Evidence map›Paper›PMID 37404180›Full record

ArticleApplied and environmental microbiology2023

The Tomato Brown Rugose Fruit Virus Movement Protein Gene Is a Novel Microbial Source Tracking Marker.

Aravind Natarajan, Brayon J Fremin, Danica T Schmidtke, Marlene K Wolfe, Soumaya Zlitni, Katherine E Graham, Erin F Brooks, Christopher J Severyn, Kathleen M Sakamoto, Norman J Lacayo and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Applied and environmental microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 2 institutions in 1 country.

Aravind Natarajan *Department of Genetics, Stanford University, Stanford, California, USA.ORCID 0000-0003-2180-7842
Brayon J Fremin *Department of Genetics, Stanford University, Stanford, California, USA.ORCID 0000-0002-5799-8655
Danica T SchmidtkeDepartment of Microbiology and Immunology, Stanford University, Stanford, California, USA.ORCID 0000-0001-9509-6188
Marlene K WolfeDepartment of Civil and Environmental Engineering, Stanford University, Stanford, California, USA.ORCID 0000-0002-6476-0450
Soumaya ZlitniDepartment of Genetics, Stanford University, Stanford, California, USA.ORCID 0000-0003-2228-8343
Katherine E GrahamDepartment of Civil and Environmental Engineering, Stanford University, Stanford, California, USA.ORCID 0000-0002-4148-1395
Erin F BrooksDepartment of Medicine (Hematology, Blood and Marrow Transplantation), Stanford University, Stanford, California, USA.ORCID 0000-0002-5834-0679
Christopher J SeverynDepartment of Pediatrics, (Hematology/Oncology/Stem Cell Transplant & Regenerative Medicine), Stanford University, Stanford, California, USA.ORCID 0000-0002-0884-6372
Kathleen M SakamotoDepartment of Pediatrics, (Hematology/Oncology/Stem Cell Transplant & Regenerative Medicine), Stanford University, Stanford, California, USA.ORCID 0000-0003-0494-8838
Norman J LacayoDepartment of Pediatrics, (Hematology/Oncology/Stem Cell Transplant & Regenerative Medicine), Stanford University, Stanford, California, USA.ORCID 0000-0003-4573-5118
Scott KuerstenIllumina, Inc., San Diego, California, USA.
Jeff KobleIllumina, Inc., San Diego, California, USA.
Glorianna CavesIllumina, Inc., San Diego, California, USA.
Inna KaplanDepartment of Medicine (Blood and Marrow Transplantation and Cellular Therapy), Stanford University, Stanford, California, USA.ORCID 0000-0001-8591-9726
Upinder SinghDepartment of Medicine (Infectious Diseases and Geographic Medicine), Stanford University, Stanford, California, USA.ORCID 0000-0003-0630-0306
Prasanna JagannathanDepartment of Microbiology and Immunology, Stanford University, Stanford, California, USA.ORCID 0000-0001-6305-758X
Andrew R RezvaniDepartment of Medicine (Blood and Marrow Transplantation and Cellular Therapy), Stanford University, Stanford, California, USA.
Ami S BhattDepartment of Genetics, Stanford University, Stanford, California, USA.ORCID 0000-0001-8099-2975
Alexandria B BoehmDepartment of Civil and Environmental Engineering, Stanford University, Stanford, California, USA.ORCID 0000-0002-8162-5090
Stanford University · USIllumina (United States) · US

Funding

Supplement to Enhance Wellness and Resiliency in the Graduate EnvironmentT32GM007276 · NIGMS · STANFORD UNIVERSITY · PI MORRISON, ASHBY J. · 1985 to 2023
$32.9M
Culture-free pathogen tracking in hospitalized patientsR01AI143757 · NIAID · STANFORD UNIVERSITY · PI BHATT, AMI SIDDHARTH · 2020 to 2023
$3.0M
Emerging novel mechanisms of antibiotic resistance in the prevalent foodborne pathogen, SalmonellaR01AI148623 · NIAID · STANFORD UNIVERSITY · PI BHATT, AMI SIDDHARTH · 2019 to 2023
$2.0M
Training in Pediatric Nonmalignant Hematology and Stem Cell BiologyT32DK098132 · NIDDK · STANFORD UNIVERSITY · PI SAKAMOTO, KATHLEEN M · 2014 to 2022
$1.9M
NIAID NIH HHS R01 AI143757NIAID NIH HHS R01 AI148623NIDDK NIH HHS T32 DK098132NIGMS NIH HHS T32 GM007276NIH HHS DGE-1656518NIH HHS DK098132NIH HHS R01 AI148623
6 · The paper itself

Abstract

Microbial source tracking (MST) identifies sources of fecal contamination in the environment using host-associated fecal markers. While there are numerous bacterial MST markers that can be used herein, there are few such viral markers. Here, we designed and tested novel viral MST markers based on tomato brown rugose fruit virus (ToBRFV) genomes. We assembled eight nearly complete genomes of ToBRFV from wastewater and stool samples from the San Francisco Bay Area in the United States. Next, we developed two novel probe-based reverse transcription-PCR (RT-PCR) assays based on conserved regions of the ToBRFV genome and tested the markers' sensitivities and specificities using human and non-human animal stool as well as wastewater. The ToBRFV markers are sensitive and specific; in human stool and wastewater, they are more prevalent and abundant than a commonly used viral marker, the pepper mild mottle virus (PMMoV) coat protein (CP) gene. We used the assays to detect fecal contamination in urban stormwater samples and found that the ToBRFV markers matched cross-assembly phage (crAssphage), an established viral MST marker, in prevalence across samples. Taken together, these results indicate that ToBRFV is a promising viral human-associated MST marker.

Indexed as

Solanum lycopersicumWastewaterAnimalsBiomarkersEnvironmental MonitoringFecesFruitBiomarkersWastewaterfecal pollutionhuman-associated markermicrobial source trackingMSTToBRFVtomato brown rugose fruit virusviruswastewater

Identifiers

PMID37404180
PMCPMC10370318
OpenAlexW4383186738

What OpenQuestion holds

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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.