Evidence map›Paper›PMID 26844868›Full record

ArticleInsect biochemistry and molecular biology2016

The putative role of Rhipicephalus microplus salivary serpins in the tick-host relationship.

Lucas Tirloni, Tae Kwon Kim, Mariana Loner Coutinho, Abid Ali, Adriana Seixas, Carlos Termignoni, Albert Mulenga, Itabajara da Silva Vaz

Open access · greenAbstract read
In one paragraph

Article in Insect biochemistry and molecular biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
6.3field-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

39 citing papers in PubMed, 86 citations in OpenAlex.

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  15. Serpins in Tick Physiology and Tick-Host Interaction.Frontiers in cellular and infection microbiology · 2022
    Review
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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

8 authors at 3 institutions in 3 countries.

Lucas TirloniCentro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil; Department of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M University, College Station, TX, USA.
Tae Kwon KimDepartment of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M University, College Station, TX, USA.
Mariana Loner CoutinhoCentro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil; Faculdade de Veterinária, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Abid AliInstitute of Biotechnology Genetic Engineering, The University of Agriculture, Peshawar, Khyber Pakhtunkhwa, Pakistan.
Adriana SeixasCentro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil; Departamento de Farmacociências, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, RS, Brazil.
Carlos TermignoniCentro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil; Departamento de Bioquímica, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Albert MulengaDepartment of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M University, College Station, TX, USA.
Itabajara da Silva VazCentro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil; Faculdade de Veterinária, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil. Electronic address: itabajara.vaz@ufrgs.br.
Universidade Federal do Rio Grande do Sul · BRTexas A&M University · USThe University of Agriculture, Peshawar · PK

Funding

Tick feeding regulation by orthologous tick saliva serine protease inhibitorsR01AI093858 · NIAID · TEXAS A&M UNIVERSITY · PI MULENGA, ALBERT · 2011 to 2014
$1.0M
Molecular Mechanisms Regulating Early Stage Tick FeedingR21AI081093 · NIAID · TEXAS A&M UNIVERSITY · PI MULENGA, ALBERT · 2011 to 2012
$404k
Serine Proteinase Inhibitors (Serpins) in Tick Feeding and PhysiologyR03AI074789 · NIAID · TEXAS A&M UNIVERSITY · PI MULENGA, ALBERT · 2008 to 2009
$229k
NIAID NIH HHS AI074789NIAID NIH HHS AI074789-01A1S1NIAID NIH HHS AI081093NIAID NIH HHS AI093858NIAID NIH HHS R01 AI093858NIAID NIH HHS R03 AI074789NIAID NIH HHS R21 AI081093
6 · The paper itself

Abstract

Inflammation and hemostasis are part of the host's first line of defense to tick feeding. These systems are in part serine protease mediated and are tightly controlled by their endogenous inhibitors, in the serpin superfamily (serine protease inhibitors). From this perspective ticks are thought to use serpins to evade host defenses during feeding. The cattle tick Rhipicephalus microplus encodes at least 24 serpins, of which RmS-3, RmS-6, and RmS-17 were previously identified in saliva of this tick. In this study, we screened inhibitor functions of these three saliva serpins against a panel of 16 proteases across the mammalian defense pathway. Our data confirm that Pichia pastoris-expressed rRmS-3, rRmS-6, and rRmS-17 are likely inhibitors of pro-inflammatory and pro-coagulant proteases. We show that rRmS-3 inhibited chymotrypsin and cathepsin G with stoichiometry of inhibition (SI) indices of 1.8 and 2.0, and pancreatic elastase with SI higher than 10. Likewise, rRmS-6 inhibited trypsin with SI of 2.6, chymotrypsin, factor Xa, factor XIa, and plasmin with SI higher than 10, while rRmS-17 inhibited trypsin, cathepsin G, chymotrypsin, plasmin, and factor XIa with SI of 1.6, 2.6, 2.7, 3.4, and 9.0, respectively. Additionally, we observed the formation of irreversible complexes between rRmS-3 and chymotrypsin, rRmS-6/rRmS-17 and trypsin, and rRmS-3/rRmS-17 and cathepsin G, which is consistent with typical mechanism of inhibitory serpins. In blood clotting assays, rRmS-17 delayed plasma clotting by 60 s in recalcification time assay, while rRmS-3 and rRmS-6 did not have any effect. Consistent with inhibitor function profiling data, 2.0 μM rRmS-3 and rRmS-17 inhibited cathepsin G-activated platelet aggregation in a dose-responsive manner by up to 96% and 95% respectively. Of significant interest, polyclonal antibodies blocked inhibitory functions of the three serpins. Also notable, antibodies to Amblyomma americanum, Ixodes scapularis, and Rhipicephalus sanguineus tick saliva proteins cross-reacted with the three R. microplus saliva serpins, suggesting the potential of these proteins as candidates for universal anti-tick vaccines.

Indexed as

AnimalsArthropod ProteinsCattleCattle DiseasesFemaleHost-Parasite InteractionsMaleMultigene FamilyRhipicephalusSalivaSerpinsTick InfestationsArthropod ProteinsSerpinsCathepsin GImmune responsePlatelet aggregation inhibitorTick saliva

Identifiers

PMID26844868
PMCPMC4808628
OpenAlexW2259014087

What OpenQuestion holds

Textmetadata
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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.