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Antimicrobial activity of hydralazine against methicillin-resistant and methicillin-susceptible Staphylococcus aureus.
Stefany Aires do Nascimento, Francisca B; do Amaral Valente Sá, Lívia Gurgel; de Andrade Neto, João B; da Silva, Lisandra Juvêncio; Rodrigues, Daniel Sampaio; de Farias Cabral, Vitória P; Barbosa, Amanda Dias; Almeida Moreira, Lara E; Braga Vasconcelos, Camille R; Cavalcanti, Bruno Coêlho; França Rios, Maria E; Silva, Jacilene; Marinho, Emmanuel Silva; Dos Santos, Helcio Silva; de Mesquita, Jacó Rl; Pinto Lobo, Marina Duarte; de Moraes, Manoel Odorico; Nobre Júnior, Hélio V; da Silva, Cecília Rocha.
Afiliação
  • Stefany Aires do Nascimento FB; School of Pharmacy, Laboratory of Bioprospection of Antimicrobial Molecules (LABIMAN), Federal University of Ceará, Fortaleza, CE, 60430-372, Brazil.
  • do Amaral Valente Sá LG; Drug Research & Development Center, Federal University of Ceará, Fortaleza, CE, 60430-275, Brazil.
  • de Andrade Neto JB; School of Pharmacy, Laboratory of Bioprospection of Antimicrobial Molecules (LABIMAN), Federal University of Ceará, Fortaleza, CE, 60430-372, Brazil.
  • da Silva LJ; Drug Research & Development Center, Federal University of Ceará, Fortaleza, CE, 60430-275, Brazil.
  • Rodrigues DS; Christus University Center (UNICHRISTUS), Fortaleza, CE, 60190-180, Brazil.
  • de Farias Cabral VP; School of Pharmacy, Laboratory of Bioprospection of Antimicrobial Molecules (LABIMAN), Federal University of Ceará, Fortaleza, CE, 60430-372, Brazil.
  • Barbosa AD; Drug Research & Development Center, Federal University of Ceará, Fortaleza, CE, 60430-275, Brazil.
  • Almeida Moreira LE; Christus University Center (UNICHRISTUS), Fortaleza, CE, 60190-180, Brazil.
  • Braga Vasconcelos CR; School of Pharmacy, Laboratory of Bioprospection of Antimicrobial Molecules (LABIMAN), Federal University of Ceará, Fortaleza, CE, 60430-372, Brazil.
  • Cavalcanti BC; Drug Research & Development Center, Federal University of Ceará, Fortaleza, CE, 60430-275, Brazil.
  • França Rios ME; School of Pharmacy, Laboratory of Bioprospection of Antimicrobial Molecules (LABIMAN), Federal University of Ceará, Fortaleza, CE, 60430-372, Brazil.
  • Silva J; Drug Research & Development Center, Federal University of Ceará, Fortaleza, CE, 60430-275, Brazil.
  • Marinho ES; School of Pharmacy, Laboratory of Bioprospection of Antimicrobial Molecules (LABIMAN), Federal University of Ceará, Fortaleza, CE, 60430-372, Brazil.
  • Dos Santos HS; Drug Research & Development Center, Federal University of Ceará, Fortaleza, CE, 60430-275, Brazil.
  • de Mesquita JR; School of Pharmacy, Laboratory of Bioprospection of Antimicrobial Molecules (LABIMAN), Federal University of Ceará, Fortaleza, CE, 60430-372, Brazil.
  • Pinto Lobo MD; Drug Research & Development Center, Federal University of Ceará, Fortaleza, CE, 60430-275, Brazil.
  • de Moraes MO; School of Pharmacy, Laboratory of Bioprospection of Antimicrobial Molecules (LABIMAN), Federal University of Ceará, Fortaleza, CE, 60430-372, Brazil.
  • Nobre Júnior HV; Drug Research & Development Center, Federal University of Ceará, Fortaleza, CE, 60430-275, Brazil.
  • da Silva CR; School of Pharmacy, Laboratory of Bioprospection of Antimicrobial Molecules (LABIMAN), Federal University of Ceará, Fortaleza, CE, 60430-372, Brazil.
Future Microbiol ; 19: 91-106, 2024 01.
Article em En | MEDLINE | ID: mdl-38294293
ABSTRACT

Background:

Staphylococcus aureus is a human pathogen responsible for high mortality rates. The development of new antimicrobials is urgent. Materials &

methods:

The authors evaluated the activity of hydralazine along with its synergism with other drugs and action on biofilms. With regard to action mechanisms, the authors evaluated cell viability, DNA damage and molecular docking.

Results:

MIC and minimum bactericidal concentration values ranged from 128 to 2048 µg/ml. There was synergism with oxacillin (50%) and vancomycin (25%). Hydralazine reduced the viability of biofilms by 50%. After exposure to hydralazine 2× MIC, 58.78% of the cells were unviable, 62.07% were TUNEL positive and 27.03% presented damage in the comet assay (p < 0.05). Hydralazine showed affinity for DNA gyrase and TyrRS.

Conclusion:

Hydralazine is a potential antibacterial.
Staphylococcus aureus is a bacterium that can cause infection. Infections of S. aureus are becoming difficult to treat, but developing new drugs is a challenge. Repurposing them may be easier. This study looks at the possibility of using hydralazine, a type of medicine used to treat high blood pressure, against S. aureus. The authors found that hydralazine can kill S. aureus and can be used with other antibiotics, including oxacillin and vancomycin. Hydralazine interferes with important processes for the multiplication and survival of this bacterium. These results are preliminary but encouraging. Further studies are needed to confirm the use of hydralazine as a new treatment for S. aureus infections.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções Estafilocócicas / Staphylococcus aureus Resistente à Meticilina Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções Estafilocócicas / Staphylococcus aureus Resistente à Meticilina Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article