Significance of transiently positive enzyme-linked immunosorbent assay results in detection of Helicobacter pylori in stool samples from children

被引:35
作者
Haggerty, TD
Perry, S
Sanchez, L
Perez-Perez, G
Parsonnet, J
机构
[1] Stanford Univ, Dept Med, Div Infect Dis & Geograph Med, Stanford, CA 94305 USA
[2] NYU, Sch Med, Dept Med, Div Infect Dis, New York, NY USA
[3] NYU, Sch Med, Dept Microbiol, Div Infect Dis, New York, NY USA
[4] Stanford Univ, Div Epidemiol, Dept Hlth Res & Policy, Stanford, CA 94305 USA
关键词
D O I
10.1128/JCM.43.5.2220-2223.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In young children, the significance of stool samples transiently positive for Helicobacter pylori antigen is unknown. As part of a larger prospective study on enteric infections, stool samples were obtained from 323 children at two time points 3 months apart and tested for H. pylori antigen using a commercially available enzyme-linked immunosorbent assay (ELISA) test. Seminested PCR for a Helicobacter-specific 16S rRNA gene was performed on all 26 pairs reverting from positive to negative (transient positives), all 4 persistent antigen-positive pairs, and 10 randomly selected persistent antigen-negative pairs. Helicobacter species were amplified from the first stool samples of 15/26 (58%) of the transient positives and 1 (25%) of 4 persistent positives. No Helicobacter species were amplified from the 10 persistent negatives. Among the 15 amplicons from transient-positive stool, H. pylori was sequenced and identified from 12 (80%; 95% confidence interval, 52% to 96%) and other Helicobacter spp. were identified from three (Helicobacter canis, Helicobacter winghamensis, and MIT 99-5504). Four of the 15 remained positive by PCR for the second (antigen-negative) stool sample, including all 3 initially identified as non-H. pylori. Helicobacter bilis was amplified from the second sample of a persistent positive. Two of eight transient positives from whom serum was available had accompanying transient elevations in anti-H. pylori antibodies. Transiently positive stool ELISAs for H. pylori are common and represent H. pylori in the majority of cases where sequences can be obtained. A not-insignificant percentage of antigen-positive stools, however, may represent other Helicobacter species.
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页码:2220 / 2223
页数:4
相关论文
共 26 条
[1]   Helicobacter pylori infection, gastric acid secretion, and infant growth [J].
Dale, A ;
Thomas, JE ;
Darboe, MK ;
Coward, WA ;
Harding, M ;
Weaver, LT .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 1998, 26 (04) :393-397
[2]   Isolation of Helicobacter canis from a colony of Bengal cats with endemic diarrhea [J].
Foley, JE ;
Marks, SL ;
Munson, L ;
Melli, A ;
Dewhirst, FE ;
Yu, SL ;
Shen, ZL ;
Fox, JG .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (10) :3271-3275
[3]  
Fox J G, 1997, Semin Gastrointest Dis, V8, P124
[4]   Hepatic Helicobacter species identified in bile and gallbladder tissue from Chileans with chronic cholecystitis [J].
Fox, JG ;
Dewhirst, FE ;
Shen, ZL ;
Feng, Y ;
Taylor, NS ;
Paster, BJ ;
Ericson, RL ;
Lau, CN ;
Correa, P ;
Araya, JC ;
Roa, I .
GASTROENTEROLOGY, 1998, 114 (04) :755-763
[5]   Novel Helicobacter species isolated from rhesus monkeys with chronic idiopathic colitis [J].
Fox, JG ;
Handt, L ;
Xu, SL ;
Shen, ZL ;
Dewhirst, FE ;
Paster, BJ ;
Dangler, C ;
Lodge, K ;
Motzel, S ;
Klein, H .
JOURNAL OF MEDICAL MICROBIOLOGY, 2001, 50 (05) :421-429
[6]   Helicobacter pylori in cathartic stools of subjects with and without cimetidine-induced hypochlorhydria [J].
Haggerty, T ;
Shmuely, H ;
Parsonnet, J .
JOURNAL OF MEDICAL MICROBIOLOGY, 2003, 52 (02) :189-191
[7]   Detection of Helicobacter pylori DNA in feces and saliva by polymerase chain reaction:: a review [J].
Kabir, S .
HELICOBACTER, 2004, 9 (02) :115-123
[8]  
Konstantopoulos N, 2001, AM J GASTROENTEROL, V96, P677, DOI 10.1111/j.1572-0241.2001.03603.x
[9]  
Leal-Herrera Y, 2003, AM J GASTROENTEROL, V98, P2395, DOI 10.1111/j.1572-0241.2003.07708.x
[10]   ATTEMPT TO FULFILL KOCH POSTULATES FOR PYLORIC CAMPYLOBACTER [J].
MARSHALL, BJ ;
ARMSTRONG, JA ;
MCGECHIE, DB ;
GLANCY, RJ .
MEDICAL JOURNAL OF AUSTRALIA, 1985, 142 (08) :436-439