Evidence map›Paper›PMID 26973816›Full record

ArticleFrontiers in cellular and infection microbiology2016

The Pathogen-Occupied Vacuoles of Anaplasma phagocytophilum and Anaplasma marginale Interact with the Endoplasmic Reticulum.

Hilary K Truchan, Chelsea L Cockburn, Kathryn S Hebert, Forgivemore Magunda, Susan M Noh, Jason A Carlyon

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
5.2field-weighted citation impact, top 5% 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

34 citing papers in PubMed, 50 citations in OpenAlex.

  1. Machine Learning-Based Detection ofPathogens (Basel, Switzerland) · 2026
    Article
  2. mBio · 2026
    Article
  3. Review
  4. Article
  5. Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Article
  7. Rab27 in tick extracellular vesicle biogenesis and infection.bioRxiv : the preprint server for biology · 2023
    Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. The Novel Zoonotic Pathogen,Pathogens (Basel, Switzerland) · 2021
    Article
  16. Article
  17. Review
  18. Article
  19. Frontiers in public health · 2020
    Article
  20. Article
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

6 authors at 3 institutions in 1 country.

Hilary K TruchanDepartment of Microbiology and Immunology, Virginia Commonwealth University School of Medicine Richmond, VA, USA.
Chelsea L CockburnDepartment of Microbiology and Immunology, Virginia Commonwealth University School of Medicine Richmond, VA, USA.
Kathryn S HebertDepartment of Microbiology and Immunology, Virginia Commonwealth University School of Medicine Richmond, VA, USA.
Forgivemore MagundaProgram in Vector Borne Diseases, Department of Veterinary Microbiology and Pathology, Washington State UniversityPullman, WA, USA; The Paul G. Allen School for Global Animal Health, Washington State UniversityPullman, WA, USA.
Susan M NohProgram in Vector Borne Diseases, Department of Veterinary Microbiology and Pathology, Washington State UniversityPullman, WA, USA; Animal Disease Research Unit, Agricultural Research Service, U. S. Department of AgriculturePullman, WA, USA.
Jason A CarlyonDepartment of Microbiology and Immunology, Virginia Commonwealth University School of Medicine Richmond, VA, USA.
Virginia Commonwealth University · USAgricultural Research Service · USWashington State University · US

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Kim Felder Rhoads · 1985 to 2026
$51.0M
Center for Clinical and Translational ResearchUL1TR000058 · NCATS · VIRGINIA COMMONWEALTH UNIVERSITY · PI MOELLER, FREDERICK GERARD · 2012 to 2015
$12.5M
The roles of Anaplasma phagocytophilum surface proteins in infectionR01AI072683 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI CARLYON, JASON A · 2007 to 2021
$5.8M
VCU Neuroscience Center Core GrantP30NS047463 · NINDS · VIRGINIA COMMONWEALTH UNIVERSITY · PI POVLISHOCK, JOHN T · 2003 to 2013
$5.0M
Antigenic variation in microbial transmissionR37AI044005 · NIAID · WASHINGTON STATE UNIVERSITY · PI PALMER, GUY HUGHES · 2009 to 2018
$3.3M
The roles of Anaplasma phagocytophilum surface proteins in infectionR37AI072683 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI Jason A Carlyon · 2022 to 2026
$2.6M
NCATS NIH HHS UL1 TR000058NCATS NIH HHS UL1TR000058NCI NIH HHS P30 CA016059NIAID NIH HHS R01 AI072683NIAID NIH HHS R37 AI072683NIAID NIH HHS R37 AI44005NINDS NIH HHS 5P30NS047463NINDS NIH HHS P30 NS047463
6 · The paper itself

Abstract

The genus Anaplasma consists of tick-transmitted obligate intracellular bacteria that invade white or red blood cells to cause debilitating and potentially fatal infections. A. phagocytophilum, a human and veterinary pathogen, infects neutrophils to cause granulocytic anaplasmosis. A. marginale invades bovine erythrocytes. Evidence suggests that both species may also infect endothelial cells in vivo. In mammalian and arthropod host cells, A. phagocytophilum and A. marginale reside in host cell derived pathogen-occupied vacuoles (POVs). While it was recently demonstrated that the A. phagocytophilum-occupied vacuole (ApV) intercepts membrane traffic from the trans-Golgi network, it is unclear if it or the A. marginale-occupied vacuole (AmV) interacts with other secretory organelles. Here, we demonstrate that the ApV and AmV extensively interact with the host endoplasmic reticulum (ER) in endothelial, myeloid, and/or tick cells. ER lumen markers, calreticulin, and protein disulfide isomerase, and the ER membrane marker, derlin-1, were pronouncedly recruited to the peripheries of both POVs. ApV association with the ER initiated early and continued throughout the infection cycle. Both the ApV and AmV interacted with the rough ER and smooth ER. However, only derlin-1-positive rough ER derived vesicles were delivered into the ApV lumen where they localized with intravacuolar bacteria. Transmission electron microscopy identified multiple ER-POV membrane contact sites on the cytosolic faces of both species' vacuoles that corresponded to areas on the vacuoles' lumenal faces where intravacuolar Anaplasma organisms closely associated. A. phagocytophilum is known to hijack Rab10, a GTPase that regulates ER dynamics and morphology. Yet, ApV-ER interactions were unhindered in cells in which Rab10 had been knocked down, demonstrating that the GTPase is dispensable for the bacterium to parasitize the ER. These data establish the ApV and AmV as pathogen-host interfaces that directly engage the ER in vertebrate and invertebrate host cells and evidence the conservation of ER parasitism between two Anaplasma species.

Indexed as

Anaplasma marginaleAnaplasma phagocytophilumAnaplasmosisAnimalsCalreticulinCell Line, TumorEndoplasmic ReticulumEndothelial CellsHEK293 CellsHL-60 CellsHost-Pathogen InteractionsHumansIxodesMembrane ProteinsMicroscopy, Electron, TransmissionMyeloid CellsCalreticulinDERL1 protein, humanMembrane ProteinsProtein Disulfide-IsomerasesRab10 protein, humanrab GTP-Binding ProteinsRNA, Small InterferingAnaplasmataceaeendoplasmic reticulumintracellular bacteriapathogen synapseRabRickettsia

Identifiers

PMID26973816
PMCPMC4771727
OpenAlexW2302539226

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.