Evidence map›Paper›PMID 11333897›Full record

ArticleJournal of virology2001

Marek's disease virus (MDV) encodes an interleukin-8 homolog (vIL-8): characterization of the vIL-8 protein and a vIL-8 deletion mutant MDV.

M S Parcells, S F Lin, R L Dienglewicz, V Majerciak, D R Robinson, H C Chen, Z Wu, G R Dubyak, P Brunovskis, H D Hunt and 2 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of virology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

64 citing papers in PubMed, 171 citations in OpenAlex.

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  15. Review
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  17. Microorganisms · 2021
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4 more citing papers are in PubMed but not listed here.

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

12 authors at 6 institutions in 2 countries.

M S ParcellsCenter of Excellence for Poultry Science, Department of Poultry Science, University of Arkansas, Fayetteville, Arkansas 72701, USA. parcells@uark.edu
S F Lin
R L Dienglewicz
V Majerciak
D R Robinson
H C Chen
Z Wu
G R Dubyak
P Brunovskis
H D Hunt
L F Lee
H J Kung
Case Western Reserve University · USDartmouth College · USUniversity of Arkansas System · USInstitute of Virology of the Slovak Academy of Sciences · SKUnited States Department of Agriculture · USUniversity of California, Davis · US

Funding

ONCOGENE ACTIVATION IN BANDT LYMPHOMAR37CA046613 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI KUNG, HSING-JIEN · 1993 to 2000
$321k
ONCOGENE ACTIVATION IN AVIAN B &T LYMPHOMAR01CA046613 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI KUNG, HSING-JIEN · 1988 to 1992
–
NCI NIH HHS CA46613
6 · The paper itself

Abstract

Chemokines induce chemotaxis, cell migration, and inflammatory responses. We report the identification of an interleukin-8 (IL-8) homolog, termed vIL-8, encoded within the genome of Marek's disease virus (MDV). The 134-amino-acid vIL-8 shares closest homology to mammalian and avian IL-8, molecules representing the prototype CXC chemokine. The gene for vIL-8 consists of three exons which map to the BamHI-L fragment within the repeats flanking the unique long region of the MDV genome. A 0.7-kb transcript encoding vIL-8 was detected in an n-butyrate-treated, MDV-transformed T-lymphoblastoid cell line, MSB-1. This induction is essentially abolished by cycloheximide and herpesvirus DNA polymerase inhibitor phosphonoacetate, indicating that vIL-8 is expressed with true late (gamma2) kinetics. Baculovirus-expressed vIL-8 was found to be secreted into the medium and shown to be functional as a chemoattractant for chicken peripheral blood mononuclear cells but not for heterophils. To characterize the function of vIL-8 with respect to MDV infection in vivo, a recombinant MDV was constructed with a deletion of all three exons and a soluble-modified green fluorescent protein (smGFP) expression cassette inserted at the site of deletion. In two in vivo experiments, the vIL-8 deletion mutant (RB1BvIL-8DeltasmGFP) showed a decreased level of lytic infection in comparison to its parent virus, an equal-passage-level parent virus, and to another recombinant MDV containing the insertion of a GFP expression cassette at the nonessential US2 gene. RB1BvIL-8DeltasmGFP retained oncogenicity, albeit at a greatly reduced level. Nonetheless, we have been able to establish a lymphoblastoid cell line from an RB1BvIL-8DeltasmGFP-induced ovarian lymphoma (MDCC-UA20) and verify the presence of a latent MDV genome lacking vIL-8. Taken together, these data describe the identification and characterization of a chemokine homolog encoded within the MDV genome that is dispensable for transformation but may affect the level of MDV in vivo lytic infection.

Indexed as

Amino Acid SequenceAnimalsAnimals, NewbornBaculoviridaeBase SequenceCell LineCell Line, TransformedChemotactic FactorsChickensCloning, MolecularCycloheximideGene DeletionGreen Fluorescent ProteinsHerpesvirus 2, GallidInterleukin-8Leukocytes, MononuclearChemotactic FactorsCycloheximideGreen Fluorescent ProteinsInterleukin-8Luminescent ProteinsPhosphonoacetic AcidRecombinant ProteinsRNA, MessengerViral Proteins

Identifiers

PMID11333897
PMCPMC114921
OpenAlexW2075702234

What OpenQuestion holds

Textmetadata
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.