Detection of Campylobacter in Stool and Determination of Significance by Culture, Enzyme Immunoassay, and PCR in Developing Countries

被引:77
作者
Platts-Mills, James A. [1 ]
Liu, Jie [1 ]
Gratz, Jean [1 ]
Mduma, Esto [2 ]
Amour, Caroline [3 ]
Swai, Ndealilia [3 ]
Taniuchi, Mami [1 ]
Begum, Sharmin [4 ]
Penataro Yori, Pablo [5 ,6 ]
Tilley, Drake H. [7 ]
Lee, Gwenyth [6 ]
Shen, Zeli [8 ]
Whary, Mark T. [8 ]
Fox, James G. [8 ]
McGrath, Monica [9 ]
Kosek, Margaret [5 ,6 ]
Haque, Rashidul [4 ]
Houpt, Eric R. [1 ]
机构
[1] Univ Virginia, Div Infect Dis & Int Hlth, Charlottesville, VA 22908 USA
[2] Haydom Lutheran Hosp, Haydom, Tanzania
[3] Kilimanjaro Clin Res Inst, Moshi, Tanzania
[4] Int Ctr Diarrhoeal Dis Res, Dhaka 1000, Bangladesh
[5] Asociac Benef PRISMA, Iquitos, Peru
[6] Johns Hopkins Bloomberg Sch Publ Hlth, Baltimore, MD USA
[7] US Naval Med Res Unit 6, Lima, Peru
[8] MIT, Cambridge, MA USA
[9] NIH, Fogarty Int Ctr, Bethesda, MD 20892 USA
基金
比尔及梅琳达.盖茨基金会; 美国国家卫生研究院;
关键词
MULTIPLEX PCR; CHILDREN; ASSAY; INFECTIONS; JEJUNI; POPULATION; ETIOLOGY; INFANTS; ANTIGEN;
D O I
10.1128/JCM.02935-13
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Campylobacter is a common bacterial enteropathogen that can be detected in stool by culture, enzyme immunoassay (EIA), or PCR. We compared culture for C. jejuni/C. coli, EIA (ProSpecT), and duplex PCR to distinguish Campylobacter jejuni/C. coli and non-jejuni/coli Campylobacter on 432 diarrheal and matched control stool samples from infants in a multisite longitudinal study of enteric infections in Tanzania, Bangladesh, and Peru. The sensitivity and specificity of culture were 8.5% and 97.6%, respectively, compared with the results of EIA and 8.7% and 98.0%, respectively, compared with the results of PCR for C. jejuni/C. coli. Most (71.6%) EIA-positive samples were positive by PCR for C. jejuni/C. coli, but 27.6% were positive for nonjejuni/coli Campylobacter species. Sequencing of 16S rRNA from 53 of these non-jejuni/coli Campylobacter samples showed that it most closely matched the 16S rRNA of C. hyointestinalis subsp. lawsonii (56%), C. troglodytis (33%), C. upsaliensis (7.7%), and C. jejuni/C. coli (2.6%). Campylobacter-negative stool spiked with each of the above-mentioned Campylobacter species revealed reactivity with EIA. PCR detection of Campylobacter species was strongly associated with diarrhea in Peru (odds ratio [OR] = 3.66, P < 0.001) but not in Tanzania (OR = 1.56, P = 0.24) or Bangladesh (OR = 1.13, P = 0.75). According to PCR, Campylobacter jejuni/C. coli infections represented less than half of all infections with Campylobacter species. In sum, in infants in developing country settings, the ProSpecT EIA and PCR for Campylobacter reveal extremely high rates of positivity. We propose the use of PCR because it retains high sensitivity, can ascertain burden, and can distinguish between Campylobacter infections at the species level.
引用
收藏
页码:1074 / 1080
页数:7
相关论文
共 28 条
[1]   New Methods for Detection of Campylobacters in Stool Samples in Comparison to Culture [J].
Bessede, Emilie ;
Delcamp, Adline ;
Sifre, Elodie ;
Buissonniere, Alice ;
Megraud, Francis .
JOURNAL OF CLINICAL MICROBIOLOGY, 2011, 49 (03) :941-944
[2]   Molecular-based detection of non-culturable and emerging campylobacteria in patients presenting with gastroenteritis [J].
Bullman, S. ;
O'Leary, J. ;
Corcoran, D. ;
Sleator, R. D. ;
Lucey, B. .
EPIDEMIOLOGY AND INFECTION, 2012, 140 (04) :684-688
[3]  
CALVA JJ, 1988, LANCET, V1, P503
[4]   Human campylobacteriosis in developing countries [J].
Coker, AO ;
Isokpehi, RD ;
Thomas, BN ;
Amisu, KO ;
Obi, CL .
EMERGING INFECTIOUS DISEASES, 2002, 8 (03) :237-243
[5]   Detection of non-jejuni and -coli Campylobacter Species from Stool Specimens with an Immunochromatographic Antigen Detection Assay [J].
Couturier, Brianne A. ;
Couturier, Marc Roger ;
Kalp, Kim J. ;
Fisher, Mark A. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2013, 51 (06) :1935-1937
[6]   Three-Hour Molecular Detection of Campylobacter, Salmonella, Yersinia, and Shigella Species in Feces with Accuracy as High as That of Culture [J].
Cunningham, Scott A. ;
Sloan, Lynne M. ;
Nyre, Lisa M. ;
Vetter, Emily A. ;
Mandrekar, Jayawant ;
Patel, Robin .
JOURNAL OF CLINICAL MICROBIOLOGY, 2010, 48 (08) :2929-2933
[7]   Detection of Campylobacter Species and Arcobacter butzleri in Stool Samples by Use of Real-Time Multiplex PCR [J].
de Boer, Richard F. ;
Ott, Alewijn ;
Gueren, Pinar ;
van Zanten, Evert ;
van Belkum, Alex ;
Kooistra-Smid, Anna M. D. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2013, 51 (01) :253-259
[8]   Evaluation of the ProSpecT Microplate Assay for detection of Campylobacter:: a routine laboratory perspective [J].
Dediste, A ;
Vandenberg, O ;
Vlaes, L ;
Ebraert, A ;
Douat, N ;
Bahwere, P ;
Butzler, JP .
CLINICAL MICROBIOLOGY AND INFECTION, 2003, 9 (11) :1085-1090
[9]   Comparison of immunochromatography, PCR and culture methods for the detection of Campylobacter bacteria [J].
Dey, Shuvra Kanti ;
Nishimura, Shuichi ;
Okitsu, Shoko ;
Hayakawa, Satoshi ;
Mizuguchi, Masashi ;
Ushijima, Hiroshi .
JOURNAL OF MICROBIOLOGICAL METHODS, 2012, 91 (03) :566-568
[10]   Rapid Detection of Campylobacter Antigen by Enzyme Immunoassay Leads to Increased Positivity Rates [J].
Giltner, Carmen L. ;
Saeki, Sandra ;
Bobenchik, April M. ;
Humphries, Romney M. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2013, 51 (02) :618-620