Evidence map›Paper›PMID 33261663›Full record

ArticleParasites & vectors2020

The intracellular bacterium Rickettsia rickettsii exerts an inhibitory effect on the apoptosis of tick cells.

Larissa Almeida Martins, Giuseppe Palmisano, Mauro Cortez, Rebeca Kawahara, José Mario de Freitas Balanco, André Fujita, Beatriz Iglesias Alonso, Darci Moraes Barros-Battesti, Gloria Regina Cardoso Braz, Lucas Tirloni and 3 more

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 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Apoptosis and autophagy promoteFrontiers in microbiology · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. The anal pore route is efficient to infectFrontiers in cellular and infection microbiology · 2023
    Article
  11. Lock and Key: WhyPathogens (Basel, Switzerland) · 2022
    Article
  12. Apoptosis and Autophagy: Current Understanding in Tick-Pathogen Interactions.Frontiers in cellular and infection microbiology · 2022
    Review
  13. Article
  14. Review
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

13 authors at 5 institutions in 3 countries.

Larissa Almeida MartinsDepartment of Parasitology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Giuseppe PalmisanoDepartment of Parasitology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Mauro CortezDepartment of Parasitology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Rebeca KawaharaDepartment of Parasitology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
José Mario de Freitas BalancoDepartment of Parasitology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
André FujitaDepartment of Computational Science, Institute of Mathematics and Statistics, University of São Paulo, São Paulo, SP, Brazil.
Beatriz Iglesias AlonsoDepartment of Parasitology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Darci Moraes Barros-BattestiDepartment of Veterinary Pathology, São Paulo State University, Jaboticabal, SP, Brazil.
Gloria Regina Cardoso BrazDepartment of Biochemistry, Institute of Chemistry, Federal University of Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Lucas TirloniRocky Mountain Laboratories, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Hamilton, MT, USA.
Eliane EstevesDepartment of Parasitology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Sirlei DaffreDepartment of Parasitology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil.
Andréa Cristina FogaçaDepartment of Parasitology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil. deafog@usp.br.
Universidade de São Paulo · BRMacquarie University · AUNational Institutes of Health · USUniversidade Estadual Paulista (Unesp) · BRUniversidade Federal do Rio de Janeiro · BR

Funding

DISEASE PREVENTION ANALYSIS OF INTESTINAL METAPLASIAF06TW002008 · FIC · UNIVERSITY OF ARIZONA · PI AICKIN, MIKEL G · 1994 to 1994
–
Conselho Nacional de Desenvolvimento Científico e Tecnológico 142029/2014-9Conselho Nacional de Desenvolvimento Científico e Tecnológico 304382/2017-5Conselho Nacional de Desenvolvimento Científico e Tecnológico 309733/2018-9Conselho Nacional de Desenvolvimento Científico e Tecnológico 573959/2008-0Fundação de Amparo à Pesquisa do Estado de São Paulo 2007/57749-2Fundação de Amparo à Pesquisa do Estado de São Paulo 2012/24105-3Fundação de Amparo à Pesquisa do Estado de São Paulo 2013/26450-2Fundação de Amparo à Pesquisa do Estado de São Paulo 2014/05855-7Fundação de Amparo à Pesquisa do Estado de São Paulo 2014/06863-3Fundação de Amparo à Pesquisa do Estado de São Paulo 2014/11513-1Fundação de Amparo à Pesquisa do Estado de São Paulo 2018/15549-1Fundação de Amparo à Pesquisa do Estado de São Paulo 2018/18257-1
6 · The paper itself

Abstract

backgroundRickettsia rickettsii is a tick-borne obligate intracellular bacterium that causes Rocky Mountain spotted fever, a life-threatening illness. To obtain an insight into the vector-pathogen interactions, we assessed the effects of infection with R. rickettsii on the proteome cells of the tick embryonic cell line BME26.

methodsThe proteome of BME26 cells was determined by label-free high-performance liquid chromatography coupled with tandem mass spectrometry analysis. Also evaluated were the effects of infection on the activity of caspase-3, assessed by the hydrolysis of a synthetic fluorogenic substrate in enzymatic assays, and on the exposition of phosphatidyserine, evaluated by live-cell fluorescence microscopy after labeling with annexin-V. Finally, the effects of activation or inhibition of caspase-3 activity on the growth of R. rickettsii in BME26 cells was determined.

resultsTick proteins of different functional classes were modulated in a time-dependent manner by R. rickettsii infection. Regarding proteins involved in apoptosis, certain negative regulators were downregulated at the initial phase of the infection (6 h) but upregulated in the middle of the exponential phase of the bacterial growth (48 h). Microorganisms are known to be able to inhibit apoptosis of the host cell to ensure their survival and proliferation. We therefore evaluated the effects of infection on classic features of apoptotic cells and observed DNA fragmentation exclusively in noninfected cells. Moreover, both caspase-3 activity and phosphatidylserine exposition were lower in infected than in noninfected cells. Importantly, while the activation of caspase-3 exerted a detrimental effect on rickettsial proliferation, its inhibition increased bacterial growth.

conclusionsTaken together, these results show that R. rickettsii modulates the proteome and exerts an inhibitory effect on apoptosis in tick cellsthat seems to be important to ensure cell colonization.

Indexed as

ApoptosisAnimalsCaspase 3Host-Pathogen InteractionsRickettsia rickettsiiTicksCaspase 3ApoptosisProteomeRickettsiaeTick

Identifiers

PMID33261663
PMCPMC7706286
OpenAlexW3108235738

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.