Evidence map›Paper›PMID 31220112›Full record

ArticlePLoS neglected tropical diseases2019

Emergence of phylogenetically diverse and fluoroquinolone resistant Salmonella Enteritidis as a cause of invasive nontyphoidal Salmonella disease in Ghana.

Cassandra Aldrich, Hassan Hartman, Nicholas Feasey, Marie Anne Chattaway, Denise Dekker, Hassan M Al-Emran, Lesley Larkin, Jacquelyn McCormick, Nimako Sarpong, Simon Le Hello and 8 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
6.3field-weighted citation impact, top 4% of its field
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

23 citing papers in PubMed, 45 citations in OpenAlex.

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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

18 authors at 10 institutions in 7 countries.

Cassandra AldrichDepartment of Infectious Disease Epidemiology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.ORCID 0000-0002-8625-9296
Hassan HartmanNational Infections Service, Public Health England, Colindale, United Kingdom.
Nicholas FeaseyLiverpool School of Tropical Medicine, Liverpool, United Kingdom.
Marie Anne ChattawayNational Infections Service, Public Health England, Colindale, United Kingdom.
Denise DekkerDepartment of Infectious Disease Epidemiology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Hassan M Al-EmranDepartment of Infectious Disease Epidemiology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Lesley LarkinNational Infections Service, Public Health England, Colindale, United Kingdom.ORCID 0000-0003-3699-9699
Jacquelyn McCormickNational Infections Service, Public Health England, Colindale, United Kingdom.
Nimako SarpongKumasi Centre for Collaborative Research in Tropical Medicine (KCCR), Kumasi, Ghana.
Simon Le HelloInstitut Pasteur, French National Reference Center for Escherichia coli, Shigella and Salmonella, Paris, France.
Yaw Adu-SarkodieDepartment of Clinical Microbiology, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.ORCID 0000-0003-2093-1534
Ursula PanznerInternational Vaccine Institute, Seoul, Republic of Korea.
Se Eun ParkInternational Vaccine Institute, Seoul, Republic of Korea.
Justin ImInternational Vaccine Institute, Seoul, Republic of Korea.
Florian MarksInternational Vaccine Institute, Seoul, Republic of Korea.
Jürgen MayDepartment of Infectious Disease Epidemiology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Timothy J DallmanNational Infections Service, Public Health England, Colindale, United Kingdom.
Daniel EibachDepartment of Infectious Disease Epidemiology, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Public Health England · GBInternational Vaccine Institute · KRGerman Center for Infection Research · DEBernhard Nocht Institute for Tropical Medicine · DEInstitut Pasteur · FRJashore University of Science and Technology · BDKumasi Centre for Collaborative Research in Tropical Medicine · GHKwame Nkrumah University of Science and Technology · GHLiverpool School of Tropical Medicine · GBLudwig-Maximilians-Universität München · DE

Funding

Wellcome TrustWellcome Trust 206194
6 · The paper itself

Abstract

backgroundSalmonella enterica serovar Enteritidis is a cause of both poultry- and egg-associated enterocolitis globally and bloodstream-invasive nontyphoidal Salmonella (iNTS) disease in sub-Saharan Africa (sSA). Distinct, multi-drug resistant genotypes associated with iNTS disease in sSA have recently been described, often requiring treatment with fluoroquinolone antibiotics. In industrialised countries, antimicrobial use in poultry production has led to frequent fluoroquinolone resistance amongst globally prevalent enterocolitis-associated lineages. METHODOLOGY/PRINCIPAL

findingsTwenty seven S. Enteritidis isolates from patients with iNTS disease and two poultry isolates, collected between 2007 and 2015 in the Ashanti region of Ghana, were whole-genome sequenced. These isolates, notable for a high rate of diminished ciprofloxacin susceptibility (DCS), were placed in the phyletic context of 1,067 sequences from the Public Health England (PHE) S. Enteritidis genome database to understand whether DCS was associated with African or globally-circulating clades of S. Enteritidis. Analysis showed four of the major S. Enteritidis clades were represented, two global and two African. All thirteen DCS isolates, containing a single gyrA mutation at codon 87, belonged to a global PT4-like clade responsible for epidemics of poultry-associated enterocolitis. Apart from two DCS isolates, which clustered with PHE isolates associated with travel to Spain and Brazil, the remaining DCS isolates, including one poultry isolate, belonged to two monophyletic clusters in which gyrA 87 mutations appear to have developed within the region. CONCLUSIONS/SIGNIFICANCE: Extensive phylogenetic diversity is evident amongst iNTS disease-associated S. Enteritidis in Ghana. Antimicrobial resistance profiles differed by clade, highlighting the challenges of devising empirical sepsis guidelines. The detection of fluoroquinolone resistance in phyletically-related poultry and human isolates is of major concern and surveillance and control measures within the region's burgeoning poultry industry are required to protect a human population at high risk of iNTS disease.

Indexed as

AdolescentAnimalsAnti-Bacterial AgentsChildChild, PreschoolCommunicable Diseases, EmergingEnterocolitisFemaleFluoroquinolonesGenetic VariationGenotypeGhanaHumansInfantMaleMicrobial Sensitivity TestsAnti-Bacterial AgentsFluoroquinolones

Identifiers

PMID31220112
PMCPMC6605661
OpenAlexW2950221586

What OpenQuestion holds

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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.