Development of a Novel Listeria Enrichment Broth for the Isolation of Pathogenic Listeria

2017 ◽  
Vol 80 (10) ◽  
pp. 1768-1776 ◽  
Author(s):  
Dongxin Liu ◽  
Yan Wang ◽  
Yi Wang ◽  
Lu Zhang ◽  
Lijuan Luo ◽  
...  

ABSTRACT Listeriosis, the disease caused by pathogenic Listeria species, can present severe symptoms in susceptible people. The goal of this study was to develop a novel enrichment broth, Listeria allose enrichment broth (LAEB), to improve isolation of Listeria monocytogenes and Listeria ivanovii from samples through incorporating a specific carbohydrate and reducing inhibitor concentrations. Other coexisting bacteria, particularly Listeria innocua, can interfere with the isolation of pathogenic Listeria in such ways as overgrowth of L. innocua and the generation of inhibitory metabolites. The incorporation of allose into the novel LAEB was effective for slowing the growth of L. innocua and other nontarget microorganisms. We determined that 35°C and pH 7.0 under aerobic conditions are optimal for Listeria growth in this medium. The novelty of the use of LAEB is the single enrichment procedure at 35°C for 24 h, obviating the need for a secondary enrichment medium. In 50 simulated samples, the sensitivity of the LAEB method (86%) was higher than that of the International Organization for Standardization (EN ISO) method (70%). In 142 naturally contaminated samples tested, the isolation rate for pathogenic Listeria with the LAEB method was 26.0% (37 of 142 samples), which was significantly higher than the 17.6% (25 of 142 samples) for the EN ISO method. Higher isolation rates and a quicker and easier protocol make the novel LAEB method an appropriate alternative for the isolation of pathogenic Listeria.

1994 ◽  
Vol 57 (12) ◽  
pp. 1048-1051 ◽  
Author(s):  
MICHAEL S. CURIALE ◽  
CATHERINE LEWUS

A common culture procedure for the detection of Listeria monocytogenes in meats and environmental samples was evaluated in a multilaboratory study using samples inoculated with both Listeria monocytogenes and Listeria innocua. Listeria monocytogenes was recovered from 5.4% of beef broth samples containing between 140 and 1400 L. monocytogenes cells per 25-ml sample in the presence of twice as many L. innocua cells; whereas L. innocua was recovered from all of the samples. Listeria monocytogenes was isolated from 100% of the samples when L. innocua was absent. Similar results were obtained for swab samples containing both L. monocytogenes and L. innocua. Listeria monocytogenes was recovered from 31% of the swabs containing 4.8 L. monocytogenes cells per swab and from 0% of the swabs containing the same number of L. monocytogenes cells and 4 L. innocua cells per swab. When the ratios of L. monocytogenes to L. innocua were 12:1, 120:1 and 1200:1, L. monocytogenes was isolated from 38%, 92% and 85% of the swabs, respectively. The recovery rates were consistent with the differences in growth rates for the two organisms in selective media. The generation times for L. monocytogenes were 74 min in primary enrichment broth and 105 min in modified secondary enrichment broth. Listeria innocua posted generation times of 53 and 81 min in the same two enrichment broths.


1990 ◽  
Vol 53 (6) ◽  
pp. 505-507 ◽  
Author(s):  
J. S. BAILEY ◽  
D. L. FLETCHER ◽  
N. A. COX

These studies examined the differences in recovery of Listeria monocytogenes from pure culture and in the populations of mixed aerobic microflora from chicken and Brie cheese incubated in University of Vermont (UVM) and Listeria enrichment broth (LEB) enrichment broths for different times and conditions. No significant differences were observed in levels of L. monocytogenes from pure cultures in UVM or LEB on any sampling day. No differences were observed in the levels of mixed microflora from Brie cheese in either UVM or LEB, but from chicken rinse the level of mixed flora competitors was significantly higher on all sampling days in LEB as compared to UVM. No differences were observed between a single enrichment in UVM or LEB for 2 d and a transfer to a secondary enrichment tube after 1 d. Overall, the level of mixed microflora capable of growing in enrichment broths was greater from chicken rinse than from Brie cheese. The ratio of L. monocytogenes to mixed microflora which survived the selective enrichments was most favorable for recovery of L. monocytogenes after 2 d of enrichment.


1993 ◽  
Vol 56 (7) ◽  
pp. 616-618 ◽  
Author(s):  
RUTH L. PETRAN ◽  
KATHERINE M. J. SWANSON

Listeria spp. have been isolated from a wide variety of sources, and in many situations Listeria innocua is more commonly found than Listeria monocytogenes. Growth of three L. monocytogenes strains was studied when inoculated simultaneously with a rhamnose negative L. innocua strain into culture media and cheese sauce. Fraser broth (FB), Trypticase™ soy broth plus 0.6% yeast extract (TSB-YE), University of Vermont medium (UVM) modified Listeria enrichment broth, and cheese sauce were inoculated (ca. 102 cells per ml) and incubated for 24 h; FB, TSB-YE, and cheese sauce at 35°C, UVM at 30°C. Growth of four rhamnose-positive, L. innocua strains was also studied in culture media. Growth of L. monocytogenes was similar to that for L. innocua in TSB-YE or cheese sauce. However, in FB and UVM, L. innocua populations were significantly higher than L. monocytogenes. This occurred when media were inoculated individually or simultaneously. This may explain in part why L. innocua is isolated more frequently than L. monocytogenes from foods and environmental samples.


2003 ◽  
Vol 66 (2) ◽  
pp. 328-330 ◽  
Author(s):  
PAULO CÉSAR ANTONIOLLO ◽  
FERNANDO da SILVA BANDEIRA ◽  
MÁRCIA MONKS JANTZEN ◽  
EDUARDA HALLAL DUVAL ◽  
WLADIMIR PADILHA da SILVA

The objective of this work was to study the occurrence of Listeria species in feces and on dressed and cooled carcasses of lambs at a packing plant in Brazil. Listeria spp. were recovered on Oxford and Palcam agars. The 35 fecal samples yielded Listeria welshimeri (20%) and Listeria innocua (8.6%). The 69 carcass samples yielded L. innocua (34.8%), Listeria monocytogenes (4.3%), and Listeria ivanovii (1.5%). More Listeria spp. were recovered with two selective agars than with either agar alone.


1987 ◽  
Vol 50 (6) ◽  
pp. 479-484 ◽  
Author(s):  
JEFFREY M. FARBER ◽  
JOAN I. SPEIRS

Monoclonal antibodies directed against antigens of Listeria spp. were produced. Three main classes of immunoglobulins were found that reacted with Listeria strains containing either the A, B, or C flagellar antigen. These antibodies reacted with Listeria monocytogenes, Listeria welshimeri, Listeria seeligeri, Listeria ivanovii and Listeria innocua, but not Listeria grayi, Listeria murrayi or Listeria denitrificans. The monoclones tested did not cross-react with any of the 30 non-Listeria cultures examined, including Staphylococcus aureus and Streptococcus faecalis. Cheese and milk samples naturally-contaminated with L. monocytogenes were found to be positive for Listeria within two working days after initiation by using the monoclonal antibodies in an enzyme immunoassay.


2001 ◽  
Vol 64 (4) ◽  
pp. 551-553 ◽  
Author(s):  
J. M. SORIANO ◽  
H. RICO ◽  
J. C. MOLTÓ ◽  
J. MAÑES

From September 1999 to March 2000, meat (pork, beef, and chicken), fish (salmon, hake, and sole), vegetable (lettuce and spinach), and Spanish potato omelette samples obtained at restaurants were collected and tested for the occurrence of Listeria spp. Listeria monocytogenes was isolated from 3 (2.9%) out of 103 studied samples. Other species isolated were Listeria grayi (13.6%), Listeria innocua (1.9%), Listeria ivanovii (5.8%), Listeria seeligeri (3.9%), and Listeria welshimeri (1.9%). Listeria was neither isolated from beef nor any type of fish.


1991 ◽  
Vol 54 (8) ◽  
pp. 602-606 ◽  
Author(s):  
A. M. LUND ◽  
E. A. ZOTTOLA ◽  
D. J. PUSCH

Methods used to isolate Listeria spp. from raw milk were compared during a 13-month period (April 1989–April 1990). Raw milk was obtained bimonthly from 12 dairy farms during this time period. Three enrichments were compared: Listeria enrichment broth (LEB); University of Vermont medium (UVM), followed by a secondary enrichment with Fraser broth; and LPALCAMY. Four selective plating media, including Listeria selective agar-Oxford formulation; Modified McBride Listeria agar (MMLA); Lithium chloride-phenylethanol-moxalactam (LPM) agar; and L-PALCAM agar, were compared. L-PALCAMY enrichment broth enhanced isolation of L. monocytogenes and other Listeria spp. The greatest numbers of positive Listeria samples were obtained on Oxford and PALCAM agars, while the poorest isolation was obtained using the combination of LEB with MMLA. L. monocytogenes was found to be present in 3.0% (9/300) of the samples analyzed. The incidence of Listeria spp. was 28.0%; Listeria innocua, 26.7%; and Listeria welshimeri, 1.7%. Listeria ivanovii was not isolated. The incidence of Listeria was highest during the warmer months of April–July, while the lowest incidences occurred in December and February. Somatic cell counts (SCC) and standard plate counts (SPC) were determined by the cooperative that supplied the raw milk. In general, a producer's milk with high SPC corresponded to a high incidence of Listeria spp., while low SPC corresponded to a low incidence. A particular producer's milk with the highest incidence of Listeria spp. also had the highest SCC.


1985 ◽  
Vol 31 (10) ◽  
pp. 938-941 ◽  
Author(s):  
Lucas Domínguez Rodriguez ◽  
Jose F. Fernández Garayzabal ◽  
Jose A. Vazquez Boland ◽  
Elias Rodriguez Ferri ◽  
Guillermo Suarez Fernández

Refrigerated mixtures of raw milk provided by a dairy which was supplied by farms from west and central Spain were tested for the presence of Listeria microorganisms. A total of 95 samples were taken at regular intervals over a 16-month period. Listeria grayi was isolated from 89.5% of the samples, Listeria monocytogenes s. str. from 45.3%, Listeria innocua from 15.8%, Listeria welshimeri from 3.1%, and Listeria seeligeri from 1.05%. Listeria ivanovii, Listeria murrayi, and Listeria denitrificans were not isolated.[Translated by the journal]


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