2019
DOI: 10.1111/jam.14244
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Characterization ofListeria monocytogenesfrom encephalitis cases of small ruminants from different geographical regions, in Greece

Abstract: Aims The aim of this study was to evaluate the genetic diversity and resistance phenotypes of Listeria monocytogenes strains isolated from clinical encephalitis cases, and compare this population to isolates derived from tank milk of healthy animals. Methods and Results A total of 57 L. monocytogenes strains isolated from ruminant's listeriosis cases (n = 31) and from tank milk of healthy ruminants (n = 26) were characterized by species PCR, molecular serotyping, PCR detection of virulence genes, pulsed‐field … Show more

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Cited by 11 publications
(9 citation statements)
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References 38 publications
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“…213 Among the 13 serovars, 1/2a, 1/2b, and 4b are the most commonly identified in human and animal clinical isolates, with a noticeable preponderance of serotype 4b in major listeriosis outbreaks 157,266,278 and ruminant neurolisteriosis cases. 155,164,251,308 All 3 serotypes, apart from being implicated in disease, were additionally isolated from food, food processing and farm environments, and animal feces. 26,89,102,152,211,234,277 More recently, molecular typing methods such as pulsed field gel electrophoresis (PFGE), 36,106,123 multilocus sequence typing (MLST), 114 and whole-genome sequencing (WGS) 161 (reviewed in Datta and Burall 54 and Datta et al 55 ) have been employed to link clinical, food, and environmental isolates in epidemiological investigations during outbreaks (PFGE), to study genetic relatedness in Lm populations (MLST), or both (WGS).…”
Section: Lm Strain Heterogeneitymentioning
confidence: 99%
“…213 Among the 13 serovars, 1/2a, 1/2b, and 4b are the most commonly identified in human and animal clinical isolates, with a noticeable preponderance of serotype 4b in major listeriosis outbreaks 157,266,278 and ruminant neurolisteriosis cases. 155,164,251,308 All 3 serotypes, apart from being implicated in disease, were additionally isolated from food, food processing and farm environments, and animal feces. 26,89,102,152,211,234,277 More recently, molecular typing methods such as pulsed field gel electrophoresis (PFGE), 36,106,123 multilocus sequence typing (MLST), 114 and whole-genome sequencing (WGS) 161 (reviewed in Datta and Burall 54 and Datta et al 55 ) have been employed to link clinical, food, and environmental isolates in epidemiological investigations during outbreaks (PFGE), to study genetic relatedness in Lm populations (MLST), or both (WGS).…”
Section: Lm Strain Heterogeneitymentioning
confidence: 99%
“…The interaction of internalin with its receptor, E-cad, has been the focus of several studies [35, 46, 47]. InlA has been used as a virulence marker for detecting L. monocytogenes in food [8, 23, 28, 41, 50].…”
Section: Introductionmentioning
confidence: 99%
“…The Listeria spp.-specific marker prs was detected in all L. monocytogenes isolates. In Greece, a limited number of studies have provided characterization data (serotypic and genotypic diversity, carriage of virulence genes, antibiotic resistance or biofilm-forming ability) of L. monocytogenes strains isolated from different sources such as meat, meat products, meat-processing environment and vegetables [42,43], soft whey-cheese and related food-processing surfaces [44], veterinary samples and raw ovine milk [19] or human clinical cases [45]. However, to our knowledge, data on L. monocytogenes isolates from bovine milk in Greece are not available.…”
Section: Pcr-serogrouping Of the L Monocytogenes Isolatesmentioning
confidence: 99%