Evidence map›Paper›PMID 29921321›Full record

ArticleParasites & vectors2018

Extracellular release of virulence factor major surface protease via exosomes in Leishmania infantum promastigotes.

Skye Marshall, Patrick H Kelly, Brajesh K Singh, R Marshall Pope, Peter Kim, Bayan Zhanbolat, Mary E Wilson, Chaoqun Yao

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Identification of potential novel proteomic markers ofFrontiers in cellular and infection microbiology · 2024
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  6. The Molecular Mechanisms Employed by the ParasiteInternational journal of molecular sciences · 2023
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  7. Tropical medicine and infectious disease · 2023
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  8. Article
  9. Review
  10. Microorganisms · 2021
    Review
  11. LmjF.22.0810 fromBiomedicines · 2020
    Article
  12. Review
  13. Extracellular Vesicles in Trypanosomatids: Host Cell Communication.Frontiers in cellular and infection microbiology · 2020
    Review
  14. Proteomic Analysis of Exosome-Like Vesicles Isolated From Saliva of the TickFrontiers in cellular and infection microbiology · 2020
    Article
  15. Immunomodulatory Properties ofFrontiers in cellular and infection microbiology · 2020
    Article
  16. Prolyl Oligopeptidase FromFrontiers in microbiology · 2020
    Article
  17. More than just exosomes: distinctJournal of extracellular vesicles · 2019
    Article
  18. Article
  19. Article
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 2 institutions in 1 country.

Skye MarshallDepartment of Biomedical Sciences and One Health Center for Zoonoses and Tropical Veterinary Medicine, Ross University School of Veterinary Medicine, St. Kitts & Nevis, West Indies, USA.
Patrick H KellyDepartment of Microbiology, University of Iowa, Iowa City, IA, USA.
Brajesh K SinghDepartment of Internal Medicine, University of Iowa, Iowa City, IA, USA.
R Marshall PopeThe Proteomics Facility, University of Iowa, Iowa City, IA, USA.
Peter KimCarver College of Medicine, University of Iowa, Iowa City, IA, USA.
Bayan ZhanbolatDepartment of Internal Medicine, University of Iowa, Iowa City, IA, USA.
Mary E WilsonDepartment of Microbiology, University of Iowa, Iowa City, IA, USA.
Chaoqun YaoDepartment of Biomedical Sciences and One Health Center for Zoonoses and Tropical Veterinary Medicine, Ross University School of Veterinary Medicine, St. Kitts & Nevis, West Indies, USA. chyao@rossvet.edu.kn.
University of Iowa · USIowa City VA Medical Center · US

Funding

Protective Immunity to Leishmania chagasiR01AI045540 · NIAID · UNIVERSITY OF IOWA · PI WILSON, MARY E · 2001 to 2011
$3.1M
Genetic Risk Factors for Visceral LeishmaniasisR01AI076233 · NIAID · UNIVERSITY OF IOWA · PI BLACKWELL, JENEFER MARY, WILSON, MARY E · 2009 to 2013
$1.6M
The Role of Exosomes in the Pathogenesis of LeishmaniasisI01BX000536 · VA · IOWA CITY VA MEDICAL CENTER · PI WILSON, MARY E · 2009 to 2023
–
Innate inflammatory cells in leishmaniasisI01BX001983 · VA · IOWA CITY VA MEDICAL CENTER · PI WILSON, MARY E · 2014 to 2022
–
BLRD VA I01 BX000536BLRD VA I01 BX001983National Institute of Allergy and Infectious Diseases R01 AI045540, AI076233NIAID NIH HHS R01 AI045540NIAID NIH HHS R01 AI076233Ross University School of Veterinary Medicine Leishmania/Marshall PGVeterans' Affairs Merit Review Grant BX001983; BX000536
6 · The paper itself

Abstract

backgroundThe Leishmania spp. protozoa are introduced into humans through a sand fly blood meal, depositing the infectious metacyclic promastigote form of the parasite into human skin. Parasites enter a variety of host cells, although a majority are found in macrophages where they replicate intracellularly during chronic leishmaniasis. Symptomatic leishmaniasis causes considerable human morbidity in endemic regions. The Leishmania spp. evade host microbicidal mechanisms partially through virulence-associated proteins such as the major surface protease (MSP or GP63), to inactivate immune factors in the host environment. MSP is a metalloprotease encoded by a tandem array of genes belonging to three msp gene classes, whose mRNAs are differentially expressed in different life stages of the parasite. Like other cells, Leishmania spp. release small membrane-bound vesicles called exosomes into their environment. The purpose of this study was to detect MSP proteins in exosomal vesicles of Leishmania spp. protozoa.

methodsUsing mass spectrometry data we determined the profile of MSP class proteins released in L. infantum exosomes derived from promastigotes in their avirulent procyclic (logarithmic) stage and virulent stationary and metacyclic stages. MSP protein isoforms belonging to each of the three msp gene classes could be identified by unique peptides.

resultsMetacyclic promastigote exosomes contained the highest, and logarithmic exosomes had the lowest abundance of total MSP. Among the MSP classes, MSPC class had the greatest variety of isoforms, but was least abundant in all exosomes. Nonetheless, all MSP classes were present at higher levels in exosomes released from stationary or metacyclic promastigotes than logarithmic promastigotes.

conclusionsThe data suggest the efficiency of exosome release may be more important than the identity of MSP isoform in determining the MSP content of Leishmania spp. exosomes.

Indexed as

AnimalsBiological TransportCricetinaeExosomesHumansLeishmania infantumLeishmaniasis, VisceralMaleMass SpectrometryMesocricetusPeptide HydrolasesProtein IsoformsProtozoan ProteinsVirulence FactorsPeptide HydrolasesProtein IsoformsProtozoan ProteinsVirulence FactorsExosomeLeishmaniaMajor surface proteasePromastigotesVirulence factors

Identifiers

PMID29921321
PMCPMC6006689
OpenAlexW2808934121

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.