TY  - CONF
AU  - Stevanović, Danijela
AU  - Paunović, Verica
AU  - Vučićević, Ljubica
AU  - Misirkić Marjanović, Maja
AU  - Perović, Vladimir
AU  - Ristić, Biljana
AU  - Bošnjak, Mihajlo
AU  - Mandić, Miloš
AU  - Harhaji-Trajković, Ljubica
AU  - Janjetović, Kristina
AU  - Kosić, Milica
AU  - Lalošević, Jovan
AU  - Nikolić, Miloš
AU  - Bonači-Nikolić, Branka
AU  - Trajković, Vladimir
PY  - 2023
UR  - https://indico.bio.bg.ac.rs/event/4/attachments/6/492/Abstract%20Book-CoMBoS2-TMB.pdf
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/6286
AB  - Introduction: Since the interaction between autophagy and virus-induced inflammation is complex,
we investigated the interplay between autophagy and inflammation in COVID-19 patients and THP-1
cells expressing SARS-Cov2 proteins NSP5 and ORF3a.
Methods: Autophagy markers in blood from 19 control subjects and 26 COVID-19 patients at hospital
admission and one week later were measured by ELISA, while cytokine levels were examined by flow cytometric bead immunoassay. The level of p62 in cells and its concentration in cell culture supernatants
was measured by immunoblot/ELISA. The mRNA levels of proinflammatory cytokines were measured
by RT-qPCR.
Results: IFN-α, TNF, IL-6, IL-8, IL-17, IL-33, and IFN-γ were elevated in COVID-19 patients at both time
points, whereasIL-10 and IL-1β were elevated at admission and one week later, respectively. Autophagy
markers LC3 and ATG5 were unchanged in COVID-19. The concentration of autophagic cargo receptor
p62 was significantly lower and positively correlated with TNF, IL-10, IL-17, and IL-33 at hospital admission, returning to normal levels after one week. The expression of SARS-CoV-2 proteins NSP5 or ORF3a
in THP-1 cells caused an autophagy-independent decrease/autophagy-inhibition-dependent increase
of intracellular and secreted p62. This was associated with an NSP5-mediated decrease inTNF/IL-10 mRNA
and an ORF3a-mediated increase inTNF/IL-1β/IL-6/IL-10/IL-33 mRNA levels. A genetic knockdown of p62
mimicked the immunosuppressive effect of NSP5, while a p62 increase in autophagy-deficient cells mirrored the immunostimulatory action of ORF3a.
Conclusion: The autophagy receptor p62 is reduced in acute COVID-19, and the balance between autophagy-independent decrease and autophagy blockade-dependent increase of p62 levels could affect
SARS-CoV-induced inflammation.
PB  - Belgrade: Institute of Molecular Genetics and Genetic Engineering, University of Belgrade
C3  - Abstract Book: CoMBoS2 - the Second Congress of Molecular Biologists of Serbia; 2023 Oct 6-8; Belgrade, Serbia
T1  - Autophagy receptor P62 regulates SARS-CoV-2-induced inflammation in COVID-19
SP  - 76
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_6286
ER  - 

@conference{
author = "Stevanović, Danijela and Paunović, Verica and Vučićević, Ljubica and Misirkić Marjanović, Maja and Perović, Vladimir and Ristić, Biljana and Bošnjak, Mihajlo and Mandić, Miloš and Harhaji-Trajković, Ljubica and Janjetović, Kristina and Kosić, Milica and Lalošević, Jovan and Nikolić, Miloš and Bonači-Nikolić, Branka and Trajković, Vladimir",
year = "2023",
abstract = "Introduction: Since the interaction between autophagy and virus-induced inflammation is complex,
we investigated the interplay between autophagy and inflammation in COVID-19 patients and THP-1
cells expressing SARS-Cov2 proteins NSP5 and ORF3a.
Methods: Autophagy markers in blood from 19 control subjects and 26 COVID-19 patients at hospital
admission and one week later were measured by ELISA, while cytokine levels were examined by flow cytometric bead immunoassay. The level of p62 in cells and its concentration in cell culture supernatants
was measured by immunoblot/ELISA. The mRNA levels of proinflammatory cytokines were measured
by RT-qPCR.
Results: IFN-α, TNF, IL-6, IL-8, IL-17, IL-33, and IFN-γ were elevated in COVID-19 patients at both time
points, whereasIL-10 and IL-1β were elevated at admission and one week later, respectively. Autophagy
markers LC3 and ATG5 were unchanged in COVID-19. The concentration of autophagic cargo receptor
p62 was significantly lower and positively correlated with TNF, IL-10, IL-17, and IL-33 at hospital admission, returning to normal levels after one week. The expression of SARS-CoV-2 proteins NSP5 or ORF3a
in THP-1 cells caused an autophagy-independent decrease/autophagy-inhibition-dependent increase
of intracellular and secreted p62. This was associated with an NSP5-mediated decrease inTNF/IL-10 mRNA
and an ORF3a-mediated increase inTNF/IL-1β/IL-6/IL-10/IL-33 mRNA levels. A genetic knockdown of p62
mimicked the immunosuppressive effect of NSP5, while a p62 increase in autophagy-deficient cells mirrored the immunostimulatory action of ORF3a.
Conclusion: The autophagy receptor p62 is reduced in acute COVID-19, and the balance between autophagy-independent decrease and autophagy blockade-dependent increase of p62 levels could affect
SARS-CoV-induced inflammation.",
publisher = "Belgrade: Institute of Molecular Genetics and Genetic Engineering, University of Belgrade",
journal = "Abstract Book: CoMBoS2 - the Second Congress of Molecular Biologists of Serbia; 2023 Oct 6-8; Belgrade, Serbia",
title = "Autophagy receptor P62 regulates SARS-CoV-2-induced inflammation in COVID-19",
pages = "76",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_6286"
}

Stevanović, D., Paunović, V., Vučićević, L., Misirkić Marjanović, M., Perović, V., Ristić, B., Bošnjak, M., Mandić, M., Harhaji-Trajković, L., Janjetović, K., Kosić, M., Lalošević, J., Nikolić, M., Bonači-Nikolić, B.,& Trajković, V.. (2023). Autophagy receptor P62 regulates SARS-CoV-2-induced inflammation in COVID-19. in Abstract Book: CoMBoS2 - the Second Congress of Molecular Biologists of Serbia; 2023 Oct 6-8; Belgrade, Serbia
Belgrade: Institute of Molecular Genetics and Genetic Engineering, University of Belgrade., 76.
https://hdl.handle.net/21.15107/rcub_ibiss_6286

Stevanović D, Paunović V, Vučićević L, Misirkić Marjanović M, Perović V, Ristić B, Bošnjak M, Mandić M, Harhaji-Trajković L, Janjetović K, Kosić M, Lalošević J, Nikolić M, Bonači-Nikolić B, Trajković V. Autophagy receptor P62 regulates SARS-CoV-2-induced inflammation in COVID-19. in Abstract Book: CoMBoS2 - the Second Congress of Molecular Biologists of Serbia; 2023 Oct 6-8; Belgrade, Serbia. 2023;:76.
https://hdl.handle.net/21.15107/rcub_ibiss_6286 .

Stevanović, Danijela, Paunović, Verica, Vučićević, Ljubica, Misirkić Marjanović, Maja, Perović, Vladimir, Ristić, Biljana, Bošnjak, Mihajlo, Mandić, Miloš, Harhaji-Trajković, Ljubica, Janjetović, Kristina, Kosić, Milica, Lalošević, Jovan, Nikolić, Miloš, Bonači-Nikolić, Branka, Trajković, Vladimir, "Autophagy receptor P62 regulates SARS-CoV-2-induced inflammation in COVID-19" in Abstract Book: CoMBoS2 - the Second Congress of Molecular Biologists of Serbia; 2023 Oct 6-8; Belgrade, Serbia (2023):76,
https://hdl.handle.net/21.15107/rcub_ibiss_6286 .

TY  - JOUR
AU  - Paunović, Verica
AU  - Vučićević, Ljubica
AU  - Misirkić Marjanović, Maja
AU  - Perović, Vladimir
AU  - Ristić, Biljana
AU  - Bošnjak, Mihajlo
AU  - Mandić, Miloš
AU  - Stevanović, Danijela
AU  - Harhaji-Trajković, Ljubica
AU  - Lalošević, Jovan
AU  - Nikolić, Miloš
AU  - Bonači-Nikolić, Branka
AU  - Trajković, Vladimir
PY  - 2023
UR  - https://www.mdpi.com/2073-4409/12/9/1282
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/5912
AB  - As autophagy can promote or inhibit inflammation, we examined autophagy-inflammation interplay in COVID-19. Autophagy markers in the blood of 19 control subjects and 26 COVID-19 patients at hospital admission and one week later were measured by ELISA, while cytokine levels were examined by flow cytometric bead immunoassay. The antiviral IFN-α and proinflammatory TNF, IL-6, IL-8, IL-17, IL-33, and IFN-γ were elevated in COVID-19 patients at both time points, while IL-10 and IL-1β were increased at admission and one week later, respectively. Autophagy markers LC3 and ATG5 were unaltered in COVID-19. In contrast, the concentration of autophagic cargo receptor p62 was significantly lower and positively correlated with TNF, IL-10, IL-17, and IL-33 at hospital admission, returning to normal levels after one week. The expression of SARS-CoV-2 proteins NSP5 or ORF3a in THP-1 monocytes caused an autophagy-independent decrease or autophagy-inhibition-dependent increase, respectively, of intracellular/secreted p62, as confirmed by immunoblot/ELISA. This was associated with an NSP5-mediated decrease in TNF/IL-10 mRNA and an ORF3a-mediated increase in TNF/IL-1β/IL-6/IL-10/IL-33 mRNA levels. A genetic knockdown of p62 mimicked the immunosuppressive effect of NSP5, and a p62 increase in autophagy-deficient cells mirrored the immunostimulatory action of ORF3a. In conclusion, the proinflammatory autophagy receptor p62 is reduced inacute COVID-19, and the balance between autophagy-independent decrease and autophagy blockade-dependent increase of p62 levels could affect SARS-CoV-induced inflammation.
PB  - Basel: MDPI
T2  - Cells
T1  - Autophagy Receptor p62 Regulates SARS-CoV-2-Induced Inflammation in COVID-19
IS  - 9
VL  - 12
DO  - 10.3390/cells12091282
SP  - 1282
ER  - 

@article{
author = "Paunović, Verica and Vučićević, Ljubica and Misirkić Marjanović, Maja and Perović, Vladimir and Ristić, Biljana and Bošnjak, Mihajlo and Mandić, Miloš and Stevanović, Danijela and Harhaji-Trajković, Ljubica and Lalošević, Jovan and Nikolić, Miloš and Bonači-Nikolić, Branka and Trajković, Vladimir",
year = "2023",
abstract = "As autophagy can promote or inhibit inflammation, we examined autophagy-inflammation interplay in COVID-19. Autophagy markers in the blood of 19 control subjects and 26 COVID-19 patients at hospital admission and one week later were measured by ELISA, while cytokine levels were examined by flow cytometric bead immunoassay. The antiviral IFN-α and proinflammatory TNF, IL-6, IL-8, IL-17, IL-33, and IFN-γ were elevated in COVID-19 patients at both time points, while IL-10 and IL-1β were increased at admission and one week later, respectively. Autophagy markers LC3 and ATG5 were unaltered in COVID-19. In contrast, the concentration of autophagic cargo receptor p62 was significantly lower and positively correlated with TNF, IL-10, IL-17, and IL-33 at hospital admission, returning to normal levels after one week. The expression of SARS-CoV-2 proteins NSP5 or ORF3a in THP-1 monocytes caused an autophagy-independent decrease or autophagy-inhibition-dependent increase, respectively, of intracellular/secreted p62, as confirmed by immunoblot/ELISA. This was associated with an NSP5-mediated decrease in TNF/IL-10 mRNA and an ORF3a-mediated increase in TNF/IL-1β/IL-6/IL-10/IL-33 mRNA levels. A genetic knockdown of p62 mimicked the immunosuppressive effect of NSP5, and a p62 increase in autophagy-deficient cells mirrored the immunostimulatory action of ORF3a. In conclusion, the proinflammatory autophagy receptor p62 is reduced inacute COVID-19, and the balance between autophagy-independent decrease and autophagy blockade-dependent increase of p62 levels could affect SARS-CoV-induced inflammation.",
publisher = "Basel: MDPI",
journal = "Cells",
title = "Autophagy Receptor p62 Regulates SARS-CoV-2-Induced Inflammation in COVID-19",
number = "9",
volume = "12",
doi = "10.3390/cells12091282",
pages = "1282"
}

Paunović, V., Vučićević, L., Misirkić Marjanović, M., Perović, V., Ristić, B., Bošnjak, M., Mandić, M., Stevanović, D., Harhaji-Trajković, L., Lalošević, J., Nikolić, M., Bonači-Nikolić, B.,& Trajković, V.. (2023). Autophagy Receptor p62 Regulates SARS-CoV-2-Induced Inflammation in COVID-19. in Cells
Basel: MDPI., 12(9), 1282.
https://doi.org/10.3390/cells12091282

Paunović V, Vučićević L, Misirkić Marjanović M, Perović V, Ristić B, Bošnjak M, Mandić M, Stevanović D, Harhaji-Trajković L, Lalošević J, Nikolić M, Bonači-Nikolić B, Trajković V. Autophagy Receptor p62 Regulates SARS-CoV-2-Induced Inflammation in COVID-19. in Cells. 2023;12(9):1282.
doi:10.3390/cells12091282 .

Paunović, Verica, Vučićević, Ljubica, Misirkić Marjanović, Maja, Perović, Vladimir, Ristić, Biljana, Bošnjak, Mihajlo, Mandić, Miloš, Stevanović, Danijela, Harhaji-Trajković, Ljubica, Lalošević, Jovan, Nikolić, Miloš, Bonači-Nikolić, Branka, Trajković, Vladimir, "Autophagy Receptor p62 Regulates SARS-CoV-2-Induced Inflammation in COVID-19" in Cells, 12, no. 9 (2023):1282,
https://doi.org/10.3390/cells12091282 . .

TY  - CHAP
AU  - Marković, Tatjana
AU  - Nikolić, Miloš
AU  - Glamočlija, Jasmina
AU  - Ćirić, Ana
AU  - Emerald, Mila
AU  - Radanović, Dragoja
AU  - Zheljazkov, Valtcho
AU  - Soković, Marina
AU  - Valtcho D., Jeliazkov (Zheljazkov)
AU  - Charles L., Cantrell
PY  - 2016
UR  - http://pubs.acs.org/doi/abs/10.1021/bk-2016-1218.ch015
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/2501
UR  - https://www.scopus.com/record/display.uri?eid=2-s2.0-84987638092&origin=resultslist&sort=plf-f&src=s&st1=%22Essential+Oils+for+the+Prevention+and+Treatment+of+Human+Opportunistic+Fungal+Diseases%22&st2=&sid=BC239BCE0A831C04144486E63BFE49F7.wsnAw8kcdt7IPYLO0V48gA%3a1610&sot=b&sdt=b&sl=103&s=TITLE-ABS-KEY%28%22Essential+Oils+for+the+Prevention+and+Treatment+of+Human+Opportunistic+Fungal+Diseases%22%29&relpos=0&citeCnt=0&searchTerm=
AB  - Human infectious diseases have significantly increased during the past decade, especially among immunocompromised patients. As high as 10% of hospital acquired systemic infections are caused by fungi. Among animal and human pathogens, the dermatomycetes group is the main cause of dermatomycoses, which are chronic but not life threatening infections that bring about considerable morbidity. Under certain circumstances Candida spp. commensals (ie, C. albicans and some non-albicans species) can become pathogenic, which causes amucous membrane infection to turn into a life-threatening systemic disease, particularly in patients with a weakened immune system. In addition to increased resistance of human pathogens to current commercial drugs, conventional treatments have many adverse side effects, thus drugs may become insufficient for treatment and this presents a serious medical problem. Hence, the development of more effective and less toxic antifungal agents, including natural products, is vitally important. Due to their biologically active secondary metabolites, many plants have been traditionally used in ethnomedicine for their therapeutic antifungal potential, with some recent experimental compounds proven to be promising. Essential oils and/or their individual constituents play an important role as potential therapeutic agents. The main advantage is their lipophilic nature, which allows the compounds to easily penetrate the plasma membrane, in addition to the ability to cure opportunistic fungal diseases without harmful effects on human and animal tissues. With growing interest in the use of essential oils in the pharmaceutical industry, systematic examination of their preventive and therapeutic properties has become increasingly important. This paper reviews the antifungal efficacy of essential oils belonging to various plant families for the prevention and treatment of common opportunistic diseases in humans (i.e., dermatomycosis and candidosis), specifically those infections caused by fungi with primary entry routes through skin and mucosa.
PB  - American Chemical Society, Washington, D.C.
T2  - Medicinal and Aromatic Crops: Production, Phytochemistry, and Utilization
T1  - Essential Oils for the Prevention and Treatment of Human Opportunistic Fungal Diseases
DO  - 10.1021/bk-2016-1218.ch015
SP  - 247
EP  - 277
ER  - 

@inbook{
author = "Marković, Tatjana and Nikolić, Miloš and Glamočlija, Jasmina and Ćirić, Ana and Emerald, Mila and Radanović, Dragoja and Zheljazkov, Valtcho and Soković, Marina and Valtcho D., Jeliazkov (Zheljazkov) and Charles L., Cantrell",
year = "2016",
abstract = "Human infectious diseases have significantly increased during the past decade, especially among immunocompromised patients. As high as 10% of hospital acquired systemic infections are caused by fungi. Among animal and human pathogens, the dermatomycetes group is the main cause of dermatomycoses, which are chronic but not life threatening infections that bring about considerable morbidity. Under certain circumstances Candida spp. commensals (ie, C. albicans and some non-albicans species) can become pathogenic, which causes amucous membrane infection to turn into a life-threatening systemic disease, particularly in patients with a weakened immune system. In addition to increased resistance of human pathogens to current commercial drugs, conventional treatments have many adverse side effects, thus drugs may become insufficient for treatment and this presents a serious medical problem. Hence, the development of more effective and less toxic antifungal agents, including natural products, is vitally important. Due to their biologically active secondary metabolites, many plants have been traditionally used in ethnomedicine for their therapeutic antifungal potential, with some recent experimental compounds proven to be promising. Essential oils and/or their individual constituents play an important role as potential therapeutic agents. The main advantage is their lipophilic nature, which allows the compounds to easily penetrate the plasma membrane, in addition to the ability to cure opportunistic fungal diseases without harmful effects on human and animal tissues. With growing interest in the use of essential oils in the pharmaceutical industry, systematic examination of their preventive and therapeutic properties has become increasingly important. This paper reviews the antifungal efficacy of essential oils belonging to various plant families for the prevention and treatment of common opportunistic diseases in humans (i.e., dermatomycosis and candidosis), specifically those infections caused by fungi with primary entry routes through skin and mucosa.",
publisher = "American Chemical Society, Washington, D.C.",
journal = "Medicinal and Aromatic Crops: Production, Phytochemistry, and Utilization",
booktitle = "Essential Oils for the Prevention and Treatment of Human Opportunistic Fungal Diseases",
doi = "10.1021/bk-2016-1218.ch015",
pages = "247-277"
}

Marković, T., Nikolić, M., Glamočlija, J., Ćirić, A., Emerald, M., Radanović, D., Zheljazkov, V., Soković, M., Valtcho D., J. (.,& Charles L., C.. (2016). Essential Oils for the Prevention and Treatment of Human Opportunistic Fungal Diseases. in Medicinal and Aromatic Crops: Production, Phytochemistry, and Utilization
American Chemical Society, Washington, D.C.., 247-277.
https://doi.org/10.1021/bk-2016-1218.ch015

Marković T, Nikolić M, Glamočlija J, Ćirić A, Emerald M, Radanović D, Zheljazkov V, Soković M, Valtcho D. J(, Charles L. C. Essential Oils for the Prevention and Treatment of Human Opportunistic Fungal Diseases. in Medicinal and Aromatic Crops: Production, Phytochemistry, and Utilization. 2016;:247-277.
doi:10.1021/bk-2016-1218.ch015 .

Marković, Tatjana, Nikolić, Miloš, Glamočlija, Jasmina, Ćirić, Ana, Emerald, Mila, Radanović, Dragoja, Zheljazkov, Valtcho, Soković, Marina, Valtcho D., Jeliazkov (Zheljazkov), Charles L., Cantrell, "Essential Oils for the Prevention and Treatment of Human Opportunistic Fungal Diseases" in Medicinal and Aromatic Crops: Production, Phytochemistry, and Utilization (2016):247-277,
https://doi.org/10.1021/bk-2016-1218.ch015 . .

TY  - JOUR
AU  - Petrović, Jovana
AU  - Glamočlija, Jasmina
AU  - Stojković, Dejan
AU  - Nikolić, Miloš
AU  - Ćirić, Ana
AU  - Fernandes, Angela
AU  - Ferreira, Isabel C. F. R.
AU  - Soković, Marina
PY  - 2014
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/2267
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/3638
AB  - Agrocybe aegerita (Brig.) Sing is a basidiomycete, white rot fungus.   Antimicrobial activities and the antiqourum effect on Pseudomonas   aeruginosa of an A. aegerita methanolic extract were investigated. The   extract showed very good antimicrobial activity against all the tested   microorganisms in a dose dependent manner. Effects of the Sub-MIC, MIC   and 2MIC of the A. aegerita methanolic extract regulated the virulence   factors in the quorum sensing (QS) test, as well as biofilm formation on   P. aeruginosa. Sub-inhibitory and inhibitory concentrations of the   extract demonstrated the reduction of virulence factors such as   pyocyanin production, twitching and swimming motility. The biofilm   forming capability of P. aeruginosa PAO1 was also reduced in a   concentration-dependent manner. Furthermore, the chemical composition of   the methanolic extract was determined considering its phenolic   composition. The methanolic extract of A. aegerita can be a very good   source of bioactive substances. This research is of great importance due   to the prevalence of drug-resistant microorganisms.
T2  - Food & Function
T1  - Bioactive composition, antimicrobial activities and the influence of Agrocybe aegerita (Brig.) Sing on certain quorum-sensing-regulated functions and biofilm formation by Pseudomonas aeruginosa
IS  - 12
VL  - 5
DO  - 10.1039/c4fo00819g
SP  - 3296
EP  - 3303
ER  - 

@article{
author = "Petrović, Jovana and Glamočlija, Jasmina and Stojković, Dejan and Nikolić, Miloš and Ćirić, Ana and Fernandes, Angela and Ferreira, Isabel C. F. R. and Soković, Marina",
year = "2014",
abstract = "Agrocybe aegerita (Brig.) Sing is a basidiomycete, white rot fungus.   Antimicrobial activities and the antiqourum effect on Pseudomonas   aeruginosa of an A. aegerita methanolic extract were investigated. The   extract showed very good antimicrobial activity against all the tested   microorganisms in a dose dependent manner. Effects of the Sub-MIC, MIC   and 2MIC of the A. aegerita methanolic extract regulated the virulence   factors in the quorum sensing (QS) test, as well as biofilm formation on   P. aeruginosa. Sub-inhibitory and inhibitory concentrations of the   extract demonstrated the reduction of virulence factors such as   pyocyanin production, twitching and swimming motility. The biofilm   forming capability of P. aeruginosa PAO1 was also reduced in a   concentration-dependent manner. Furthermore, the chemical composition of   the methanolic extract was determined considering its phenolic   composition. The methanolic extract of A. aegerita can be a very good   source of bioactive substances. This research is of great importance due   to the prevalence of drug-resistant microorganisms.",
journal = "Food & Function",
title = "Bioactive composition, antimicrobial activities and the influence of Agrocybe aegerita (Brig.) Sing on certain quorum-sensing-regulated functions and biofilm formation by Pseudomonas aeruginosa",
number = "12",
volume = "5",
doi = "10.1039/c4fo00819g",
pages = "3296-3303"
}

Petrović, J., Glamočlija, J., Stojković, D., Nikolić, M., Ćirić, A., Fernandes, A., Ferreira, I. C. F. R.,& Soković, M.. (2014). Bioactive composition, antimicrobial activities and the influence of Agrocybe aegerita (Brig.) Sing on certain quorum-sensing-regulated functions and biofilm formation by Pseudomonas aeruginosa. in Food & Function, 5(12), 3296-3303.
https://doi.org/10.1039/c4fo00819g

Petrović J, Glamočlija J, Stojković D, Nikolić M, Ćirić A, Fernandes A, Ferreira ICFR, Soković M. Bioactive composition, antimicrobial activities and the influence of Agrocybe aegerita (Brig.) Sing on certain quorum-sensing-regulated functions and biofilm formation by Pseudomonas aeruginosa. in Food & Function. 2014;5(12):3296-3303.
doi:10.1039/c4fo00819g .

Petrović, Jovana, Glamočlija, Jasmina, Stojković, Dejan, Nikolić, Miloš, Ćirić, Ana, Fernandes, Angela, Ferreira, Isabel C. F. R., Soković, Marina, "Bioactive composition, antimicrobial activities and the influence of Agrocybe aegerita (Brig.) Sing on certain quorum-sensing-regulated functions and biofilm formation by Pseudomonas aeruginosa" in Food & Function, 5, no. 12 (2014):3296-3303,
https://doi.org/10.1039/c4fo00819g . .