Evidence map›Paper›PMID 40038190›Full record

ArticleBrazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]2025

Establishment of a cell line from the hematophagous Bat Desmodus rotundus susceptible to Lyssavirus rabies.

Lina Violet-Lozano, Bruna Paredes-Galarza, Raíssa Gasparetto, Arthur Tonietto Mangini, Francine B Timm, Alanis S Melgarejo, Bruno A Prandi, André Witt, Martha T Oliveira, Helena Beatriz de Carvalho Ruthner Batista and 2 more

Abstract read
In one paragraph

Article in Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology], 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Chiropteran (Animals : an open access journal from MDPI · 2026
    Article
  2. 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

12 authors.

Lina Violet-LozanoFederal University of Rio Grande Do Sul (UFRGS), Virology Laboratory, Department of Microbiology, Immunology and Parasitology, Institute of Basic Health Sciences (ICBS), Porto Alegre, RS, Brazil. linaviolet14@gmail.com.ORCID http://orcid.org/0000-0003-1404-5501
Bruna Paredes-GalarzaFederal University of Rio Grande Do Sul (UFRGS), Virology Laboratory, Department of Microbiology, Immunology and Parasitology, Institute of Basic Health Sciences (ICBS), Porto Alegre, RS, Brazil.ORCID http://orcid.org/0009-0008-1490-8710
Raíssa GasparettoFederal University of Rio Grande Do Sul (UFRGS), Virology Laboratory, Department of Microbiology, Immunology and Parasitology, Institute of Basic Health Sciences (ICBS), Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0003-2433-9933
Arthur Tonietto ManginiFederal University of Rio Grande Do Sul (UFRGS), Virology Laboratory, Department of Microbiology, Immunology and Parasitology, Institute of Basic Health Sciences (ICBS), Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0001-6815-5509
Francine B TimmFederal University of Rio Grande Do Sul (UFRGS), Virology Laboratory, Department of Microbiology, Immunology and Parasitology, Institute of Basic Health Sciences (ICBS), Porto Alegre, RS, Brazil.ORCID http://orcid.org/0009-0001-7851-1279
Alanis S MelgarejoFederal University of Rio Grande Do Sul (UFRGS), Virology Laboratory, Department of Microbiology, Immunology and Parasitology, Institute of Basic Health Sciences (ICBS), Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0003-1696-099X
Bruno A PrandiFederal University of Rio Grande Do Sul (UFRGS), Virology Laboratory, Department of Microbiology, Immunology and Parasitology, Institute of Basic Health Sciences (ICBS), Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0002-6022-8686
André WittSecretariat of Agriculture, Livestock and Irrigation/RS - Animal Health Defense Division, Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0002-7211-2680
Martha T OliveiraFederal University of Rio Grande Do Sul (UFRGS), Virology Laboratory, Department of Microbiology, Immunology and Parasitology, Institute of Basic Health Sciences (ICBS), Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0002-4778-459X
Helena Beatriz de Carvalho Ruthner BatistaRabies Diagnostic Sector, Pasteur Institute, Sao Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-3202-132X
Paulo Michel RoeheFederal University of Rio Grande Do Sul (UFRGS), Virology Laboratory, Department of Microbiology, Immunology and Parasitology, Institute of Basic Health Sciences (ICBS), Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0002-2370-7661
Ana Cláudia FrancoFederal University of Rio Grande Do Sul (UFRGS), Virology Laboratory, Department of Microbiology, Immunology and Parasitology, Institute of Basic Health Sciences (ICBS), Porto Alegre, RS, Brazil.ORCID http://orcid.org/0000-0001-7747-5125

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Desmodus rotundus bats are the main reservoir for Lyssavirus rabies (RABV) in the Americas, however, knowledge of virus-host interactions in this species is very limited due to challenges associated with establishing in vivo experimental infections. In this context, cell culture becomes a valuable tool for expanding knowledge on the dynamics of RABV infection in its natural host in the Americas. This study aimed to develop and characterize a cell line from D. rotundus bat and to evaluate its susceptibility to RABV. Primary cultures of D. rotundus fetal kidney cells were immortalized using the plasmid pSV1 containing the Large T and Small T antigen gene sequences of Simian Virus 40 (SV40). The obtained clones were selected by limiting dilution and transfection was confirmed by PCR for Large T SV40 gene. The resulting cell line was named FKDR (Fetal Kidney Desmodus Rotundus). The growth curve, senescence assay, and karyotype analysis of the primary and FKDR cell cultures were performed. The susceptibility of FKDR cells to RABV was determined through direct fluorescent antibody test (dFAT), and compared with that of BHK-21, Tb1Lu, and CaroPe cells. Once immortalized, the cell adopted a fusiform appearance and showed the absence of senescence markers, chromosomal anomalies, and accelerated cell growth, compared to the primary fetal cell. The FKDR and the other cell lines used for RABV infections exhibited positive staining by immunofluorescence but no cytopathic effect. The cell line described here holds potential for studies of RABV infections in D. rotundus bats.

Indexed as

ChiropteraLyssavirusRabiesRabies virusAnimalsCell LineKidneyCell cultureFKDR cellPasteur vaccine (PV) strainsRabies virus

Identifiers

PMID40038190
PMCPMC12095102

What Socratic holds

Textmetadata
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 Socratic graph.