.

摘要

金黄色葡萄球菌感染很常见,死亡率很高,而且该细菌容易产生耐药性,使情况更加复杂。金黄色葡萄球菌是一种很好的研究案例,说明了细菌有可能成为共生菌、定殖菌、潜伏菌或致病菌;这些状态是由金黄色葡萄球菌和宿主之间的相互作用决定的。这种相互作用是多方面的,不断发展的,例如金黄色葡萄球菌在人类和其他动物宿主之间的传播,以及疫苗开发的缺乏成功,就是例证。在这篇综述中,我们研究了理解导致感染的金黄色葡萄球菌-宿主相互作用的最新进展。我们重新审视了中性粒细胞在控制感染中的主要作用,总结了新的免疫逃逸分子的发现,以及赋予已知毒力因子的新功能的发现。我们探讨了细菌和宿主代谢之间令人着迷的交叉点,其中双向的串扰可以影响免疫反应和感染结果。这篇综述还评估了金黄色葡萄球菌令人惊讶的基因组可塑性,它作为一种多哺乳动物共生菌和机会性病原体的双重性,以及我们对其他细菌在塑造金黄色葡萄球菌定植中的作用的不断发展的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dff/9882747/239a97b0034e/41579_2023_852_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dff/9882747/379c9a6996c6/41579_2023_852_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dff/9882747/8cb152ec33b3/41579_2023_852_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dff/9882747/c9cc89705849/41579_2023_852_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dff/9882747/239a97b0034e/41579_2023_852_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dff/9882747/379c9a6996c6/41579_2023_852_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dff/9882747/8cb152ec33b3/41579_2023_852_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dff/9882747/c9cc89705849/41579_2023_852_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dff/9882747/239a97b0034e/41579_2023_852_Fig4_HTML.jpg

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本文引用的文献

[1]
Non-protective immune imprint underlies failure of Staphylococcus aureus IsdB vaccine.

Cell Host Microbe. 2022-8-10

[2]
Niche-specific genome degradation and convergent evolution shaping adaptation during severe infections.

Elife. 2022-6-14

[3]
Staphylococcal Complement Evasion Protein Sbi Stabilises C3d Dimers by Inducing an N-Terminal Helix Swap.

Front Immunol. 2022

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Whole-genome and transcriptome analysis enhances precision cancer treatment options.

Ann Oncol. 2022-9

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Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin.

Science. 2022-6-17

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Genome wide association study of Escherichia coli bloodstream infection isolates identifies genetic determinants for the portal of entry but not fatal outcome.

PLoS Genet. 2022-3

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Infect Immun. 2022-4-21

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Clin Microbiol Infect. 2022-7

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Proc Natl Acad Sci U S A. 2022-1-25

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Species-Scale Genomic Analysis of Staphylococcus aureus Genes Influencing Phage Host Range and Their Relationships to Virulence and Antibiotic Resistance Genes.

mSystems. 2022-2-22

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