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金黄色葡萄球菌感染糖尿病溃疡的优化小鼠模型。

An optimized mouse model of Staphylococcus aureus infected diabetic ulcers.

机构信息

School of Medicine, Life and Health Sciences Research Institute (ICVS), University of Minho, Campus de Gualtar, 4710-057, Braga, Portugal.

ICVS/3B's-PT Government Associate Laboratory, Braga, Guimarães, Portugal.

出版信息

BMC Res Notes. 2022 Sep 7;15(1):293. doi: 10.1186/s13104-022-06170-5.

DOI:10.1186/s13104-022-06170-5
PMID:36071445
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9450231/
Abstract

OBJECTIVE

Diabetic foot infection (DFI) represents a major healthcare burden, for which treatment is challenging owing to the pathophysiological alterations intrinsic to diabetes and the alarming increase of antimicrobial resistance. Novel therapies targeting DFI are therefore a pressing research need for which proper models of disease are required.

RESULTS

Here, we present an optimized diabetic mouse model of methicillin-resistant Staphylococcus aureus (MRSA)-infected wounds, that resemble key features of DFI, such as pathogen invasion through wound bed and surrounding tissue, necrosis, persistent inflammation and impaired wound healing. Thus, in a time-efficient manner and using simple techniques, this model represents a suitable approach for studying emerging therapies targeting DFI caused by MRSA.

摘要

目的

糖尿病足感染(DFI)是一个主要的医疗保健负担,由于糖尿病内在的病理生理改变以及抗菌药物耐药性的惊人增加,治疗具有挑战性。因此,针对 DFI 的新型治疗方法是迫切需要研究的,这需要有适当的疾病模型。

结果

在这里,我们提出了一种优化的耐甲氧西林金黄色葡萄球菌(MRSA)感染伤口的糖尿病小鼠模型,该模型类似于 DFI 的关键特征,如病原体通过伤口床和周围组织的入侵、坏死、持续炎症和受损的伤口愈合。因此,这种模型以高效的方式并使用简单的技术,代表了研究针对由 MRSA 引起的 DFI 的新兴治疗方法的合适方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7dc/9450231/6c4e36412d5a/13104_2022_6170_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7dc/9450231/ae0ad6b1e567/13104_2022_6170_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7dc/9450231/6c4e36412d5a/13104_2022_6170_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7dc/9450231/ae0ad6b1e567/13104_2022_6170_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7dc/9450231/6c4e36412d5a/13104_2022_6170_Fig2_HTML.jpg

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本文引用的文献

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Biology (Basel). 2021 Apr 26;10(5):372. doi: 10.3390/biology10050372.
2
PB@PDA@Ag nanosystem for synergistically eradicating MRSA and accelerating diabetic wound healing assisted with laser irradiation.用于协同根除耐甲氧西林金黄色葡萄球菌并在激光照射辅助下加速糖尿病伤口愈合的PB@PDA@Ag纳米系统。
Biomaterials. 2020 Jun;243:119936. doi: 10.1016/j.biomaterials.2020.119936. Epub 2020 Mar 3.
3
Protocol to Create Chronic Wounds in Diabetic Mice.
Trichophyton mentagrophytes delays wound healing in ob/ob mice.
须癣毛癣菌会延迟ob/ob小鼠的伤口愈合。
Int Wound J. 2024 Dec;21(12):e70118. doi: 10.1111/iwj.70118.
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Gellan gum spongy-like hydrogel-based dual antibiotic therapy for infected diabetic wounds.基于结冷胶海绵状水凝胶的双重抗生素疗法治疗感染性糖尿病伤口。
Bioeng Transl Med. 2023 Mar 21;8(3):e10504. doi: 10.1002/btm2.10504. eCollection 2023 May.
在糖尿病小鼠中创建慢性伤口的方案。
J Vis Exp. 2019 Sep 25(151). doi: 10.3791/57656.
4
Emergence of community-acquired methicillin-resistant Staphylococcus aureus EMRSA-15 clone as the predominant cause of diabetic foot ulcer infections in Portugal.社区获得性耐甲氧西林金黄色葡萄球菌 EMRSA-15 克隆的出现成为葡萄牙糖尿病足溃疡感染的主要原因。
Eur J Clin Microbiol Infect Dis. 2020 Jan;39(1):179-186. doi: 10.1007/s10096-019-03709-6. Epub 2019 Oct 10.
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