Evidence map›Paper›PMID 28389276›Full record

ArticleClinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases2017

Whole genome sequencing of Shigella sonnei through PulseNet Latin America and Caribbean: advancing global surveillance of foodborne illnesses.

K S Baker, J Campos, M Pichel, A Della Gaspera, F Duarte-Martínez, E Campos-Chacón, H M Bolaños-Acuña, C Guzmán-Verri, A E Mather, S Diaz Velasco and 19 more

Abstract read
In one paragraph

Article in Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
–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

31 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  13. Outbreak of Central American born Shigella sonnei in two youth camps in Belgium in the summer of 2019.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2021
    Article
  14. Article
  15. Whole genome sequence analysis ofMicrobial genomics · 2021
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  19. Antimicrobial Resistance Dynamics in ChileanFrontiers in microbiology · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

29 authors.

K S BakerUniversity of Liverpool, Department of Functional and Comparative Genomics, Liverpool, England, United Kingdom; Wellcome Trust Sanger Institute, Pathogen Variation Programme, Hinxton, England, United Kingdom. Electronic address: kbaker@liverpool.ac.uk.
J CamposInstituto Nacional de Enfermedades Infecciosas, ANLIS, Buenos Aires, Argentina.
M PichelInstituto Nacional de Enfermedades Infecciosas, ANLIS, Buenos Aires, Argentina.
A Della GasperaInstituto Nacional de Enfermedades Infecciosas, ANLIS, Buenos Aires, Argentina.
F Duarte-MartínezInstituto Costarricense de Investigación y Enseñanza en Nutrición y Salud (Inciensa), Costa Rica.
E Campos-ChacónInstituto Costarricense de Investigación y Enseñanza en Nutrición y Salud (Inciensa), Costa Rica.
H M Bolaños-AcuñaInstituto Costarricense de Investigación y Enseñanza en Nutrición y Salud (Inciensa), Costa Rica.
C Guzmán-VerriPrograma de Investigación en Enfermedades Tropicales, Escuela de Medicina Veterinaria, Universidad Nacional, Heredia, Costa Rica; Centro de Investigación en Enfermedades Tropicales, Facultad de Microbiología, Universidad de Costa Rica, San José, Costa Rica.
A E MatherWellcome Trust Sanger Institute, Pathogen Variation Programme, Hinxton, England, United Kingdom; University of Cambridge, Department of Veterinary Medicine, Cambridge, England, United Kingdom.
S Diaz VelascoNational Institute of Heath, Lima, Peru.
M L Zamudio RojasNational Institute of Heath, Lima, Peru.
J L ForbesterWellcome Trust Sanger Institute, Pathogen Variation Programme, Hinxton, England, United Kingdom.
T R ConnorOrganisms and Environment Division, Cardiff University School of Biosciences, Sir Martin Evans Building, Cardiff, Wales, United Kingdom.
K H KeddyCentre for Enteric Diseases, National Institute for Communicable Diseases and Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
A M SmithCentre for Enteric Diseases, National Institute for Communicable Diseases and Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
E A López de DelgadoDepartment of Bacteriology, National Institute of Hygiene 'Rafael Rangel', Ciudad University, Los Chaguaramos, Venezuela.
G AngiolilloDepartment of Bacteriology, National Institute of Hygiene 'Rafael Rangel', Ciudad University, Los Chaguaramos, Venezuela.
N CuaicalDepartment of Bacteriology, National Institute of Hygiene 'Rafael Rangel', Ciudad University, Los Chaguaramos, Venezuela.
J FernándezMolecular Genetics Laboratory, Institute of Public Health of Chile, Santiago, Chile.
C AguayoMolecular Genetics Laboratory, Institute of Public Health of Chile, Santiago, Chile.
M Morales AguilarDepartment of Foodborne Diseases, National Health Laboratory of Guatemala, Laboratorio Nacional de Salud, Barcenas, Guatemala.
C ValenzuelaDepartment of Foodborne Diseases, National Health Laboratory of Guatemala, Laboratorio Nacional de Salud, Barcenas, Guatemala.
A J Morales MedranoDepartment of Foodborne Diseases, National Health Laboratory of Guatemala, Laboratorio Nacional de Salud, Barcenas, Guatemala.
A SirokBacteriology Laboratory, Departamento de Laboratorios de Salud Pública (DLSP), Ministerio de Salud Pública (MSP), Montevideo, Uruguay.
N Weiler GustafsonDepartment of Bacteriology, Laboratorio Central de Salud Pública, Asuncion, Paraguay.
P L Diaz GuevaraGrupo de Microbiología, Instituto Nacional de Salud, Bogotá, Colombia.
L A MontañoGrupo de Microbiología, Instituto Nacional de Salud, Bogotá, Colombia.
E PerezPan American Health Organization/World Health Organization, Department of Health Emergencies, Washington, DC, United States.
N R ThomsonWellcome Trust Sanger Institute, Pathogen Variation Programme, Hinxton, England, United Kingdom; London School of Hygiene and Tropical Medicine, London, England, United Kingdom. Electronic address: nrt@sanger.ac.uk.

Funding

Integrating the world's microbiology laboratories into a global microbial surveillance systemU01CA207167 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI STELLING, JOHN · 2016 to 2018
$1.3M
NCI NIH HHS U01 CA207167World Health Organization 001
6 · The paper itself

Abstract

objectivesShigella sonnei is a globally important diarrhoeal pathogen tracked through the surveillance network PulseNet Latin America and Caribbean (PNLA&C), which participates in PulseNet International. PNLA&C laboratories use common molecular techniques to track pathogens causing foodborne illness. We aimed to demonstrate the possibility and advantages of transitioning to whole genome sequencing (WGS) for surveillance within existing networks across a continent where S. sonnei is endemic.

methodsWe applied WGS to representative archive isolates of S. sonnei (n = 323) from laboratories in nine PNLA&C countries to generate a regional phylogenomic reference for S. sonnei and put this in the global context. We used this reference to contextualise 16 S. sonnei from three Argentinian outbreaks, using locally generated sequence data. Assembled genome sequences were used to predict antimicrobial resistance (AMR) phenotypes and identify AMR determinants.

resultsS. sonnei isolates clustered in five Latin American sublineages in the global phylogeny, with many (46%, 149 of 323) belonging to previously undescribed sublineages. Predicted multidrug resistance was common (77%, 249 of 323), and clinically relevant differences in AMR were found among sublineages. The regional overview showed that Argentinian outbreak isolates belonged to distinct sublineages and had different epidemiologic origins.

conclusionsLatin America contains novel genetic diversity of S. sonnei that is relevant on a global scale and commonly exhibits multidrug resistance. Retrospective passive surveillance with WGS has utility for informing treatment, identifying regionally epidemic sublineages and providing a framework for interpretation of prospective, locally sequenced outbreaks.

Indexed as

Dysentery, BacillaryFoodborne DiseasesCaribbean RegionDisease OutbreaksDNA, BacterialDrug Resistance, BacterialHumansLatin AmericaPublic Health SurveillanceRetrospective StudiesShigella sonneiWhole Genome SequencingDNA, BacterialAntimicrobial resistanceCentral AmericaDiarrhoeal diseaseEpidemiologyGenomicsShigellosisSouth America

Identifiers

PMID28389276
PMCPMC5667938

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LicenceCC BY
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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.