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In vitro activity of hydroxychloroquine in combination with antibiotics against intracellular uropathogenic Escherichia coli
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Abstract
Background
Two pathophysiological concepts may explain recurrent UTI: a reinfection by a bacterial strain from the digestive microbiota or a relapse from
Escherichia coli
persisting within the superficial urothelial cells as intracellular bacterial communities (IBC). Hydroxychloroquine (HCQ)-antibiotic combination is effective against intracellular adherent-invasive
E. coli
isolated from patients with Crohn’s disease. We hypothesized that HCQ may enhanced antibiotic efficacy against
E. coli
IBC.
Methods
UTI89 reference strain and two clinical
E. coli
strains forming IBCs (VITALE#2157, VITALE#2206) were used in this study. MIC, MBC and time killing curves (4xMIC) were performed for AZYTHROMYCIN (AZT), CIPROFLOXACIN (CIP), DOXYCYCLINE (DC), FOSFMOMYCIN (FF) and HCQ.
In vitro
activity of antibiotics alone and combined with HCQ was evaluated on intracellular bacterial survival assay using a model of urothelium cells (HTB-9).
Results
Time-killing curves showed that CIP has a bactericidal activity at H6 (-4.6 log
10
CFU/mL) with regrowth at H24 against 2157, and a bactericidal activity at H6 without regrowth at H24 against 2206 (-3.3 log
10
CFU/mL) and UTI89 (-3.4 log
10
CFU/mL); DC, AZT and FF demonstrated bacteriostatic activity at H24 regardless of the strain. We observed a significant decrease in the number of intracellular bacteria at H42 with CIP (-1.83 log
10
/ 10
6
cells). DC, FF, and AZT exposure did not reduce IBC formation at H42 (P>0.05). IBC formation after HCQ-antibiotic combination exposure was not significantly different (P>0.05) from antibiotic exposure alone, regardless of the antibiotic or strain studied.
Conclusions
In conclusion, HCQ exposure does not enhance antibiotics activity against intracellular uropathogenic
E. coli
.
Highlights
Using an
in vitro
model of superficial urothelium monolayer, we observed a significant decrease in intracellular uropathogenic
Escherichia coli
in response to ciprofloxacin exposure.
Hydroxychloroquine exposure does not enhance antibiotics activity against intracellular uropathogenic
Escherichia coli
.
Title: In vitro
activity of hydroxychloroquine in combination with antibiotics against intracellular uropathogenic
Escherichia coli
Description:
Abstract
Background
Two pathophysiological concepts may explain recurrent UTI: a reinfection by a bacterial strain from the digestive microbiota or a relapse from
Escherichia coli
persisting within the superficial urothelial cells as intracellular bacterial communities (IBC).
Hydroxychloroquine (HCQ)-antibiotic combination is effective against intracellular adherent-invasive
E.
coli
isolated from patients with Crohn’s disease.
We hypothesized that HCQ may enhanced antibiotic efficacy against
E.
coli
IBC.
Methods
UTI89 reference strain and two clinical
E.
coli
strains forming IBCs (VITALE#2157, VITALE#2206) were used in this study.
MIC, MBC and time killing curves (4xMIC) were performed for AZYTHROMYCIN (AZT), CIPROFLOXACIN (CIP), DOXYCYCLINE (DC), FOSFMOMYCIN (FF) and HCQ.
In vitro
activity of antibiotics alone and combined with HCQ was evaluated on intracellular bacterial survival assay using a model of urothelium cells (HTB-9).
Results
Time-killing curves showed that CIP has a bactericidal activity at H6 (-4.
6 log
10
CFU/mL) with regrowth at H24 against 2157, and a bactericidal activity at H6 without regrowth at H24 against 2206 (-3.
3 log
10
CFU/mL) and UTI89 (-3.
4 log
10
CFU/mL); DC, AZT and FF demonstrated bacteriostatic activity at H24 regardless of the strain.
We observed a significant decrease in the number of intracellular bacteria at H42 with CIP (-1.
83 log
10
/ 10
6
cells).
DC, FF, and AZT exposure did not reduce IBC formation at H42 (P>0.
05).
IBC formation after HCQ-antibiotic combination exposure was not significantly different (P>0.
05) from antibiotic exposure alone, regardless of the antibiotic or strain studied.
Conclusions
In conclusion, HCQ exposure does not enhance antibiotics activity against intracellular uropathogenic
E.
coli
.
Highlights
Using an
in vitro
model of superficial urothelium monolayer, we observed a significant decrease in intracellular uropathogenic
Escherichia coli
in response to ciprofloxacin exposure.
Hydroxychloroquine exposure does not enhance antibiotics activity against intracellular uropathogenic
Escherichia coli
.
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