CoChat
Sign Up
Cited by 25Antibiotic Resistance in BacteriaEscherichia coli research studiesSalmonella and Campylobacter epidemiology

Extended-spectrum β-lactamase-producing E. coli from retail meat and workers: genetic diversity, virulotyping, pathotyping and the antimicrobial effect of silver nanoparticles

Open access
Ahmed, Heba A., Elsohaby, Ibrahim, Elamin, Amina M., El-Ghafar, Abeer E. Abd, Elsaid, Gamilat A., Elbarbary, Mervat, Mohsen, Rasha A., El Feky, Tamer M. +1 more·2023·BMC Microbiology
DOI 10.1186/s12866-023-02948-0PMC PMC10405496
Open this paper in CoChat — free accountOpen PDF

Abstract

Background: The spread of extended-spectrum β -lactamases (ESBL) producing E. coli from food animals and the environment to humans has become a significant public health concern. The objectives of this study were to determine the occurrence, pathotypes, virulotypes, genotypes, and antimicrobial resistance patterns of ESBL-producing E. coli in retail meat samples and workers in retail meat shops in Egypt and to evaluate the bactericidal efficacy of silver nanoparticles (AgNPs-H 2 O 2 ) against multidrug resistant (MDR) ESBL-producing E. coli . Results: A total of 250 retail meat samples and 100 human worker samples (hand swabs and stool) were examined for the presence of ESBL- producing E. coli . Duck meat and workers’ hand swabs were the highest proportion of ESBL- producing E. coli isolates (81.1%), followed by camel meat (61.5%). Pathotyping revealed that the isolates belonged to groups A and B1. Virulotyping showed that the most prevalent virulence gene was Shiga toxin 2 ( stx2 ) associated gene (36.9%), while none of the isolates harbored stx1 gene. Genotyping of the identified isolates from human and meat sources by REP-PCR showed 100% similarity within the same cluster between human and meat isolates. All isolates were classified as MDR with an average multiple antibiotic resistance (MAR) index of 0.7. AgNPs-H 2 O 2 at concentrations of 0.625, 1.25, 2.5 and 5 μg/mL showed complete bacterial growth inhibition. Conclusions: Virulent MDR ESBL-producing E. coli were identified in retail meat products in Egypt, posing significant public health threats. Regular monitoring of ESBL-producing E. coli frequency and antimicrobial resistance profile in retail meat products is crucial to enhance their safety. AgNPs-H 2 O 2 is a promising alternative for treating MDR ESBL-producing E. coli infections and reducing antimicrobial resistance risks.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1186/s12866-023-02948-0

Cites

1 of 1 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Studies have revealed the presence of MDR bacteria, including methicillin-resistant S. aureus (MRSA), ESBL-producing Enterobacteriaceae, and MDR-Salmonella, in meat products.

    “Studies have revealed the presence of MDR bacteria, including methicillin-resistant S. aureus (MRSA), ESBL-producing Enterobacteriaceae, and MDR-Salmonella, in meat products [63,76,77,78,79].”

    From A Systematic Review on Antimicrobial Resistance in Ghana from a One Health Perspective (2024) · cites this paper as [76]

    The Conclusions (page not provided) report MDR ESBL-producing E. coli in retail meat, supporting the ESBL-producing Enterobacteriaceae portion of the claim. The paper does not report MRSA or MDR Salmonella in meat products; searches for both terms found no supporting passage. (LLM, conf=0.88)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 95

  1. [1]Allen HK Donato J Wang HH Cloud-Hansen KA Davies J Handelsman J Call of the wild: antibiotic resistance genes in natural environments Nat Rev Microbiol 2010 8 4 251 9 10.1038/nrmicro2312 20190823 · DOI · Paper page
  2. [2]Gutkind GO Di Conza J Power P Radice M β-lactamase-mediated resistance: a biochemical, epidemiological and genetic overview Curr Pharm Design 2013 19 2 164 208 10.2174/138161213804070320 22894615 · DOI
  3. [3]Ewers C Bethe A Semmler T Guenther S Wieler LH Extended-spectrum β-lactamase-producing and AmpC-producing Escherichia coli from livestock and companion animals, and their putative impact on public health: a global perspective Clin Microbiol Infect 2012 18 7 646 55 10.1111/j.1469-0691.2012.03850.x 22519858 · DOI
  4. [4]Abayneh M Tesfaw G Woldemichael K Yohannis M Abdissa A Assessment of extended-spectrum β-lactamase (ESBLs) – producing Escherichia coli from minced meat of cattle and swab samples and hygienic status of meat retailer shops in Jimma town, Southwest Ethiopia BMC Infect Dis 2019 19 1 897 10.1186/s12879-019-4554-6 31660887 PMC6819479 · DOI
  5. [5]Fulham M, Power M, Gray R. Diversity and distribution of Escherichia coli in three species of free-ranging australian Pinniped pups. Front Mar Sci. 2020;7. 10.3389/fmars.2020.571171 · DOI
  6. [6]Gordon DM Clermont O Tolley H Denamur E Assigning Escherichia coli strains to phylogenetic groups: multi-locus sequence typing versus the PCR triplex method Environ Microbiol 2008 10 10 2484 96 10.1111/j.1462-2920.2008.01669.x 18518895 · DOI
  7. [7]Clermont O Christenson JK Daubié A-S Gordon DM Denamur E Development of an allele-specific PCR for Escherichia coli B2 sub-typing, a rapid and easy to perform substitute of multilocus sequence typing J Microbiol Methods 2014 101 24 7 10.1016/j.mimet.2014.03.008 24685601 · DOI
  8. [8]Sabat AJ Budimir A Nashev D Sá-Leão R van Dijl J Laurent F Overview of molecular typing methods for outbreak detection and epidemiological surveillance Euro Surveill 2013 18 4 20380 10.2807/ese.18.04.20380-en 23369389 · DOI
  9. [9]Franco A Leekitcharoenphon P Feltrin F Alba P Cordaro G Iurescia M Emergence of a clonal lineage of Multidrug-Resistant ESBL-Producing Salmonella Infantis transmitted from broilers and broiler meat to humans in Italy between 2011 and 2014 PLoS ONE 2016 10 12 e0144802 10.1371/journal.pone.0144802 PMC4696813 26716443 · DOI
  10. [10]Tyrrell JM Wootton M Toleman MA Howe RA Woodward M Walsh TR Genetic & virulence profiling of ESBL-positive E. coli from nosocomial & veterinary sources Vet Microbiol 2016 186 37 43 10.1016/j.vetmic.2016.02.007 27016755 · DOI
  11. [11]Peirano G Pitout JDD Extended-spectrum β-Lactamase-producing Enterobacteriaceae: update on Molecular Epidemiology and Treatment Options Drugs 2019 79 14 1529 41 10.1007/s40265-019-01180-3 31407238 · DOI
  12. [12]Brolund A Sandegren L Characterization of ESBL disseminating plasmids Infect Dis 2016 48 1 18 25 10.3109/23744235.2015.1062536 26135711 · DOI
  13. [13]Kempf I Jouy E Chauvin C Colistin use and colistin resistance in bacteria from animals Int J Antimicrob Agents 2016 48 6 598 606 10.1016/j.ijantimicag.2016.09.016 27836380 · DOI
  14. [14]Clemente L Manageiro V Correia I Amaro A Albuquerque T Themudo P Revealing mcr-1-positive ESBL-producing Escherichia coli strains among Enterobacteriaceae from food-producing animals (bovine, swine and poultry) and meat (bovine and swine), Portugal, 2010–2015 Int J Food Microbiol 2019 296 37 42 10.1016/j.ijfoodmicro.2019.02.006 30844701 · DOI
  15. [15]Poirel L Jayol A Nordmanna P Polymyxins Antibacterial activity, susceptibility testing, and resistance mechanisms encoded by plasmids or chromosomes Clin Microbiol Rev 2017 30 2 557 96 10.1128/CMR.00064-16 28275006 PMC5355641 · DOI
  16. [16]Klein NC Cunha BA Third-generation cephalosporins Med Clin North Am 1995 79 4 705 19 10.1016/S0025-7125(16)30034-7 7791418 · DOI
  17. [19]Paterson DL Bonomo RA Extended-spectrum β-lactamases: a clinical update Clin Microbiol Rev 2005 18 4 657 86 10.1128/CMR.18.4.657-686.2005 16223952 PMC1265908 · DOI
  18. [20]Cantón R, Novais A, Valverde A, Machado E, Peixe L, Baquero F, et al. Prevalence and spread of extended-spectrum β-lactamase-producing Enterobacteriaceae in Europe. Clinical Microbiology and Infection. 2008;14:144 − 53; 10.1111/j.1469-0691.2007.01850.x 18154538 · DOI
  19. [21]Belmar Campos C Fenner I Wiese N Lensing C Christner M Rohde H Prevalence and genotypes of extended spectrum beta-lactamases in Enterobacteriaceae isolated from human stool and chicken meat in Hamburg Ger Int J Med microbiology: IJMM 2014 304 5–6 678 84 10.1016/j.ijmm.2014.04.012 24856867 · DOI
  20. [22]Franci G Falanga A Galdiero S Palomba L Rai M Morelli G Silver nanoparticles as potential antibacterial agents Molecules 2015 20 5 8856 74 10.3390/molecules20058856 25993417 PMC6272636 · DOI
  21. [23]Jones N Ray B Ranjit KT Manna AC Antibacterial activity of ZnO nanoparticle suspensions on a broad spectrum of microorganisms FEMS Microbiol Lett 2008 279 1 71 6 10.1111/j.1574-6968.2007.01012.x 18081843 · DOI
  22. [24]Lazar V Quorum sensing in biofilms – how to destroy the bacterial citadels or their cohesion/power? Anaerobe 2011 17 6 280 5 10.1016/j.anaerobe.2011.03.023 21497662 · DOI
  23. [25]Hu Q, Tu J, Han X, Zhu Y, Ding C, Yu S. Development of multiplex PCR assay for rapid detection of Riemerella anatipestifer, Escherichia coli, and Salmonella enterica simultaneously from ducks. Journal of Microbiological Methods. 2011;87(1):64 – 9; 10.1016/j.mimet.2011.07.007 21791228 · DOI
  24. [27]Jeong YW Kim TE Kim JH Kwon HJ Pathotyping avian pathogenic Escherichia coli strains in Korea J Vet Sci 2012 13 2 145 52 10.4142/jvs.2012.13.2.145 22705736 PMC3386339 · DOI
  25. [28]Yamamoto S Terai A Yuri K Kurazono H Takeda Y Yoshida O Detection of urovirulence factors in Escherichia coli by multiplex polymerase chain reaction FEMS Immunol Med Microbiol 1995 12 2 85 90 10.1111/j.1574-695X.1995.tb00179.x 8589667 · DOI
  26. [29]Yamamoto T Echeverria P Detection of the enteroaggregative Escherichia coli heat-stable enterotoxin 1 gene sequences in enterotoxigenic E. coli strains pathogenic for humans Infect Immun 1996 64 4 1441 5 10.1128/iai.64.4.1441-1445.1996 8606115 PMC173940 · DOI
  27. [30]Dipineto L Santaniello A Fontanella M Lagos K Fioretti A Menna LF Presence of Shiga toxin-producing Escherichia coli O157:H7 in living layer hens Lett Appl Microbiol 2006 43 3 293 5 10.1111/j.1472-765X.2006.01954.x 16910934 · DOI
  28. [31]Schmidt H, Scheef J, Morabito S, Caprioli A, Wieler LH, Karch H. A new Shiga toxin 2 variant (Stx2f) from Escherichia coli isolated from pigeons. Applied and environmental microbiology. 2000;66(3):1205-8; 10.1128/AEM.66.3.1205-1208.2000 PMC91964 10698793 · DOI
  29. [32]Siqueira AK Ribeiro MG Leite Dda S Tiba MR Moura C Lopes MD Virulence factors in Escherichia coli strains isolated from urinary tract infection and pyometra cases and from feces of healthy dogs Res Vet Sci 2009 86 2 206 10 10.1016/j.rvsc.2008.07.018 18783807 · DOI
  30. [33]Wang G Clark CG Rodgers FG Detection in Escherichia coli of the genes encoding the major virulence factors, the genes defining the O157:H7 serotype, and components of the type 2 Shiga toxin family by multiplex PCR J Clin Microbiol 2002 40 10 3613 9 10.1128/JCM.40.10.3613-3619.2002 12354854 PMC130888 · DOI
  31. [34]Mohapatra BR Broersma K Mazumder A Comparison of five rep-PCR genomic fingerprinting methods for differentiation of fecal Escherichia coli from humans, poultry and wild birds FEMS Microbiol Lett 2007 277 1 98 106 10.1111/j.1574-6968.2007.00948.x 17986090 · DOI
  32. [35]Hunter PR Reproducibility and indices of discriminatory power of microbial typing methods J Clin Microbiol 1990 28 9 1903 5 10.1128/jcm.28.9.1903-1905.1990 2229371 PMC268075 · DOI
  33. [36]CLSI Methods for Dilution Antimicrobial susceptibility tests for Bacteria that grow aerobically; approved Standard—Ninth Edition 2012 Wayne, PA Clinical and Laboratory Standards Institute
  34. [37]Krumperman PH Multiple antibiotic resistance indexing of Escherichia coli to identify high-risk sources of fecal contamination of foods Appl Environ Microbiol 1983 46 1 165 70 10.1128/aem.46.1.165-170.1983 6351743 PMC239283 · DOI
  35. [39]Xia Y Liang Z Su X Xiong Y Characterization of carbapenemase genes in Enterobacteriaceae species exhibiting decreased susceptibility to carbapenems in a university hospital in Chongqing, China Ann Lab Med 2012 32 4 270 5 10.3343/alm.2012.32.4.270 22779068 PMC3384808 · DOI
  36. [40]Colom K Pérez J Alonso R Fernández-Aranguiz A Lariño E Cisterna R Simple and reliable multiplex PCR assay for detection of blaTEM, bla(SHV) and blaOXA-1 genes in Enterobacteriaceae FEMS Microbiol Lett 2003 223 2 147 51 10.1016/s0378-1097(03)00306-9 12829279 · DOI
  37. [41]Gray JT Hungerford LL Fedorka-Cray PJ Headrick ML Extended-spectrum-cephalosporin resistance in Salmonella enterica isolates of animal origin Antimicrob Agents Chemother 2004 48 8 3179 81 10.1128/aac.48.8.3179-3181.2004 15273145 PMC478523 · DOI
  38. [42]Jouini A Vinué L Slama KB Sáenz Y Klibi N Hammami S Characterization of CTX-M and SHV extended-spectrum beta-lactamases and associated resistance genes in Escherichia coli strains of food samples in Tunisia J Antimicrob Chemother 2007 60 5 1137 41 10.1093/jac/dkm316 17855726 · DOI
  39. [43]Randall LP Cooles SW Osborn MK Piddock LJ Woodward MJ Antibiotic resistance genes, integrons and multiple antibiotic resistance in thirty-five serotypes of Salmonella enterica isolated from humans and animals in the UK J Antimicrob Chemother 2004 53 2 208 16 10.1093/jac/dkh070 14729766 · DOI
  40. [44]Ibekwe AM Murinda SE Graves AK Genetic diversity and Antimicrobial Resistance of Escherichia coli from Human and Animal sources uncovers multiple resistances from human sources PLoS ONE 2011 6 6 e20819 10.1371/journal.pone.0020819 21687635 PMC3110821 · DOI
  41. [45]Keyes K Hudson C Maurer JJ Thayer S White DG Lee MD Detection of florfenicol resistance genes in Escherichia coli isolated from sick chickens Antimicrob Agents Chemother 2000 44 2 421 4 10.1128/AAC.44.2.421-424.2000 10639375 PMC89696 · DOI
  42. [46]Doublet B Lailler R Meunier D Brisabois A Boyd D Mulvey MR Variant Salmonella genomic island 1 antibiotic resistance gene cluster in Salmonella enterica serovar Albany Emerg Infect Dis 2003 9 5 585 91 10.3201/eid0905.020609 12737743 PMC2972765 · DOI
  43. [47]Rebelo AR Bortolaia V Kjeldgaard JS Pedersen SK Leekitcharoenphon P Hansen IM Multiplex PCR for detection of plasmid-mediated colistin resistance determinants, mcr-1, mcr-2, mcr-3, mcr-4 and mcr-5 for surveillance purposes Euro Surveill 2018 23 6 17 00672 10.2807/1560-7917.ES.2018.23.6.17-00672 29439754 PMC5824125 · DOI
  44. [48]El-Gohary FA Abdel-Hafez LJM Zakaria AI Shata RR Tahoun A El-Mleeh A Enhanced antibacterial activity of silver nanoparticles combined with hydrogen peroxide against Multidrug-Resistant pathogens isolated from dairy farms and beef slaughterhouses in Egypt Infect Drug Resist 2020 13 3485 99 10.2147/idr.S271261 33116668 PMC7550212 · DOI
  45. [49]Hamilton-Miller JM Calculating MIC50 J Antimicrob Chemother 1991 27 6 863 4 10.1093/jac/27.6.863 1938695 · DOI
  46. [50]Gu Z Eils R Schlesner M Complex heatmaps reveal patterns and correlations in multidimensional genomic data Bioinformatics 2016 32 18 2847 9 10.1093/bioinformatics/btw313 27207943 · DOI
  47. [51]Yassin AK Gong J Kelly P Lu G Guardabassi L Wei L Antimicrobial resistance in clinical Escherichia coli isolates from poultry and livestock, China PLoS ONE 2017 12 9 e0185326 10.1371/journal.pone.0185326 28934348 PMC5608385 · DOI
  48. [52]Tansawai U Walsh TR Niumsup PR Extended spectrum ß-lactamase-producing Escherichia coli among backyard poultry farms, farmers, and environments in Thailand Poult Sci 2019 98 6 2622 31 10.3382/ps/pez009 30690545 · DOI
  49. [53]Kürekci C Osek J Aydın M Tekeli İO Kurpas M Wieczorek K Evaluation of bulk tank raw milk and raw chicken meat samples as source of ESBL producing Escherichia coli in Turkey: recent insights J Food Saf 2019 39 2 e12605 10.1111/jfs.12605 · DOI
  50. [54]Cantón R Novais A Valverde A Machado E Peixe L Baquero F Prevalence and spread of extended-spectrum β-lactamase-producing Enterobacteriaceae in Europe Clin Microbiol Infect 2008 14 s1 144 53 10.1111/j.1469-0691.2007.01850.x 18154538 · DOI
  51. [55]Randall LP Lodge MP Elviss NC Lemma FL Hopkins KL Teale CJ Evaluation of meat, fruit and vegetables from retail stores in five United Kingdom regions as sources of extended-spectrum beta-lactamase (ESBL)-producing and carbapenem-resistant Escherichia coli Int J Food Microbiol 2017 241 283 90 10.1016/j.ijfoodmicro.2016.10.036 27821357 · DOI
  52. [56]Rao M Laidlaw A Li L Young K Tamber S Isolation of third generation cephalosporin resistant Enterobacteriaceae from retail meats and detection of extended spectrum beta-lactamase activity J Microbiol Methods 2021 189 106314 10.1016/j.mimet.2021.106314 34461553 · DOI
  53. [57]EFSA ECDC The European Union Summary Report on Antimicrobial Resistance in zoonotic and indicator bacteria from humans, animals and food in 2017/2018 EFSA J 2020 18 3 e06007 32874244 PMC7448042
  54. [58]El-Ghareeb WR Abdel-Raheem M Al-Marri SM Alaql TA Fayez FM Isolation and identification of extended spectrum β-lactamases (ESBLs) Escherichia coli from minced camel meat in Eastern province, Saudi Arabia Thai J Veterinary Med 2020 50 2 155 61 10.56808/2985-1130.3013 · DOI
  55. [59]I.C.M.S. Micro-organisms in Foods 6: Microbial Ecology of Food Commodities. Springer US; 2000.
  56. [60]Niumsup PR Tansawai U Na-udom A Jantapalaboon D Assawatheptawee K Kiddee A Prevalence and risk factors for intestinal carriage of CTX-M-type ESBLs in Enterobacteriaceae from a thai community Eur J Clin Microbiol Infect Dis 2018 37 1 69 75 10.1007/s10096-017-3102-9 28918585 · DOI
  57. [61]Martínez-Vázquez AV Mandujano A Cruz-Gonzalez E Guerrero A Vazquez J Cruz-Pulido WL Evaluation of Retail Meat as a source of ESBL Escherichia coli in Tamaulipas Mexico Antibiot 2022 10.3390/antibiotics11121795 PMC9774973 36551452 · DOI
  58. [62]Barrios-Villa E Cortés-Cortés G Lozano Zarain P Romero-Romero S Lara Flores N Estepa V Characterization of extended-spectrum and CMY-2 -lactamases, and associated virulence genes in from food of animal origin in México Br Food J 2018 120 7 1457 73 10.1108/BFJ-02-2018-0104 · DOI
  59. [63]Baran A, Adıgüzel M, Yüksel M. Prevalence of antibiotic-resistant and extended-spectrum beta-lactamase-producing Escherichia coli in chicken meat from eastern Turkey. Pakistan Veterinary Journal. 2020;40(3).
  60. [64]Abdallah HM Reuland EA Wintermans BB al Naiemi N Koek A Abdelwahab AM Extended-spectrum β-Lactamases and/or Carbapenemases-Producing Enterobacteriaceae isolated from Retail Chicken meat in Zagazig, Egypt PLoS ONE 2015 10 8 e0136052 10.1371/journal.pone.0136052 26284654 PMC4540287 · DOI
  61. [65]Johnson RP Clarke RC Wilson JB Read SC Rahn K Renwick SA Growing concerns and recent outbreaks involving Non-O157:H7 serotypes of Verotoxigenic Escherichia coli J Food Prot 1996 59 10 1112 22 10.4315/0362-028x-59.10.1112 31195470 · DOI
  62. [66]Johannes L Römer W Shiga toxins–from cell biology to biomedical applications Nat Rev Microbiol 2010 8 2 105 16 10.1038/nrmicro2279 20023663 · DOI
  63. [67]Brusa V, Aliverti V, Aliverti F, Ortega E, de la Torre J, Linares L, et al. Shiga toxin-producing Escherichia coli in beef retail markets from Argentina. Front Cell Infect Microbiol. 2013;2. 10.3389/fcimb.2012.00171 PMC3548221 23346554 · DOI
  64. [68]Hoang Minh S Kimura E Hoang Minh D Honjoh K Miyamoto T Virulence characteristics of Shiga toxin-producing Escherichia coli from raw meats and clinical samples Microbiol Immunol 2015 59 3 114 22 10.1111/1348-0421.12235 25644201 · DOI
  65. [69]Nong F Zhang P Meng J Xie Q Li Y Pan Y Characterization of shiga-toxin producing Escherichia coli (STEC) isolated from retail raw meats in Southeast China Food Control 2021 126 108061 10.1016/j.foodcont.2021.108061 · DOI
  66. [70]Ali SS Sonbol FI Sun J Hussein MA Hafez AE Abdelkarim EA Molecular characterization of virulence and drug resistance genes-producing Escherichia coli isolated from chicken meat: metal oxide nanoparticles as novel antibacterial agents Microb Pathog 2020 143 104164 10.1016/j.micpath.2020.104164 32198092 · DOI
  67. [71]Werber D Fruth A Buchholz U Prager R Kramer MH Ammon A Strong association between shiga toxin-producing Escherichia coli O157 and virulence genes stx2 and eae as possible explanation for predominance of serogroup O157 in patients with haemolytic uraemic syndrome Eur J Clin Microbiol Infect Dis 2003 22 12 726 30 10.1007/s10096-003-1025-0 14614596 · DOI
  68. [72]Ferreira JC Penha Filho RAC Kuaye APY Andrade LN Chang Y-F Darini ALC Virulence potential of commensal multidrug resistant Escherichia coli isolated from poultry in Brazil Infect Genet Evol 2018 65 251 6 10.1016/j.meegid.2018.07.037 30071311 · DOI
  69. [73]Dorado-García A Smid JH Van Pelt W Bonten MJ Fluit AC van den Bunt G Molecular relatedness of ESBL/AmpC-producing Escherichia coli from humans, animals, food and the environment: a pooled analysis J Antimicrob Chemother 2018 73 2 339 47 10.1093/jac/dkx397 29165596 · DOI
  70. [74]Kluytmans JAJW Overdevest ITMA Willemsen I Kluytmans-van den Bergh MFQ van der Zwaluw K Heck M Extended-spectrum β-Lactamase–producing Escherichia coli from Retail Chicken meat and humans: comparison of strains, plasmids, resistance genes, and virulence factors Clin Infect Dis 2012 56 4 478 87 10.1093/cid/cis929 23243181 · DOI
  71. [75]Kawamura K Goto K Nakane K Arakawa Y Molecular epidemiology of extended-spectrum β-lactamases and Escherichia coli isolated from retail foods including chicken meat in Japan Foodborne Pathog Dis 2014 11 2 104 10 10.1089/fpd.2013.1608 24093132 · DOI
  72. [76]Börjesson S Ny S Egervärn M Bergström J Rosengren à Englund S Limited dissemination of extended-spectrum β-Lactamase– and plasmid-encoded AmpC–Producing < em > Escherichia coli from Food and Farm Animals, Sweden Emerg Infect Disease J 2016 22 4 634 10.3201/eid2204.151142 PMC4806949 26982890 · DOI
  73. [77]Falgenhauer L, Imirzalioglu C, Oppong K, Akenten CW, Hogan B, Krumkamp R, et al. Detection and characterization of ESBL-Producing Escherichia coli from humans and poultry in Ghana. Front Microbiol. 2019;9. 10.3389/fmicb.2018.03358 PMC6340976 30697208 · DOI
  74. [78]de Been M Lanza VF de Toro M Scharringa J Dohmen W Du Y Dissemination of Cephalosporin Resistance genes between Escherichia coli strains from farm animals and humans by specific plasmid lineages PLoS Genet 2014 10 12 e1004776 10.1371/journal.pgen.1004776 25522320 PMC4270446 · DOI
  75. [79]Wang H McEntire JC Zhang L Li X Doyle M The transfer of antibiotic resistance from food to humans: facts, implications and future directions Rev Sci Tech 2012 31 1 249 60 10.20506/rst.31.1.2117 22849280 · DOI
  76. [80]Grave K Torren-Edo J Mackay D Comparison of the sales of veterinary antibacterial agents between 10 european countries J Antimicrob Chemother 2010 65 9 2037 40 10.1093/jac/dkq247 20587611 · DOI
  77. [81]Moawad AA Hotzel H Awad O Tomaso H Neubauer H Hafez HM Occurrence of Salmonella enterica and Escherichia coli in raw chicken and beef meat in northern Egypt and dissemination of their antibiotic resistance markers Gut Pathog 2017 9 57 10.1186/s13099-017-0206-9 29075329 PMC5648511 · DOI
  78. [82]Hassen B Abbassi MS Ruiz-Ripa L Mama OM Hassen A Torres C High prevalence of mcr-1 encoding colistin resistance and first identification of blaCTX-M-55 in ESBL/CMY-2-producing Escherichia coli isolated from chicken faeces and retail meat in Tunisia Int J Food Microbiol 2020 318 108478 10.1016/j.ijfoodmicro.2019.108478 31855787 · DOI
  79. [83]Uz Zaman T Albladi M Siddique MI Aljohani SM Balkhy HH Insertion element mediated mgrB disruption and presence of ISKpn28 in colistin-resistant Klebsiella pneumoniae isolates from Saudi Arabia Infect Drug Resist 2018 11 1183 7 10.2147/IDR.S161146 30147346 PMC6101004 · DOI
  80. [84]Cao L Li X Xu Y Shen J Prevalence and molecular characteristics of mcr-1 colistin resistance in Escherichia coli: isolates of clinical infection from a Chinese University Hospital Infect Drug Resist 2018 11 1597 603 10.2147/IDR.S166726 30310295 PMC6165781 · DOI
  81. [85]Carroll LM Gaballa A Guldimann C Sullivan G Henderson LO Wiedmann M Identification of Novel Mobilized Colistin Resistance Gene mcr-9 in a Multidrug-Resistant, Colistin-Susceptible Salmonella enterica Serotype Typhimurium isolate mBio 2019 10 3 e00853 19 10.1128/mBio.00853-19 31064835 PMC6509194 · DOI · Paper page
  82. [86]Haenni M Métayer V Gay E Madec JY Increasing trends in mcr-1 prevalence among extended-spectrum-β-lactamase-producing Escherichia coli isolates from french calves despite decreasing exposure to colistin Antimicrob Agents Chemother 2016 60 10 6433 4 10.1128/AAC.01147-16 27503658 PMC5038315 · DOI
  83. [87]Perrin-Guyomard A Bruneau M Houée P Deleurme K Legrandois P Poirier C Prevalence of mcr-1 in commensal Escherichia coli from French livestock, 2007 to 2014 Eurosurveillance 2016 21 6 30135 10.2807/1560-7917.ES.2016.21.6.30135 26898350 · DOI
  84. [88]Adiguzel MC Baran A Wu Z Cengiz S Dai L Oz C Prevalence of Colistin Resistance in Escherichia coli in Eastern Turkey and genomic characterization of an mcr-1 positive strain from Retail Chicken meat Microb Drug Resist 2020 27 3 424 32 10.1089/mdr.2020.0209 32721263 · DOI
  85. [89]Rahman MM Husna A Elshabrawy HA Alam J Runa NY Badruzzaman ATM Isolation and molecular characterization of multidrug-resistant Escherichia coli from chicken meat Sci Rep 2020 10 1 21999 10.1038/s41598-020-78367-2 33319793 PMC7738667 · DOI
  86. [90]Overdevest I Willemsen I Rijnsburger M Eustace A Xu L Hawkey P Extended-spectrum β-lactamase genes of Escherichia coli in chicken meat and humans, the Netherlands Emerg Infect Dis 2011 17 7 1216 22 10.3201/eid1707.110209 21762575 PMC3381403 · DOI
  87. [91]Guo S Aung KT Leekitcharoenphon P Tay MYF Seow KLG Zhong Y Prevalence and genomic analysis of ESBL-producing Escherichia coli in retail raw meats in Singapore J Antimicrob Chemother 2020 76 3 601 5 10.1093/jac/dkaa461 33331642 · DOI
  88. [92]Lim EJ Ho SX Cao DY Lau QC Koh TH Hsu LY Extended-spectrum beta-lactamase-producing Enterobacteriaceae in Retail Chicken meat in Singapore Ann Acad Med Singapore 2016 45 12 557 9 10.47102/annals-acadmedsg.V45N12p557 28062884 · DOI
  89. [93]Oteo J Hernández JM Espasa M Fleites A Sáez D Bautista V Emergence of OXA-48-producing Klebsiella pneumoniae and the novel carbapenemases OXA-244 and OXA-245 in Spain J Antimicrob Chemother 2013 68 2 317 21 10.1093/jac/dks383 23034714 · DOI
  90. [94]van der Bij AK Pitout JD The role of international travel in the worldwide spread of multiresistant Enterobacteriaceae J Antimicrob Chemother 2012 67 9 2090 100 10.1093/jac/dks214 22678728 · DOI
  91. [95]Mohammed ASA Mourad MI Alsewy FZ Azzam NFAEM Combination of silver nanoparticles with ineffective antibiotics against extended spectrum beta-lactamases producing isolates at Alexandria Main University Hospital, Egypt Beni-Suef Univ J Basic Appl Sci 2021 10 1 58 10.1186/s43088-021-00147-2 · DOI
  92. [96]Castillo RR Lozano D González B Manzano M Izquierdo-Barba I Vallet-Regí M Advances in mesoporous silica nanoparticles for targeted stimuli-responsive drug delivery: an update Expert Opin Drug Deliv 2019 16 4 415 39 10.1080/17425247.2019.1598375 30897978 PMC6667337 · DOI
  93. [97]Ansari MA Khan HM Khan AA Cameotra SS Pal R Antibiofilm efficacy of silver nanoparticles against biofilm of extended spectrum β-lactamase isolates of Escherichia coli and Klebsiella pneumoniae Appl Nanosci 2014 4 7 859 68 10.1007/s13204-013-0266-1 · DOI
  94. [98]Vazquez-Muñoz R Meza-Villezcas A Fournier PGJ Soria-Castro E Juarez-Moreno K Gallego-Hernández AL Enhancement of antibiotics antimicrobial activity due to the silver nanoparticles impact on the cell membrane PLoS ONE 2019 14 11 e0224904 10.1371/journal.pone.0224904 31703098 PMC6839893 · DOI
  95. [99]Shafreen RB Seema S Ahamed AP Thajuddin N Ali Alharbi S Inhibitory effect of Biosynthesized Silver Nanoparticles from Extract of Nitzschia palea against curli-mediated biofilm of Escherichia coli Appl Biochem Biotechnol 2017 183 4 1351 61 10.1007/s12010-017-2503-7 28573605 · DOI

Cited by

Sorted by citations

Authors
Ahmed, H. A., Elsohaby, I., Elamin, A. M., El-Ghafar, A. E. A., Elsaid, G. A., Elbarbary, M., Mohsen, R. A., El Feky, T. M., & El Bayomi, R. M.
Affiliations
  • Zagazig University (EG)
  • City University of Hong Kong (HK)
  • Animal Health Research Institute (TW)
Corresponding author
Ahmed, Heba A.
ORCID
Venue
BMC Microbiology
Publisher
Springer Science and Business Media LLC
Published
2023-08-07
Volume
23
Issue
1
Pages
212-212
ISSN
1471-2180 (ISSN-L)
DOI
10.1186/s12866-023-02948-0
PMC
PMC10405496
OpenAlex
W4385634909
Cited by
25
References
1
Citations by year
2026: 6 · 2025: 11 · 2024: 8
FWCI
2.14
Type
journal article
Language
en
Open access
Licence
Locations
  • BMC Microbiology (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • CityU Scholars (submittedVersion, cc-by)
  • Greater South Information System
Funders
Zagazig University
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Antibiotic Resistance in Bacteria
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Escherichia coli research studies
  • Life Sciences › Agricultural and Biological Sciences › Food Science › Salmonella and Campylobacter epidemiology
Keywords
extended-spectrum beta-lactamase, Escherichia coli, retail meat, antimicrobial resistance, multidrug resistance, pathotyping, Shiga toxin 2, REP-PCR genotyping, silver nanoparticles, hydrogen peroxide, duck meat, camel meat, food safety
MeSH terms
beta-Lactamases, Egypt, Escherichia coli, Food Contamination, Humans, Meat, Silver, Drug Resistance, Bacterial, Metal Nanoparticles, Genotyping Techniques

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review