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Published on: August 9, 2011
Viability and Virulence of Listeria monocytogenes in Poultry
Sarah Panera-Martínez1,2, Rosa Capita1,2, Camino García-Fernández2
1Department of Food Hygiene and Technology, Veterinary Faculty, University of León, 24071 León, Spain.
Abstract:
The prevalence of Listeria monocytogenes in 30 samples of poultry was determined using culture-dependent (isolation on OCLA and confirmation by conventional polymerase chain reaction -PCR-, OCLA&PCR) and culture-independent (real-time polymerase chain reaction, q-PCR) methods. L. monocytogenes was detected in 15 samples (50.0%) by OCLA&PCR and in 20 (66.7%) by q-PCR. The concentrations (log10 cfu/g) of L. monocytogenes (q-PCR) ranged from 2.40 to 5.22 (total cells) and from <2.15 to 3.93 (viable cells). The two methods, q-PCR using a viability marker (v-PCR) and OCLA&PCR (gold standard), were compared for their capacity to detect viable cells of L. monocytogenes, with the potential to cause human disease. The values for sensitivity, specificity and efficiency of the v-PCR were 100%, 66.7% and 83.3%, respectively. The agreement between the two methods (kappa coefficient) was 0.67. The presence of nine virulence genes (hlyA, actA, inlB, inlA, inlC, inlJ, prfA, plcA and iap) was studied in 45 L. monocytogenes isolates (three from each positive sample) using PCR. All the strains harbored between six and nine virulence genes. Fifteen isolates (33.3% of the total) did not show the potential to form biofilm on a polystyrene surface, as determined by a crystal violet assay. The remaining strains were classified as weak (23 isolates, 51.1% of the total), moderate (one isolate, 2.2%) or strong (six isolates, 13.3%) biofilm producers. The strains were tested for susceptibility to a panel of 15 antibiotics. An average of 5.11 ± 1.30 resistances per isolate was observed. When the values for resistance and for reduced susceptibility were taken jointly, this figure rose to 6.91 ± 1.59. There was a prevalence of resistance or reduced susceptibility of more than 50.0% for oxacillin, cefoxitin, cefotaxime, cefepime ciprofloxacin, enrofloxacin and nitrofurantoin. For the remaining antibiotics tested, the corresponding values ranged from 0.0% for chloramphenicol to 48.9% for rifampicin. The high prevalence and level of L. monocytogenes with numerous virulence factors in poultry underline how crucial it is to follow correct hygiene procedures during the processing of this foodstuff in order to reduce the risk of human listeriosis.
Insights
Listeria monocytogenes is prevalent in poultry, detected by both culture-dependent and culture-independent methods. This pathogen possesses numerous virulence factors and antibiotic resistance, highlighting the need for strict hygiene in poultry processing to prevent human listeriosis.
Area of Science:
- Food Microbiology
- Food Safety
- Bacteriology
Background:
- Listeria monocytogenes is a significant foodborne pathogen.
- Poultry is a common vehicle for foodborne illnesses.
- Accurate detection and characterization of L. monocytogenes are crucial for public health.
Purpose of the Study:
- To determine the prevalence of L. monocytogenes in poultry samples.
- To compare culture-dependent and culture-independent detection methods.
- To characterize virulence factors, biofilm formation, and antibiotic resistance of L. monocytogenes isolates from poultry.
Main Methods:
- Culture-dependent methods: isolation on OCLA and confirmation by conventional PCR (OCLA&PCR).
- Culture-independent method: real-time PCR (q-PCR) with a viability marker (v-PCR).
- PCR for virulence genes, crystal violet assay for biofilm, and antibiotic susceptibility testing.
Main Results:
- L. monocytogenes was detected in 50% of samples by OCLA&PCR and 66.7% by q-PCR.
- All isolates possessed 6-9 virulence genes. Biofilm production varied, with 33.3% unable to form biofilms.
- High prevalence of antibiotic resistance/reduced susceptibility observed for several antibiotics, including oxacillin, ciprofloxacin, and nitrofurantoin.
Conclusions:
- The study highlights the significant presence of L. monocytogenes in poultry, with substantial virulence potential and antibiotic resistance.
- Culture-independent methods like q-PCR offer higher detection rates compared to traditional methods.
- Strict hygiene practices during poultry processing are essential to mitigate the risk of human listeriosis.
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