Evidence map›Paper›PMID 34273394›Full record

ArticleInternational journal for parasitology2021

PpSP32-like protein as a marker of human exposure to Phlebotomus argentipes in Leishmania donovani foci in Bangladesh.

Petra Sumova, Chizu Sanjoba, Laura Willen, Nikola Polanska, Yoshitsugu Matsumoto, Eisei Noiri, Shyamal Kumar Paul, Yusuf Ozbel, Petr Volf

Open access · hybridAbstract read
In one paragraph

Article in International journal for parasitology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

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  5. Comparative Analysis ofMicroorganisms · 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

9 authors at 5 institutions in 4 countries.

Petra SumovaDepartment of Parasitology, Faculty of Science, Charles University, Vinicna7, Prague 12844, Czech Republic. Electronic address: sumovap@natur.cuni.cz.
Chizu SanjobaLaboratory of Molecular Immunology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
Laura WillenDepartment of Parasitology, Faculty of Science, Charles University, Vinicna7, Prague 12844, Czech Republic.
Nikola PolanskaDepartment of Parasitology, Faculty of Science, Charles University, Vinicna7, Prague 12844, Czech Republic.
Yoshitsugu MatsumotoLaboratory of Molecular Immunology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
Eisei NoiriHemodialysis and Apheresis, Nephrology 107 Lab, The University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.
Shyamal Kumar PaulDepartment of Microbiology, Mymensingh Medical College, Mymensingh 2206, Bangladesh.
Yusuf OzbelDepartment of Parasitology, Faculty of Medicine, Ege University, 35100 Bornova, Izmir, Turkey.
Petr VolfDepartment of Parasitology, Faculty of Science, Charles University, Vinicna7, Prague 12844, Czech Republic.
Charles University · CZThe University of Tokyo · JPEge University · TRMymensingh Medical College Hospital · BDUniversity of Tokyo Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phlebotomus argentipes is a predominant vector of Leishmania donovani, the protozoan parasite causing visceral leishmaniasis in the Indian subcontinent. In hosts bitten by P. argentipes, sand fly saliva elicits the production of specific anti-salivary protein antibodies. Here, we have utilised these antibodies as markers of human exposure to P. argentipes in a visceral leishmaniasis endemic area in Pabna district, Bangladesh. The use of whole salivary gland homogenate as an antigen to detect these antibodies has several limitations, therefore it is being superseded by the use of specific recombinant salivary proteins. We have identified three major P. argentipes salivary antigenic proteins recognised by sera of bitten humans, expressed them in a recombinant form (rPagSP04, rPagSP05 and rPagSP06) and tested their applicability in ELISA and immunoblot. One of them, PpSP32-like protein rPagSP06, was identified as the most promising antigen, showing highest resemblance and correlation with the IgG response to P. argentipes salivary gland homogenate. Furthermore, we have validated the applicability of rPagSP06 in a large cohort of 585 individuals and obtained a high correlation coefficient for anti-rPagSP06 and anti-P. argentipes saliva IgG responses. The anti-rPagSP06 and anti-P. argentipes salivary gland homogenate IgG responses followed a similar right-skewed distribution. This is the first report of screening human sera for anti-P. argentipes saliva antibodies using recombinant salivary protein. The rPagSP06 was proven to be a valid antigen for screening human sera for exposure to P. argentipes bites in a visceral leishmaniasis endemic area.

Indexed as

Insect ProteinsPhlebotomusSalivary Proteins and PeptidesAnimalsBangladeshBites and StingsHumansLeishmania donovaniSalivaInsect ProteinsSalivary Proteins and PeptidesBangladeshIgG antibodiesLeishmania donovaniMarker of exposurePhlebotomus argentipesSalivary glands

Identifiers

PMID34273394
PMCPMC8575019
OpenAlexW3184760912

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.