NATURE REVIEWS MICROBIOLOGY自然综述：微生物学
NATURE REVIEWS MICROBIOLOGY(英文缩写 NAT REV MICROBIOL),ISSN 1740-1526,eISSN 1740-1534,中文译名:自然综述：微生物学 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。
发文量统计区间：2025-09-27 至 2026-09-27，按本站收录文献的发表日期统计。
期刊介绍
历年影响因子趋势
| JCR 数据年份 | 影响因子 | JCR 分区 |
|---|---|---|
| 2021 | 78.297 | Q1 |
| 2022 | 88.100 | Q1 |
| 2023 | 69.200 | Q1 |
| 2024 | 103.300 | Q1 |
| 2025 | 104.600 | Q1 |
NATURE REVIEWS MICROBIOLOGY 最新收录文献
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7. Klebsiella genus as driver of human disease: from infections to non-communicable disorders.
PMID:日期:2026-10-01Klebsiella spp. are pathobionts associated with acute infections, including pneumonia and infections in the urinary tract and bloodstream, often acquired in health-care settings. They represent a global threat owing to the prevalence of multidrug-resistant strains. Moreover, Klebsiella spp., similarly to other members of the human gut microbiota, can contribute to the pathogenesis of non-communicable disorders. In this Review, we describe the taxonomical and molecular characteristics of the Klebsiella genus, as well as its epidemiology and impact as an infectious agent. We also review current evidence that associates Klebsiella spp. with different non-communicable disorders, including chronic inflammatory and metabolic disorders and cancer. We discuss different approaches to target Klebsiella spp., including tailored antibiotics, faecal microbiota transplantation, live biotherapeutic products and bacteriophages. Finally, we discuss the importance of preventative measures, such as epidemiological surveillance, infection control practices and lifestyle interventions, to reduce the spread of Klebsiella spp. in health-care settings and the broader community.
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8. Antimicrobial stewardship in LMICs: from paper promises to purpose-driven people.
PMID:日期:2026-10-01该文献暂无摘要。
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9. Mechanisms of HIV-1 assembly, release and maturation.
PMID:日期:2026-10-01Over the past decade, major advances in structural biology and in vitro and cell-based technologies have enhanced our understanding of HIV-1 assembly, release and maturation. The cryo-electron microscopy revolution, alongside developments in single-molecule approaches and live-cell imaging techniques, have enabled researchers to visualize biological complexes at remarkably high resolution, reconstitute biochemical processes under physiologically relevant conditions and directly observe these processes in cells and virions. Effective integration of these methods with both classical and novel molecular virology approaches has yielded a wealth of basic knowledge that has driven the development of potent inhibitors targeting virus maturation and highlighted mechanisms by which events that take place late in the virus replication cycle prime newly formed virus particles for infection of a new host cell. This Review outlines the recent progress in elucidating the molecular underpinnings of the late stages of the HIV-1 replication cycle and highlights the interplay between virology, host cell biology and the development of antiretroviral compounds with therapeutic potential.
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10. Infection cycles of viruses of the phylum Nucleocytoviricota.
PMID:日期:2026-10-01The phylum Nucleocytoviricota, formerly known as nucleocytoplasmic large DNA viruses (NCLDVs), comprises evolutionarily related viruses with remarkably diverse genome sizes, coding capacities and virion morphologies. These viruses infect hosts across the eukaryotic tree of life, from protists to humans, and are believed to have emerged during the early stages of eukaryotic evolution. How the basic aspects of virus-host interaction have evolved in different lineages and whether they share a conserved infection cycle remain unclear. In this Review, we synthesize the information on the infection cycles of model representatives from the major orders within the phylum, revealing both shared traits and lineage-specific innovations. We compare the information available for the extensively studied poxviruses, asfiviruses, iridoviruses and chloroviruses with insights from the rapidly expanding literature on the mimiviruses, pandoraviruses, marseilleviruses and pithoviruses. We provide an overview of the molecular details underlying the key stages of Nucleocytoviricota infection cycles: entry via membrane fusion, formation of viral factories organized via phase separation, genome replication, virion morphogenesis through a crescent intermediate, and egress. We highlight outstanding questions in the field, unify concepts across traditionally separated research areas, and provide a conceptual framework to guide future cell biology studies on large double-stranded DNA viruses.