Evidence map›Paper›PMID 26022221›Full record

ArticleParasites & vectors2015

Phlebotomus papatasi SP15: mRNA expression variability and amino acid sequence polymorphisms of field populations.

Marcelo Ramalho-Ortigão, Iliano V Coutinho-Abreu, Valdir Q Balbino, Carlos Alberto S Figueiredo, Rami Mukbel, Hussan Dayem, Hanafi A Hanafi, Shabaan S El-Hossary, Emad El-Din Y Fawaz, Mahmoud Abo-Shehada and 11 more

Abstract read
In one paragraph

Article in Parasites & vectors, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
  2. Comparative Analysis ofMicroorganisms · 2024
    Article
  3. Review
  4. Article
  5. Article
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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

21 authors.

Marcelo Ramalho-OrtigãoDepartment of Entomology, Kansas State University, Manhattan, KS, 66506, USA. mortigao@k-state.edu.
Iliano V Coutinho-AbreuLaboratory of Malaria and Vector Research, NIAID-NIH, 12735 Twinbrook Parkway, Rockville, MD, 20852, USA. vieiracoutinhi2@niaid.nih.gov.
Valdir Q BalbinoDepartment of Genetics, Universidade Federal de Pernambuco, Recife, PE, Brazil. Valdir@ufpe.br.
Carlos Alberto S FigueiredoDepartment of Genetics, Universidade Federal de Pernambuco, Recife, PE, Brazil. cjsantifigo@hotmail.com.
Rami MukbelFaculty of Veterinary Medicine, Jordan University of Science and Technology, Irbid, 22110, Jordan. rmmukbel@just.edu.jo.
Hussan DayemFaculty of Veterinary Medicine, Jordan University of Science and Technology, Irbid, 22110, Jordan. hdayem@just.edu.jo.
Hanafi A HanafiFaculty of Veterinary Medicine, Jordan University of Science and Technology, Irbid, 22110, Jordan. hanafi.ahmed.hanafi@gmail.com.
Shabaan S El-HossaryVector Biology Research Program, U.S. Naval Medical Research Unit No. 3 (NAMRU-3), Cairo, Egypt. shabaan.elhossary.ctr.eg@med.navy.mil.
Emad El-Din Y FawazVector Biology Research Program, U.S. Naval Medical Research Unit No. 3 (NAMRU-3), Cairo, Egypt. EmadEl-Din.Fawaz.eg@med.navy.mil.
Mahmoud Abo-ShehadaFaculty of Veterinary Medicine, Jordan University of Science and Technology, Irbid, 22110, Jordan. mnshehada@hotmail.com.
David F HoelDepartment of Biostatistics, Uniformed Services University of the Health Sciences, Bethesda, MD, 20814, USA. David.Hoel@usuhs.edu.
Gwen StaybackEck Institute for Global Health, Department of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA. gstaybac@nd.edu.
Mariha WadsworthEck Institute for Global Health, Department of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA. mwadswor@nd.edu.
Douglas A ShoueEck Institute for Global Health, Department of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA. dshoue@nd.edu.
Jenica AbrudanDepartment of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, USA. jenica.abrudan@gmail.com.
Neil F LoboEck Institute for Global Health, Department of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA. nlobo@nd.edu.
Andrew R MahonDepartment of Biology, Central Michigan University, Mount Pleasant, Detroit, MI, 48859, USA. mahon2a@cmich.edu.
Scott J EmrichEck Institute for Global Health, Department of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA. semrich@nd.edu.
Shaden KamhawiLaboratory of Malaria and Vector Research, NIAID-NIH, 12735 Twinbrook Parkway, Rockville, MD, 20852, USA. SKAMHAWI@niaid.nih.gov.
Frank H CollinsEck Institute for Global Health, Department of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA. frank@nd.edu.
Mary Ann McDowellEck Institute for Global Health, Department of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA. mcdowell.11@nd.edu.

Funding

P. papatasi midgut molecules: gene function and assessing TBV candidatesR01AI074691 · NIAID · UNIVERSITY OF NOTRE DAME · PI MCDOWELL, MARY A, RAMALHO-ORTIGAO, JOSE MARCELO · 2008 to 2010
$1.0M
NIAID NIH HHS R01 AI074691NIAID NIH HHS R01AI074691
6 · The paper itself

Abstract

backgroundThe Phlebotomus papatasi salivary protein PpSP15 was shown to protect mice against Leishmania major, suggesting that incorporation of salivary molecules in multi-component vaccines may be a viable strategy for anti-Leishmania vaccines.

methodsHere, we investigated PpSP15 predicted amino acid sequence variability and mRNA profile of P. papatasi field populations from the Middle East. In addition, predicted MHC class II T-cell epitopes were obtained and compared to areas of amino acid sequence variability within the secreted protein.

resultsThe analysis of PpSP15 expression from field populations revealed significant intra- and interpopulation variation.. In spite of the variability detected for P. papatasi populations, common epitopes for MHC class II binding are still present and may potentially be used to boost the response against Le. major infections.

conclusionsConserved epitopes of PpSP15 could potentially be used in the development of a salivary gland antigen-based vaccine.

Indexed as

Amino Acid SequenceAnimalsGenetic VariationInsect ProteinsMolecular Sequence DataPhlebotomusPolymorphism, GeneticRNA, MessengerSequence AlignmentInsect ProteinsRNA, Messenger

Identifiers

PMID26022221
PMCPMC4472253

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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.