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Emergence of Macrolide Resistance Gene mph (B) in Streptococcus uberis and Cooperative Effects with rdmC -Like Gene
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0378-1097(92)90369-yopenalex-snapshot
Purification and characterization of macrolide 2′-phosphotransferase type II from a strain of Escherichia coli highly resistant to macrolide antibiotics
inferredcites →https://doi.org/10.1016/0378-1119(89)90421-6openalex-snapshot
Production of a hybrid macrolide antibiotic in Streptomyces ambofaciens and Streptomyces lividans by introduction of a cloned carbomycin biosynthetic gene from Streptomyces thermotolerans
inferredcites →https://doi.org/10.1016/s0167-4838(00)00089-3openalex-snapshot
Modifications of aclacinomycin T by aclacinomycin methyl esterase (RdmC) and aclacinomycin-10-hydroxylase (RdmB) from Streptomyces purpurascens
inferredcites →https://doi.org/10.1016/s0378-1097(00)00429-8openalex-snapshot
A transposon carrying the gene mphB for macrolide 2′-phosphotransferase II
inferredcites →https://doi.org/10.1016/s0378-1097(03)00961-3openalex-snapshot
The role of histidine residues conserved in the putative ATP-binding region of macrolide 2′-phosphotransferase II
inferredcites →https://doi.org/10.1016/s0378-1097(98)00003-2openalex-snapshot
Expression of the mphB gene for macrolide 2′-phosphotransferase II from Escherichia coli in Staphylococcus aureus
inferredcites →https://doi.org/10.1016/s0749-0720(02)00067-1openalex-snapshot
Mastitis therapy and pharmacology
inferredcites →https://doi.org/10.1053/tvjl.1998.0298openalex-snapshot
Streptococcus uberis: A Permanent Barrier to the Control of Bovine Mastitis?
inferredcites →https://doi.org/10.1111/j.1365-2885.1992.tb00986.xopenalex-snapshot
Pharmacokinetics of spiramycin after intravenous, intramuscular and subcutaneous administration in lactating cows
inferredcites →https://doi.org/10.1111/j.1574-6968.1985.tb01618.xopenalex-snapshot
Sequence-specific endonuclease from the transformable cyanobacteriumAnacystis nidulansR2
inferredcites →https://doi.org/10.1111/j.1574-6968.2007.00643.xopenalex-snapshot
Resistance phenotypes conferred by macrolide phosphotransferases
inferredcites →https://doi.org/10.1128/aac.28.3.421openalex-snapshot
Plasmid-mediated resistance to lincomycin by inactivation in Staphylococcus haemolyticus
inferredcites →https://doi.org/10.1128/aac.38.9.1899openalex-snapshot
Contribution of VanY D,D-carboxypeptidase to glycopeptide resistance in Enterococcus faecalis by hydrolysis of peptidoglycan precursors
inferredcites →https://doi.org/10.1128/aac.39.10.2359openalex-snapshot
Nucleotide sequence and characterization of erythromycin resistance determinant that encodes macrolide 2'-phosphotransferase I in Escherichia coli
inferredcites →https://doi.org/10.1128/aac.40.11.2562openalex-snapshot
Detection of erythromycin-resistant determinants by PCR
inferredcites →https://doi.org/10.1128/aac.43.12.2823openalex-snapshot
Nomenclature for Macrolide and Macrolide-Lincosamide-Streptogramin B Resistance Determinants
inferredcites →https://doi.org/10.1128/aac.45.1.1-12.2001openalex-snapshot
Macrolide Resistance Conferred by Base Substitutions in 23S rRNA
inferredcites →https://doi.org/10.1128/iai.71.1.132-139.2003openalex-snapshot
The Hyaluronic Acid Capsule of Streptococcus uberis Is Not Required for the Development of Infection and Clinical Mastitis
inferredcites →https://doi.org/10.1128/jb.178.1.306-308.1996openalex-snapshot
AcrAB efflux pump plays a major role in the antibiotic resistance phenotype of Escherichia coli multiple-antibiotic-resistance (Mar) mutants
inferredcites →https://doi.org/10.1128/jb.179.22.6929-6936.1997openalex-snapshot
Streptothricin biosynthesis is catalyzed by enzymes related to nonribosomal peptide bond formation
inferredcites →https://doi.org/10.1128/mmbr.69.2.326-356.2005openalex-snapshot
The TetR Family of Transcriptional Repressors
inferredcites →https://doi.org/10.1136/vr.148.22.683openalex-snapshot
Aetiology of clinical mastitis in six Somerset dairy herds
inferredcites →https://doi.org/10.1248/bpb.22.227openalex-snapshot
Nucleotide Sequence of the Gene Cluster Containing the mphB Gene for Macrolide 2'-Phosphotransferase II.
inferredcites →https://doi.org/10.1542/peds.65.1.187openalex-snapshot
National Committee for Clinical Laboratory Standards
inferredcites →https://doi.org/10.2174/1567204052931113openalex-snapshot
Macrolide Antibiotics: Binding Site, Mechanism of Action, Resistance
inferredcites →https://doi.org/10.2174/1568026033452159openalex-snapshot
Macrolide Antibiotics: Binding Site, Mechanism of Action, Resistance
inferredcites →https://doi.org/10.3168/jds.s0022-0302(06)72330-xopenalex-snapshot
Prevalence of Mastitis Pathogens and Their Resistance Against Antimicrobial Agents in Dairy Cows in Brandenburg, Germany
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.4601470openalex-extracted
Application of MALDI-TOF Ms to Identify and Detect Antimicrobial-Resistant Streptococcus Uberis Associated with Bovine Mastitis
inferred← citeshttps://doi.org/10.1002/prot.26621openalex-snapshot
TetR and OmpR family regulators in natural product biosynthesis and resistance
inferred← citeshttps://doi.org/10.1007/978-3-030-46721-0_10openalex-snapshot
Molecular Biology Perspective of Susceptibility and Resistance in Main Target Pathogens in the Respective Species and Antimicrobials of Concern
inferred← citeshttps://doi.org/10.1007/s11356-016-7521-4openalex-snapshot
Presence and distribution of Macrolides-Lincosamide-Streptogramin resistance genes and potential indicator ARGs in the university ponds in Guangzhou, China
inferred← citeshttps://doi.org/10.1016/b978-0-443-14170-6.00027-5openalex-snapshot
Association of antimicrobial biodegradation with the evolution of antimicrobial resistance in ecosystems
inferred← citeshttps://doi.org/10.1016/j.biortech.2017.03.104openalex-snapshot
Occurrence of antibiotic resistance genes and mobile genetic elements in enterococci and genomic DNA during anaerobic digestion of pharmaceutical waste sludge with different pretreatments
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2017.05.149openalex-snapshot
Organic compounds stimulate horizontal transfer of antibiotic resistance genes in mixed wastewater treatment systems
inferred← citeshttps://doi.org/10.1016/j.foodres.2025.117352openalex-snapshot
Mobile genetic elements potentially drive adaptive evolution of pork-derived multidrug-resistant Salmonella Derby ST40 lineages: An integrated analysis
inferred← citeshttps://doi.org/10.1016/j.ijmm.2015.04.005openalex-snapshot
Virulence factors and mechanisms of antimicrobial resistance in Shigella strains from periurban areas of Lima (Peru)
inferred← citeshttps://doi.org/10.1016/j.jgar.2017.03.015openalex-snapshot
The novel mef (C)– mph (G) macrolide resistance genes are conveyed in the environment on various vectors
inferred← citeshttps://doi.org/10.1016/j.jwpe.2025.109195openalex-snapshot
Diversity and resistome shifts in combined clinical-domestic effluent following submerged aerated filter treatment: Insights from culture-dependent and independent methods
inferred← citeshttps://doi.org/10.1016/j.plasmid.2026.102773openalex-snapshot
Enhanced resistance to macrolides and tetracyclines due to cooperation among plasmid-encoded genes associated with IS26 mobile genetic elements
inferred← citeshttps://doi.org/10.1016/j.tvjl.2014.02.028openalex-snapshot
Macrolides and lincosamides in cattle and pigs: Use and development of antimicrobial resistance
inferred← citeshttps://doi.org/10.1016/j.vetmic.2024.110319openalex-snapshot
Genomic analyses of Streptococcus uberis reveal high diversity but few antibiotic resistance genes
inferred← citeshttps://doi.org/10.1016/j.watres.2014.05.045openalex-snapshot
Abundance and distribution of Macrolide-Lincosamide-Streptogramin resistance genes in an anaerobic-aerobic system treating spiramycin production wastewater
inferred← citeshttps://doi.org/10.1038/s41467-022-28658-1openalex-snapshot
Different gut microbial communities correlate with efficacy of albendazole-ivermectin against soil-transmitted helminthiases
inferred← citeshttps://doi.org/10.1093/jac/dkaf341openalex-snapshot
Azithromycin resistance in non-typhoidal Salmonella : a review
inferred← citeshttps://doi.org/10.1111/1462-2920.12578openalex-snapshot
Functional characterization and phylogenetic analysis of acquired and intrinsic macrolide phosphotransferases in the B acillus cereus group
inferred← citeshttps://doi.org/10.1128/9781555819804.ch8openalex-snapshot
Antimicrobial Resistance inStreptococcusspp.
inferred← citeshttps://doi.org/10.1128/aac.00781-08openalex-snapshot
Genetic Elements Responsible for Erythromycin Resistance in Streptococci
inferred← citeshttps://doi.org/10.1128/aem.03257-13openalex-snapshot
Characterization of a Multiresistant Mosaic Plasmid from a Fish Farm Sediment Exiguobacterium sp. Isolate Reveals Aggregation of Functional Clinic-Associated Antibiotic Resistance Genes
inferred← citeshttps://doi.org/10.1128/microbiolspec.arba-0008-2017openalex-snapshot
Antimicrobial Resistance inStreptococcusspp
inferred← citeshttps://doi.org/10.1155/2010/169739openalex-snapshot
Intravitreal Ampicillin Sodium for Antibiotic-Resistant Endophthalmitis:Streptococcus uberisFirst Human Intraocular Infection Report
inferred← citeshttps://doi.org/10.1590/0074-02760150356openalex-snapshot
The prevalence of genotypes that determine resistance to macrolides, lincosamides, and streptogramins B compared with spiramycin susceptibility among erythromycin-resistant Staphylococcus epidermidis
inferred← citeshttps://doi.org/10.21608/ejmm.2019.282380openalex-snapshot
Phenotypic and Genotypic Characterization of Macrolide, Lincosamide and Streptogramin Resistance among Nosocomial Staphylococci Isolated from Intensive Care Units
inferred← citeshttps://doi.org/10.2903/j.efsa.2012.2740openalex-snapshot
Guidance on the assessment of bacterial susceptibility to antimicrobials of human and veterinary importance
inferred← citeshttps://doi.org/10.3168/jds.2019-17141openalex-snapshot
Different distribution of antimicrobial resistance genes and virulence profiles of Staphylococcus aureus strains isolated from clinical mastitis in six countries
inferred← citeshttps://doi.org/10.3168/jds.2022-22267openalex-snapshot
Invited review: Antimicrobial resistance in bovine mastitis pathogens: A review of genetic determinants and prevalence of resistance in European countries
inferred← citeshttps://doi.org/10.3390/microorganisms12071332openalex-snapshot
Application of MALDI-TOF MS to Identify and Detect Antimicrobial-Resistant Streptococcus uberis Associated with Bovine Mastitis
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