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Effect of Temperature on the Expression of Classical Enterotoxin Genes among Staphylococci Associated with Bovine Mastitis

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s11250-011-9882-5openalex-snapshot
Detection of superantigenic toxin genes in Staphylococcus aureus strains from subclinical bovine mastitis
inferredcites →https://doi.org/10.1007/s40588-018-0094-xopenalex-snapshot
Staphylococcus aureus as a Foodborne Pathogen
inferredcites →https://doi.org/10.1016/0168-1605(90)90036-5openalex-snapshot
Temperature limits of growth, TNase and enterotoxin production of Staphylococcus aureus strains isolated from foods
inferredcites →https://doi.org/10.1016/0168-1605(96)00952-xopenalex-snapshot
Enterotoxin production by coagulase-negative staphylococci isolated from goats' milk and cheese
inferredcites →https://doi.org/10.1016/j.fm.2009.06.007openalex-snapshot
Differential temporal expression of the staphylococcal enterotoxins genes during cell growth
inferredcites →https://doi.org/10.1016/j.fm.2014.05.020openalex-snapshot
Expression and production of staphylococcal enterotoxin C is substantially reduced in milk
inferredcites →https://doi.org/10.1016/j.idairyj.2013.01.003openalex-snapshot
Production of staphylococcal enterotoxin C in milk
inferredcites →https://doi.org/10.1016/j.idairyj.2014.05.001openalex-snapshot
Factors affecting staphylococcal enterotoxin Cbovine production in milk
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2005.10.013openalex-snapshot
Distribution of newly described enterotoxin-like genes in Staphylococcus aureus from food
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2008.03.024openalex-snapshot
Classical enterotoxigenic characteristics of Staphylococcus aureus strains isolated from bovine subclinical mastitis in Van, Turkey
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2013.02.005openalex-snapshot
Enterotoxigenic potential of coagulase-negative staphylococci
inferredcites →https://doi.org/10.1016/j.mimet.2014.10.014openalex-snapshot
Molecular analysis of Staphylococcus aureus pathogenicity islands (SaPI) and their superantigens combination of food samples
inferredcites →https://doi.org/10.1016/j.vetmic.2010.06.021openalex-snapshot
Detection of classical and newly described staphylococcal superantigen genes in coagulase-negative staphylococci isolated from bovine intramammary infections
inferredcites →https://doi.org/10.1016/s0022-2836(05)80360-2openalex-snapshot
Basic Local Alignment Search Tool
inferredcites →https://doi.org/10.1016/s0147-619x(02)00157-9openalex-snapshot
Mobile genetic elements and bacterial toxinoses: the superantigen-encoding pathogenicity islands of Staphylococcus aureus
inferredcites →https://doi.org/10.1016/s0167-7012(00)00241-4openalex-snapshot
How to optimize the drop plate method for enumerating bacteria
inferredcites →https://doi.org/10.1016/s0168-1605(00)00377-9openalex-snapshot
Staphylococcal enterotoxins
inferredcites →https://doi.org/10.1016/s1286-4579(01)01414-9openalex-snapshot
Pathogenicity and resistance islands of staphylococci
inferredcites →https://doi.org/10.1017/s0022029917000851openalex-snapshot
Characterisation ofStaphylococcus aureusstrains isolated from mastitis bovine milk in Argentina
inferredcites →https://doi.org/10.1017/s0950268800050949openalex-snapshot
Staphylococcal food poisoning in the United Kingdom, 1969–90
inferredcites →https://doi.org/10.1089/fpd.2009.0478openalex-snapshot
Polymerase Chain Reaction Detection of Enterotoxins Genes in Coagulase-Negative Staphylococci Isolated from Brazilian Minas Cheese
inferredcites →https://doi.org/10.1089/fpd.2018.2544openalex-snapshot
Effects of Temperature Abuse on the Growth and Staphylococcal Enterotoxin A Gene ( sea ) Expression of Staphylococcus aureus in Milk
inferredcites →https://doi.org/10.1111/j.1365-2672.2005.02569.xopenalex-snapshot
EnterotoxigenicStaphylococcus aureusin bulk milk in Norway
inferredcites →https://doi.org/10.1111/j.1574-6976.2011.00311.xopenalex-snapshot
Staphylococcus aureus and its food poisoning toxins: characterization and outbreak investigation
inferredcites →https://doi.org/10.1111/j.1600-065x.2008.00681.xopenalex-snapshot
The bacterial superantigen and superantigen‐like proteins
inferredcites →https://doi.org/10.1128/aem.00803-12openalex-snapshot
Elevated Enterotoxin A Expression and Formation in Staphylococcus aureus and Its Association with Prophage Induction
inferredcites →https://doi.org/10.1128/aem.54.2.566-569.1988openalex-snapshot
A quantitative study of enterotoxin production by sheep milk staphylococci
inferredcites →https://doi.org/10.1128/aem.67.12.5551-5557.2001openalex-snapshot
Enterotoxigenic Potential ofStaphylococcus intermedius
inferredcites →https://doi.org/10.1128/iai.61.1.356-359.1993openalex-snapshot
Staphylococcal enterotoxin A gene (sea) expression is not affected by the accessory gene regulator (agr)
inferredcites →https://doi.org/10.1128/iai.61.10.4254-4262.1993openalex-snapshot
Characterization of novel type C staphylococcal enterotoxins: biological and evolutionary implications
inferredcites →https://doi.org/10.1128/iai.65.6.2346-2352.1997openalex-snapshot
Characterization of the canine type C enterotoxin produced by Staphylococcus intermedius pyoderma isolates
inferredcites →https://doi.org/10.1128/jcm.38.8.2998-3003.2000openalex-snapshot
Genetic and Serologic Evaluation of Capsule Production by Bovine Mammary Isolates ofStaphylococcus aureusand OtherStaphylococcusspp. from Europe and the United States
inferredcites →https://doi.org/10.1145/1978942.1978963openalex-snapshot
The aligned rank transform for nonparametric factorial analyses using only anova procedures
inferredcites →https://doi.org/10.1145/3472749.3474784openalex-snapshot
An Aligned Rank Transform Procedure for Multifactor Contrast Tests
inferredcites →https://doi.org/10.1186/1471-2180-10-147openalex-snapshot
Acetic acid increases the phage-encoded enterotoxin A expression in Staphylococcus aureus
inferredcites →https://doi.org/10.1271/bbb.120391openalex-snapshot
Temperature Dependence of the Production of Staphylococcal Enterotoxin A byStaphylococcus aureus
inferredcites →https://doi.org/10.14202/ijoh.2021.70-77openalex-snapshot
Molecular detection of Staphylococcus aureus enterotoxin genes isolated from mastitic milk and humans in El-Behira, Egypt
inferredcites →https://doi.org/10.1590/s1517-83822009000200009openalex-snapshot
Detection of methicillin resistance and slime factor production of Staphylococcus aureus in bovine mastitis
inferredcites →https://doi.org/10.18637/jss.v069.i01openalex-snapshot
Least-Squares Means: The R Package lsmeans
inferredcites →https://doi.org/10.18637/jss.v069.i07openalex-snapshot
Recovering a Basic Space from Issue Scales inR
inferredcites →https://doi.org/10.18637/jss.v082.i13openalex-snapshot
lmerTest Package: Tests in Linear Mixed Effects Models
inferredcites →https://doi.org/10.2478/pjvs-2014-0058openalex-snapshot
Distribution of classical enterotoxin genes in staphylococci from milk of cows withand without mastitis and the cowshed environment
inferredcites →https://doi.org/10.3168/jds.2012-5864openalex-snapshot
Enterotoxin genes in coagulase-negative and coagulase-positive staphylococci isolated from bovine milk
inferredcites →https://doi.org/10.3168/jds.2015-9589openalex-snapshot
Bovine Staphylococcus aureus: Subtyping, evolution, and zoonotic transfer
inferredcites →https://doi.org/10.3168/jds.2016-11252openalex-snapshot
Short communication: Pasteurization as a means of inactivating staphylococcal enterotoxins A, B, and C in milk
inferredcites →https://doi.org/10.3168/jds.2018-15255openalex-snapshot
Effect of heat treatment on activity of staphylococcal enterotoxins of type A, B, and C in milk
inferredcites →https://doi.org/10.3390/toxins11030141openalex-snapshot
Staphylococcal Enterotoxin C Is an Important Virulence Factor for Mastitis
inferredcites →https://doi.org/10.3390/toxins12090584openalex-snapshot
Staphylococcal Enterotoxin C—An Update on SEC Variants, Their Structure and Properties, and Their Role in Foodborne Intoxications
inferredcites →https://doi.org/10.3390/toxins7124889openalex-snapshot
Prophage-Encoded Staphylococcal Enterotoxin A: Regulation of Production in Staphylococcus aureus Strains Representing Different Sea Regions
inferredcites →https://doi.org/10.3390/tropicalmed4020088openalex-snapshot
The One Health Approach—Why Is It So Important?
inferredcites →https://doi.org/10.4161/viru.2.6.18122openalex-snapshot
The formation ofStaphylococcus aureusenterotoxin in food environments and advances in risk assessment
inferredcites →https://doi.org/10.4172/2157-7110.1000128openalex-snapshot
Study of Staphylococcus aureus in raw and pasteurized milk consumed in the Reconcavo area of the State of Bahia, Brazil

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.4755342openalex-extracted
Comprehensive Analysis of Antimicrobial Resistance, Biofilm Formation and Virulence Factors of Staphylococci Isolated from Bovine Mastitis
inferred← citeshttps://doi.org/10.1007/s10068-025-01949-1openalex-snapshot
Evaluation of the antimicrobial and antibiofilm properties of Quercus phillyraeoides essential oil against Staphylococcus aureus
inferred← citeshttps://doi.org/10.1016/j.azn.2025.07.004openalex-snapshot
Confronting bacterial mastitis: From pathogen diversity to sustainable control in the post-antibiotic era
inferred← citeshttps://doi.org/10.1016/j.micpath.2025.107410openalex-snapshot
Staphylococcus species from bovine milk: Prevalence, antibiogram profile, and carriage of methicillin resistance and virulence genes
inferred← citeshttps://doi.org/10.1080/10408398.2025.2528165openalex-snapshot
Staphylococcus aureus in food safety: antimicrobial resistance, detection technologies, and future perspectives
inferred← citeshttps://doi.org/10.1186/s12866-024-03415-0openalex-snapshot
Coagulase-negative staphylococci from bovine milk: Antibiogram profiles and virulent gene detection
inferred← citeshttps://doi.org/10.1186/s12866-025-03870-3openalex-snapshot
Virulence traits, agr typing, multidrug resistance patterns, and biofilm ability of MDR Staphylococcus aureus recovered from clinical and subclinical mastitis in dairy cows
inferred← citeshttps://doi.org/10.2139/ssrn.4933938openalex-snapshot
Comprehensive Analysis of Antimicrobial Resistance, Biofilm Formation and Virulence Factors of Staphylococci Isolated from Bovine Mastitis
inferred← citeshttps://doi.org/10.3390/ani12030301openalex-snapshot
Characterization of Virulence Factors in Enterotoxin-Producing Staphylococcus aureus from Bulk Tank Milk
inferred← citeshttps://doi.org/10.3390/pathogens12070954openalex-snapshot
Impact of the Food-Related Stress Conditions on the Expression of Enterotoxin Genes among Staphylococcus aureus
inferred← citeshttps://doi.org/10.3390/toxins14100718openalex-snapshot
Co-Occurrence of Staphylococcus aureus and Ochratoxin A in Pasteurized Milk
inferred← citeshttps://doi.org/10.5433/1679-0359.2022v43n5p2309openalex-snapshot
Characterization of coagulase-positive Staphylococcus spp., antimicrobial resistance profile, and presence of enterotoxin-producing genes in goat milk in Paraná State
inferred← citeshttps://doi.org/10.5937/ffr0-55906openalex-snapshot
Presence of Staphylococcus aureus enterotoxin genes in milk and dairy products: A review
inferred← citeshttps://doi.org/10.6084/m9.figshare.26333216openalex-snapshot
Additional file 1 of Coagulase-negative staphylococci from bovine milk: Antibiogram profiles and virulent gene detection
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