Evidence map›Paper›PMID 34467469›Full record

ArticleBrazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]2021

Occurrence of genes associated with virulence in Escherichia coli isolates from chicken carcasses at different stages of processing at a slaughterhouse.

João Juliano Pinheiro, Luiz Eduardo de Souza Gazal, Gabriella Oliveira de Araujo, Kelly Cristina Tagliari de Brito, Ivonete Fatima Tazzo, Rafael Tonini Mesquita, Renata Katsuko Takayama Kobayashi, Luciana Kazue Otutumi, José Matheus Beltrami, Lissandra Souto Cavalli and 1 more

Erratum issuedAbstract read
In one paragraph

Article in Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology], 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

João Juliano PinheiroLaboratory of Avian Health and Technological Innovation, Institute for Veterinary Research Desidério Finamor (IPVDF), Postgraduate Program in Animal Health, Department of Agricultural Diagnosis and Research, Secretariat of Agriculture, Livestock and Rural Development of Rio Grande Do Sul, Estrada do Conde, 6000, Sans Souci, Eldorado do Sul, RS, 92990-000, Brazil.
Luiz Eduardo de Souza GazalBacteriology Laboratory, Department of Microbiology, Center for Biological Sciences, State University of Londrina, Rodovia Celso Garcia Cid, Km 380, S/N Campus Universitário, Londrina, PR, 86057-970, Brazil.
Gabriella Oliveira de AraujoLaboratory of Avian Health and Technological Innovation, Institute for Veterinary Research Desidério Finamor (IPVDF), Postgraduate Program in Animal Health, Department of Agricultural Diagnosis and Research, Secretariat of Agriculture, Livestock and Rural Development of Rio Grande Do Sul, Estrada do Conde, 6000, Sans Souci, Eldorado do Sul, RS, 92990-000, Brazil.
Kelly Cristina Tagliari de BritoLaboratory of Avian Health and Technological Innovation, Institute for Veterinary Research Desidério Finamor (IPVDF), Postgraduate Program in Animal Health, Department of Agricultural Diagnosis and Research, Secretariat of Agriculture, Livestock and Rural Development of Rio Grande Do Sul, Estrada do Conde, 6000, Sans Souci, Eldorado do Sul, RS, 92990-000, Brazil. kellybritofepagro@gmail.com.
Ivonete Fatima TazzoDepartment of Agricultural Diagnosis and Research, Secretariat of Agriculture, Livestock and Rural Development of Rio Grande do Sul, Rua Gonçalves Dias, 570, Menino Deus, Porto Alegre, RS, 90130-060, Brazil.
Rafael Tonini MesquitaLaboratory of Avian Health and Technological Innovation, Institute for Veterinary Research Desidério Finamor (IPVDF), Postgraduate Program in Animal Health, Department of Agricultural Diagnosis and Research, Secretariat of Agriculture, Livestock and Rural Development of Rio Grande Do Sul, Estrada do Conde, 6000, Sans Souci, Eldorado do Sul, RS, 92990-000, Brazil.
Renata Katsuko Takayama KobayashiBacteriology Laboratory, Department of Microbiology, Center for Biological Sciences, State University of Londrina, Rodovia Celso Garcia Cid, Km 380, S/N Campus Universitário, Londrina, PR, 86057-970, Brazil.
Luciana Kazue OtutumiPostgraduate Program in Animal Science With Emphasis On Bioactive Products, Universidade Paranaense, Umuarama, PR, Brazil.
José Matheus BeltramiMaster in Animal Science, Universidade Paranaense, UNIPAR, Umuarama, PR, Brazil.
Lissandra Souto CavalliDepartment of Agricultural Diagnosis and Research, Secretariat of Agriculture, Livestock and Rural Development of Rio Grande do Sul, Rua Gonçalves Dias, 570, Menino Deus, Porto Alegre, RS, 90130-060, Brazil.
Benito Guimarães de BritoLaboratory of Avian Health and Technological Innovation, Institute for Veterinary Research Desidério Finamor (IPVDF), Postgraduate Program in Animal Health, Department of Agricultural Diagnosis and Research, Secretariat of Agriculture, Livestock and Rural Development of Rio Grande Do Sul, Estrada do Conde, 6000, Sans Souci, Eldorado do Sul, RS, 92990-000, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Escherichia coli is a bacterium frequently found in chicken carcasses, causing carcass condemnation with losses to the industry and when present in food, it carries a risk to public health as there is evidence that some strains pathogenic to birds (APEC - Avian Pathogenic E. coli) have zoonotic potential. Carcass contamination can occur at the slaughterhouse, but the influence of the different stages of processing in the selection of potential extraintestinal pathogenic E. coli strains is unknown. This study aimed to analyze the influence of the processing steps in the slaughterhouse on the detection of E. coli isolates carrying APEC predictor's virulence-associated genes (VAGs), and to relate their presence with post-mortem condemnation. A sample consisted of four pooled carcasses collected at seven different stages of slaughter (before scalding, after scalding, after plucking, before evisceration/after shower wash, after evisceration, after pre-coolers, and after packing) from 15 batches of broilers. The total samples obtained was 105 pools with four carcasses each, totaling 420 carcasses analyzed. Enterobacteriaceae were counted from each pool and E. coli were subsequently selected, which were submitted to pentaplex PCR to identify the five VAG APEC predictor's: iroN, ompT, hlyF, iss, and iutA. The Enterobacteriaceae count demonstrated a reduction of 4.25 log CFU per gram of carcass from the first to the last stage analyzed, with scalding and pre-cooling by immersion being the procedures that contributed most to this reduction. The presence of VAGs and potential APEC (presence of two or more of these gene predictors) was observed at all points evaluated in the slaughterhouse, which suggested that bacteria carrying these genes could reach the consumer.

Indexed as

Escherichia coliEscherichia coli InfectionsPoultry DiseasesVirulenceAbattoirsAnimalsChickensAvian Pathogenic Escherichia coli (APEC)CondemnationEnterobacteriaceaeSlaughterhouseVirulence factor

Identifiers

PMID34467469
PMCPMC8578229

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.