Effects of α and β-adrenergic signaling on innate immunity and Porphyromonas gingivalis virulence in an invertebrate model

Bibliographic Details
Main Author: Moraes, Renata Mendonça
Publication Date: 2022
Other Authors: Garcia, Maíra Terra [UNESP], Stossi, Fabio, Junqueira, Juliana Campos [UNESP], Anbinder, Ana Lia [UNESP], Barros, Patrícia Pimentel de [UNESP]
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://hdl.handle.net/11449/237077
Summary: To investigate the role of adrenergic signaling (AS) in the host immune response and Porphyromonas gingivalis virulence, we compared norepinephrine (NE) and isoproterenol (ISO) responses in Galleria mellonella. P. gingivalis infection was evaluated by survival; humoral immune responses (i.e., melanization and cecropin and gloverin mRNA expression); cellular immune responses (i.e., hemocyte count, nodulation by histology); and P. gingivalis recovery (CFU/mL). P. gingivalis was cultivated in the presence of ISO (PgISO) or NE and injected into the larvae for survival evaluation. Finally, we co-injected ISO and PgISO to evaluate the concomitant effects on the immune response and bacterial virulence. None of the ligands were toxic to the larvae; ISO increased hemocyte number, even after P. gingivalis infection, by mobilizing sessile hemocytes in a β-adrenergic-specific manner, while NE showed the opposite effect. ISO treatment reduced larval mortality and the number of recovered bacteria, while NE increased mortality and showed no effect on bacterial recovery. ISO and NE had similar effects on melanization and decreased the expression of cecropin. Although co-cultivation with NE and ISO increased the gene expression of bacterial virulence factors in vitro, only the injection of PgISO increased larval death, which was partially reversed by circulating ISO. Therefore, α- and β-adrenergic signaling had opposite effects after P. gingivalis infection. Ultimately, the catecholamine influence on the immune response overcame the effect of more virulent strains. The effect of AS directly on the pathogen found in vitro did not translate to the in vivo setting.
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spelling Effects of α and β-adrenergic signaling on innate immunity and Porphyromonas gingivalis virulence in an invertebrate modelGalleria mellonellaPorphyromonas gingivalisAdrenergic signalingInvertebratesInnate immunityTo investigate the role of adrenergic signaling (AS) in the host immune response and Porphyromonas gingivalis virulence, we compared norepinephrine (NE) and isoproterenol (ISO) responses in Galleria mellonella. P. gingivalis infection was evaluated by survival; humoral immune responses (i.e., melanization and cecropin and gloverin mRNA expression); cellular immune responses (i.e., hemocyte count, nodulation by histology); and P. gingivalis recovery (CFU/mL). P. gingivalis was cultivated in the presence of ISO (PgISO) or NE and injected into the larvae for survival evaluation. Finally, we co-injected ISO and PgISO to evaluate the concomitant effects on the immune response and bacterial virulence. None of the ligands were toxic to the larvae; ISO increased hemocyte number, even after P. gingivalis infection, by mobilizing sessile hemocytes in a β-adrenergic-specific manner, while NE showed the opposite effect. ISO treatment reduced larval mortality and the number of recovered bacteria, while NE increased mortality and showed no effect on bacterial recovery. ISO and NE had similar effects on melanization and decreased the expression of cecropin. Although co-cultivation with NE and ISO increased the gene expression of bacterial virulence factors in vitro, only the injection of PgISO increased larval death, which was partially reversed by circulating ISO. Therefore, α- and β-adrenergic signaling had opposite effects after P. gingivalis infection. Ultimately, the catecholamine influence on the immune response overcame the effect of more virulent strains. The effect of AS directly on the pathogen found in vitro did not translate to the in vivo setting.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)PreprintSão Paulo State University (Unesp), Institute of Science and Technology, Bioscience and Diagnosis Department, São José dos Campos, Brazil.São Paulo State University (Unesp), Institute of Science and Technology, Bioscience and Diagnosis Department, São José dos Campos, BrazilDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas and GCC Center for Advanced Microscopy and Image Informatics, Houston, Texas.São Paulo State University (Unesp), Institute of Science and Technology, Bioscience and Diagnosis Department, São José dos Campos, Brazil e Multicampi School of Medical Sciences, Federal University of Rio Grande do Norte (UFRN), Caicó, RN, BrazilSão Paulo State University (Unesp), Institute of Science and Technology, Bioscience and Diagnosis Department, São José dos Campos, Brazil.São Paulo State University (Unesp), Institute of Science and Technology, Bioscience and Diagnosis Department, São José dos Campos, Brazil.FAPESP 2017/26461-5FAPESP 2018/ 21701-0FAPESP 2018/25933-3NIH (DK56338, CA125123)CPRIT (RP170719)Taylo&FrancisUniversidade Estadual Paulista (Unesp)Moraes, Renata MendonçaGarcia, Maíra Terra [UNESP]Stossi, FabioJunqueira, Juliana Campos [UNESP]Anbinder, Ana Lia [UNESP]Barros, Patrícia Pimentel de [UNESP]2022-10-17T19:00:41Z2022-10-17T19:00:41Z2022-09-19info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdf2150-5608http://hdl.handle.net/11449/23707710.1080/21505594.2022.2123302387360439844864398130303575282912802486281558128032202054105590060979679430082730000-0002-4484-59320000-0002-1193-29090000-0001-6029-54780000-0003-4885-28110000-0001-6646-68560000-0003-3930-4274engVirulenceinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESP2024-11-07T13:18:59Zoai:repositorio.unesp.br:11449/237077Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-11-07T13:18:59Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Effects of α and β-adrenergic signaling on innate immunity and Porphyromonas gingivalis virulence in an invertebrate model
title Effects of α and β-adrenergic signaling on innate immunity and Porphyromonas gingivalis virulence in an invertebrate model
spellingShingle Effects of α and β-adrenergic signaling on innate immunity and Porphyromonas gingivalis virulence in an invertebrate model
Moraes, Renata Mendonça
Galleria mellonella
Porphyromonas gingivalis
Adrenergic signaling
Invertebrates
Innate immunity
title_short Effects of α and β-adrenergic signaling on innate immunity and Porphyromonas gingivalis virulence in an invertebrate model
title_full Effects of α and β-adrenergic signaling on innate immunity and Porphyromonas gingivalis virulence in an invertebrate model
title_fullStr Effects of α and β-adrenergic signaling on innate immunity and Porphyromonas gingivalis virulence in an invertebrate model
title_full_unstemmed Effects of α and β-adrenergic signaling on innate immunity and Porphyromonas gingivalis virulence in an invertebrate model
title_sort Effects of α and β-adrenergic signaling on innate immunity and Porphyromonas gingivalis virulence in an invertebrate model
author Moraes, Renata Mendonça
author_facet Moraes, Renata Mendonça
Garcia, Maíra Terra [UNESP]
Stossi, Fabio
Junqueira, Juliana Campos [UNESP]
Anbinder, Ana Lia [UNESP]
Barros, Patrícia Pimentel de [UNESP]
author_role author
author2 Garcia, Maíra Terra [UNESP]
Stossi, Fabio
Junqueira, Juliana Campos [UNESP]
Anbinder, Ana Lia [UNESP]
Barros, Patrícia Pimentel de [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Moraes, Renata Mendonça
Garcia, Maíra Terra [UNESP]
Stossi, Fabio
Junqueira, Juliana Campos [UNESP]
Anbinder, Ana Lia [UNESP]
Barros, Patrícia Pimentel de [UNESP]
dc.subject.por.fl_str_mv Galleria mellonella
Porphyromonas gingivalis
Adrenergic signaling
Invertebrates
Innate immunity
topic Galleria mellonella
Porphyromonas gingivalis
Adrenergic signaling
Invertebrates
Innate immunity
description To investigate the role of adrenergic signaling (AS) in the host immune response and Porphyromonas gingivalis virulence, we compared norepinephrine (NE) and isoproterenol (ISO) responses in Galleria mellonella. P. gingivalis infection was evaluated by survival; humoral immune responses (i.e., melanization and cecropin and gloverin mRNA expression); cellular immune responses (i.e., hemocyte count, nodulation by histology); and P. gingivalis recovery (CFU/mL). P. gingivalis was cultivated in the presence of ISO (PgISO) or NE and injected into the larvae for survival evaluation. Finally, we co-injected ISO and PgISO to evaluate the concomitant effects on the immune response and bacterial virulence. None of the ligands were toxic to the larvae; ISO increased hemocyte number, even after P. gingivalis infection, by mobilizing sessile hemocytes in a β-adrenergic-specific manner, while NE showed the opposite effect. ISO treatment reduced larval mortality and the number of recovered bacteria, while NE increased mortality and showed no effect on bacterial recovery. ISO and NE had similar effects on melanization and decreased the expression of cecropin. Although co-cultivation with NE and ISO increased the gene expression of bacterial virulence factors in vitro, only the injection of PgISO increased larval death, which was partially reversed by circulating ISO. Therefore, α- and β-adrenergic signaling had opposite effects after P. gingivalis infection. Ultimately, the catecholamine influence on the immune response overcame the effect of more virulent strains. The effect of AS directly on the pathogen found in vitro did not translate to the in vivo setting.
publishDate 2022
dc.date.none.fl_str_mv 2022-10-17T19:00:41Z
2022-10-17T19:00:41Z
2022-09-19
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv 2150-5608
http://hdl.handle.net/11449/237077
10.1080/21505594.2022.2123302
3873604398448643
9813030357528291
2802486281558128
0322020541055900
6097967943008273
0000-0002-4484-5932
0000-0002-1193-2909
0000-0001-6029-5478
0000-0003-4885-2811
0000-0001-6646-6856
0000-0003-3930-4274
identifier_str_mv 2150-5608
10.1080/21505594.2022.2123302
3873604398448643
9813030357528291
2802486281558128
0322020541055900
6097967943008273
0000-0002-4484-5932
0000-0002-1193-2909
0000-0001-6029-5478
0000-0003-4885-2811
0000-0001-6646-6856
0000-0003-3930-4274
url http://hdl.handle.net/11449/237077
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Virulence
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Taylo&Francis
publisher.none.fl_str_mv Taylo&Francis
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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