Suppr超能文献

鲍曼不动杆菌与大鼠模型中的骨髓炎无关:一项初步研究。

Acinetobacter baumannii is not associated with osteomyelitis in a rat model: a pilot study.

机构信息

Division of Geographic Medicine and Infectious Diseases, Tufts Medical Center, Tufts University, Boston, MA, USA.

出版信息

Clin Orthop Relat Res. 2011 Jan;469(1):274-82. doi: 10.1007/s11999-010-1488-0. Epub 2010 Jul 29.

Abstract

BACKGROUND

Multidrug resistant Acinetobacter baumannii (MDR AB) with and without Staphylococcus aureus (SA) is a commonly isolated organism in infected segmental bone defects in combat-related trauma in Iraq and Afghanistan. Although MDR AB in visceral infections is a therapeutic challenge, control of infection appears more common for combat-related osteomyelitis.

QUESTIONS/PURPOSES: Using a rat model, we explored the virulence of MDR AB in segmental bone defects alone and in combination with SA.

METHODS

Segmental defects in 60 rat femurs were created, stabilized, and inoculated with MDR AB alone and 60 with MDR AB and SA. We performed qualitative and quantitative bacteriology and radiographic assessments at 2, 4, and 8 weeks for MDR AB and at 1, 2, and 3 weeks for MDR AB and SA.

RESULTS

Quantitative bacteriology revealed a 3- to 5-log decrease in MDR AB from the initial inoculum. After polymicrobial inoculation, only 10 of 60 animals had positive cultures for MDR AB, whereas 59 of 60 animals had positive cultures for SA. Recovered SA were 2 to 5 log greater than the initial inoculum, while there again was a 3- to 5-log decrease in MDR AB. MDR AB alone did not cause bony lysis, but there was radiographic evidence of new bone formation in 67% of the segmental defects. Osteolysis was noted with MDR AB and SA.

CONCLUSIONS

MDR AB did not appear to cause or contribute to clinically apparent osteomyelitis in this pilot study.

CLINICAL RELEVANCE

Resolution of infections in combat-related segmental bone defects inoculated with MDR AB may be attributable to low virulence. Additional studies are needed to confirm low virulence and bone formation with MDR AB.

摘要

背景

在伊拉克和阿富汗与战斗相关的创伤中,感染性节段性骨缺损中经常分离出耐多药鲍曼不动杆菌(MDR AB)和金黄色葡萄球菌(SA)。尽管内脏感染中的 MDR AB 是治疗上的挑战,但与战斗相关的骨髓炎似乎更容易控制感染。

问题/目的:我们使用大鼠模型,单独和组合 SA 研究 MDR AB 在节段性骨缺损中的毒力。

方法

在 60 只大鼠股骨中创建节段性缺损,稳定并接种 MDR AB 单独和 60 只 MDR AB 和 SA。我们对 MDR AB 进行定性和定量细菌学和放射学评估,时间为 2、4 和 8 周,对 MDR AB 和 SA 进行评估的时间为 1、2 和 3 周。

结果

定量细菌学显示 MDR AB 从初始接种物减少了 3-5 对数级。在混合接种后,仅 60 只动物中有 10 只 MDR AB 培养阳性,而 60 只动物中有 59 只 SA 培养阳性。回收的 SA 比初始接种物高 2-5 个对数级,而 MDR AB 再次减少了 3-5 个对数级。MDR AB 单独不会引起骨溶解,但在 67%的节段性缺损中有新骨形成的放射学证据。在 MDR AB 和 SA 中观察到溶骨性。

结论

在这项初步研究中,MDR AB 似乎不会引起或导致临床上明显的骨髓炎。

临床相关性

在接种 MDR AB 的与战斗相关的节段性骨缺损感染中,感染的解决可能归因于低毒力。需要进一步的研究来证实 MDR AB 的低毒力和骨形成。

相似文献

1
Acinetobacter baumannii is not associated with osteomyelitis in a rat model: a pilot study.
Clin Orthop Relat Res. 2011 Jan;469(1):274-82. doi: 10.1007/s11999-010-1488-0. Epub 2010 Jul 29.
2
Bioburden Increases Heterotopic Ossification Formation in an Established Rat Model.
Clin Orthop Relat Res. 2015 Sep;473(9):2840-7. doi: 10.1007/s11999-015-4272-3.
3
Characterization of a chronic infection in an internally-stabilized segmental defect in the rat femur.
J Orthop Res. 2005 Jul;23(4):816-23. doi: 10.1016/j.orthres.2005.01.009. Epub 2005 Apr 7.
5
A rabbit osteomyelitis model to simulate multibacterial war wound infections.
Mil Med. 2013 Jun;178(6):696-700. doi: 10.7205/MILMED-D-12-00550.
9
The Role of MDR-Acinetobacter baumannii in Orthopedic Surgical Site Infections.
Surg Infect (Larchmt). 2015 Oct;16(5):518-22. doi: 10.1089/sur.2014.187. Epub 2015 Jun 26.

引用本文的文献

1
Choosing the right animal model for osteomyelitis research: Considerations and challenges.
J Orthop Translat. 2023 Nov 29;43:47-65. doi: 10.1016/j.jot.2023.10.001. eCollection 2023 Nov.
2
Skeletal infections: microbial pathogenesis, immunity and clinical management.
Nat Rev Microbiol. 2022 Jul;20(7):385-400. doi: 10.1038/s41579-022-00686-0. Epub 2022 Feb 15.
3
Staphylococcus aureus and Acinetobacter baumannii Inhibit Osseointegration of Orthopedic Implants.
Infect Immun. 2022 Mar 17;90(3):e0066921. doi: 10.1128/iai.00669-21. Epub 2022 Jan 31.
4
The Mechanisms of Disease Caused by .
Front Microbiol. 2019 Jul 17;10:1601. doi: 10.3389/fmicb.2019.01601. eCollection 2019.
5
Osteomyelitis due to multiple rare infections in a patient with idiopathic CD4 lymphocytopenia.
Intractable Rare Dis Res. 2017 Aug;6(3):206-210. doi: 10.5582/irdr.2017.01029.
6
A composite critical-size rabbit mandibular defect for evaluation of craniofacial tissue regeneration.
Nat Protoc. 2016 Oct;11(10):1989-2009. doi: 10.1038/nprot.2016.122. Epub 2016 Sep 22.
8
Bioburden Increases Heterotopic Ossification Formation in an Established Rat Model.
Clin Orthop Relat Res. 2015 Sep;473(9):2840-7. doi: 10.1007/s11999-015-4272-3.
10
A silver ion-doped calcium phosphate-based ceramic nanopowder-coated prosthesis increased infection resistance.
Clin Orthop Relat Res. 2013 Aug;471(8):2532-9. doi: 10.1007/s11999-013-2894-x.

本文引用的文献

1
Infectious complications of damage control orthopedics in war trauma.
J Trauma. 2009 Oct;67(4):758-61. doi: 10.1097/TA.0b013e3181af6aa6.
4
Osteomyelitis in military personnel wounded in Iraq and Afghanistan.
J Trauma. 2008 Feb;64(2 Suppl):S163-8; discussion S168. doi: 10.1097/TA.0b013e318160868c.
5
Multidrug-resistant Acinetobacter baumannii osteomyelitis from Iraq.
Emerg Infect Dis. 2008 Mar;14(3):512-4. doi: 10.3201/eid1403.070128.
7
Impact of multi-drug-resistant Acinetobacter baumannii on clinical outcomes.
Eur J Clin Microbiol Infect Dis. 2007 Nov;26(11):793-800. doi: 10.1007/s10096-007-0371-8.
8
Infectious complications of open type III tibial fractures among combat casualties.
Clin Infect Dis. 2007 Aug 15;45(4):409-15. doi: 10.1086/520029. Epub 2007 Jul 5.
10
Bacteriology of war wounds at the time of injury.
Mil Med. 2006 Sep;171(9):826-9. doi: 10.7205/milmed.171.9.826.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验