Evidence map›Paper›PMID 30148847›Full record

ArticlePLoS neglected tropical diseases2018

Evidence for transovarial transmission of tick-borne rickettsiae circulating in Northern Mongolia.

Thomas C Moore, Laura A Pulscher, Luke Caddell, Michael E von Fricken, Benjamin D Anderson, Battsetseg Gonchigoo, Gregory C Gray

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.8field-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

26 citing papers in PubMed, 69 citations in OpenAlex.

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  14. What do we know about the microbiome ofFrontiers in cellular and infection microbiology · 2022
    Review
  15. Metagenomic profiles ofFrontiers in microbiology · 2022
    Article
  16. Article
  17. Pathogens (Basel, Switzerland) · 2021
    Article
  18. Article
  19. Article
  20. Current debates and advances in tick microbiome research.Current research in parasitology & vector-borne diseases · 2021
    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

7 authors at 3 institutions in 1 country.

Thomas C MooreDivision of Infectious Diseases and Duke Global Health Institute, Duke University, Durham, North Carolina, United States of America.ORCID 0000-0001-6145-5736
Laura A PulscherDivision of Infectious Diseases and Duke Global Health Institute, Duke University, Durham, North Carolina, United States of America.ORCID 0000-0002-3996-5585
Luke CaddellMiller School of Medicine, University of Miami, Miami, Florida, United States of America.
Michael E von FrickenDepartment of Global and Community Health, George Mason University, Fairfax, Virginia, United States of America.ORCID 0000-0003-2938-4549
Benjamin D AndersonDivision of Infectious Diseases and Duke Global Health Institute, Duke University, Durham, North Carolina, United States of America.
Battsetseg GonchigooInstitute of Veterinary Medicine, Ulaanbaatar, Mongolia.
Gregory C GrayDivision of Infectious Diseases and Duke Global Health Institute, Duke University, Durham, North Carolina, United States of America.
Duke University · USGeorge Mason University · USUniversity of Miami · US

Funding

One Health Innovation Fellowships for Zoonotic Disease Research In MongoliaD43TW009373 · FIC · UNIVERSITY OF FLORIDA · PI GRAY, GREGORY CHARLES · 2013 to 2017
$1.6M
FIC NIH HHS D43 TW009373
6 · The paper itself

Abstract

Transstadial transmission of tick-borne rickettsiae has been well documented. Few studies, however, have evaluated the role of transovarial transmission of tick-borne rickettsiae, particularly in nature within the host-vector ecosystem. This cross-sectional study aimed to understand the role of transovarial transmission of tick-borne rickettsiae among feeding ticks at different life stages. Tick eggs laid by engorged wild-caught adult female ticks were pooled and tested for Rickettsia spp. and Anaplasma/Ehrlichia spp. using molecular techniques, while adult fed ticks were tested individually. Additionally, larval and nymphal ticks were collected in the wild from small mammals, pooled and tested for Rickettsia spp. and Anaplasma/Ehrlichia spp. There were 38 fed adult and 618 larvae/nymphs (60 pools total) Dermacentor spp. ticks collected from livestock and rodents. All individual adult ticks and tick pools were positive for Rickettsia spp. While none of the larvae/nymphs were positive for Anaplasma/Ehrlichia spp., two adult fed ticks were positive. Rickettsia spp. DNA was detected in 91% (30/33) of the pooled eggs tested, and one pool of eggs tested positive for Anaplasma/Ehrlichia spp. Sequencing data revealed Rickettsia spp. shared ≥99% identity with R. raoultii ompA. Anaplasma/Ehrlichia spp. shared ≥89% identity with A. ovis 16S ribosomal RNA. This study identified potential transovarial transmission of Rickettsia spp. and Anaplasma spp. among D. nuttalli ticks. Additional studies are needed to further assess the proportion of transovarial transmission occurring in nature to better understand the burden and disease ecology of tick-borne rickettsiae in Mongolia.

Indexed as

AnimalsDermacentorFemaleHost-Pathogen InteractionsLarvaMongoliaNymphOvaryRickettsia

Identifiers

PMID30148847
PMCPMC6128658
OpenAlexW2889353810

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.