Evidence map›Paper›PMID 33050923›Full record

ArticleParasites & vectors2020

Diminished adherence of Biomphalaria glabrata embryonic cell line to sporocysts of Schistosoma mansoni following programmed knockout of the allograft inflammatory factor.

Fernanda Sales Coelho, Rutchanee Rodpai, André Miller, Shannon E Karinshak, Victoria H Mann, Omar Dos Santos Carvalho, Roberta Lima Caldeira, Marina de Moraes Mourão, Paul J Brindley, Wannaporn Ittiprasert

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. CRISPR/Cas9-germline editing ofScience advances · 2025
    Article
  5. International journal of molecular sciences · 2025
    Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. 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

10 authors at 4 institutions in 3 countries.

Fernanda Sales CoelhoGrupo de Pesquisa Em Helmintologia E Malacologia Médica, Instituto René Rachou, Fundação Oswaldo Cruz, Belo Horizonte, MG, Brazil.
Rutchanee RodpaiDepartment of Microbiology, Immunology and Tropical Medicine, School of Medicine and Health Sciences, George Washington University, Washington, D.C., USA.
André MillerSchistosomiasis Resource Center, Biomedical Research Institute, Rockville, MD, USA.
Shannon E KarinshakDepartment of Microbiology, Immunology and Tropical Medicine, School of Medicine and Health Sciences, George Washington University, Washington, D.C., USA.
Victoria H MannDepartment of Microbiology, Immunology and Tropical Medicine, School of Medicine and Health Sciences, George Washington University, Washington, D.C., USA.
Omar Dos Santos CarvalhoGrupo de Pesquisa Em Helmintologia E Malacologia Médica, Instituto René Rachou, Fundação Oswaldo Cruz, Belo Horizonte, MG, Brazil.
Roberta Lima CaldeiraGrupo de Pesquisa Em Helmintologia E Malacologia Médica, Instituto René Rachou, Fundação Oswaldo Cruz, Belo Horizonte, MG, Brazil.
Marina de Moraes MourãoGrupo de Pesquisa Em Helmintologia E Malacologia Médica, Instituto René Rachou, Fundação Oswaldo Cruz, Belo Horizonte, MG, Brazil. marina.mourao@fiocruz.br.
Paul J BrindleyDepartment of Microbiology, Immunology and Tropical Medicine, School of Medicine and Health Sciences, George Washington University, Washington, D.C., USA. pbrindley@gwu.edu.
Wannaporn IttiprasertDepartment of Microbiology, Immunology and Tropical Medicine, School of Medicine and Health Sciences, George Washington University, Washington, D.C., USA. wannaporni@gwu.edu.ORCID http://orcid.org/0000-0001-9411-8883
Fundação Oswaldo Cruz · BRGeorge Washington University · USBiomedical Research Institute · USKhon Kaen University · TH

Funding

NIAID NIH HHS HHSN272201000005CNIAID NIH HHS HHSN272201000005IWellcome TrustWellcome Trust 107475/Z/15/Z
6 · The paper itself

Abstract

backgroundLarval development in an intermediate host gastropod snail of the genus Biomphalaria is an obligatory component of the life-cycle of Schistosoma mansoni. Understanding of the mechanism(s) of host defense may hasten the development of tools that block transmission of schistosomiasis. The allograft inflammatory factor 1, AIF, which is evolutionarily conserved and expressed in phagocytes, is a marker of macrophage activation in both mammals and invertebrates. AIF enhances cell proliferation and migration. The embryonic cell line, termed Bge, from Biomphalaria glabrata is a versatile resource for investigation of the snail-schistosome relationship since Bge exhibits a hemocyte-like phenotype. Hemocytes perform central roles in innate and cellular immunity in gastropods and in some cases can kill the parasite. However, the Bge cells do not kill the parasite in vitro.

methodsBge cells were transfected by electroporation with plasmid pCas-BgAIFx4, encoding the Cas9 nuclease and a guide RNA specific for exon 4 of the B. glabrata AIF (BgAIF) gene. Transcript levels for Cas9 and for BgAIF were monitored by reverse-transcription-PCR and, in parallel, adhesion of gene-edited Bge cells during co-culture with of schistosome sporocysts was assessed.

resultsGene knockout manipulation induced gene-disrupting indels, frequently 1-2 bp insertions and/or 8-30 bp deletions, at the programmed target site; a range from 9 to 17% of the copies of the BgAIF gene in the Bge population of cells were mutated. Transcript levels for BgAIF were reduced by up to 73% (49.5 ± 20.2% SD, P ≤ 0.05, n = 12). Adherence by BgAIF gene-edited (ΔBgAIF) Bge to sporocysts diminished in comparison to wild type cells, although cell morphology did not change. Specifically, as scored by a semi-quantitative cell adherence index (CAI), fewer ΔBgAIF than control wild type cells adhered to sporocysts; control CAI, 2.66 ± 0.10, ΔBgAIF, 2.30 ± 0.22 (P ≤ 0.01).

conclusionsThe findings supported the hypothesis that BgAIF plays a role in the adherence of B. glabrata hemocytes to sporocysts during schistosome infection in vitro. This demonstration of the activity of programmed gene editing will enable functional genomics approaches using CRISPR/Cas9 to investigate additional components of the snail-schistosome host-parasite relationship.

Indexed as

BiomphalariaAnimalsCalcium-Binding ProteinsCell AdhesionCell LineCRISPR-Cas SystemsGene EditingGene Knockout TechniquesHemocytesHost-Parasite InteractionsHumansMicrofilament ProteinsSchistosoma mansoniSchistosomiasisAIF1 protein, humanCalcium-Binding ProteinsMicrofilament ProteinsAllograft inflammatory factorBgeBiomphalaria glabrata embryonic cell lineCell adhesionCRISPR/Cas9Gene editing

Identifiers

PMID33050923
PMCPMC7552541
OpenAlexW3092115723

What OpenQuestion holds

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Registered trials

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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.