实验动物与比较医学

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金黄色葡萄球菌4种感染疾病动物模型的研究进展

许静茹1,2(), 范思思1,2, 丘淑琪1, 闫娜娜1()(), 范克伟1   

  1. 1. 龙岩学院生命科学学院 福建省家畜传染病防控与生物技术重点实验室, 龙岩 364000
    2. 福建农林大学动物科学学院, 福州 350002
  • 出版日期:2026-09-07
  • 通讯作者:
    闫娜娜(1995—),女,博士,讲师,研究方向:动物病原学与免疫学。E-mail: 。ORCID: 0000-0001-8550-2816;
  • 作者简介:

    许静茹(2002—),女,硕士,研究方向:动物病原学与免疫学。E-mail:

  • 基金资助:
    福建省第四批“创新之星”人才项目(闽科专函〔2023〕110号); 福建省科技计划项目“基于GEM表面展示技术的新型PEDV亚单位疫苗研究与开发”(2020N5012); 福建省林业科技项目“福建梅花山虎园野生动物疫源疫病本底调查、监测预警及防控技术研究”(2024FKJ06); 龙岩市科技创新联合资金社会发展科技项目“华南虎源猪圆环病毒流行病学调查及跨物种传播风险评估”(2023LYF17119); 新罗区产学研科技联合创新项目“猪源性重要人兽共患病原菌的监测与感染风险评估”(2022XLXYZ009)

Research Progress on Animal Models of Four Staphylococcus aureus Infection

XU Jingru1,2(), FAN Sisi1,2, QIU Shuqi1, YAN Nana1()(), FAN Kewei1   

  1. 1. Fujian Provincial Key Laboratory for Prevention and Control of Animal Infectious Diseases and Biotechnology, College of Life Sciences, Longyan University, Longyan 364000, China
    2. College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou 350002, China
  • Published:2026-09-07
  • Correspondence to:
    YAN Nana (ORCID:0000-0001-8550-2816), E-mail: ;

摘要:

金黄色葡萄球菌(Staphylococcus aureusS. aureus)是一种临床高发的革兰氏阳性致病菌,可导致皮肤软组织感染、肺炎、败血症及心内膜炎等疾病。耐甲氧西林金黄色葡萄球菌(Methicillin-resistant Staphylococcus aureus,MRSA)等耐药表型的出现与流行使临床治疗面临巨大挑战。动物模型是深入解析其致病机制、耐药机制与评估新型抗感染策略的重要工具。皮肤软组织感染模型、骨髓炎与植入物相关感染模型、肺炎模型以及心内膜炎模型作为金黄色葡萄球菌感染研究中四类成熟的常见模型,本文系统阐述了这四类模型的实验动物选择依据、主流建模方法、应用场景以及各自的优势与局限。模型常用动物包括小鼠、大鼠、兔、猪等;皮肤软组织感染模型造模快、成本低,但难以模拟复杂的慢性病灶;骨髓炎与内置物相关感染模型多用于模拟细菌生物膜形成及慢性感染,肺炎模型多用于研究急性肺损伤与药效评价;感染性心内膜炎模型多用于研究赘生物形成与深部感染药效。但这些现有模型普遍存在缺陷,实验动物与人类免疫系统存在固有差异,多数动物模型因采用高接种剂量和短周期,难以完全复现临床慢性感染过程等。未来可通过发展人源化及器官芯片等体外系统克服物种差异,整合共病因素以提升临床相关性,并采用多模态动态评估与伦理替代方案。本综述旨在为合理选择、优化和应用金黄色葡萄球菌感染动物模型提供系统的理论参考,以推动抗感染研究。

关键词: 金黄色葡萄球菌, 动物模型, 致病机制, 耐药性, 防治策略

Abstract:

Staphylococcus aureus is a highly prevalent Gram-positive pathogenic bacterium in clinical settings, capable of causing skin and soft tissue infections, pneumonia, sepsis, endocarditis and other illnesses. The emergence and spread of drug-resistant phenotypes such as methicillin-resistant Staphylococcus aureus (MRSA) have posed formidable challenges to clinical treatment. Animal models serve as vital tools for dissecting its pathogenic and resistance mechanisms, as well as evaluating novel anti-infective strategies. Four well-established and widely adopted models for S. aureus infection research include skin and soft tissue infection models, osteomyelitis and implant-associated infection models, pneumonia models, and infective endocarditis models. This review systematically elaborates on animal selection criteria, mainstream modeling protocols, application scenarios, and the respective advantages and limitations of these four model types. Common experimental animals encompass mice, rats, rabbits, pigs and so forth. Skin and soft tissue infection models feature rapid construction and low costs yet fail to recapitulate complex chronic lesions. Osteomyelitis and implant-associated infection models are primarily utilized to mimic bacterial biofilm formation and chronic infection, while pneumonia models are applied to investigate acute lung injury and assess drug efficacy. Infective endocarditis models are suitable for exploring vegetation formation and therapeutic effects against deep-seated infection. Nevertheless, current models share inherent drawbacks: there are innate discrepancies in immune system composition and response between laboratory animals and humans, and most models adopt high bacterial inoculation doses with short experimental cycles, making full recapitulation of clinical chronic infection unachievable. Future improvements can be realized by developing humanized animal models and organ-on-a-chip in vitro systems to bridge interspecies gaps, incorporating comorbidities to boost clinical relevance, and implementing multimodal dynamic assessment alongside ethical alternative approaches. This review provides systematic theoretical references for the rational selection, optimization and application of animal models of S. aureus infection, so as to facilitate anti-infective research progress.

Key words: Staphylococcus aureus, Animal model, Pathogenic mechanism, Drug resistance, Prevention and control strategies

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