Synergism between molecules derived from Garcinia brasiliensis and antimicrobial drugs on field isolates of Mycoplasma hyopneumoniae.

Antimicrobials Bioactive compounds Minimum inhibitory concentration Swine enzootic pneumonia

Journal

Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]
ISSN: 1678-4405
Titre abrégé: Braz J Microbiol
Pays: Brazil
ID NLM: 101095924

Informations de publication

Date de publication:
28 Nov 2023
Historique:
received: 28 09 2023
accepted: 02 11 2023
pubmed: 28 11 2023
medline: 28 11 2023
entrez: 27 11 2023
Statut: aheadofprint

Résumé

Mycoplasma hyopneumoniae (M. hyopneumoniae) is one of the smallest free-living bacteria found in nature; it has an extremely small genome and lacks a cell wall. It is the main etiological agent of porcine enzootic pneumonia (EP), a chronic respiratory disease with worldwide distribution that causes significant losses in swine production. Due to the great economic impact caused by EP, new strategies for treating and controlling this agent are researched. The objective of this study was to verify the anti-M. hyopneumoniae activity of compounds derived from Garcinia brasiliensis and the synergism with the main antimicrobials used in the treatment of EP; this is the first study assessing the synergism between bioactive molecules and antimicrobial compounds in vitro against isolates of M. hyopneumoniae. The minimum inhibitory concentrations (MICs) of the antimicrobials tiamulin, valnemulin, and enrofloxacin, as well as the bioactive compounds guttiferone-A (Gut-A), 7-epiculsone (7-Epic), copper 7-epiculsone (7-Epic-Cu), and benzophenone, were determined. Subsequently, the interactions of antibiotics with the compounds were evaluated using the checkerboard method. Three field M. hyopneumoniae isolates were used, and the J strain was used as a control. The MIC values of the antimicrobials compared to the field isolates were equal to and lower than those of the reference strain J. Among the compounds used, 7-Epic-Cu showed the lowest MIC value. Synergistic association was observed for Gut-A with tiamulin and valnemulin, whereas 7-Epic and 7-Epic-Cu showed synergistic action with enrofloxacin. No synergistic effect was observed for benzophenone. Despite being an initial study, the results suggest that these combinations hold promise for the treatment of infections caused by M. hyopneumoniae.

Identifiants

pubmed: 38012513
doi: 10.1007/s42770-023-01175-z
pii: 10.1007/s42770-023-01175-z
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2023. The Author(s) under exclusive licence to Sociedade Brasileira de Microbiologia.

Références

Liu L, Ruiwensli L, Zhang R, Wang J, Han Q, Wang J, Yu W (2019) Rapid and sensitive detection of Mycoplasma hyopneumoniae by recombinase polymerase amplification assay. J Microbiol Methods:56–61. https://doi.org/10.1016/j.mimet.2019.02.015
Rosales M, Ramírez A, Tavío M, Poveda C, Poveda J (2020) Antimicrobial susceptibility profiles of porcine mycoplasmas isolated from samples collected in southern Europe. BMC Vet Res. https://doi.org/10.1186/s12917-020-02512-2
Almeida L, Murata R, Santos M, Nagem T, Alencar S et al (2008) Antimicrobial activity of Rheedia brasiliensis and 7-epiclusianone against Streptococcus mutans. Phytomedicine 15:886–891. https://doi.org/10.1016/j.phymed.2007.12.003
doi: 10.1016/j.phymed.2007.12.003 pubmed: 18276126
Gustafson K, Mckee C (1992) The guttiferones, HIV-inhibtory benzophenones from Symphonia globulifera, Garcinia livingstonei, Garcinia ovalifolia and Clusia rosea. Tetrahedron 48:10093–10102. https://doi.org/10.1016/S0040-4020(01)89039-6
doi: 10.1016/S0040-4020(01)89039-6
Ngouela S, Lenta N, Noungoue T, Ngoupayo J, Boyom F, Tsamo E et al (2006) Anti-plasmodial and antioxidant activities of constituents of the seed shells of Symphonia globulifera Linn f. Phytochemistry 67:302–306. https://doi.org/10.1016/j.phytochem.2005.11.004
doi: 10.1016/j.phytochem.2005.11.004 pubmed: 16368120
Neves S, Coelho P, Cordeiro B, Veloso P, Rodrigues e Silva M, dos Santos H et al (2007) Antianaphylactic properties of 7-epiclusianone, a tetraprenylated benzophenone isolated from Garcinia brasiliensis. Planta Med 73:644–649. https://doi.org/10.1055/s-2007-981534
doi: 10.1055/s-2007-981534 pubmed: 17562491
Santa-Cecília V, Freitas S, Vilela C, Veloso C, Da Rocha Q, Moreira C et al (2011) Antinociceptive and anti-inflammatory properties of 7-epiclusianone, a prenylated benzophenone from Garcinia brasiliensis. Eur J Pharmacol 670:280–285. https://doi.org/10.1016/j.ejphar.2011.08.032
doi: 10.1016/j.ejphar.2011.08.032 pubmed: 21924261
Maia N, Barros M, Oliveira L, Cardoso S, Santos M, Pieri F, Ramalho T, Cunha E, Scatamburlo M (2018) Synergism of plant compound with traditional antimicrobials against Streptococcus spp. isolated From bovine mastitis. Front Microbiol. https://doi.org/10.3389/fmicb.2018.01203
Aranda M, Gómez G, Barros M, Santos M, Oliveira L, Pena J, Moeira M (2019) Antimicrobial and synergistic activity of 2,2′,4-trihydroxybenzophenone against bacterial pathogens of poultry. Front Microbiol. https://doi.org/10.3389/fmicb.2019.00490
Barros M, Perciano P, Santos M, Oliveira L, Costa E, Moreira M (2017) Antibacterial activity of 7-epiclusianone and its novel copper metal complex on Streptococcus spp. isolated from bovine mastitis and their cytotoxicity in MAC-T cells. Molecules 22(5):823. https://doi.org/10.3390/molecules22050823
doi: 10.3390/molecules22050823 pubmed: 28513553 pmcid: 6154111
Naldoni FJ, Claudino ALR, Cruz JW, Chavasco JK, Silva FE, Veloso MP et al (2009) Antimicrobial activity of benzophenones and extracts from the fruits of Garcinia brasiliensis. J Med Food 12:403–407
doi: 10.1089/jmf.2007.0622 pubmed: 19459744
Gonzaga N, Souza L, Santos M, Assao V, Rycrof A, Ndrew R, Deeney A, Fietto J, Bressan G, Moreira M, Silva-júnior A (2019) Antimicrobial susceptibility and genetic profile of Mycoplasma hyopneumoniae isolates from Brazil. Braz J Microbiol:18–19. https://doi.org/10.1007/s42770-019-00185-0
Cook B, Beddow J, Manso-Silván L, Maglennon G, Rycroft A (2016) Selective medium for culture of Mycoplasma hyopneumoniae. Vet Microbiol 195:158–164. https://doi.org/10.1016/j.vetmic.2016.09.022
doi: 10.1016/j.vetmic.2016.09.022 pubmed: 27771062 pmcid: 5081061
Clinical and Laboratory Standards Institute [CLSI] (2012) Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically; approved standard—nine edition. Clinical and Laboratory Standards Institute, Wayne, PA
Klein U, Jong A, Moyaert H (2017) Antimicrobial susceptibility monitoring of Mycoplasma hyopneumoniae and Mycoplasma bovis isolated in Europe. Vet Microbiol:188–193. https://doi.org/10.1016/j.vetmic.2017.04.012
Hannan P (2000) Guidelines and recommendations for antimicrobial minimum inhibitory concentration (MIC) testing against veterinary mycoplasma species. Vet Res 31(4):373–395. https://doi.org/10.1051/vetres:2000100
doi: 10.1051/vetres:2000100 pubmed: 10958240
Brahim M, Fadli M, Hassani L, Boulay B, Markouk M, Bekkouche K, Abbad A et al (2015) Chenopodium ambrosioides var. ambrosioides used in Moroccan traditional medicine can enhance the antimicrobial activity of conventional antibiotics. Ind Crops Prod:37–43. https://doi.org/10.1016/j.indcrop.2015.03.067
Biavatti M (2009) Synergy: an old wisdom, a new paradigm for pharmacotherapy. Braz J Pharm Sci 45(3). https://doi.org/10.1590/S1984-82502009000300002
Thongkamkoon M, Narongsak W, Kobayashi H, Pathanasophon P, Kishima M, Yamamoto K (2013) In vitro susceptibility of Mycoplasma hyopneumoniae field isolates and occurrence of fluoroquinolone, macrolides and lincomycin resistance. J Vet Med Sci 75(8):1067–1070. https://doi.org/10.1292/jvms.12-0520
doi: 10.1292/jvms.12-0520 pubmed: 23503167
Ribeiro V, Santana R (2019) Development of antimicrobial composites based on SEBS/PP added with copper particles. Federal University of Rio Grande do Sul, School of Engineering, Programa de Pós-Graduação em Engenharia de Materiais (PPGE3M)

Auteurs

Bruna Araújo Euzébio Alves Jacob Lopes (BAEAJ)

Department of Microbiology, Federal University of Viçosa, Viçosa, MG, Brazil.

Leonardo Teófilo Toledo (LT)

Department de Veterinary, Federal University of Viçosa, Viçosa, MG, Brazil.

Jessica Lobo Albuquerque Caldeira (JLA)

Department de Veterinary, Federal University of Viçosa, Viçosa, MG, Brazil.

Fábio Assad Feres Rodrigues (FAF)

Department of Biochemistry, Federal University of Viçosa, Viçosa, MG, Brazil.

Mariana de Barros (M)

Department de Veterinary, Federal University of Viçosa, Viçosa, MG, Brazil.

Luiz Fernando Lino de Souza (LFL)

Department de Veterinary, Federal University of Viçosa, Viçosa, MG, Brazil.

Natália Fialho Gonzaga (NF)

Department de Veterinary, Federal University of Viçosa, Viçosa, MG, Brazil.

Marcelo Henrique Dos Santos (MH)

Department of Chemistry, Federal University of Viçosa, Viçosa, Brazil.

Abelardo Silva-Júnior (A)

Institute of Biological and Health Sciences, Federal University of Alagoas, Maceió, AL, Brazil.

Maria Aparecida Scatamburlo Moreira (MAS)

Department de Veterinary, Federal University of Viçosa, Viçosa, MG, Brazil. masm@ufv.br.

Classifications MeSH