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Quantitative and ecological aspects of Listeria monocytogenes population heterogeneity

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inferredcites →https://doi.org/10.1002/bit.260270311openalex-snapshot
Kinetics of ethanol inhibition in alcohol fermentation
inferredcites →https://doi.org/10.1006/fmic.1997.0125openalex-snapshot
When is simple good enough: a comparison of the Gompertz, Baranyi, and three-phase linear models for fitting bacterial growth curves
inferredcites →https://doi.org/10.1007/217.1438-2385openalex-snapshot
European Food Research and Technology
inferredcites →https://doi.org/10.1007/bf00029864openalex-snapshot
A cold-regulated cyanobacterial gene cluster encodes RNA-binding protein and ribosomal protein S21
inferredcites →https://doi.org/10.1007/bf01584196openalex-snapshot
Modeling bacterial survival in unfavorable environments
inferredcites →https://doi.org/10.1007/bf01584209openalex-snapshot
A decision support system for prediction of microbial spoilage in foods
inferredcites →https://doi.org/10.1007/bf01639726openalex-snapshot
Listeriosis — History and actual developments
inferredcites →https://doi.org/10.1007/s00203-011-0716-7openalex-snapshot
Factors affecting survival of Listeria monocytogenes and Listeria innocua in soil samples
inferredcites →https://doi.org/10.1007/s00203-013-0878-6openalex-snapshot
Different assembly of acid and salt tolerance response in two dairy Listeria monocytogenes wild strains
inferredcites →https://doi.org/10.1007/s00217-012-1698-7openalex-snapshot
Inactivation of microorganisms in orange juice by high-pressure homogenization combined with its inherent heating effect
inferredcites →https://doi.org/10.1007/s00248-013-0364-3openalex-snapshot
Listeria monocytogenes Can Form Biofilms in Tap Water and Enter Into the Viable but Non-Cultivable State
inferredcites →https://doi.org/10.1016/0168-1605(93)90109-topenalex-snapshot
Behaviour of Listeria monocytogenes during the maturation of naturally and artificially contaminated salami: effect of lactic-acid bacteria starter cultures
inferredcites →https://doi.org/10.1016/0168-1605(96)00987-7openalex-snapshot
Quantitative risk analysis and the production of microbiologically safe food: an introduction
inferredcites →https://doi.org/10.1016/0168-1605(96)00991-9openalex-snapshot
Application of predictive microbiology to estimate the number of Bacillus cereus in pasteurised milk at the point of consumption
inferredcites →https://doi.org/10.1016/0378-1097(96)00204-2openalex-snapshot
Characterization of a barotolerant mutant of the yeast Saccharomyces cerevisiae: importance of trehalose content and membrane fluidity
inferredcites →https://doi.org/10.1016/j.cell.2007.01.023openalex-snapshot
Timescales of Genetic and Epigenetic Inheritance
inferredcites →https://doi.org/10.1016/j.cell.2012.06.036openalex-snapshot
Prophage Excision Activates Listeria Competence Genes that Promote Phagosomal Escape and Virulence
inferredcites →https://doi.org/10.1016/j.copbio.2010.11.012openalex-snapshot
Bacterial SOS response: a food safety perspective
inferredcites →https://doi.org/10.1016/j.femsle.2004.05.040openalex-snapshot
Antimicrobial effects of sanitizers against planktonic and sessile Listeria monocytogenes cells according to the growth phase
inferredcites →https://doi.org/10.1016/j.fm.2007.10.008openalex-snapshot
Heat and acid tolerance of Listeria monocytogenes after exposure to single and multiple sublethal stresses
inferredcites →https://doi.org/10.1016/j.fm.2009.06.006openalex-snapshot
Resistance of Listeria monocytogenes, Escherichia coli O157:H7 and Campylobacter jejuni after exposure to repetitive cycles of mild bactericidal treatments
inferredcites →https://doi.org/10.1016/j.fm.2009.12.002openalex-snapshot
Prediction of time to growth of Listeria monocytogenes using Monte Carlo simulation or regression analysis, influenced by sublethal heat and recovery conditions
inferredcites →https://doi.org/10.1016/j.fm.2010.04.015openalex-snapshot
Modelling: One word for many activities and uses
inferredcites →https://doi.org/10.1016/j.fm.2012.10.009openalex-snapshot
Evaluation of the strain variability of Salmonella enterica acid and heat resistance
inferredcites →https://doi.org/10.1016/j.fm.2014.04.008openalex-snapshot
Individual cell heterogeneity as variability source in population dynamics of microbial inactivation
inferredcites →https://doi.org/10.1016/j.fm.2014.04.015openalex-snapshot
Biofilm-associated persistence of food-borne pathogens
inferredcites →https://doi.org/10.1016/j.fm.2014.06.019openalex-snapshot
Modeling transfer of Escherichia coli O157:H7 and Listeria monocytogenes during preparation of fresh-cut salads: Impact of cutting and shredding practices
inferredcites →https://doi.org/10.1016/j.foodcont.2011.10.002openalex-snapshot
Adherence kinetics, resistance to benzalkonium chloride and microscopic analysis of mixed biofilms formed by Listeria monocytogenes and Pseudomonas putida
inferredcites →https://doi.org/10.1016/j.foodres.2014.08.044openalex-snapshot
Acquired acid adaptation of Listeria monocytogenes during its planktonic growth enhances subsequent survival of its sessile population to disinfection with natural organic compounds
inferredcites →https://doi.org/10.1016/j.foodres.2015.03.001openalex-snapshot
Impact of growth conditions and role of sigB on Listeria monocytogenes fitness in single and mixed biofilms cultured with Lactobacillus plantarum
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2004.03.031openalex-snapshot
Interactions in biofilms between Listeria monocytogenes and resident microorganisms from food industry premises
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2004.11.038openalex-snapshot
GInaFiT, a freeware tool to assess non-log-linear microbial survivor curves
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2005.08.014openalex-snapshot
A systematic approach to determine global thermal inactivation parameters for various food pathogens
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2006.12.016openalex-snapshot
Quantifying the effects of heating temperature, and combined effects of heating medium pH and recovery medium pH on the heat resistance of Salmonella typhimurium
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2008.12.025openalex-snapshot
Quantitative risk assessment: Is more complex always better?
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2009.05.007openalex-snapshot
Influence of pH, type of acid and recovery media on the thermal inactivation of Listeria innocua
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2010.10.020openalex-snapshot
Efficiency of different sanitation methods on Listeria monocytogenes biofilms formed under various environmental conditions
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2010.10.029openalex-snapshot
Mixed species biofilms of Listeria monocytogenes and Lactobacillus plantarum show enhanced resistance to benzalkonium chloride and peracetic acid
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2011.01.001openalex-snapshot
Effect of acid tolerance response (ATR) on attachment of Listeria monocytogenes Scott A to stainless steel under extended exposure to acid or/and salt stress and resistance of sessile cells to subsequent strong acid challenge
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2011.07.012openalex-snapshot
Variability in biofilm production by Listeria monocytogenes correlated to strain origin and growth conditions
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2011.09.023openalex-snapshot
Modelling of growth, growth/no-growth interface and nonthermal inactivation areas of Listeria in foods
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2012.03.029openalex-snapshot
Disease burden of foodborne pathogens in the Netherlands, 2009
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2012.07.027openalex-snapshot
Adaptive acid tolerance response of Listeria monocytogenes strains under planktonic and immobilized growth conditions
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2013.03.003openalex-snapshot
Modeling the Listeria innocua micropopulation lag phase and its variability
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2013.05.025openalex-snapshot
Diversity assessment of Listeria monocytogenes biofilm formation: Impact of growth condition, serotype and strain origin
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2013.07.001openalex-snapshot
Emergence of pulsed electric fields resistance in Salmonella enterica serovar Typhimurium SL1344
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2013.07.012openalex-snapshot
A predictive model for assessment of decontamination effects of lactic acid and chitosan used in combination on Vibrio parahaemolyticus in shrimps
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2013.08.011openalex-snapshot
Isolation and quantification of highly acid resistant variants of Listeria monocytogenes
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2013.11.013openalex-snapshot
Impact of acid adaptation on attachment of Listeria monocytogenes to stainless steel during long-term incubation under low or moderate temperature conditions and on subsequent recalcitrance of attached cells to lethal acid treatments
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2014.10.021openalex-snapshot
Quantifying variability on thermal resistance of Listeria monocytogenes
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2015.04.021openalex-snapshot
Performance of stress resistant variants of Listeria monocytogenes in mixed species biofilms with Lactobacillus plantarum
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2015.05.006openalex-snapshot
Quantifying strain variability in modeling growth of Listeria monocytogenes
inferredcites →https://doi.org/10.1016/j.ijmm.2010.11.006openalex-snapshot
Contribution of Listeria monocytogenes RecA to acid and bile survival and invasion of human intestinal Caco-2 cells
inferredcites →https://doi.org/10.1016/j.jinf.2010.08.007openalex-snapshot
A large outbreak of Listeria monocytogenes infection with short incubation period in a tertiary care hospital
inferredcites →https://doi.org/10.1016/j.meegid.2015.08.008openalex-snapshot
The evolution and epidemiology of Listeria monocytogenes in Europe and the United States
inferredcites →https://doi.org/10.1016/j.micinf.2007.05.001openalex-snapshot
Listeriology (1926–2007): the rise of a model pathogen
inferredcites →https://doi.org/10.1016/j.micpath.2013.04.007openalex-snapshot
Virulence aspects of Listeria monocytogenes LO28 high pressure-resistant variants
inferredcites →https://doi.org/10.1016/j.tim.2008.05.006openalex-snapshot
Modulation of stress and virulence in Listeria monocytogenes
inferredcites →https://doi.org/10.1016/j.tim.2014.03.008openalex-snapshot
Bacterial persisters: formation, eradication, and experimental systems
inferredcites →https://doi.org/10.1016/s0168-1605(00)00223-3openalex-snapshot
Mathematical modelling of the growth rate and lag time for Listeria monocytogenes
inferredcites →https://doi.org/10.1016/s0168-1605(00)00224-5openalex-snapshot
Modelling the growth rate of Listeria monocytogenes with a multiplicative type model including interactions between environmental factors
inferredcites →https://doi.org/10.1016/s0168-1605(00)00225-7openalex-snapshot
Separation of uncertainty and variability in quantitative microbial risk assessment models
inferredcites →https://doi.org/10.1016/s0168-1605(00)00362-7openalex-snapshot
Structural model requirements to describe microbial inactivation during a mild heat treatment
inferredcites →https://doi.org/10.1016/s0168-1605(01)00624-9openalex-snapshot
On calculating sterility in thermal preservation methods: application of the Weibull frequency distribution model
inferredcites →https://doi.org/10.1016/s0168-1605(01)00640-7openalex-snapshot
Modelling the growth kinetics of Listeria as a function of temperature, pH and organic acid concentration
inferredcites →https://doi.org/10.1016/s0168-1605(01)00742-5openalex-snapshot
On the use of the Weibull model to describe thermal inactivation of microbial vegetative cells
inferredcites →https://doi.org/10.1016/s0168-1605(02)00003-xopenalex-snapshot
Variation among Escherichia coli O157:H7 strains relative to their growth, survival, thermal inactivation, and toxin production in broth
inferredcites →https://doi.org/10.1016/s0168-1605(03)00049-7openalex-snapshot
Predicting thermal inactivation in media of different pH of Salmonella grown at different temperatures
inferredcites →https://doi.org/10.1016/s0168-1605(98)00189-5openalex-snapshot
Validation of predictive models describing the growth of Listeria monocytogenes
inferredcites →https://doi.org/10.1016/s0168-1605(99)00205-6openalex-snapshot
Survival of osmotic and acid stress by Listeria monocytogenes strains of clinical or meat origin
inferredcites →https://doi.org/10.1016/s0740-0020(14)00320-7openalex-snapshot
International Journal of Food Microbiology
inferredcites →https://doi.org/10.1016/s0958-6946(01)00125-xopenalex-snapshot
Bacterial stress response in Listeria monocytogenes: jumping the hurdles imposed by minimal processing
inferredcites →https://doi.org/10.1017/s0950268805005376openalex-snapshot
Nationwide outbreak of listeriosis due to contaminated meat
inferredcites →https://doi.org/10.1023/b:bile.0000019559.84305.47openalex-snapshot
Determination of stable housekeeping genes, differentially regulated target genes and sample integrity: BestKeeper – Excel-based tool using pair-wise correlations
inferredcites →https://doi.org/10.1038/nrm2198openalex-snapshot
Lessons from 50 years of SOS DNA-damage-induced mutagenesis
inferredcites →https://doi.org/10.1038/nrmicro1460openalex-snapshot
Microbial cell individuality and the underlying sources of heterogeneity
inferredcites →https://doi.org/10.1038/nrmicro2171openalex-snapshot
Listeria monocytogenes — from saprophyte to intracellular pathogen
inferredcites →https://doi.org/10.1046/j.1365-2672.1998.00334.xopenalex-snapshot
Heat resistance of Listeria monocytogenes in dairy products as affected by the growth medium
inferredcites →https://doi.org/10.1046/j.1365-2672.2002.01541.xopenalex-snapshot
Acid stress in the food pathogen Bacillus cereus
inferredcites →https://doi.org/10.1046/j.1365-2672.2003.02013.xopenalex-snapshot
Evaluation of the pH-dependent, stationary-phase acid tolerance in Listeria monocytogenes and Salmonella Typhimurium DT104 induced by culturing in media with 1% glucose: a comparative study with Escherichia coli O157:H7
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03636.xopenalex-snapshot
The CtsR regulator of Listeria monocytogenes contains a variant glycine repeat region that affects piezotolerance, stress resistance, motility and virulence
inferredcites →https://doi.org/10.1051/vetres:2002022openalex-snapshot
Environmental and physico-chemical factors induce VBNC state in Listeria monocytogenes
inferredcites →https://doi.org/10.1056/nejmoa1215837openalex-snapshot
Multistate Outbreak of Listeriosis Associated with Cantaloupe
inferredcites →https://doi.org/10.1080/09168451.2014.915729openalex-snapshot
Cell motility and biofilm formation in Bacillus subtilis are affected by the ribosomal proteins, S11 and S21
inferredcites →https://doi.org/10.1080/10409230701648502openalex-snapshot
Mutation as a Stress Response and the Regulation of Evolvability
inferredcites →https://doi.org/10.1089/cmb.2009.0238openalex-snapshot
Ray: Simultaneous Assembly of Reads from a Mix of High-Throughput Sequencing Technologies
inferredcites →https://doi.org/10.1089/fpd.2006.3.196openalex-snapshot
Characterization of a Spontaneous, Pressure-Tolerant Listeria monocytogenes Scott A cts R Deletion Mutant
inferredcites →https://doi.org/10.1089/fpd.2010.0631openalex-snapshot
Large Listeriosis Outbreak Linked to Cheese Made from Pasteurized Milk, Germany, 2006–2007
inferredcites →https://doi.org/10.1089/fpd.2015.1939openalex-snapshot
Multi-Province Listeriosis Outbreak Linked to Contaminated Deli Meat Consumed Primarily in Institutional Settings, Canada, 2008
inferredcites →https://doi.org/10.1089/fpd.2015.1966openalex-snapshot
Estimates of Foodborne Illness–Related Hospitalizations and Deaths in Canada for 30 Specified Pathogens and Unspecified Agents
inferredcites →https://doi.org/10.1093/genetics/173.1.1openalex-snapshot
Chaos and Order in Spontaneous Mutation
inferredcites →https://doi.org/10.1093/nar/30.9.1886openalex-snapshot
Over-representation of repeats in stress response genes: a strategy to increase versatility under stressful conditions?
inferredcites →https://doi.org/10.1099/00221287-147-8-2275openalex-snapshot
Starvation survival in Listeria monocytogenes: characterization of the response and the role of known and novel components
inferredcites →https://doi.org/10.1099/mic.0.035196-0openalex-snapshot
The SOS response of Listeria monocytogenes is involved in stress resistance and mutagenesis
inferredcites →https://doi.org/10.1101/gr.229202openalex-snapshot
BLAT —The BLAST -Like Alignment Tool
inferredcites →https://doi.org/10.1111/ele.12159openalex-snapshot
The form of a trade‐off determines the response to competition
inferredcites →https://doi.org/10.1111/j.1365-2621.2008.01839.xopenalex-snapshot
Biofilms in the food industry: problems and potential solutions
inferredcites →https://doi.org/10.1111/j.1365-2672.1994.tb01644.xopenalex-snapshot
Heat resistance of different serovars of Listeria monocytogenes
inferredcites →https://doi.org/10.1111/j.1365-2672.1996.tb01946.xopenalex-snapshot
Indices for performance evaluation of predictive models in food microbiology
inferredcites →https://doi.org/10.1111/j.1365-2672.2008.03873.xopenalex-snapshot
The growth limits of a large number ofListeria monocytogenesstrains at combinations of stresses show serotype- and niche-specific traits
inferredcites →https://doi.org/10.1111/j.1365-2672.2008.03909.xopenalex-snapshot
Effects of repeated cycles of acid challenge and growth on the phenotype and virulence ofSalmonella enterica
inferredcites →https://doi.org/10.1111/j.1365-2672.2012.05434.xopenalex-snapshot
Role of glutamate metabolism in bacterial responses towards acid and other stresses
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05264.xopenalex-snapshot
Different genetic programmes within identical bacteria under identical conditions: the phenomenon of bistability greatly modifies our view on bacterial populations
inferredcites →https://doi.org/10.1111/j.1472-765x.1990.tb00119.xopenalex-snapshot
Heat resistance of Listeria: strain differences and effects of meat type and curing salts
inferredcites →https://doi.org/10.1111/j.1472-765x.1992.tb00691.xopenalex-snapshot
Induced acid tolerance in Listeria monocytogenes
inferredcites →https://doi.org/10.1111/j.1472-765x.1996.tb01123.xopenalex-snapshot
The effect of temperature and growth rate on the susceptibility of Listeria monocytogenes to environmental stress conditions
inferredcites →https://doi.org/10.1111/j.1753-4887.1981.tb06752.xopenalex-snapshot
Proceedings of the National Academy of Sciences of the United States of America
inferredcites →https://doi.org/10.1126/science.1099390openalex-snapshot
Bacterial Persistence as a Phenotypic Switch
inferredcites →https://doi.org/10.1128/aem.00004-14openalex-snapshot
Transcriptional and Phenotypic Responses of Listeria monocytogenes to Chlorine Dioxide
inferredcites →https://doi.org/10.1128/aem.00227-12openalex-snapshot
Characterization of the Intracellular Glutamate Decarboxylase System: Analysis of Its Function, Transcription, and Role in the Acid Resistance of Various Strains of Listeria monocytogenes
inferredcites →https://doi.org/10.1128/aem.00703-11openalex-snapshot
Comparing Nonsynergy Gamma Models and Interaction Models To Predict Growth of Emetic Bacillus cereus for Combinations of pH and Water Activity Values
inferredcites →https://doi.org/10.1128/aem.00876-06openalex-snapshot
General Model, Based on Two Mixed Weibull Distributions of Bacterial Resistance, for Describing Various Shapes of Inactivation Curves
inferredcites →https://doi.org/10.1128/aem.00900-15openalex-snapshot
Phenotypic Heterogeneity, a Phenomenon That May Explain Why Quorum Sensing Does Not Always Result in Truly Homogenous Cell Behavior
inferredcites →https://doi.org/10.1128/aem.01018-14openalex-snapshot
Reservoirs of Listeria Species in Three Environmental Ecosystems
inferredcites →https://doi.org/10.1128/aem.01286-15openalex-snapshot
Spatial and Temporal Factors Associated with an Increased Prevalence of Listeria monocytogenes in Spinach Fields in New York State
inferredcites →https://doi.org/10.1128/aem.01801-06openalex-snapshot
Piezotolerant Small-Colony Variants with Increased Thermotolerance, Antibiotic Susceptibility, and Low Invasiveness in a Clonal Staphylococcus aureus Population
inferredcites →https://doi.org/10.1128/aem.02184-13openalex-snapshot
Survival of Bactericidal Antibiotic Treatment by a Persister Subpopulation of Listeria monocytogenes
inferredcites →https://doi.org/10.1128/aem.02434-09openalex-snapshot
Population Diversity of Listeria monocytogenes LO28: Phenotypic and Genotypic Characterization of Variants Resistant to High Hydrostatic Pressure
inferredcites →https://doi.org/10.1128/aem.02617-10openalex-snapshot
Isolation of Highly Heat-Resistant Listeria monocytogenes Variants by Use of a Kinetic Modeling-Based Sampling Scheme
inferredcites →https://doi.org/10.1128/aem.02824-15openalex-snapshot
The Connection between Persistent, Disinfectant-Resistant Listeria monocytogenes Strains from Two Geographically Separate Iberian Pork Processing Plants: Evidence from Comparative Genome Analysis
inferredcites →https://doi.org/10.1128/aem.03715-12openalex-snapshot
Genome Sequencing Identifies Two Nearly Unchanged Strains of Persistent Listeria monocytogenes Isolated at Two Different Fish Processing Plants Sampled 6 Years Apart
inferredcites →https://doi.org/10.1128/aem.60.1.195-203.1994openalex-snapshot
Evaluation of Data Transformations and Validation of a Model for the Effect of Temperature on Bacterial Growth
inferredcites →https://doi.org/10.1128/aem.62.4.1252-1256.1996openalex-snapshot
Influence of environmental parameters on phosphatidylcholine phospholipase C production in Listeria monocytogenes: a convenient method to differentiate L. monocytogenes from other Listeria species
inferredcites →https://doi.org/10.1128/aem.62.5.1693-1698.1996openalex-snapshot
Adaptive acid tolerance response in Listeria monocytogenes: isolation of an acid-tolerant mutant which demonstrates increased virulence
inferredcites →https://doi.org/10.1128/aem.63.3.945-950.1997openalex-snapshot
Escherichia coli mutants resistant to inactivation by high hydrostatic pressure
inferredcites →https://doi.org/10.1128/aem.68.7.3183-3189.2002openalex-snapshot
Characterization of a Listeria monocytogenes Scott A Isolate with High Tolerance towards High Hydrostatic Pressure
inferredcites →https://doi.org/10.1128/aem.71.12.8390-8396.2005openalex-snapshot
Contingency Locus in ctsR of Listeria monocytogenes Scott A: a Strategy for Occurrence of Abundant Piezotolerant Isolates within Clonal Populations
inferredcites →https://doi.org/10.1128/aem.71.6.2940-2948.2005openalex-snapshot
Influence of Stress on Individual Lag Time Distributions of Listeria monocytogenes
inferredcites →https://doi.org/10.1128/aem.72.1.124-134.2006openalex-snapshot
Development of a Microbial Model for the Combined Effect of Temperature and pH on Spoilage of Ground Meat, and Validation of the Model under Dynamic Temperature Conditions
inferredcites →https://doi.org/10.1128/cmr.12.1.147openalex-snapshot
Antiseptics and Disinfectants: Activity, Action, and Resistance
inferredcites →https://doi.org/10.1128/cmr.15.2.167-193.2002openalex-snapshot
Biofilms: Survival Mechanisms of Clinically Relevant Microorganisms
inferredcites →https://doi.org/10.1128/eissn.1098-5336openalex-snapshot
Applied and Environmental Microbiology
inferredcites →https://doi.org/10.1128/iai.60.1.219-230.1992openalex-snapshot
Nucleotide sequence of the lecithinase operon of Listeria monocytogenes and possible role of lecithinase in cell-to-cell spread
inferredcites →https://doi.org/10.1128/jb.00980-12openalex-snapshot
Virulence or Niche Factors: What's in a Name?
inferredcites →https://doi.org/10.1128/jb.01544-12openalex-snapshot
Inactivation of Ribosomal Protein Genes in Bacillus subtilis Reveals Importance of Each Ribosomal Protein for Cell Proliferation and Cell Differentiation
inferredcites →https://doi.org/10.1128/jb.149.1.1-5.1982openalex-snapshot
Relationship between temperature and growth rate of bacterial cultures
inferredcites →https://doi.org/10.1128/jb.179.22.7063-7071.1997openalex-snapshot
Temperature-dependent regulation of the ribosomal small-subunit protein S21 in the cyanobacterium Anabaena variabilis M3
inferredcites →https://doi.org/10.1128/mmbr.00038-10openalex-snapshot
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS
inferredcites →https://doi.org/10.1128/mmbr.05028-11openalex-snapshot
Culture History and Population Heterogeneity as Determinants of Bacterial Adaptation: the Adaptomics of a Single Environmental Transition
inferredcites →https://doi.org/10.1128/mmbr.62.2.275-293.1998openalex-snapshot
Short-Sequence DNA Repeats in Prokaryotic Genomes
inferredcites →https://doi.org/10.1128/mmbr.67.3.429-453.2003openalex-snapshot
Surviving the Acid Test: Responses of Gram-Positive Bacteria to Low pH
inferredcites →https://doi.org/10.1146/annurev-food-041715-033128openalex-snapshot
Impact of Pathogen Population Heterogeneity and Stress-Resistant Variants on Food Safety
inferredcites →https://doi.org/10.1146/annurev.micro.62.081307.163002openalex-snapshot
Bistability, Epigenetics, and Bet-Hedging in Bacteria
inferredcites →https://doi.org/10.1146/foodopenalex-snapshot
Annual Review of Food Science and Technology
inferredcites →https://doi.org/10.1186/1471-2164-7-126openalex-snapshot
Lactobacillus plantarum gene clusters encoding putative cell-surface protein complexes for carbohydrate utilization are conserved in specific gram-positive bacteria
inferredcites →https://doi.org/10.1186/1471-2164-9-75openalex-snapshot
The RAST Server: Rapid Annotations using Subsystems Technology
inferredcites →https://doi.org/10.1201/9781420017410openalex-snapshot
Kinetic Modeling of Reactions In Foods
inferredcites →https://doi.org/10.1371/journal.pone.0028590openalex-snapshot
Generation of Variants in Listeria monocytogenes Continuous-Flow Biofilms Is Dependent on Radical-Induced DNA Damage and RecA-Mediated Repair
inferredcites →https://doi.org/10.1371/journal.pone.0073603openalex-snapshot
Characterisation of the Transcriptomes of Genetically Diverse Listeria monocytogenes Exposed to Hyperosmotic and Low Temperature Conditions Reveal Global Stress-Adaptation Mechanisms
inferredcites →https://doi.org/10.1371/journal.pone.0075969openalex-snapshot
Biotic and Abiotic Soil Properties Influence Survival of Listeria monocytogenes in Soil
inferredcites →https://doi.org/10.1371/journal.pone.0077276openalex-snapshot
Co-Culture with Listeria monocytogenes within a Dual-Species Biofilm Community Strongly Increases Resistance of Pseudomonas putida to Benzalkonium Chloride
inferredcites →https://doi.org/10.2807/esm.11.06.00630-enopenalex-snapshot
Surveillance of listeriosis in Finland during 1995-2004
inferredcites →https://doi.org/10.3201/eid0304.970411openalex-snapshot
Quantitative Risk Assessment: An Emerging Tool for Emerging Foodborne Pathogens
inferredcites →https://doi.org/10.3201/eid1701.09-1101p1openalex-snapshot
Foodborne Illness Acquired in the United States—Major Pathogens
inferredcites →https://doi.org/10.3389/fcimb.2013.00087openalex-snapshot
Listeria monocytogenes, a down-to-earth pathogen
inferredcites →https://doi.org/10.3389/fmicb.2014.00258openalex-snapshot
The importance of the viable but non-culturable state in human bacterial pathogens
inferredcites →https://doi.org/10.3389/fmicb.2015.00422openalex-snapshot
Diversity of acid stress resistant variants of Listeria monocytogenes and the potential role of ribosomal protein S21 encoded by rpsU
inferredcites →https://doi.org/10.34218/ijommopenalex-snapshot
INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY
inferredcites →https://doi.org/10.4315/0362-028x-60.10.1201openalex-snapshot
Listeria monocytogenes Survival in Soil and Incidence in Agricultural Soils
inferredcites →https://doi.org/10.4315/0362-028x-61.6.683openalex-snapshot
Heat Resistance and Fatty Acid Composition of Listeria monocytogenes: Effect of pH, Acidulant, and Growth Temperature
inferredcites →https://doi.org/10.4315/0362-028x-64.3.410openalex-snapshot
Heat Resistance of Listeria monocytogenes
inferredcites →https://doi.org/10.4315/0362-028x-64.9.1362openalex-snapshot
Role of the Glutamate Decarboxylase Acid Resistance System in the Survival of Listeria monocytogenes LO28 in Low pH Foods
inferredcites →https://doi.org/10.4315/0362-028x-65.11.1717openalex-snapshot
Biofilm Formation by Acid-Adapted and Nonadapted Listeria monocytogenes in Fresh Beef Decontamination Washings and Its Subsequent Inactivation with Sanitizers
inferredcites →https://doi.org/10.4315/0362-028x-65.11.1811openalex-snapshot
Listeria monocytogenes Virulence and Pathogenicity, a Food Safety Perspective
inferredcites →https://doi.org/10.4315/0362-028x-65.4.709openalex-snapshot
Control of Listeria monocytogenes in the Food-Processing Environment
inferredcites →https://doi.org/10.4315/0362-028x-66.9.1611openalex-snapshot
Thermal Inactivation, Growth, and Survival Studies of Listeria monocytogenes Strains Belonging to Three Distinct Genotypic Lineages
inferredcites →https://doi.org/10.4315/0362-028x-67.10.2189openalex-snapshot
Occurrence of Listeria monocytogenes in Green Table Olives
inferredcites →https://doi.org/10.4315/0362-028x-69.11.2640openalex-snapshot
Growth and Stress Resistance Variation in Culture Broth among Listeria monocytogenes Strains of Various Serotypes and Origins
inferredcites →https://doi.org/10.4315/0362-028x-71.10.2007openalex-snapshot
Inactivation Kinetics of Three Listeria monocytogenes Strains under High Hydrostatic Pressure
inferredcites →https://doi.org/10.4315/0362-028x-72.12.2618openalex-snapshot
Modeling Penicillium expansum Resistance to Thermal and Chlorine Treatments
inferredcites →https://doi.org/10.4315/0362-028x.jfp-11-417openalex-snapshot
Annual Cost of Illness and Quality-Adjusted Life Year Losses in the United States Due to 14 Foodborne Pathogens
inferredcites →https://doi.org/10.4315/0362-028x.jfp-13-150openalex-snapshot
Listeria monocytogenes Persistence in Food-Associated Environments: Epidemiology, Strain Characteristics, and Implications for Public Health
inferredcites →https://doi.org/10.5281/zenodo.3521934openalex-snapshot
Acid tolerance in Listeria monocytogenes: the adaptive acid tolerance response (ATR) and growth-phase-dependent acid resistance

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4671025openalex-extracted
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2024.110680openalex-snapshot
Stress resistant rpsU variants of Listeria monocytogenes can become underrepresented due to enrichment bias
inferred← citeshttps://doi.org/10.18174/582186openalex-snapshot
Listeria monocytogenes stress resistant variants : impact on high hydrostatic pressure processing efficacy
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