Sensitivity of PCR Targeting Mycobacterium ulcerans by Use of Fine-Needle Aspirates for Diagnosis of Buruli Ulcer

被引:40
作者
Phillips, R. O. [2 ,3 ]
Sarfo, F. S. [3 ]
Osei-Sarpong, F. [4 ]
Boateng, A. [4 ]
Tetteh, I. [3 ]
Lartey, A. [3 ]
Adentwe, E. [4 ]
Opare, W. [5 ]
Asiedu, K. B. [6 ]
Wansbrough-Jones, M. [1 ]
机构
[1] Univ London, St Georges Hosp & Med Sch, London SW17 0RE, England
[2] Kwame Nkrumah Univ Sci & Technol, Kumasi, Ghana
[3] Komfo Anokye Teaching Hosp, Kumasi, Ghana
[4] Tepa Govt Hosp, Tepa, Ghana
[5] Natl Buruli Ulcer Control Programme, Accra, Ghana
[6] WHO, CH-1211 Geneva, Switzerland
关键词
INFECTION; SPECIMENS; SEQUENCE;
D O I
10.1128/JCM.01842-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In a previous study, we reported that the sensitivity of PCR targeting the IS2404 insertion sequence of Mycobacterium ulcerans was 98% when it was applied to 4-mm punch biopsy samples of Buruli lesions. Fine-needle aspiration (FNA) is a less traumatic sampling technique for nonulcerated lesions, and we have studied the sensitivity of PCR using FNA samples. Fine-needle aspirates were taken with a 21-gauge needle from 43 patients diagnosed clinically with M. ulcerans disease. Four-millimeter punch biopsies were obtained for microscopy, culture, and PCR targeting the IS2404 insertion sequence. The sensitivity of PCR using samples obtained by FNA was 86% (95% confidence interval [95% CI], 72 to 94%) compared with that for PCR using punch biopsy samples. In this study, the sensitivities of culture and microscopy for punch biopsy samples were 44% (95% CI, 29 to 60%) and 26% (95% CI, 14 to 41%), respectively. This demonstrates that PCR on an FNA sample is a viable minimally invasive technique to diagnose M. ulcerans lesions.
引用
收藏
页码:924 / 926
页数:3
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