Evidence map›Paper›PMID 19358735›Full record

ArticleRetrovirology2009

Conservation of Nef function across highly diverse lineages of SIVsmm.

Jan Schmökel, Hui Li, Elizabeth Bailes, Michael Schindler, Guido Silvestri, Beatrice H Hahn, Cristian Apetrei, Frank Kirchhoff

Open access · goldAbstract read
In one paragraph

Article in Retrovirology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

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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

8 authors at 7 institutions in 3 countries.

Jan SchmökelInstitute of Virology, University of Ulm, 89081 Ulm, Germany. jan.schmoekel@uniklinik-ulm.de
Hui Li
Elizabeth Bailes
Michael Schindler
Guido Silvestri
Beatrice H Hahn
Cristian Apetrei
Frank Kirchhoff
University of Alabama at Birmingham · USLeibniz Institute of Virology (LIV) · DEQueen's Medical Centre · GBTechnische Hochschule Ulm · DETulane University · USUniversität Ulm · DEUniversity of Pennsylvania · US

Funding

ZCM:A NOVEL BROAD-SPECTRUM MICROBICIDE FOR SEXUALLY TRANSMITTED INFECTIONSP51RR000164 · NCRR · TULANE UNIVERSITY OF LOUISIANA · PI VEAZEY, RONALD S. · 1985 to 2011
$100.1M
TNF AND MCP-1 IN RETROVIRUS-INDUCED BRAIN DISEASEP20RR020159 · NCRR · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI PAHAR, BAPI · 2004 to 2011
$16.1M
Natural SIV Reservoirs and Human Zoonotic RiskR37AI050529 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI HAHN, BEATRICE H · 2008 to 2017
$5.7M
Pathogenesis of New SIVsm Lineages in Rhesus MacaquesR01AI065325 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI APETREI, CRISTIAN · 2006 to 2009
$2.6M
Role of specific Nef functions in AIDS pathogenesisR01AI067057 · NIAID · UNIVERSITY OF ULM · PI KIRCHHOFF, FRANK · 2006 to 2008
$558k
NCRR NIH HHS P20 RR020159NCRR NIH HHS P51 RR000164NIAID NIH HHS R01 AI065325NIAID NIH HHS R01 AI067057NIAID NIH HHS R37 AI050529
6 · The paper itself

Abstract

backgroundSIVsmm is a simian immunodeficiency virus that persists efficiently without causing disease in naturally infected sooty mangabeys (SMs) but induces AIDS upon cross-species transmission to humans and macaques. Current phylogenetic data indicate that SIVsmm strains comprise a highly diverse group of viruses that can be subdivided into different lineages. Since only certain SIVsmm strains have successfully crossed the species barrier to humans and macaques, the question has been raised whether there are lineage specific differences in SIVsmm biology. In the present study we examined whether representatives of five different SIVsmm lineages show differences in the function of the accessory Nef protein, which plays an important role in viral persistence, transmission and pathogenesis.

resultsWe found that nef alleles from all SIVsmm lineages down-modulated CD4, MHC-I, CD28 and CD3 and up-regulated the invariant chain (Ii) associated with immature MHC-II molecules in human-derived cells. Moreover, they generally suppressed the responsiveness of virally infected T cells to activation, enhanced virion infectivity and promoted virus replication in human peripheral blood mononuclear cells. The functional activity of these nef alleles in the various assays varied substantially between different strains of SIVsmm but quantitative analyses did not reveal any significant lineage-specific differences in Nef function.

conclusionNef alleles from different lineages of SIVsmm do not require adaptive changes to be functionally active in human cells. Strain rather than lineage-specific differences in Nef function may impact the virological and immunological feature of SIVsmm in SMs and possibly affected viral fitness and pathogenicity in human and macaque hosts.

Indexed as

AllelesAmino Acid SequenceAnimalsCell LineHIV-2HumansJurkat CellsMolecular Sequence Datanef Gene Products, Human Immunodeficiency VirusPhylogenySequence AlignmentSimian Immunodeficiency VirusViral Regulatory and Accessory ProteinsVirus Replicationnef Gene Products, Human Immunodeficiency VirusNEF protein, SIVViral Regulatory and Accessory Proteins

Identifiers

PMID19358735
PMCPMC2678078
OpenAlexW2003677831

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.