• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Wistar 大鼠慢性暗色丝孢霉病模型的构建。

A chronic chromoblastomycosis model by Fonsecaea monophora in Wistar rat.

机构信息

Department of Dermatology, the Second Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.

出版信息

Med Mycol. 2010 Feb;48(1):201-6. doi: 10.3109/13693780902785320.

DOI:10.3109/13693780902785320
PMID:19255903
Abstract

Chromoblastomycosis is a chronic, cutaneous and subcutaneous infection characterized by verrucose lesions. It is primarily caused by Fonsecaea monophora in southern China and responds poorly to available therapies. In order to investigate the pathogenicity of Fonsecaea monophora, we established a chronic chromoblastomycosis animal model in Wistar rats. Suspensions of 2x10(6) cfu conidia and hyphal fragments were intracutaneous (ic) and subcutaneous (sc) on either side of the backs of the rats. Small nodules were formed at the inoculation sites within the first week after inoculation. By the second week, the nodules had enlarged and become soft, and pus could be aspirated from them. In the fourth week, the nodules in the ic inoculated group had ulcerated and sclerotic bodies were observed in smears prepared from all animals. In the 3rd month after inoculation, the nodules at the sites of the ic inoculation had become flat, with a thin black crust on the surface. For the ic inoculated group, sequential biopsy studies revealed extensive necrosis with neutrophil infiltration and sclerotic bodies and some debris of fungi in the 1st month, sclerotic bodies inside multinucleated giant cells by the 2nd month and widespread granulomatous inflammations in the 3rd month.

摘要

着色芽生菌病是一种慢性皮肤和皮下感染,其特征为疣状病变。它主要由中国南方的单端孢霉引起,对现有疗法反应不佳。为了研究单端孢霉的致病性,我们在 Wistar 大鼠中建立了慢性着色芽生菌病动物模型。在大鼠背部两侧的皮内(ic)和皮下(sc)接种 2x10(6)cfu 分生孢子和菌丝片段的悬浮液。接种后第一周内接种部位形成小结节。到第二周,结节已经增大并且变软,可以从其中抽吸脓液。第四周时,ic 接种组的结节已经溃疡,并且从所有动物制备的涂片上观察到硬化体。接种后 3 个月,ic 接种部位的结节变得平坦,表面有一层薄薄的黑色结痂。对于 ic 接种组,连续活检研究显示第 1 个月广泛的坏死伴中性粒细胞浸润和硬化体,以及一些真菌碎片,第 2 个月在多核巨细胞内有硬化体,第 3 个月广泛的肉芽肿性炎症。

相似文献

1
A chronic chromoblastomycosis model by Fonsecaea monophora in Wistar rat.Wistar 大鼠慢性暗色丝孢霉病模型的构建。
Med Mycol. 2010 Feb;48(1):201-6. doi: 10.3109/13693780902785320.
2
Chromoblastomycosis due to Fonsecaea monophora in a man with nephritic syndrome.由单端孢霉引起的暗色丝孢霉病于肾病综合征患者。
Mycopathologia. 2015 Jun;179(5-6):447-52. doi: 10.1007/s11046-014-9856-z. Epub 2015 Jan 10.
3
Local phagocytic responses after murine infection with different forms of Fonsecaea pedrosoi and sclerotic bodies originating from an inoculum of conidiogenous cells.不同形式的佩德罗索外瓶霉感染鼠后局部吞噬反应和来自分生孢子细胞接种物的硬化体。
Mycoses. 2011 May;54(3):202-11. doi: 10.1111/j.1439-0507.2009.01792.x.
4
Chromoblastomycosis caused by a meristematic mutant of Fonsecaea monophora.由单孢瓶霉的分生组织突变体引起的着色芽生菌病。
Med Mycol. 2009 Feb;47(1):77-80. doi: 10.1080/13693780802322588. Epub 2008 Sep 15.
5
Chromoblastomycosis due to Fonsecaea pedrosoi: an old wine in a rare bottle.裴氏瓶霉引起的着色芽生菌病:珍稀瓶中的陈酿。
J Infect Dev Ctries. 2015 Mar 15;9(3):325-9. doi: 10.3855/jidc.5312.
6
Molecular diversity of Fonsecaea (Chaetothyriales) causing chromoblastomycosis in southern China.在中国南方引起着色芽生菌病的瓶霉属(座囊菌目)的分子多样性
Med Mycol. 2009 Feb;47(1):27-33. doi: 10.1080/13693780802468209. Epub 2008 Oct 25.
7
Successful treatment of chromoblastomycosis of 36 years duration caused by Fonsecaea monophora.成功治疗由单端孢霉引起的 36 年病程的着色芽生菌病。
Med Mycol. 2010 Mar;48(2):390-3. doi: 10.1080/13693780903008813.
8
Chromoblastomycosis caused by Fonsecaea: clinicopathology, susceptibility and molecular identification of seven consecutive cases in Southern China.中国南方地区由 Fonsecaea 引起的着色芽生菌病:七例连续病例的临床病理、易感性和分子鉴定。
Clin Microbiol Infect. 2013 Nov;19(11):1023-8. doi: 10.1111/1469-0691.12067. Epub 2012 Nov 15.
9
Molecular identification of chromoblastomycosis clinical isolates in Guangdong.广东着色芽生菌病临床分离株的分子鉴定
Med Mycol. 2017 Nov 1;55(8):851-858. doi: 10.1093/mmy/myw140.
10
Successful treatment for chromoblastomycosis caused by Fonsecaea monophora: a report of three cases in Guangdong, China.单孢瓶霉引起的着色芽生菌病的成功治疗:中国广东三例报告
Mycoses. 2009 Mar;52(2):176-81. doi: 10.1111/j.1439-0507.2008.01547.x. Epub 2008 Jun 21.

引用本文的文献

1
Reviewing the Etiologic Agents, Microbe-Host Relationship, Immune Response, Diagnosis, and Treatment in Chromoblastomycosis.探讨着色芽生菌病的病因、微生物-宿主关系、免疫反应、诊断和治疗。
J Immunol Res. 2021 Nov 1;2021:9742832. doi: 10.1155/2021/9742832. eCollection 2021.
2
[Long-pulsed 1064 nm Nd: YAG laser combined with terbinafine against chromoblastomycosis caused by and the effect of laser therapy in a Wistar rat model].[长脉冲1064纳米钕:钇铝石榴石激光联合特比萘芬治疗裴氏着色芽生菌引起的着色芽生菌病及在Wistar大鼠模型中的激光治疗效果]
Nan Fang Yi Ke Da Xue Xue Bao. 2019 Jun 30;39(6):712-717. doi: 10.12122/j.issn.1673-4254.2019.06.13.
3
Challenges in the therapy of chromoblastomycosis.
黑曲霉病治疗的挑战。
Mycopathologia. 2013 Jun;175(5-6):477-88. doi: 10.1007/s11046-013-9648-x. Epub 2013 May 2.
4
Taenia taeniaeformis in rat favors protracted skin lesions caused by Sporothrix schenckii infection: Dectin-1 and IL-17 are dispensable for clearance of this fungus.猪带绦虫有利于孢子丝菌感染引起的迁延性皮肤损伤:Dectin-1 和 IL-17 对于清除这种真菌是可有可无的。
PLoS One. 2012;7(12):e52514. doi: 10.1371/journal.pone.0052514. Epub 2012 Dec 20.
5
DNA-hsp65 vaccine as therapeutic strategy to treat experimental chromoblastomycosis caused by Fonsecaea pedrosoi.DNA-hsp65 疫苗作为治疗由佩德罗索拟青霉引起的实验性着色芽生菌病的治疗策略。
Mycopathologia. 2013 Jun;175(5-6):463-75. doi: 10.1007/s11046-012-9599-7. Epub 2012 Nov 22.
6
Prolonged infection by Fonsecaea pedrosoi after antigenic co-stimulation at different sites in experimental murine chromoblastomycosis.实验性暗色丝孢霉病中不同部位抗原协同刺激后,匐形青霉感染持续存在。
Virulence. 2010 Jan-Feb;1(1):29-36. doi: 10.4161/viru.1.1.9920.
7
Melanized fungi in human disease.人类疾病中的黑化真菌。
Clin Microbiol Rev. 2010 Oct;23(4):884-928. doi: 10.1128/CMR.00019-10.