Evidence map›Paper›PMID 19439374›Full record

ArticleMolecular and biochemical parasitology2009

Biomphalaria glabrata peroxiredoxin: effect of schistosoma mansoni infection on differential gene regulation.

Matty Knight, Nithya Raghavan, Cheri Goodall, Carolyn Cousin, Wannaporn Ittiprasert, Ahmed Sayed, Andre Miller, David L Williams, Christopher J Bayne

Abstract read
In one paragraph

Article in Molecular and biochemical parasitology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.6field-weighted citation impact, top 6% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

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  6. Roles of catalase and glutathione peroxidase in the tolerance of a pulmonate gastropod to anoxia and reoxygenation.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2016
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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

9 authors at 5 institutions in 2 countries.

Matty KnightBiomedical Research Institute, 12111 Parklawn Drive, Rockville, MD 20852, USA. mknight@afbr-bri.com
Nithya Raghavan
Cheri Goodall
Carolyn Cousin
Wannaporn Ittiprasert
Ahmed Sayed
Andre Miller
David L Williams
Christopher J Bayne
Biomedical Research Institute · USOregon State University · USAin Shams University · EGRush University Medical Center · USUniversity of the District of Columbia · US

Funding

UNDERLYING MECHANISMS OF SCHISTOSOME/SNAIL COMPATIBILITYR01AI016137 · NIAID · OREGON STATE UNIVERSITY · PI BAYNE, CHRISTOPHER JEFFREY · 1989 to 2012
$3.1M
A gene map for Biomphalaria glabrata, a S. mansoni hostR01AI063480 · NIAID · BIOMEDICAL RESEARCH INSTITUTE · PI KNIGHT, MATTY · 2005 to 2009
$2.8M
NIAID NIH HHS NIH-R01 AI63480-01A1NIAID NIH HHS R01 AI016137NIAID NIH HHS R01 AI063480
6 · The paper itself

Abstract

To identify gene(s) that may be associated with resistance/susceptibility in the intermediate snail host Biomphalaria glabrata to Schistosoma mansoni infection, a snail albumen gland cDNA library was differentially screened and a partial cDNA encoding an antioxidant enzyme thioredoxin peroxidase (Tpx), or peroxiredoxin (Prx), was identified. The 753bp full-length, single-copy, constitutively expressed gene now referred to as BgPrx4 was later isolated. BgPrx4 is a 2-Cys peroxiredoxin containing the conserved peroxidatic cysteine (C(P)) in the N-terminus and the resolving cysteine (C(R)) in the C-terminus. Sequence analysis of BgPrx4 from both resistant and susceptible snails revealed the presence of several (at least 7) single nucleotide polymorphisms (SNPs). Phylogenetic analysis indicated BgPrx4 to resemble a homolog of human peroxiredoxin, PRDX4. Northern analysis of hepatopancreas RNA from both resistant and susceptible snails showed that upon parasite exposure there were qualitative changes in gene expression. Quantitative real-time RT-PCR analysis showed differences in the levels of BgPrx4 transcript induction following infection, with the transcript up-regulated in resistant snails during the early phase (5h) of infection compared to susceptible snails in which it was down-regulated within the early time period. While there was an increase in transcription in susceptible snails later (48h) post-infection, this never reached the levels detected in resistant snails. A similar trend - higher, earlier up-regulation in the resistant snails but lower, slower protein expression in susceptible snails - was observed by Western blot analysis. Enzymatic analysis of the purified, recombinant BgPrx4 revealed the snail sequence to function as Prx but with an unusual ability to use both thioredoxin and glutathione as substrates.

Indexed as

Gene Expression RegulationAmino Acid SequenceAnimalsBiomphalariaDNAGlutathioneMolecular Sequence DataPeroxiredoxinsPhylogenySchistosoma mansoniSchistosomiasis mansoniSequence AlignmentSequence Analysis, DNASequence Homology, Amino AcidThioredoxinsDNAGlutathionePeroxiredoxinsThioredoxins

Identifiers

PMID19439374
PMCPMC2705950
OpenAlexW2169542946

What OpenQuestion holds

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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.