Evaluation of chromogenic media for the detection of Listeria species in food

被引:27
作者
Greenwood, M
Willis, C
Doswell, P
Allen, G
Pathak, K
机构
[1] Southampton Gen Hosp, Hlth Protect Agcy, Wessex Environm Microbiol Serv, Southampton SO16 6YD, Hants, England
[2] Royal Preston Hosp, Food & Environm Microbiol Serv NW, Preston, Lancs, England
[3] Ctr Infect, Hlth Protect Agcy, Food Safety Microbiol Lab, Food Water & Environm Lab, London, England
关键词
chromogenic agar; detection; enumeration; food; Listeria; media;
D O I
10.1111/j.1365-2672.2005.02734.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: The aim of this study was to evaluate the performance of chromogenic agars, Agar Listeria according to Ottaviani and Agosti (ALOA) and Rapid L. mono agar, compared with Oxford agar for the enumeration and detection of Listeria species in food. Methods and Results: A total of 170 food samples were examined using the three plating media. Listeria species were isolated from 63 samples. In contrast to Oxford agar, detection of Listeria colonies on chromogenic media was as good after 24 h of incubation of plates as after 48 h. While there was no significant difference in recovery of Listeria monocytogenes on the three media, recovery of other Listeria species was significantly poorer on Rapid L. mono agar compared with Oxford and ALOA agars. Recovery of species other than L. monocytogenes was significantly improved by including a secondary enrichment stage in the detection method. Conclusions: Using chromogenic agars, presumptive identification of L. monocytogenes is possible after 24 h, compared with 3-4 days using Oxford agar. However, the poor detection of species other than L. monocytogenes on Rapid L. mono agar is a disadvantage of this medium. Significance and Impact of the Study: This study provides new information regarding the isolation of Listeria species other than L. monocytogenes from food using chromogenic plating media. This is important, as nonpathogenic Listeria species act as markers for the likelihood of presence of L. monocytogenes and allow preventive action to be taken to avoid its presence.
引用
收藏
页码:1340 / 1345
页数:6
相关论文
共 18 条
[1]  
*BRIT STAND I, 1997, 112901997 BSENISO BR
[2]  
*BRIT STAND I, 2001, 1664922001 BSISO BRI
[3]  
*BRIT STAND I, 1998, 112901998 BSENISO BR
[4]  
*BRIT STAND I, 2001, 1664912001 BSISO BRI
[5]   LISTERIA-MENINGITIS AND PATE [J].
CUMBER, PM ;
MUMARBASHI, W ;
PALMER, S ;
HUTTON, RD .
JOURNAL OF CLINICAL PATHOLOGY, 1991, 44 (04) :339-339
[6]   DETECTION OF LISTERIA-MONOCYTOGENES IN SAMPLES CONTAINING LISTERIA-INNOCUA [J].
CURIALE, MS ;
LEWUS, C .
JOURNAL OF FOOD PROTECTION, 1994, 57 (12) :1048-1051
[7]  
*HLTH PROT AG, 2004, CDR WKLY, V14
[8]   Evaluation and interlaboratory validation of a selective agar for phosphatidylinositol-specific phospholipase C activity using a chromogenic substrate to detect Listeria monocytogenes from foods [J].
Jinneman, KC ;
Hunt, JM ;
Eklund, CA ;
Wernberg, JS ;
Sado, PN ;
Johnson, JM ;
Richter, RS ;
Torres, ST ;
Ayotte, E ;
Eliasberg, SJ ;
Istafanos, P ;
Bass, D ;
Kexel-Calabresa, N ;
Lin, W ;
Barton, CN .
JOURNAL OF FOOD PROTECTION, 2003, 66 (03) :441-445
[9]   LISTERIA-IVANOVII INFECTION [J].
LESSING, MPA ;
CURTIS, GDW ;
BOWLER, ICJ .
JOURNAL OF INFECTION, 1994, 29 (02) :230-231
[10]   HUMAN LISTERIOSIS AND PATE - A POSSIBLE ASSOCIATION [J].
MCLAUCHLIN, J ;
HALL, SM ;
VELANI, SK ;
GILBERT, RJ .
BRITISH MEDICAL JOURNAL, 1991, 303 (6805) :773-775