Selection, characterization, and application of DNA aptamers for the capture and detection of Salmonella enterica serovars

被引:213
作者
Joshi, Raghavendra [1 ]
Janagama, Harish [1 ]
Dwivedi, Hari P. [2 ]
Kumar, T. M. A. Senthil [1 ]
Jaykus, Lee-Ann [2 ]
Schefers, Jeremy [1 ]
Sreevatsan, Srinand [1 ,3 ]
机构
[1] Univ Minnesota, Coll Vet Med, Dept Vet Populat Med, St Paul, MN 55108 USA
[2] N Carolina State Univ, Dept Food Sci, Raleigh, NC 27695 USA
[3] Univ Minnesota, Coll Vet Med, Vet & Biomed Sci Dept, St Paul, MN 55108 USA
关键词
Salmonella; Pre-analytical processing; Aptamers; Food borne pathogens; Detection; REAL-TIME PCR; TETRATHIONATE BROTH ENRICHMENT; POLYMERASE-CHAIN-REACTION; IN-VITRO SELECTION; IMMUNOMAGNETIC SEPARATION; RESISTANT SALMONELLA; RAPID DETECTION; FECAL SAMPLES; ENVIRONMENTAL-SAMPLES; NEWPORT INFECTIONS;
D O I
10.1016/j.mcp.2008.10.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Sensitive and specific pre-analytical sample processing methods are needed to enhance our ability to detect and quantify food borne pathogens from complex food and environmental samples. In this study, DNA aptamers were selected and evaluated for the capture and detection of Salmonella enterica serovar. Typhimurium. A total of 66 candidate sequences were enriched against S. Typhimurium outer membrane proteins (OMPs) with counter-selection against Escherichia coli OMPs and lipopolysaccharides (LPS). Specificity of the selected aptamers was evaluated by gel-shift analysis against S. Typhimurium OMP. Five Salmonella-specific aptamer candidates were selected for further characterization. A dilution-to-extinction capture protocol using pure cultures of S. Typhimurium further narrowed the field to two candidates (aptamers 33 and 45) which showed low-end detection limits of 10-40 CFU. DNase protection assays applied to these aptamers confirmed sequence-specific binding to S. Typhimurium OMP preparations, while South-Western blot analysis combined with mass spectrometry identified putative membrane proteins as targets for aptamer binding. Aptamer 33 was bound to magnetic beads and used for the capture of S. Typhimurium seeded into whole carcass chicken rinse samples, followed by detection using quantitative real-time RT-PCR. In a pull-down assay format, detection limits were 10(1)-10(2) CFU S. Typhimurium/9 mL rinsate, while in a recirculation format, detection limits were 10(2)-10(3) CFU/25 mL rinsate. Reproducible detection at <10(1) S. typhimurium CFU/g was also achieved in spike-and-recovery experiments using bovine feces. The pull-down analysis using aptamer 33 was validated on 3 naturally infected chicken litter samples confirming their applicability in the field. This study demonstrates the applicability of Salmonella specific aptamers for pre-analytical sample processing as applied to food and environmental sample matrices. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:20 / 28
页数:9
相关论文
共 47 条
[1]   Rapid PCR detection of Salmonella in horse faecal samples [J].
Amavisit, P ;
Browning, GF ;
Lightfoot, D ;
Church, S ;
Anderson, GA ;
Whithear, KG ;
Markham, PF .
VETERINARY MICROBIOLOGY, 2001, 79 (01) :63-74
[2]   PROTEIN COMPOSITION OF OUTER MEMBRANE OF SALMONELLA-TYPHIMURIUM - EFFECT OF LIPOPOLYSACCHARIDE MUTATIONS [J].
AMES, GF ;
SPUDICH, EN ;
NIKAIDO, H .
JOURNAL OF BACTERIOLOGY, 1974, 117 (02) :406-416
[3]   Outer membrane protein P6 of nontypeable Haemophilus influenzae is a potent and selective inducer of human macrophage proinflammatory cytokines [J].
Berenson, CS ;
Murphy, TF ;
Wrona, CT ;
Sethi, S .
INFECTION AND IMMUNITY, 2005, 73 (05) :2728-2735
[4]  
Brody E N, 2000, J Biotechnol, V74, P5, DOI 10.1016/S1389-0352(99)00004-5
[5]   In vitro selection of DNA aptamers to anthrax spores with electrochemiluminescence detection [J].
Bruno, JG ;
Kiel, JL .
BIOSENSORS & BIOELECTRONICS, 1999, 14 (05) :457-464
[6]   Detection of salmonellae in chicken feces by a combination of tetrathionate broth enrichment, capillary PCR, and capillary gel electrophoresis [J].
Carli, KT ;
Unal, CB ;
Caner, V ;
Eyigor, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (05) :1871-1876
[7]   The evaluation of a fluorogenic polymerase chain reaction assay for the detection of Salmonella species in food commodities [J].
Chen, S ;
Yee, A ;
Griffiths, M ;
Larkin, C ;
Yamashiro, CT ;
Behari, R ;
PaszkoKolva, C ;
Rahn, K ;
DeGrandis, SA .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 1997, 35 (03) :239-250
[8]   Rapid identification of Salmonella serovars in feces by specific detection of virulence genes, invA and spvC, by an enrichment broth culture-multiplex PCR combination assay [J].
Chiu, CH ;
Ou, JT .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (10) :2619-2622
[9]   Biosensors for the detection of bacteria [J].
Deisingh, AK ;
Thompson, M .
CANADIAN JOURNAL OF MICROBIOLOGY, 2004, 50 (02) :69-77
[10]   Implementation of real-time PCR to tetrathionate broth enrichment step of Salmonella detection in poultry [J].
Eyigor, A ;
Carli, KT ;
Unal, CB .
LETTERS IN APPLIED MICROBIOLOGY, 2002, 34 (01) :37-41