Evidence map›Paper›PMID 35189916›Full record

ArticleVirology journal2022

Rare isolation of human-tropic recombinant porcine endogenous retroviruses PERV-A/C from Göttingen minipigs.

Sabrina Halecker, Ludwig Krabben, Yannick Kristiansen, Luise Krüger, Lars Möller, Dietmar Becher, Michael Laue, Benedikt Kaufer, Christian Reimer, Joachim Denner

Open access · goldAbstract read
In one paragraph

Article in Virology journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.1field-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

14 citing papers in PubMed, 19 citations in OpenAlex.

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  6. [Xenotransplantation of solid organs].Chirurgie (Heidelberg, Germany) · 2024
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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

10 authors at 4 institutions in 1 country.

Sabrina HaleckerInstitute of Virology, Free University Berlin, Berlin, Germany.
Ludwig KrabbenInstitute of Virology, Free University Berlin, Berlin, Germany.
Yannick KristiansenRobert Koch Institute, Berlin, Germany.
Luise KrügerRobert Koch Institute, Berlin, Germany.
Lars MöllerCentre for Biological Threats and Special Pathogens ZBS 4: Advanced Light and Electron Microscopy, Robert Koch Institute, Berlin, Germany.
Dietmar BecherMICROMUN, Privates Institut Für Mikrobiologische Forschung GmbH, Greifswald, Germany.
Michael LaueCentre for Biological Threats and Special Pathogens ZBS 4: Advanced Light and Electron Microscopy, Robert Koch Institute, Berlin, Germany.
Benedikt KauferInstitute of Virology, Free University Berlin, Berlin, Germany.
Christian ReimerDepartment of Animal Sciences, Animal Breeding and Genetics Group, University of Göttingen, Albrecht-Thaer-Weg 3, 37075, Göttingen, Germany.
Joachim DennerInstitute of Virology, Free University Berlin, Berlin, Germany. Joachim.Denner@fu-berlin.de.ORCID http://orcid.org/0000-0003-3244-6085
Freie Universität Berlin · DERobert Koch Institute · DEMicromun · DEUniversitätsmedizin Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPorcine endogenous retroviruses (PERVs) can infect human cells and pose a risk for xenotransplantation when pig cells, tissues or organs are transplanted to human recipients. Xenotransplantation holds great promise to overcome the shortage of human donor organs after solving the problems of rejection, functionality and virus safety. We recently described the transmission of a human-tropic recombinant PERV-A/C, designated PERV-F, from peripheral blood mononuclear cells (PBMCs) of a Göttingen Minipig (GöMP) to human 293 cells (Krüger et al., in Viruses 12(1):38, 2019). The goal of this study was to characterize PERV-F in more detail and to analyze the probability of virus isolation from other animals.

methodsThe recombination site in the envelope (env) gene, the long terminal repeats (LTR), the proteins and the morphology of the recombinant PERV-F were characterized by polymerase chain reaction (PCR), sequencing, Western blot analysis, immunofluorescence, and transmissible electron microscopy. Mitogen-stimulated PBMCs from 47 additional pigs, including 17 new GöMP, were co-cultured with highly susceptible human 293 T cells, and the PERV-A/C prevalence and PERV transmission was analyzed by PCR.

resultsPERV-F, isolated from a GöMP, is an infectious human-tropic PERV-A/C virus with a novel type of recombination in the env gene. The length of the LTR of PERV-F increased after passaging on human cells. In a few minipigs, but not in German landrace pigs, PERV-A/C were found. There was no transmission of human-tropic PERV-A/C from additional 47 pigs, including 17 GöMP, to human cells.

conclusionThese data show that human-tropic recombinant PERV-A/C proviruses can only be found in a very small number of minipigs, but not in other pigs, and that their isolation as infectious virus able to replicate on human cells is an extremely rare event, even when using highly susceptible 293 cells.

Indexed as

Endogenous RetrovirusesAnimalsHumansLeukocytes, MononuclearProvirusesSwineSwine, MiniatureTransplantation, HeterologousCopy numberLong terminal repeatsPorcine endogenous retrovirusesRecombinationXenotransplantation

Identifiers

PMID35189916
PMCPMC8862210
OpenAlexW4212885549

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.