Evidence map›Paper›PMID 30657756›Full record

ArticlePLoS neglected tropical diseases2019

Naja annulifera Snake: New insights into the venom components and pathogenesis of envenomation.

Felipe Silva-de-França, Isadora Maria Villas-Boas, Solange Maria de Toledo Serrano, Bruno Cogliati, Sonia Aparecida de Andrade Chudzinski, Priscila Hess Lopes, Eduardo Shigueo Kitano, Cinthya Kimori Okamoto, Denise V Tambourgi

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.9field-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

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Africanized honeybee venom (Frontiers in immunology · 2024
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  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Immunological Responses to Envenomation.Frontiers in immunology · 2021
    Review
  10. Article
  11. Article
  12. Toxins · 2020
    Article
  13. Article
  14. Review
  15. 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

9 authors at 2 institutions in 1 country.

Felipe Silva-de-FrançaImmunochemistry Laboratory, Butantan Institute, São Paulo, Brazil.
Isadora Maria Villas-BoasImmunochemistry Laboratory, Butantan Institute, São Paulo, Brazil.
Solange Maria de Toledo SerranoSpecial Laboratory of Applied Toxinology, Butantan Institute, São Paulo, Brazil.
Bruno CogliatiDepartment of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil.
Sonia Aparecida de Andrade ChudzinskiSpecial Laboratory of Applied Toxinology, Butantan Institute, São Paulo, Brazil.
Priscila Hess LopesImmunochemistry Laboratory, Butantan Institute, São Paulo, Brazil.
Eduardo Shigueo KitanoSpecial Laboratory of Applied Toxinology, Butantan Institute, São Paulo, Brazil.
Cinthya Kimori OkamotoImmunochemistry Laboratory, Butantan Institute, São Paulo, Brazil.
Denise V TambourgiImmunochemistry Laboratory, Butantan Institute, São Paulo, Brazil.ORCID 0000-0003-1896-9074
Instituto Butantan · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNaja annulifera is a medically important venomous snake occurring in some of the countries in Sub-Saharan Africa. Accidental bites result in severe coagulation disturbances, systemic inflammation and heart damage, as reported in dogs, and death, by respiratory arrest, in humans. Despite the medical importance of N. annulifera, little is known about its venom composition and the pathogenesis of envenomation. In this paper, the toxic, inflammatory and immunogenic properties of N. annulifera venom were analyzed. METHODOLOGY/PRINCIPAL

findingsVenom proteomic analysis identified 79 different proteins, including Three Finger Toxins, Cysteine Rich Secretory Proteins, Metalloproteinases, Phospholipases A2 (PLA2), Hyaluronidase, L-amino-acid oxidase, Cobra Venom Factor and Serine Proteinase. The presence of PLA2, hyaluronidase, fibrinogenolytic and anticoagulant activities was detected using functional assays. The venom was cytotoxic to human keratinocytes. In an experimental murine model of envenomation, it was found that the venom induced local changes, such as swelling, which was controlled by anti-inflammatory drugs. Moreover, the venom caused death, which was preceded by systemic inflammation and pulmonary hemorrhage. The venom was shown to be immunogenic, inducing a strong humoral immune response, with the production of antibodies able to recognize venom components with high molecular weight and to neutralize its lethal activity. CONCLUSIONS/SIGNIFICANCE: The results obtained in this study demonstrate that N. annulifera venom contains toxins able to induce local and systemic inflammation, which can contribute to lung damage and death. Moreover, the venom is immunogenic, an important feature that must be considered during the production of a therapeutic anti-N. annulifera antivenom.

Indexed as

AnimalsAntiveninsElapid VenomsFemaleHyaluronoglucosaminidaseL-Amino Acid OxidaseMaleMetalloproteasesMiceMice, Inbred BALB CNajaPhospholipases A2ProteomicsSerine ProteasesAntiveninscobra venom factorElapid VenomsHyaluronoglucosaminidaseL-Amino Acid OxidaseMetalloproteasesPhospholipases A2Serine Proteases

Identifiers

PMID30657756
PMCPMC6338361
OpenAlexW2909175222

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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.