Analyze Diet
The Journal of antimicrobial chemotherapy2018; 73(4); 867-872; doi: 10.1093/jac/dkx489

Emergence of blaCTX-M-55 associated with fosA, rmtB and mcr gene variants in Escherichia coli from various animal species in France.

Abstract: In Asian countries, blaCTX-M-55 is the second most common ESBL-encoding gene. blaCTX-M-55 frequently co-localizes with fosA and rmtB genes on epidemic plasmids, which remain sporadic outside Asia. During 2010-13, we investigated CTX-M-55-producing Escherichia coli isolates and their co-resistance to fosfomycin, aminoglycosides, fluoroquinolones and colistin as part of a global survey of ESBLs in animals in France. blaCTX-M-55, fosA, rmtB and plasmidic quinolone and colistin resistance genes were characterized by PCR, sequencing and hybridization experiments. Plasmids were classified according to their incompatibility groups and subtypes. Genotyping was performed by MLST and repetitive extragenic palindromic sequence-based PCR. Twenty-one E. coli isolates from bovines (n = 16), dogs (n = 2), horses (n = 2) and a monkey harboured blaCTX-M-55, were MDR and belonged to ST744 (n = 9) and 10 other clones. blaCTX-M-55 was mostly located on IncF (n = 19), but also on IncI1 (n = 2) plasmids. On IncF33:A1:B1 plasmids, blaCTX-M-55 co-localized with the rmtB and aac(6')-Ib genes and in one isolate with the fosA3 allele. Ten IncF46:A-:B20 plasmids, which were found in different clones from unrelated animals, also carried the mcr-3 gene. blaCTX-M-55-carrying IncF18:A-:B1 plasmids were found in different animal species from distinct locations and periods, and one additionally carried the fosA4 gene. One isolate harboured the mcr-1 gene, which did not co-localize with blaCTX-M-55. A large diversity of E. coli clones and plasmid types supported the spread of blaCTX-M-55, together with atypical resistance genes, in various animal species in France. fosA and rmtB genes are emerging among animals in Europe and this issue is of concern for public health.
Publication Date: 2018-01-18 PubMed ID: 29340602DOI: 10.1093/jac/dkx489Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research article focuses on the emergence of the blaCTX-M-55 gene in Escherichia coli isolates from various animal species in France, investigating instances of co-resistance to several types of antibiotics. Throughout their study, the researchers found a wide diversity of E. coli clones and plasmids responsible for spreading the blaCTX-M-55 gene, along with other unconventional resistance genes.

Research Methodology

  • The researchers conducted a thorough examination of CTX-M-55-producing E. coli isolates in animals from 2010 to 2013, across France. They also looked for co-resistance to other antibiotics like fosfomycin, aminoglycosides, fluoroquinolones, and colistin.
  • The characterization of blaCTX-M-55, fosA, rmtB and plasmidic quinolone, and colistin resistance genes was done through methods like PCR (Polymerase Chain Reaction), sequencing, and hybridization experiments.
  • The plasmids, which are independent genetic structures in cells capable of replication, were categorized based on their incompatibility groups and subtypes.
  • Genotyping of the isolates was carried out using MLST (Multi Locus Sequence Typing) and repetitive extragenic palindromic sequence-based PCR.

Research Findings

  • The investigators identified twenty-one E. coli isolates from different animals- bovines, dogs, horses, and a monkey- that carried the blaCTX-M-55 gene. These isolates were multi-drug resistant (MDR) and connected to the clone ST744 and ten other clones.
  • The blaCTX-M-55 gene was primarily found on IncF plasmids, and to a lesser extent on IncI1 plasmids. When present on IncF33:A1:B1 plasmids, the blaCTX-M-55 gene typically co-localized with the rmtB and aac(6′)-Ib genes, another gene, fosA3, was also co-localized in one isolate.
  • The blaCTX-M-55 gene was also found on blaCTX-M-55-carrying IncF18:A-:B1 plasmids in different animal species from various locations and time periods. Plasmid IncF18:A-:B1 also carried the fosA4 gene in one distinct instance.
  • One isolate was found to harbour the mcr-1 gene that did not co-localize with the blaCTX-M-55 gene.

Conclusions and Public Health Implications

  • The research discovered a considerable diversity of E. coli clones and plasmid types instrumental in amplifying the spread of the blaCTX-M-55 gene, alongside other non-typical resistance genes, across various animal species in France.
  • Additionally, the study emphasized that the fosA and rmtB genes are progressively emerging among animal populations in Europe, presenting concerning implications for public health, as this development could challenge the efficacy of existing antibiotic treatments.

Cite This Article

APA
Lupo A, Saras E, Madec JY, Haenni M. (2018). Emergence of blaCTX-M-55 associated with fosA, rmtB and mcr gene variants in Escherichia coli from various animal species in France. J Antimicrob Chemother, 73(4), 867-872. https://doi.org/10.1093/jac/dkx489

Publication

ISSN: 1460-2091
NlmUniqueID: 7513617
Country: England
Language: English
Volume: 73
Issue: 4
Pages: 867-872

Researcher Affiliations

Lupo, Agnese
  • Université de Lyon - ANSES, Unité Antibiorésistance et Virulence Bactériennes, Lyon, France.
Saras, Estelle
  • Université de Lyon - ANSES, Unité Antibiorésistance et Virulence Bactériennes, Lyon, France.
Madec, Jean-Yves
  • Université de Lyon - ANSES, Unité Antibiorésistance et Virulence Bactériennes, Lyon, France.
Haenni, Marisa
  • Université de Lyon - ANSES, Unité Antibiorésistance et Virulence Bactériennes, Lyon, France.

MeSH Terms

  • Animals
  • Cattle
  • Dogs
  • Drug Resistance, Bacterial
  • Escherichia coli / drug effects
  • Escherichia coli / genetics
  • Escherichia coli / isolation & purification
  • Escherichia coli Infections / microbiology
  • Escherichia coli Infections / veterinary
  • Escherichia coli Proteins / genetics
  • France
  • Genotype
  • Genotyping Techniques
  • Haplorhini
  • Horses
  • Methyltransferases / genetics
  • Multilocus Sequence Typing
  • Nucleic Acid Hybridization
  • Plasmids / analysis
  • Plasmids / classification
  • Polymerase Chain Reaction
  • Sequence Analysis, DNA
  • beta-Lactamases / genetics

Citations

This article has been cited 57 times.
  1. Zhang S, Guo X, Wang Y, Zhong Z, Wang M, Jia R, Chen S, Liu M, Zhu D, Zhao X, Wu Y, Yang Q, Huang J, Ou X, Mao S, Gao Q, Sun D, Tian B, Cheng A. Implications of different waterfowl farming on cephalosporin resistance: Investigating the role of bla(CTX-M-55). Poult Sci 2023 Jul 15;102(10):102929.
    doi: 10.1016/j.psj.2023.102929pubmed: 37562134google scholar: lookup
  2. Abo-Almagd EE, Sabala RF, Abd-Elghany SM, Jackson CR, Ramadan H, Imre K, Morar A, Herman V, Sallam KI. β-Lactamase Producing Escherichia coli Encoding bla(CTX-M) and bla(CMY) Genes in Chicken Carcasses from Egypt. Foods 2023 Feb 1;12(3).
    doi: 10.3390/foods12030598pubmed: 36766128google scholar: lookup
  3. Higgins O, Chueiri A, O'Connor L, Lahiff S, Burke L, Morris D, Pfeifer NM, Santamarina BG, Berens C, Menge C, Caniça M, Manageiro V, Kisand V, Hassan MM, Gardner B, van Vliet AHM, La Ragione RM, Gonzalez-Zorn B, Smith TJ. Portable Differential Detection of CTX-M ESBL Gene Variants, bla(CTX-M-1) and bla(CTX-M-15), from Escherichia coli Isolates and Animal Fecal Samples Using Loop-Primer Endonuclease Cleavage Loop-Mediated Isothermal Amplification. Microbiol Spectr 2023 Feb 14;11(1):e0331622.
    doi: 10.1128/spectrum.03316-22pubmed: 36511696google scholar: lookup
  4. Hamame A, Davoust B, Hasnaoui B, Mwenebitu DL, Rolain JM, Diene SM. Screening of colistin-resistant bacteria in livestock animals from France. Vet Res 2022 Nov 22;53(1):96.
    doi: 10.1186/s13567-022-01113-1pubmed: 36414994google scholar: lookup
  5. Mhaya A, Trabelsi R, Aillerie S, M'Zali F, Bégu D, Tounsi S, Gdoura R, Arpin C. Detection of Clones B2-ST131-C2 and A-ST617 in Escherichia coli Producing Both CTX-M-15 and CTX-M-27 from Tunisian Community Patients. Antibiotics (Basel) 2022 Sep 29;11(10).
    doi: 10.3390/antibiotics11101329pubmed: 36289987google scholar: lookup
  6. Anyanwu MU, Jaja IF, Nwobi OC, Mgbeahuruike AC, Ikpendu CN, Okafor NA, Oguttu JW. Epidemiology and Traits of Mobile Colistin Resistance (mcr) Gene-Bearing Organisms from Horses. Microorganisms 2022 Jul 25;10(8).
  7. Perestrelo S, Correia Carreira G, Valentin L, Fischer J, Pfeifer Y, Werner G, Schmiedel J, Falgenhauer L, Imirzalioglu C, Chakraborty T, Käsbohrer A. Comparison of approaches for source attribution of ESBL-producing Escherichia coli in Germany. PLoS One 2022;17(7):e0271317.
    doi: 10.1371/journal.pone.0271317pubmed: 35839265google scholar: lookup
  8. Soncini JGM, Cerdeira L, Sano E, Koga VL, Tizura AT, Tano ZN, Nakazato G, Kobayashi RKT, Aires CAM, Lincopan N, Vespero EC. Genomic insights of high-risk clones of ESBL-producing Escherichia coli isolated from community infections and commercial meat in southern Brazil. Sci Rep 2022 Jun 7;12(1):9354.
    doi: 10.1038/s41598-022-13197-ypubmed: 35672430google scholar: lookup
  9. Menck-Costa MF, Baptista AAS, Gazal LES, Justino L, Sanches MS, de Souza M, Nishio EK, Queiroz Dos Santos B, Cruz VD, Berbert JVM, Gonçalves BC, Andrade G, Vespero EC, Nakazato G, Kobayashi RKT. High-Frequency Detection of fosA3 and bla (CTX-M-55) Genes in Escherichia coli From Longitudinal Monitoring in Broiler Chicken Farms. Front Microbiol 2022;13:846116.
    doi: 10.3389/fmicb.2022.846116pubmed: 35663865google scholar: lookup
  10. Aworh MK, Ekeng E, Nilsson P, Egyir B, Owusu-Nyantakyi C, Hendriksen RS. Extended-Spectrum ß-Lactamase-Producing Escherichia coli Among Humans, Beef Cattle, and Abattoir Environments in Nigeria. Front Cell Infect Microbiol 2022;12:869314.
    doi: 10.3389/fcimb.2022.869314pubmed: 35463650google scholar: lookup
  11. Lima LS, Proietti-Junior AA, Rodrigues YC, da Silva Vieira MC, Lima LNGC, de Oliveira Souza C, Dias Gonçalves V, de Oliveira Lima M, Dos Prazeres Rodrigues D, Lima KVB. High Genetic Diversity and Antimicrobial Resistance in Escherichia coli Highlight Arapaima gigas (Pisces: Arapaimidae) as a Reservoir of Quinolone-Resistant Strains in Brazilian Amazon Rivers. Microorganisms 2022 Apr 13;10(4).
  12. Sonnevend Á, Alali WQ, Mahmoud SA, Ghazawi A, Bharathan G, Melegh S, Rizvi TA, Pál T. Molecular Characterization of MCR-1 Producing Enterobacterales Isolated in Poultry Farms in the United Arab Emirates. Antibiotics (Basel) 2022 Feb 24;11(3).
    doi: 10.3390/antibiotics11030305pubmed: 35326769google scholar: lookup
  13. Nagy BJ, Balázs B, Benmazouz I, Gyüre P, Kövér L, Kaszab E, Bali K, Lovas-Kiss Á, Damjanova I, Majoros L, Tóth Á, Bányai K, Kardos G. Comparison of Extended-Spectrum Beta-Lactamase-Producing Escherichia coli Isolates From Rooks (Corvus frugilegus) and Contemporary Human-Derived Strains: A One Health Perspective. Front Microbiol 2021;12:785411.
    doi: 10.3389/fmicb.2021.785411pubmed: 35095799google scholar: lookup
  14. Clemente L, Leão C, Moura L, Albuquerque T, Amaro A. Prevalence and Characterization of ESBL/AmpC Producing Escherichia coli from Fresh Meat in Portugal. Antibiotics (Basel) 2021 Nov 1;10(11).
    doi: 10.3390/antibiotics10111333pubmed: 34827270google scholar: lookup
  15. Qin J, Zhao Y, Wang A, Chi X, Wen P, Li S, Wu L, Bi S, Xu H. Comparative genomic characterization of multidrug-resistant Citrobacter spp. strains in Fennec fox imported to China. Gut Pathog 2021 Oct 13;13(1):59.
    doi: 10.1186/s13099-021-00458-wpubmed: 34645508google scholar: lookup
  16. Lee S, An JU, Guk JH, Song H, Yi S, Kim WH, Cho S. Prevalence, Characteristics and Clonal Distribution of Extended-Spectrum β-Lactamase- and AmpC β-Lactamase-Producing Escherichia coli Following the Swine Production Stages, and Potential Risks to Humans. Front Microbiol 2021;12:710747.
    doi: 10.3389/fmicb.2021.710747pubmed: 34367116google scholar: lookup
  17. Ramadan H, Soliman AM, Hiott LM, Elbediwi M, Woodley TA, Chattaway MA, Jenkins C, Frye JG, Jackson CR. Emergence of Multidrug-Resistant Escherichia coli Producing CTX-M, MCR-1, and FosA in Retail Food From Egypt. Front Cell Infect Microbiol 2021;11:681588.
    doi: 10.3389/fcimb.2021.681588pubmed: 34327151google scholar: lookup
  18. He WY, Zhang XX, Gao GL, Gao MY, Zhong FG, Lv LC, Cai ZP, Si XF, Yang J, Liu JH. Clonal spread of Escherichia coli O101: H9-ST10 and O101: H9-ST167 strains carrying fosA3 and bla (CTX-M-14) among diarrheal calves in a Chinese farm, with Australian Chroicocephalus as the possible origin of E. coli O101: H9-ST10. Zool Res 2021 Jul 18;42(4):461-468.
  19. Li L, Olsen RH, Song A, Xiao J, Wang C, Meng H, Shi L. First Report of a Foodborne Salmonella enterica Serovar Gloucester (4:i:l,w) ST34 Strain Harboring bla (CTX-M-) (55) and qnrS Genes Located in IS26-Mediated Composite Transposon. Front Microbiol 2021;12:646101.
    doi: 10.3389/fmicb.2021.646101pubmed: 33959109google scholar: lookup
  20. Salgado-Caxito M, Benavides JA, Adell AD, Paes AC, Moreno-Switt AI. Global prevalence and molecular characterization of extended-spectrum β-lactamase producing-Escherichia coli in dogs and cats - A scoping review and meta-analysis. One Health 2021 Jun;12:100236.
    doi: 10.1016/j.onehlt.2021.100236pubmed: 33889706google scholar: lookup
  21. Soliman AM, Ramadan H, Zarad H, Sugawara Y, Yu L, Sugai M, Shimamoto T, Hiott LM, Frye JG, Jackson CR, Shimamoto T. Coproduction of Tet(X7) Conferring High-Level Tigecycline Resistance, Fosfomycin FosA4, and Colistin Mcr-1.1 in Escherichia coli Strains from Chickens in Egypt. Antimicrob Agents Chemother 2021 May 18;65(6).
    doi: 10.1128/AAC.02084-20pubmed: 33820767google scholar: lookup
  22. Hounmanou YMG, Bortolaia V, Dang STT, Truong D, Olsen JE, Dalsgaard A. ESBL and AmpC β-Lactamase Encoding Genes in E. coli From Pig and Pig Farm Workers in Vietnam and Their Association With Mobile Genetic Elements. Front Microbiol 2021;12:629139.
    doi: 10.3389/fmicb.2021.629139pubmed: 33776959google scholar: lookup
  23. Cao C, Niu Q, Chen J, Xu X, Sheng H, Cui S, Liu B, Yang B. Epidemiology and Characterization of CTX-M-55-Type Extended-Spectrum β-Lactamase-Producing Salmonella enterica Serovar Enteritidis Isolated from Patients in Shanghai, China. Microorganisms 2021 Jan 27;9(2).
    doi: 10.3390/microorganisms9020260pubmed: 33513880google scholar: lookup
  24. Sadek M, Ortiz de la Rosa JM, Abdelfattah Maky M, Korashe Dandrawy M, Nordmann P, Poirel L. Genomic Features of MCR-1 and Extended-Spectrum β-Lactamase-Producing Enterobacterales from Retail Raw Chicken in Egypt. Microorganisms 2021 Jan 19;9(1).
    doi: 10.3390/microorganisms9010195pubmed: 33477851google scholar: lookup
  25. Zurfluh K, Treier A, Schmitt K, Stephan R. Mobile fosfomycin resistance genes in Enterobacteriaceae-An increasing threat. Microbiologyopen 2020 Dec;9(12):e1135.
    doi: 10.1002/mbo3.1135pubmed: 33128341google scholar: lookup
  26. Apostolakos I, Feudi C, Eichhorn I, Palmieri N, Fasolato L, Schwarz S, Piccirillo A. High-resolution characterisation of ESBL/pAmpC-producing Escherichia coli isolated from the broiler production pyramid. Sci Rep 2020 Jul 7;10(1):11123.
    doi: 10.1038/s41598-020-68036-9pubmed: 32636426google scholar: lookup
  27. Chandler JC, Anders JE, Blouin NA, Carlson JC, LeJeune JT, Goodridge LD, Wang B, Day LA, Mangan AM, Reid DA, Coleman SM, Hopken MW, Bisha B. The Role of European Starlings (Sturnus vulgaris) in the Dissemination of Multidrug-Resistant Escherichia coli among Concentrated Animal Feeding Operations. Sci Rep 2020 May 15;10(1):8093.
    doi: 10.1038/s41598-020-64544-wpubmed: 32415136google scholar: lookup
  28. Song J, Oh SS, Kim J, Park S, Shin J. Clinically Relevant Extended-Spectrum β-Lactamase-Producing Escherichia coli Isolates From Food Animals in South Korea. Front Microbiol 2020;11:604.
    doi: 10.3389/fmicb.2020.00604pubmed: 32390965google scholar: lookup
  29. Renzhammer R, Loncaric I, Roch FF, Pinior B, Käsbohrer A, Spergser J, Ladinig A, Unterweger C. Prevalence of Virulence Genes and Antimicrobial Resistances in E. coli Associated with Neonatal Diarrhea, Postweaning Diarrhea, and Edema Disease in Pigs from Austria. Antibiotics (Basel) 2020 Apr 24;9(4).
    doi: 10.3390/antibiotics9040208pubmed: 32344550google scholar: lookup
  30. Dantas Palmeira J, Ferreira HMN. Extended-spectrum beta-lactamase (ESBL)-producing Enterobacteriaceae in cattle production - a threat around the world. Heliyon 2020 Jan;6(1):e03206.
    doi: 10.1016/j.heliyon.2020.e03206pubmed: 32042963google scholar: lookup
  31. Gelbíčová T, Baráková A, Florianová M, Jamborová I, Zelendová M, Pospíšilová L, Koláčková I, Karpíšková R. Dissemination and Comparison of Genetic Determinants of mcr-Mediated Colistin Resistance in Enterobacteriaceae via Retailed Raw Meat Products. Front Microbiol 2019;10:2824.
    doi: 10.3389/fmicb.2019.02824pubmed: 31921017google scholar: lookup
  32. Feng C, Wen P, Xu H, Chi X, Li S, Yu X, Lin X, Wu S, Zheng B. Emergence and Comparative Genomics Analysis of Extended-Spectrum-β-Lactamase-Producing Escherichia coli Carrying mcr-1 in Fennec Fox Imported from Sudan to China. mSphere 2019 Nov 20;4(6).
    doi: 10.1128/mSphere.00732-19pubmed: 31748247google scholar: lookup
  33. Poirel L, Vuillemin X, Kieffer N, Mueller L, Descombes MC, Nordmann P. Identification of FosA8, a Plasmid-Encoded Fosfomycin Resistance Determinant from Escherichia coli, and Its Origin in Leclercia adecarboxylata. Antimicrob Agents Chemother 2019 Nov;63(11).
    doi: 10.1128/AAC.01403-19pubmed: 31481445google scholar: lookup
  34. Zhang CZ, Ding XM, Lin XL, Sun RY, Lu YW, Cai RM, Webber MA, Ding HZ, Jiang HX. The Emergence of Chromosomally Located bla (CTX-M-55) in Salmonella From Foodborne Animals in China. Front Microbiol 2019;10:1268.
    doi: 10.3389/fmicb.2019.01268pubmed: 31231347google scholar: lookup
  35. Gay E, Bour M, Cazeau G, Jarrige N, Martineau C, Madec JY, Haenni M. Antimicrobial Usages and Antimicrobial Resistance in Commensal Escherichia coli From Veal Calves in France: Evolution During the Fattening Process. Front Microbiol 2019;10:792.
    doi: 10.3389/fmicb.2019.00792pubmed: 31031738google scholar: lookup
  36. Mueller L, Cimen C, Poirel L, Descombes MC, Nordmann P. Prevalence of fosfomycin resistance among ESBL-producing Escherichia coli isolates in the community, Switzerland. Eur J Clin Microbiol Infect Dis 2019 May;38(5):945-949.
    doi: 10.1007/s10096-019-03531-0pubmed: 30877486google scholar: lookup
  37. Tuo H, Yang Y, Tao X, Liu D, Li Y, Xie X, Li P, Gu J, Kong L, Xiang R, Lei C, Wang H, Zhang A. The Prevalence of Colistin Resistant Strains and Antibiotic Resistance Gene Profiles in Funan River, China. Front Microbiol 2018;9:3094.
    doi: 10.3389/fmicb.2018.03094pubmed: 30619173google scholar: lookup
  38. García-Meniño I, García V, Mora A, Díaz-Jiménez D, Flament-Simon SC, Alonso MP, Blanco JE, Blanco M, Blanco J. Swine Enteric Colibacillosis in Spain: Pathogenic Potential of mcr-1 ST10 and ST131 E. coli Isolates. Front Microbiol 2018;9:2659.
    doi: 10.3389/fmicb.2018.02659pubmed: 30455680google scholar: lookup
  39. Birgy A, Madhi F, Hogan J, Doit C, Gaschignard J, Caseris M, Bidet P, Cohen R, Bonacorsi S. CTX-M-55-, MCR-1-, and FosA-Producing Multidrug-Resistant Escherichia coli Infection in a Child in France. Antimicrob Agents Chemother 2018 Apr;62(4).
    doi: 10.1128/AAC.00127-18pubmed: 29378715google scholar: lookup
  40. Oh JY, Kwak SM, Kim JY, Ro WB, Lee KJ, Chae JC. Case Report: Transferable IncX4 plasmid carrying mcr-1 in colistin-resistant Escherichia coli from a healthy pet dog in South Korea. Front Vet Sci 2025;12:1746399.
    doi: 10.3389/fvets.2025.1746399pubmed: 41675125google scholar: lookup
  41. Guitor AK, Wang S, Tuck OT, Firek B, Mostacci N, Jauhal A, Chen LX, Dziegiel AH, Baker S, Duong VT, Mather AE, Corander J, Kantele A, Shenhav L, Hilty M, Morowitz MJ, Sachdeva R, Banfield JF. Megaplasmids associate with Escherichia coli and other Enterobacteriaceae. bioRxiv 2025 Oct 22;.
    doi: 10.1101/2025.09.30.679422pubmed: 41280017google scholar: lookup
  42. Yassara S, Zeouk I, Jaouhar S, Sbiti M, Bekhti K. Extended-spectrum beta-lactamases: definition, history, an update on their genetic environment and detection methods. J Med Microbiol 2025 Jun;74(6).
    doi: 10.1099/jmm.0.002033pubmed: 40554694google scholar: lookup
  43. Zhang S, Yang J, Yang Q, Li Q, Zhong Z, Wang M, Jia R, Chen S, Liu M, Zhu D, Zhao X, Wu Y, Yang Q, Huang J, Ou X, Sun D, Tian B, Wu Z, He Y, Cheng A. High prevalence of plasmid-mediated Fosfomycin resistance in waterfowl-derived Escherichia coli strains: insights into genetic context and transmission dynamics in China. Front Vet Sci 2025;12:1481822.
    doi: 10.3389/fvets.2025.1481822pubmed: 40191084google scholar: lookup
  44. Juscele F, Saidenberg ABS, Christoffersen LEB, Edslev SM, Hallstrøm S, Nacarato JR, Barbosa FB, Cunha MP, Esposito F, Lincopan NH, Stegger M, Knöbl T. Escherichia coli in Brazilian Poultry Fecal Samples: Co-Carriage of Fosfomycin and ESBL Resistance. Antibiotics (Basel) 2025 Mar 6;14(3).
    doi: 10.3390/antibiotics14030269pubmed: 40149080google scholar: lookup
  45. Gonzales-Zubiate FA, Tambor JHM, Valencia-Bacca J, Villota-Burbano MF, Cardenas-Arias A, Esposito F, Moura Q, Fuga B, Sano E, Pariona JGM, Jacome MPO, Lincopan N. Pandemic one health clones of Escherichia coli and Klebsiella pneumoniae producing CTX-M-14, CTX-M-27, CTX-M-55 and CTX-M-65 ESβLs among companion animals in northern Ecuador. Front Cell Infect Microbiol 2023;13:1259764.
    doi: 10.3389/fcimb.2023.1259764pubmed: 39840255google scholar: lookup
  46. Caderhoussin A, Couvin D, Gruel G, Quétel I, Pot M, Arquet R, Dereeper A, Bambou JC, Talarmin A, Ferdinand S. The fly route of extended-spectrum-β-lactamase-producing Enterobacteriaceae dissemination in a cattle farm: from the ecosystem to the molecular scale. Front Antibiot 2024;3:1367936.
    doi: 10.3389/frabi.2024.1367936pubmed: 39816254google scholar: lookup
  47. Loncaric I, Szostak MP, Cabal-Rosel A, Grünzweil OM, Riegelnegg A, Misic D, Müller E, Feßler AT, Braun SD, Schwarz S, Monecke S, Ehricht R, Ruppitsch W, Spergser J, Lewis A, Bloom PH, Saggese MD. Molecular characterization, virulence and antimicrobial and biocidal susceptibility of selected bacteria isolated from the cloaca of nestling ospreys (Pandion haliaetus) from Mono Lake, California, USA. PLoS One 2024;19(9):e0311306.
    doi: 10.1371/journal.pone.0311306pubmed: 39331631google scholar: lookup
  48. Morgan G, Pinchbeck G, Haldenby S, Schmidt V, Williams N. Raw meat diets are a major risk factor for carriage of third-generation cephalosporin-resistant and multidrug-resistant E. coli by dogs in the UK. Front Microbiol 2024;15:1460143.
    doi: 10.3389/fmicb.2024.1460143pubmed: 39314877google scholar: lookup
  49. Iwan E, Zając M, Bomba A, Olejnik M, Skarżyńska M, Wasiński B, Wieczorek K, Tłuścik K, Wasyl D. Phylogenetics and Mobilization of Genomic Traits of Cephalosporin-Resistant Escherichia coli Originated from Retail Meat. Pathogens 2024 Aug 19;13(8).
    doi: 10.3390/pathogens13080700pubmed: 39204300google scholar: lookup
  50. Li X, Hu H, Zhu Y, Wang T, Lu Y, Wang X, Peng Z, Sun M, Chen H, Zheng J, Tan C. Population structure and antibiotic resistance of swine extraintestinal pathogenic Escherichia coli from China. Nat Commun 2024 Jul 10;15(1):5811.
    doi: 10.1038/s41467-024-50268-2pubmed: 38987310google scholar: lookup
  51. Smith CM, Anacker M, Bevis DL, Dutton NAM, Powell D, McLaughlin RW. Isolation of a CTX-M-55 (ESBL)-Producing Escherichia coli Strain of the Global ST6448 Clone from a Captive Orangutan in the USA. Curr Microbiol 2024 May 17;81(7):177.
    doi: 10.1007/s00284-024-03693-xpubmed: 38758473google scholar: lookup
  52. Wang W, Wei X, Arbab S, Wu L, Lu N, Zhu Q, Bai Y, Zhang J. Multidrug-Resistant Escherichia coli Isolate of Chinese Bovine Origin Carrying the bla(CTX-M-55) Gene Located in IS26-Mediated Composite Translocatable Units. Microorganisms 2023 Nov 17;11(11).
  53. Mattioni Marchetti V, Hrabak J, Bitar I. Fosfomycin resistance mechanisms in Enterobacterales: an increasing threat. Front Cell Infect Microbiol 2023;13:1178547.
    doi: 10.3389/fcimb.2023.1178547pubmed: 37469601google scholar: lookup
  54. Zhang LJ, Yang JT, Chen HX, Liu WZ, Ding YL, Chen RA, Zhang RM, Jiang HX. F18:A-:B1 Plasmids Carrying bla(CTX-M-55) Are Prevalent among Escherichia coli Isolated from Duck-Fish Polyculture Farms. Antibiotics (Basel) 2023 May 25;12(6).
    doi: 10.3390/antibiotics12060961pubmed: 37370280google scholar: lookup
  55. Tate H, Li C, Nyirabahizi E, Tyson GH, Zhao S, Rice-Trujillo C, Jones SB, Ayers S, M'ikanatha NM, Hanna S, Ruesch L, Cavanaugh ME, Laksanalamai P, Mingle L, Matzinger SR, McDermott PF. A National Antimicrobial Resistance Monitoring System Survey of Antimicrobial-Resistant Foodborne Bacteria Isolated from Retail Veal in the United States. J Food Prot 2021 Oct 1;84(10):1749-1759.
    doi: 10.4315/JFP-21-005pubmed: 34015113google scholar: lookup
  56. Wachino JI, Doi Y, Arakawa Y. Aminoglycoside Resistance: Updates with a Focus on Acquired 16S Ribosomal RNA Methyltransferases. Infect Dis Clin North Am 2020 Dec;34(4):887-902.
    doi: 10.1016/j.idc.2020.06.002pubmed: 33011054google scholar: lookup
  57. Poirel L, Madec JY, Lupo A, Schink AK, Kieffer N, Nordmann P, Schwarz S. Antimicrobial Resistance in Escherichia coli. Microbiol Spectr 2018 Jul;6(4).