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Browsing by Author "Ranin, Jovana (57219407010)"

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    Carbapenem-Resistant Acinetobacter baumannii: Biofilm-Associated Genes, Biofilm-Eradication Potential of Disinfectants, and Biofilm-Inhibitory Effects of Selenium Nanoparticles
    (2023)
    Smitran, Aleksandra (55865631000)
    ;
    Lukovic, Bojana (57189443662)
    ;
    Bozic, LJiljana (57202649173)
    ;
    Jelic, Dijana (23034961300)
    ;
    Jovicevic, Milos (57223044336)
    ;
    Kabic, Jovana (57215669275)
    ;
    Kekic, Dusan (36696225200)
    ;
    Ranin, Jovana (57219407010)
    ;
    Opavski, Natasa (6507364674)
    ;
    Gajic, Ina (55428924700)
    This study aimed to investigate the biofilm-production ability of carbapenem-resistant Acinetobacter baumannii (CRAB), the biofilm-eradication potential of 70% ethanol and 0.5% sodium hypochlorite, the effects of selenium nanoparticles (SeNPs) against planktonic and biofilm-embedded CRAB, and the relationship between biofilm production and bacterial genotypes. A total of 111 CRAB isolates were tested for antimicrobial susceptibility, biofilm formation, presence of the genes encoding carbapenemases, and biofilm-associated virulence factors. The antibiofilm effects of disinfectants and SeNPs against CRAB isolates were also tested. The vast majority of the tested isolates were biofilm producers (91.9%). The bap, ompA, and csuE genes were found in 57%, 70%, and 76% of the CRAB isolates, with the csuE being significantly more common among biofilm producers (78.6%) compared to non-biofilm-producing CRAB (25%). The tested disinfectants showed a better antibiofilm effect on moderate and strong biofilm producers than on weak producers (p < 0.01). The SeNPs showed an inhibitory effect against all tested planktonic (MIC range: 0.00015 to >1.25 mg/mL) and biofilm-embedded CRAB, with a minimum biofilm inhibitory concentration of less than 0.15 mg/mL for 90% of biofilm producers. In conclusion, SeNPs might be used as promising therapeutic and medical device coating agents, thus serving as an alternative approach for the prevention of biofilm-related infections. © 2023 by the authors.
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    Publication
    Carbapenem-Resistant Acinetobacter baumannii: Biofilm-Associated Genes, Biofilm-Eradication Potential of Disinfectants, and Biofilm-Inhibitory Effects of Selenium Nanoparticles
    (2023)
    Smitran, Aleksandra (55865631000)
    ;
    Lukovic, Bojana (57189443662)
    ;
    Bozic, LJiljana (57202649173)
    ;
    Jelic, Dijana (23034961300)
    ;
    Jovicevic, Milos (57223044336)
    ;
    Kabic, Jovana (57215669275)
    ;
    Kekic, Dusan (36696225200)
    ;
    Ranin, Jovana (57219407010)
    ;
    Opavski, Natasa (6507364674)
    ;
    Gajic, Ina (55428924700)
    This study aimed to investigate the biofilm-production ability of carbapenem-resistant Acinetobacter baumannii (CRAB), the biofilm-eradication potential of 70% ethanol and 0.5% sodium hypochlorite, the effects of selenium nanoparticles (SeNPs) against planktonic and biofilm-embedded CRAB, and the relationship between biofilm production and bacterial genotypes. A total of 111 CRAB isolates were tested for antimicrobial susceptibility, biofilm formation, presence of the genes encoding carbapenemases, and biofilm-associated virulence factors. The antibiofilm effects of disinfectants and SeNPs against CRAB isolates were also tested. The vast majority of the tested isolates were biofilm producers (91.9%). The bap, ompA, and csuE genes were found in 57%, 70%, and 76% of the CRAB isolates, with the csuE being significantly more common among biofilm producers (78.6%) compared to non-biofilm-producing CRAB (25%). The tested disinfectants showed a better antibiofilm effect on moderate and strong biofilm producers than on weak producers (p < 0.01). The SeNPs showed an inhibitory effect against all tested planktonic (MIC range: 0.00015 to >1.25 mg/mL) and biofilm-embedded CRAB, with a minimum biofilm inhibitory concentration of less than 0.15 mg/mL for 90% of biofilm producers. In conclusion, SeNPs might be used as promising therapeutic and medical device coating agents, thus serving as an alternative approach for the prevention of biofilm-related infections. © 2023 by the authors.
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    Publication
    HCV Treatment Outcomes in PWID: Impact of Addiction History on SVR12
    (2024)
    Milošević, Ivana (58456808200)
    ;
    Beronja, Branko (58610945200)
    ;
    Filipović, Ana (58487006900)
    ;
    Mitrović, Nikola (55110096400)
    ;
    Simić, Jelena (57201274633)
    ;
    Knežević, Nataša (59170791600)
    ;
    Ranin, Jovana (57219407010)
    ;
    Todorović, Nevena (58688792000)
    ;
    Stevanović, Olja (57201195181)
    ;
    Radovanović-Spurnić, Aleksandra (57191847101)
    ;
    Katanić, Nataša (57190964860)
    ;
    Hristović, Dejan (7801380935)
    ;
    Nikolić, Nataša (58288723700)
    People who inject drugs (PWIDs) experience high rates of hepatitis C virus (HCV) infection, primarily due to needle sharing and limited healthcare access, resulting in a disproportionate disease burden within this population. This prospective study evaluated treatment outcomes in 432 adult patients with chronic hepatitis C (CHC) treated with direct-acting antivirals (DAAs) at the University Clinical Center of Serbia. Patients were categorized into two groups based on a history of drug addiction: PWIDs (163, 37.7%) and non-PWIDs (269, 62.3%). The PWID group was further categorized into subpopulations of problematic PWIDs (39, 23.9%), ex-PWIDs (124, 76.1%), and PWIDs on OST (96, 58.9%). The PWID group demonstrated significantly lower treatment adherence, with an intention-to-treat (ITT) rate of 82.8%, compared to 96.3% in the control group (p < 0.001). In contrast, no significant differences were observed in per-protocol (PP) outcomes between the two groups. Additionally, PWIDs were significantly younger (p < 0.001) and had higher rates of psychiatric disorders (p < 0.001), alcohol abuse (p < 0.001), and HCV genotype 1a (p < 0.001). Advanced fibrosis was predictor of PP treatment failure among PWIDs, while mood disorders and alcohol use disorder were associated with interruptions before the scheduled completion time. For non-PWIDs, older age and advanced fibrosis emerged as key predictors of PP treatment failure. The loss to follow-up was most commonly observed in the problematic PWID subgroup (p = 0.001). These findings highlight the importance of addressing barriers in PWIDs through integrated care strategies that concurrently manage addiction and HCV. © 2024 by the authors.
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    Publication
    HCV Treatment Outcomes in PWID: Impact of Addiction History on SVR12
    (2024)
    Milošević, Ivana (58456808200)
    ;
    Beronja, Branko (58610945200)
    ;
    Filipović, Ana (58487006900)
    ;
    Mitrović, Nikola (55110096400)
    ;
    Simić, Jelena (57201274633)
    ;
    Knežević, Nataša (59170791600)
    ;
    Ranin, Jovana (57219407010)
    ;
    Todorović, Nevena (58688792000)
    ;
    Stevanović, Olja (57201195181)
    ;
    Radovanović-Spurnić, Aleksandra (57191847101)
    ;
    Katanić, Nataša (57190964860)
    ;
    Hristović, Dejan (7801380935)
    ;
    Nikolić, Nataša (58288723700)
    People who inject drugs (PWIDs) experience high rates of hepatitis C virus (HCV) infection, primarily due to needle sharing and limited healthcare access, resulting in a disproportionate disease burden within this population. This prospective study evaluated treatment outcomes in 432 adult patients with chronic hepatitis C (CHC) treated with direct-acting antivirals (DAAs) at the University Clinical Center of Serbia. Patients were categorized into two groups based on a history of drug addiction: PWIDs (163, 37.7%) and non-PWIDs (269, 62.3%). The PWID group was further categorized into subpopulations of problematic PWIDs (39, 23.9%), ex-PWIDs (124, 76.1%), and PWIDs on OST (96, 58.9%). The PWID group demonstrated significantly lower treatment adherence, with an intention-to-treat (ITT) rate of 82.8%, compared to 96.3% in the control group (p < 0.001). In contrast, no significant differences were observed in per-protocol (PP) outcomes between the two groups. Additionally, PWIDs were significantly younger (p < 0.001) and had higher rates of psychiatric disorders (p < 0.001), alcohol abuse (p < 0.001), and HCV genotype 1a (p < 0.001). Advanced fibrosis was predictor of PP treatment failure among PWIDs, while mood disorders and alcohol use disorder were associated with interruptions before the scheduled completion time. For non-PWIDs, older age and advanced fibrosis emerged as key predictors of PP treatment failure. The loss to follow-up was most commonly observed in the problematic PWID subgroup (p = 0.001). These findings highlight the importance of addressing barriers in PWIDs through integrated care strategies that concurrently manage addiction and HCV. © 2024 by the authors.

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