Literature DB >> 32687033

mcr-Positive Escherichia coli ST131-H22 from Poultry in Brazil.

Andre Becker S Saidenberg, Marc Stegger, Lance Bradley Price, Thor Bech Johannesen, Maliha Aziz, Marcos P V Cunha, Andrea M Moreno, Terezinha Knöbl.   

Abstract

Escherichia coli sequence type (ST) 131 is of concern because it can acquire antimicrobial resistance and cause extraintestinal infections. E. coli ST131-H22 sublineage appears capable of being transmitted to humans through poultry. We report on multidrug-resistant ST131-H22 poultry isolates in Brazil closely related to international human and poultry isolates.

Entities:  

Keywords:  Antimicrobial resistance; Brazil; Escherichia coli; MDR; ST131; avian pathogenic Escherichia coli; colistin; phylogenetic analyses; poultry; virulence factors; zoonoses

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Substances:

Year:  2020        PMID: 32687033      PMCID: PMC7392447          DOI: 10.3201/eid2608.191724

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


The pandemic, extraintestinal, pathogenic Escherichia coli multilocus sequence type (MLST) 131 lineage has emerged extensively, gaining notoriety for its extensively multidrug-resistant ST131-H30 sublineage (). Whereas ST131-H30 appears to be transmitted primarily from person to person, the H22 sublineage may be transmitted zoonotically through poultry and cause urinary tract infections and urosepsis (,). We report isolating ST131-H22 strains that are multidrug resistant (MDR), meaning that they are resistant to >3 classes of antimicrobials (), carrying mobile colistin-resistance (mcr) determinants from poultry in Brazil, the largest poultry-exporting country in the world. We collected 64 E. coli strains from poultry with colibacillosis cases from 2 different farms in the same geographic region of Brazil and screened them by PCR for the ST131 clonal group (). PCR detected 6 ST131 isolates (2 from the first farm, 4 from the second), which we whole-genome sequenced (BioProject no. PRJNA398035). We determined phenotypic antimicrobial susceptibility with disk diffusion testing, except for isolates carrying the mcr gene, which we tested using broth microdilution (). We trimmed the reads and used QUAST (http://quast.sourceforge.net) to evaluate the quality of assemblies (contig lengths and expected genome sizes). We assembled DNA sequences with SPAdes (http://cab.spbu.ru/software/spades), then determined the serotype, phylogroup, MLST, fimH protein type, virulence gene profile, plasmid replicons, and markers of antimicrobial resistance for each isolate in silico using the ABRicate virulence factors database (https://github.com/tseemann/abricate) and ResFinder/PlasmidFinder tools from CGE (https://cge.cbs.dtu.dk/services). Genes were identified with a minimum of >95% of identity and coverage. We identified all isolates as O25:H4-ST131-H22, all belonging to phylogroup B2. We generated a maximum-likelihood phylogeny tree on the basis of core-genome single-nucleotide polymorphisms, including the 6 isolates from Brazil and 140 ST131-H22 sequences from EnteroBase (http://enterobase.warwick.ac.uk) and a previous study (), using the Northern Arizona SNP Pipeline (https://tgennorth.github.io/NASP/) aligned against E. coli JJ1886 ST131-H30 (GenBank accession no. CP006784) (Appendix). The 6 isolates from poultry were nested within a clade of intermingled poultry and human clinical isolates within the overall international isolates (Figure, panel A). The isolates from Brazil were closely related to ST131-H22 avian pathogenic E. coli isolates from poultry in the United States and those from a human urinary tract infection in Australia (Figure, panel B). Identical virulence factors and plasmid replicons were observed among 4 β-lactamase positive isolates and between 2 isolates missing the β-lactamase genes but carrying mcr colistin–resistance determinants. All 6 isolates had MDR profiles, phenotypically confirmed (data not shown except for those from colistin microdilution method) (Figure, panel B).
Figure

Phylogenetic analysis of Escherichia coli ST131-H22 isolates from poultry in Brazil and reference sequences. A) Unrooted phylogeny of 146 E. coli ST131-H22 isolates based on core genome single-nucleotide polymorphisms with the host origin outlined. The cluster containing closely related isolates to the 6 isolates from Brazil is highlighted. B) Rooted phylogeny of closely related isolates from retail meat with APEC and a human isolate with our 6 APEC isolates. The highlighted cluster includes a partial depiction of the tree including the data on host, country, and disease (urinary tract infection or other). Clusters containing the study’s isolates have their individual identification in parenthesis. Asterisks indicate farm origins (*, farm 1; **, farm 2). Virulence factors profiles are identified as groups A: cvi/cva, ent, fimA-H, ibeA, irp1/2, iroN, iucD,iss, kpsM, ompA, tsh; B: cvi/cva, ent, fimA-H, ibeA, irp1/2, iroN, iucD, iss, kpsM, ompA; and C: cvi/cva, ent, fimA-H, fyuA, ibeA, irp1/2, iroN, iucD, iss, kpsM, ompA, tsh. Plasmid profiles are identified by group: 1: IncFIB, IncFIC(FII), Incl1; 2: IncFIB, IncFIC(FII), IncFII, Incl1; 3: IncFIB, IncFIC(FII), IncFII, IncHI2, IncHI2A, Incl1; 4: IncFIB, IncFIC(FII), Incl1, IncN; 5: IncFIB, IncFIC(FII), IncFII, IncFII(pCoo), IncHI2, IncHI2A; 6: IncFIB, IncFIC(FII), IncFII, IncHI2, IncHI2A; 7: IncFIB, IncFII, Incl1, IncX1; and 8: IncFIB, IncFIC(FII), IncFII, Incl1, IncX1. Phenotypic colistin-resistance is indicated by the symbol # for the 2 colistin-resistance mcr genes positive isolates, showing resistance according to 2018 Clinical Laboratory Standards Institute (https://clsi.org/) clinical breakpoints. APEC, avian pathogenic E. coli; ID, identification; ST, sequence type; UTI, urinary tract infection.

Phylogenetic analysis of Escherichia coli ST131-H22 isolates from poultry in Brazil and reference sequences. A) Unrooted phylogeny of 146 E. coli ST131-H22 isolates based on core genome single-nucleotide polymorphisms with the host origin outlined. The cluster containing closely related isolates to the 6 isolates from Brazil is highlighted. B) Rooted phylogeny of closely related isolates from retail meat with APEC and a human isolate with our 6 APEC isolates. The highlighted cluster includes a partial depiction of the tree including the data on host, country, and disease (urinary tract infection or other). Clusters containing the study’s isolates have their individual identification in parenthesis. Asterisks indicate farm origins (*, farm 1; **, farm 2). Virulence factors profiles are identified as groups A: cvi/cva, ent, fimA-H, ibeA, irp1/2, iroN, iucD,iss, kpsM, ompA, tsh; B: cvi/cva, ent, fimA-H, ibeA, irp1/2, iroN, iucD, iss, kpsM, ompA; and C: cvi/cva, ent, fimA-H, fyuA, ibeA, irp1/2, iroN, iucD, iss, kpsM, ompA, tsh. Plasmid profiles are identified by group: 1: IncFIB, IncFIC(FII), Incl1; 2: IncFIB, IncFIC(FII), IncFII, Incl1; 3: IncFIB, IncFIC(FII), IncFII, IncHI2, IncHI2A, Incl1; 4: IncFIB, IncFIC(FII), Incl1, IncN; 5: IncFIB, IncFIC(FII), IncFII, IncFII(pCoo), IncHI2, IncHI2A; 6: IncFIB, IncFIC(FII), IncFII, IncHI2, IncHI2A; 7: IncFIB, IncFII, Incl1, IncX1; and 8: IncFIB, IncFIC(FII), IncFII, Incl1, IncX1. Phenotypic colistin-resistance is indicated by the symbol # for the 2 colistin-resistance mcr genes positive isolates, showing resistance according to 2018 Clinical Laboratory Standards Institute (https://clsi.org/) clinical breakpoints. APEC, avian pathogenic E. coli; ID, identification; ST, sequence type; UTI, urinary tract infection. The ST131-H22 lineage, while currently not as common as the H30 sublineage as a cause of community-acquired infections, does present a public health challenge because it colonizes poultry flocks, contaminating retail poultry products, and carries mcr colistin–resistance genes (). The enormity and rapid growth of poultry production, in which many developing countries use antimicrobials extensively (), and its zoonotic potential, make ST131-H22 worthy of specific attention (). Findings from our phylogenetic analyses of a global collection of ST131-H22 isolates from humans and poultry support findings from previous studies (,) and underscore the zoonotic potential of this virulent sublineage. Given that Brazil annually processes 13.8 million poultry products and exports 3.8 million kilograms (), these findings warrant further examination to assess potential zoonotic spillover in Brazil and poultry-importing countries. Until such studies are conducted, the zoonotic potential of ST131-H22 in flocks in Brazil cannot be quantified. The discovery of mcr mobile colistin resistance determinants in food animals has renewed attention to the potential risks of widespread antimicrobial use in livestock. In Latin America, mcr-5 has been found in poultry in Paraguay (). The description of the mcr-9 homologue from humans in the United States and horses in Sweden has raised attention to another mcr gene with potential for global spread (). Both mcr variants in this study, 153_Br and 157_Br, showed phenotypic resistance () and came from the same farm (Figure, panel B). Interestingly, 153_Br carried both mcr-5.1 and mcr-9 variants. These isolates may portend a more widespread problem within poultry flocks in Brazil. Isolates from this study showed resistance to all of the World Health Organization’s highest priority critically important antimicrobial classes (Figure, panel B) (). Analysis of the absence of tetracycline resistance (tet[B]/[D]) in 1 of our isolates (Figure, panel B) indicates partial plasmid loss (data not shown). Use of colistin as a growth promoter in livestock was banned in Brazil in November 2016, although it continued being therapeutically used in poultry up to 2018 (). Therefore, mcr-encoding H22 strains could be selected out of the population over time. Further restrictions will have to be implemented to combat the growing resistance of E. coli in poultry in Brazil to critically important antimicrobial drugs (). Our findings suggest that poultry in Brazil may serve as a reservoir for MDR extraintestinal pathogenic E. coli carrying mobile colistin-resistance determinants. These findings highlight the need for better antimicrobial stewardship and surveillance systems to determine the prevalence of MDR E. coli ST131-H22 in these poultry flocks and clarify the risks posed to domestic and international poultry consumers.

Appendix

Additional information on mcr-positive Escherichia coli ST131-H22 from poultry connected to international isolates, Brazil.
  7 in total

1.  Global trends in antimicrobial use in food animals.

Authors:  Thomas P Van Boeckel; Charles Brower; Marius Gilbert; Bryan T Grenfell; Simon A Levin; Timothy P Robinson; Aude Teillant; Ramanan Laxminarayan
Journal:  Proc Natl Acad Sci U S A       Date:  2015-03-19       Impact factor: 11.205

2.  Various conjugative plasmids carrying the mcr-5 gene in Escherichia coli isolates from healthy chickens in Paraguay.

Authors:  Kristina Nesporova; Ivana Jamborova; Adam Valcek; Matej Medvecky; Ivan Literak; Monika Dolejska
Journal:  J Antimicrob Chemother       Date:  2019-11-01       Impact factor: 5.790

3.  ST131 fimH22 Escherichia coli isolate with a blaCMY-2/IncI1/ST12 plasmid obtained from a patient with bloodstream infection: highly similar to E. coli isolates of broiler origin.

Authors:  Louise Roer; Søren Overballe-Petersen; Frank Hansen; Thor B Johannesen; Marc Stegger; Valeria Bortolaia; Pimlapas Leekitcharoenphon; Helle B Korsgaard; Anne Mette Seyfarth; Joël Mossong; Pierre Wattiau; Cécile Boland; Dennis S Hansen; Henrik Hasman; Anette M Hammerum; Rene S Hendriksen
Journal:  J Antimicrob Chemother       Date:  2019-03-01       Impact factor: 5.790

4.  Rapid identification of major Escherichia coli sequence types causing urinary tract and bloodstream infections.

Authors:  M Doumith; M Day; H Ciesielczuk; R Hope; A Underwood; R Reynolds; J Wain; D M Livermore; N Woodford
Journal:  J Clin Microbiol       Date:  2014-10-29       Impact factor: 5.948

5.  A link between the newly described colistin resistance gene mcr-9 and clinical Enterobacteriaceae isolates carrying blaSHV-12 from horses in Sweden.

Authors:  Stefan Börjesson; Christina Greko; Mattias Myrenås; Annica Landén; Oskar Nilsson; Karl Pedersen
Journal:  J Glob Antimicrob Resist       Date:  2019-09-05       Impact factor: 4.035

Review 6.  Escherichia coli and urinary tract infections: the role of poultry-meat.

Authors:  A R Manges
Journal:  Clin Microbiol Infect       Date:  2015-12-08       Impact factor: 8.067

7.  Escherichia coli ST131-H22 as a Foodborne Uropathogen.

Authors:  Cindy M Liu; Marc Stegger; Maliha Aziz; Timothy J Johnson; Kara Waits; Lora Nordstrom; Lori Gauld; Brett Weaver; Diana Rolland; Sally Statham; Joseph Horwinski; Sanjeev Sariya; Gregg S Davis; Evgeni Sokurenko; Paul Keim; James R Johnson; Lance B Price
Journal:  MBio       Date:  2018-08-28       Impact factor: 7.867

  7 in total
  8 in total

Review 1.  Avian Pathogenic Escherichia coli (APEC): An Overview of Virulence and Pathogenesis Factors, Zoonotic Potential, and Control Strategies.

Authors:  Dipak Kathayat; Dhanashree Lokesh; Sochina Ranjit; Gireesh Rajashekara
Journal:  Pathogens       Date:  2021-04-12

2.  Prevalence and Antibiotic Resistance Characteristics of Extraintestinal Pathogenic Escherichia coli among Healthy Chickens from Farms and Live Poultry Markets in China.

Authors:  Ming Zou; Ping-Ping Ma; Wen-Shuang Liu; Xiao Liang; Xu-Yong Li; You-Zhi Li; Bao-Tao Liu
Journal:  Animals (Basel)       Date:  2021-04-13       Impact factor: 2.752

3.  Genomic comparisons of Escherichia coli ST131 from Australia.

Authors:  Dmitriy Li; Ethan R Wyrsch; Paarthiphan Elankumaran; Monika Dolejska; Marc S Marenda; Glenn F Browning; Rhys N Bushell; Jessica McKinnon; Piklu Roy Chowdhury; Nola Hitchick; Natalie Miller; Erica Donner; Barbara Drigo; Dave Baker; Ian G Charles; Timothy Kudinha; Veronica M Jarocki; Steven Philip Djordjevic
Journal:  Microb Genom       Date:  2021-12

4.  WHO Critical Priority Escherichia coli as One Health Challenge for a Post-Pandemic Scenario: Genomic Surveillance and Analysis of Current Trends in Brazil.

Authors:  Bruna Fuga; Fábio P Sellera; Louise Cerdeira; Fernanda Esposito; Brenda Cardoso; Herrison Fontana; Quézia Moura; Adriana Cardenas-Arias; Elder Sano; Rosineide M Ribas; Albalúcia C Carvalho; Maria Cristina B Tognim; Marcia Maria C de Morais; Ana Judith P G Quaresma; Ângela Patrícia Santana; Joice N Reis; Marcelo Pilonetto; Eliana Carolina Vespero; Raquel R Bonelli; Aloysio M F Cerqueira; Thaís C M Sincero; Nilton Lincopan
Journal:  Microbiol Spectr       Date:  2022-03-02

Review 5.  Worldwide Prevalence of mcr-mediated Colistin-Resistance Escherichia coli in Isolates of Clinical Samples, Healthy Humans, and Livestock-A Systematic Review and Meta-Analysis.

Authors:  Carlos Bastidas-Caldes; Jacobus H de Waard; María Soledad Salgado; María José Villacís; Marco Coral-Almeida; Yoshimasa Yamamoto; Manuel Calvopiña
Journal:  Pathogens       Date:  2022-06-08

6.  Host Colonization as a Major Evolutionary Force Favoring the Diversity and the Emergence of the Worldwide Multidrug-Resistant Escherichia coli ST131.

Authors:  Richard Bonnet; Racha Beyrouthy; Marisa Haenni; Marie-Hélène Nicolas-Chanoine; Guillaume Dalmasso; Jean-Yves Madec
Journal:  mBio       Date:  2021-08-24       Impact factor: 7.867

7.  Insights and genetic features of extended-spectrum beta-lactamase producing Escherichia coli isolates from two hospitals in Ghana.

Authors:  Samiratu Mahazu; Wakana Sato; Alafate Ayibieke; Isaac Prah; Takaya Hayashi; Toshihiko Suzuki; Shiroh Iwanaga; Anthony Ablordey; Ryoichi Saito
Journal:  Sci Rep       Date:  2022-02-03       Impact factor: 4.379

8.  Colistin-resistant Enterobacter kobei carrying mcr-9.1 and blaCTX-M-15 infecting a critically endangered franciscana dolphin (Pontoporia blainvillei), Brazil.

Authors:  Danny Fuentes-Castillo; Fábio P Sellera; Daphne W Goldberg; Herrison Fontana; Fernanda Esposito; Brenda Cardoso; Joana Ikeda; Anneliese Kyllar; José L Catão-Dias; Nilton Lincopan
Journal:  Transbound Emerg Dis       Date:  2021-05-06       Impact factor: 4.521

  8 in total

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