TY - JOUR
T1 - Antimicrobial and antibiofilm activity of human recombinant H1 histones against bacterial infections
AU - Arévalo-Jaimes, Betsy Verónica
AU - Salinas-Pena, Mónica
AU - Ponte, Inmaculada
AU - Jordan, Albert
AU - Roque, Alicia
AU - Torrents, Eduard
N1 - Publisher Copyright:
Copyright © 2024 Arévalo-Jaimes et al.
PY - 2024/10/29
Y1 - 2024/10/29
N2 - Histones possess significant antimicrobial potential, yet their activity against biofilms remains underexplored. Moreover, concerns regarding adverse effects limit their clinical implementation. We investigated the antibacterial efficacy of human recombinant histone H1 subtypes against Pseudomonas aeruginosa PAO1, both planktonic and in biofilms. After the in vitro tests, toxicity and efficacy were assessed in a P. aeruginosa PAO1 infection model using Galleria mellonella larvae. Histones were also evaluated in combination with ciprofloxacin (Cpx) and gentamicin (Gm). Our results demonstrate antimicrobial activity of all three histones against P. aeruginosa PAO1, with H1.0 and H1.4 showing efficacy at lower concentrations. The bactericidal effect was associated with a mechanism of membrane disruption. In vitro studies using static and dynamic models showed that H1.4 had antibiofilm potential by reducing cell biomass. Neither H1.0 nor H1.4 showed toxicity in G. mellonella larvae, and both increased larvae survival when infected with P. aeruginosa PAO1. Although in vitro synergism was observed between ciprofloxacin and H1.0, no improvement over the antibiotic alone was noted in vivo. Differences in antibacterial and antibiofilm activity were attributed to sequence and structural variations among histone subtypes. Moreover, the efficacy of H1.0 and H1.4 was influenced by the presence and strength of the extracellular matrix. These findings suggest histones hold promise for combating acute and chronic infections caused by pathogens such as P. aeruginosa.
AB - Histones possess significant antimicrobial potential, yet their activity against biofilms remains underexplored. Moreover, concerns regarding adverse effects limit their clinical implementation. We investigated the antibacterial efficacy of human recombinant histone H1 subtypes against Pseudomonas aeruginosa PAO1, both planktonic and in biofilms. After the in vitro tests, toxicity and efficacy were assessed in a P. aeruginosa PAO1 infection model using Galleria mellonella larvae. Histones were also evaluated in combination with ciprofloxacin (Cpx) and gentamicin (Gm). Our results demonstrate antimicrobial activity of all three histones against P. aeruginosa PAO1, with H1.0 and H1.4 showing efficacy at lower concentrations. The bactericidal effect was associated with a mechanism of membrane disruption. In vitro studies using static and dynamic models showed that H1.4 had antibiofilm potential by reducing cell biomass. Neither H1.0 nor H1.4 showed toxicity in G. mellonella larvae, and both increased larvae survival when infected with P. aeruginosa PAO1. Although in vitro synergism was observed between ciprofloxacin and H1.0, no improvement over the antibiotic alone was noted in vivo. Differences in antibacterial and antibiofilm activity were attributed to sequence and structural variations among histone subtypes. Moreover, the efficacy of H1.0 and H1.4 was influenced by the presence and strength of the extracellular matrix. These findings suggest histones hold promise for combating acute and chronic infections caused by pathogens such as P. aeruginosa.
KW - Galleria mellonella
KW - Antimicrobial peptides
KW - Biofilm
KW - Proteins
KW - Toxicity
KW - Treatment
KW - Biofilms/drug effects
KW - Ciprofloxacin/pharmacology
KW - Humans
KW - Recombinant Proteins/pharmacology
KW - Anti-Bacterial Agents/pharmacology
KW - Histones/metabolism
KW - Larva/drug effects
KW - Moths/microbiology
KW - Microbial Sensitivity Tests
KW - Animals
KW - Gentamicins/pharmacology
KW - Pseudomonas Infections/drug therapy
KW - Pseudomonas aeruginosa/drug effects
KW - toxicity
KW - treatment
KW - proteins
KW - biofilm
KW - antimicrobial peptides
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=uab_pure&SrcAuth=WosAPI&KeyUT=WOS:001345219400001&DestLinkType=FullRecord&DestApp=WOS_CPL
UR - http://www.scopus.com/inward/record.url?scp=85210105932&partnerID=8YFLogxK
U2 - 10.1128/msystems.00704-24
DO - 10.1128/msystems.00704-24
M3 - Article
C2 - 39470247
SN - 2379-5077
VL - 9
JO - mSystems
JF - mSystems
IS - 11
M1 - e00704-24
ER -