Evidence map›Paper›PMID 30670612›Full record

ArticlemBio2019

Genomic Analyses of Acute Flaccid Myelitis Cases among a Cluster in Arizona Provide Further Evidence of Enterovirus D68 Role.

Jolene R Bowers, Michael Valentine, Veronica Harrison, Viacheslav Y Fofanov, John Gillece, Josie Delisle, Bethany Patton, James Schupp, Krystal Sheridan, Darrin Lemmer and 17 more

Open access · goldAbstract read
In one paragraph

Article in mBio, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
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

27 authors at 6 institutions in 1 country.

Jolene R BowersPathogen and Microbiome Division, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Michael ValentinePathogen and Microbiome Division, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Veronica HarrisonPathogen and Microbiome Division, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Viacheslav Y FofanovSchool of Informatics Computing and Cyber Systems, Northern Arizona University, Flagstaff, Arizona, USA.
John GillecePathogen and Microbiome Division, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Josie DelislePathogen and Microbiome Division, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Bethany PattonPathogen and Microbiome Division, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
James SchuppPathogen and Microbiome Division, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Krystal SheridanPathogen and Microbiome Division, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Darrin LemmerPathogen and Microbiome Division, Translational Genomics Research Institute, Flagstaff, Arizona, USA.
Scott OstdiekPhoenix Children's Hospital, Phoenix, Arizona, USA.
Harlori K BainsPhoenix Children's Hospital, Phoenix, Arizona, USA.
Jennifer HeimPhoenix Children's Hospital, Phoenix, Arizona, USA.
Tammy SylvesterMaricopa County Department of Public Health, Phoenix, Arizona, USA.
Siru PrasaiMaricopa County Department of Public Health, Phoenix, Arizona, USA.
Melissa KretschmerMaricopa County Department of Public Health, Phoenix, Arizona, USA.
Nicole FowleMaricopa County Department of Public Health, Phoenix, Arizona, USA.
Kenneth KomatsuArizona Department of Health Services, Phoenix, Arizona, USA.
Shane BradyArizona Department of Health Services, Phoenix, Arizona, USA.
Susan RobinsonArizona Department of Health Services, Phoenix, Arizona, USA.
Kathryn FitzpatrickArizona Department of Health Services, Phoenix, Arizona, USA.
Gholamabbas Amin OstovarMaricopa Integrated Health System, Phoenix, Arizona, USA.
Eric AlsopNeurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.
Elizabeth HutchinsNeurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.
Kendall JensenNeurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, USA.
Paul KeimPathogen and Microbiome Division, Translational Genomics Research Institute, Flagstaff, Arizona, USA.ORCID 0000-0003-0089-5820
David M EngelthalerPathogen and Microbiome Division, Translational Genomics Research Institute, Flagstaff, Arizona, USA dengelthaler@tgen.org.ORCID 0000-0001-5945-059X
Translational Genomics Research Institute · USArizona Department of Health Services · USMaricopa County Department of Public Health · USPhoenix Children's Hospital · USNorthern Arizona University · USValleywise Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enteroviruses are a common cause of respiratory and gastrointestinal illness, and multiple subtypes, including poliovirus, can cause neurologic disease. In recent years, enterovirus D68 (EV-D68) has been associated with serious neurologic illnesses, including acute flaccid myelitis (AFM), frequently preceded by respiratory disease. A cluster of 11 suspect cases of pediatric AFM was identified in September 2016 in Phoenix, AZ. To determine if these cases were associated with EV-D68, we performed multiple genomic analyses of nasopharyngeal (NP) swabs and cerebrospinal fluid (CSF) material from the patients, including real-time PCR and amplicon sequencing targeting the EV-D68 VP1 gene and unbiased microbiome and metagenomic sequencing. Four of the 11 patients were classified as confirmed cases of AFM, and an additional case was classified as probable AFM. Real-time PCR and amplicon sequencing detected EV-D68 virus RNA in the three AFM patients from which NP swabs were collected, as well as in a fourth patient diagnosed with acute disseminated encephalomyelitis, a disease that commonly follows bacterial or viral infections, including enterovirus. No other obvious etiological causes for AFM were identified by 16S or RNA and DNA metagenomic sequencing in these cases, strengthening the likelihood that EV-D68 is an etiological factor. Herpes simplex viral DNA was detected in the CSF of the fourth case of AFM and in one additional suspect case from the cluster. Multiple genomic techniques, such as those described here, can be used to diagnose patients with suspected EV-D68 respiratory illness, to aid in AFM diagnosis, and for future EV-D68 surveillance and epidemiology.

Indexed as

Cluster AnalysisPhylogenyArizonaCentral Nervous System Viral DiseasesCerebrospinal FluidEnterovirus D, HumanHumansMolecular EpidemiologyMyelitisNasopharynxNeuromuscular DiseasesReal-Time Polymerase Chain ReactionRNA, ViralSequence Analysis, DNARNA, Viralacute flaccid myelitisAFMenterovirusEV-D68genomicsmetagenomics

Identifiers

PMID30670612
PMCPMC6343034
OpenAlexW2911746116

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.