Evaluation of an immunochromatography strip assay for the detection of Salmonella sp from poultry

被引:26
作者
Bautista, DA
Elankumaran, S
Arking, JA
Heckert, RA
机构
[1] Univ Maryland, Virginia Maryland Reg Coll Vet Med, College Pk, MD 20742 USA
[2] New Horizons Diagnost Corp, Columbia, MD 21045 USA
关键词
D O I
10.1177/104063870201400514
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The present study was conducted to evaluate the sensitivity and specificity of an immunochromatography-based diagnostic kit for Salmonella, The analytical sensitivity of the test when using pure colonies of different Salmonella species was in the range of 1 X 104 to 1 X 101 colony-forming units per milliliter. The strip detected 19 of 22 strains of Salmonella spp. but failed to detect S. worthington, S. choleraesuis var, kunzendorf, and S. johannesburg. The strip did not detect 27 different enteric bacteria, including Escherichia coli O157:H7, Campylobacter jejuni, Shigella sonnei, and Vibrio parahaemolyticus. In direct testing of feces (n=66) from chickens infected with Salmonella typhimurium, the strip had a sensitivity of 12.3% and a specificity of 100%. Evaluation of the strip assay (n=510) after sample pre-enrichment in 2% buffered peptone water (BPW) yielded a sensitivity of 93.8% and specificity of 89% when compared to isolation and identification with xylose-lysine-tergitol 4 (XLT4) selective plating media. Subsequent enrichment in Hajna tetrathionate (TT) broth yielded a higher sensitivity (94.7%) and specificity (96.8%). The agreement (kappa) between the strip test and isolation was 0.004 in direct fecal testing, 0.82 in BPW, and 0.89 in TT broth. The assay could detect Salmonella sp. as early as 18-48 hours during pre-enrichment and enrichment compared to isolation on XLT4, which required an overnight incubation step for the presumptive isolation and identification of Salmonella.
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页码:427 / 430
页数:4
相关论文
共 13 条
[1]  
Andrews WH, 1996, J AOAC INT, V79, P4
[2]  
Bird CB, 1999, J AOAC INT, V82, P625
[3]   Evaluation of salmonella serotype distributions from commercial broiler hatcheries and grower houses [J].
Byrd, JA ;
DeLoach, JR ;
Corrier, DE ;
Nisbet, DJ ;
Stanker, LH .
AVIAN DISEASES, 1999, 43 (01) :39-47
[4]  
Ferris K. E., 1998, Proceedings One Hundred and Second Annual Meeting of the United States Animal Health Association, Minneapolis, Minnesota, USA, 3-9 October, 1998., P584
[5]   Improved plating media for the detection of Salmonella species with typical and atypical hydrogen sulfide production [J].
Mallinson, ET ;
Miller, RG ;
de Rezende, CE ;
Ferris, KE ;
deGraft-Hanson, J ;
Joseph, SW .
JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2000, 12 (01) :83-87
[6]   Novel detection techniques for human pathogens that contaminate poultry [J].
Mandrell, RE ;
Wachtel, MR .
CURRENT OPINION IN BIOTECHNOLOGY, 1999, 10 (03) :273-278
[7]   Food-related illness and death in the United States [J].
Mead, PS ;
Slutsker, L ;
Dietz, V ;
McCaig, LF ;
Bresee, JS ;
Shapiro, C ;
Griffin, PM ;
Tauxe, RV .
EMERGING INFECTIOUS DISEASES, 1999, 5 (05) :607-625
[8]  
Peplow MO, 1999, APPL ENVIRON MICROB, V65, P1055
[9]   A PRIMER ON THE PRECISION AND ACCURACY OF THE CLINICAL EXAMINATION [J].
SACKETT, DL .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1992, 267 (19) :2638-2644
[10]  
Swayne D.E., 1998, AM ASS AVIAN PATHOLO, P4