中华皮肤科杂志 ›› 2017, Vol. 50 ›› Issue (10): 724-728.doi: 10.3760/cma.j.issn.0412-4030.2017.10.007

• 论著 • 上一篇    下一篇

疣状瓶霉致nu/nu BALB/c小鼠皮下慢性感染模型的建立

陈瑶 董碧麟 章旭 陈柳青 李东升 童中胜   

  1. 430022 武汉市第一医院皮肤科
  • 收稿日期:2017-02-03 修回日期:2017-03-02 发布日期:2017-09-29
  • 通讯作者: 董碧麟 E-mail:augustusdong@126.com
  • 基金资助:
    国家自然科学基金(81301376)

Establishment of an athymic BALB/c mouse model with chronic infection due to Phialophora verrucosa

Chen Yao, Dong Bilin, Zhang Xu, Chen Liuqing, Li Dongsheng, Tong Zhongsheng   

  1. Department of Dermatology, Wuhan No.1 Hospital, Wuhan 430022, China
  • Received:2017-02-03 Revised:2017-03-02 Published:2017-09-29
  • Contact: Bi-Lin DONG E-mail:augustusdong@126.com
  • Supported by:
    National Natural Science Foundation of China(81301376)

摘要: 目的 建立疣状瓶霉(Phialophora verrucosa,P. verrucosa)致无胸腺(nu/nu)BALB/c小鼠皮下慢性感染模型,探讨T淋巴细胞在抵御形成侵袭性感染中的作用。方法 经皮下接种100 μl P. verrucosa菌丝或孢子悬液(CFU = 5.0 × 108/ml)至足垫,每3天测量其肿胀程度。分析BALB/c和nu/nu BALB/c小鼠感染灶的病理特征。通过组织真菌培养分析P. verrucosa在上述两类小鼠感染灶内的存活状态。结果 BALB/c小鼠接种菌丝或孢子12 d内足垫呈一过性肿胀,50 d后基本恢复正常;nu/nu BALB/c小鼠接种菌丝或孢子后足垫肿胀明显、伴反复破溃和结痂,迁延不愈。病理提示,BALB/c小鼠菌丝或孢子接种灶均表现为局限性感染特征,灶内P. verrucosa亦维持接种时形态;nu/nu BALB/c小鼠菌丝或孢子接种灶中,P. verrucosa以单一菌丝或伴硬壳细胞混合形态形成侵袭性感染。真菌培养提示,P. verrucosa在BALB/c小鼠足垫21 d后接种灶中不能生长;在nu/nu BALB/c小鼠接种灶中则可持续存活。结论 以nu/nu BALB/c小鼠成功建立P. verrucosa致皮下暗色丝孢霉病实验室模型;与BALB/c小鼠相比,nu/nu BALB/c小鼠更易感染。

Abstract: Chen Yao, Dong Bilin, Zhang Xu, Chen Liuqing, Li Dongsheng, Tong Zhongsheng Department of Dermatology, Wuhan No.1 Hospital, Wuhan 430022, China Corresponding author: Dong Bilin, Email: augustusdong@126.com 【Abstract】 Objective To establish an athymic(nu/nu)BALB/c mouse model with chronic subcutaneous infection due to Phialophora verrucosa (P. verrucosa), and to explore the role of T lymphocytes in defensing against invasive infection due to P. verrucosa. Methods Six immunocompetent BALB/c mice and 6 nu/nu BALB/c mice were subcutaneously inoculated with 100 μl of P. verrucosa hyphae suspensions at a concentration of 5.0 × 108 colony-forming unit (CFU)/ml into one footpad, while another 6 immunocompetent BALB/c mice and 6 nu/nu BALB/c mice were subcutaneously inoculated with 100 μl of 5.0 × 108 CFU/ml P. verrucosa conidium suspensions into one footpad. The degree of footpad swelling was measured with a vernier caliper every 3 days. Histopathological characteristics of infected footpads were further analyzed. Biopsy tissues were also subjected to fungal culture to analyze the growth of P. verrucosa in infection foci in mice. Results After the treatment with hyphae or conidium suspensions, the BALB/c mice experienced transient footpad swelling within 12 days, and basically recovered after 50 days. However, the nu/nu BALB/c mice experienced persistent footpad swelling with recurrent ulceration and crusting. As pathological examination revealed, all the inoculation loci in BALB/c mice experienced local infection, and the morphology of P. verrucosa in the infected foci was not changed over time. However, invasive infections due to P. verrucosa hyphae alone or a mixture of P. verrucosa hyphae and sclerotic cells were observed in all the inoculation loci in nu/nu BALB/c mice. The fungal culture showed that P. verrucosa could not grow in the footpads of BALB/c mice after 21 days, while P. verrucosa could persistently grow in the footpads of nu/nu BALB/c mice. Conclusion An experimental model with subcutaneous phaeohyphomycosis due to P. verrucosa has been successfully established by using nu/nu BALB/c mice, and the nu/nu BALB/c mice are more susceptible to P. verrucosa infection compared with the immunocompetent BALB/c mice.

Key words: 瓶霉菌属;模型, 动物;黑霉病;小鼠, 裸;疣状瓶霉;nu/nu BALB/c

中图分类号: 

  • Phialophora

引用本文

陈瑶 董碧麟 章旭 陈柳青 李东升 童中胜. 疣状瓶霉致nu/nu BALB/c小鼠皮下慢性感染模型的建立[J]. 中华皮肤科杂志, 2017,50(10):724-728. doi:10.3760/cma.j.issn.0412-4030.2017.10.007

Chen Yao, Dong Bilin, Zhang Xu, Chen Liuqing, Li Dongsheng, Tong Zhongsheng. Establishment of an athymic BALB/c mouse model with chronic infection due to Phialophora verrucosa[J]. Chinese Journal of Dermatology, 2017, 50(10): 724-728.doi:10.3760/cma.j.issn.0412-4030.2017.10.007