@article{MTMT:34824870,
	title = {Shewanella baltica in a Microbial Fuel Cell for Sensing of Biological Oxygen Demand (BOD) of Wastewater},
	url = {https://m2.mtmt.hu/api/publication/34824870},
	author = {Dang, Nga Phuong and Petrich, Chris and Pasztor, Dorina and Schneider, György and Calay, Rajnish Kaur},
	doi = {10.1080/00032719.2024.2341087},
	journal-iso = {ANAL LETT},
	journal = {ANALYTICAL LETTERS},
	unique-id = {34824870},
	issn = {0003-2719},
	abstract = {Geobacter and Shewanella are the most characterized electroactive bacteria genera. Unlike genus Geobacter that is strictly anaerobic, Shewanella can grow under both oxic and anoxic environments and is capable of metabolizing a wider substrate range. In the present study, the use of strain Shewanella baltica 20 in MFC-based biosensor for BOD monitoring is reported. The S. baltica strain 20 was isolated from river sediment in Hungary. The bacterium could form a biofilm, oxidized glucose, and transferred electrons to produce current when they were enriched on the anode in an air cathode microbial fuel cell (MFC). The tested MFC system demonstrated linearity in the current response to glucose from 50 to 300 mg/L. The electrical efficiency was determined from the polarization curve using the method of Varying Circuit Resistance (VCR) with an external load probed from 10 ohm to 220 k ohm. The maximum power production was 1.2 mW/m2 at an external load of 40 k ohm. Studying the effect of external resistors on the MFC performance showed that the MFC reached higher saturation for 500 mg/L of glucose at lower resistances of 100 and 470 ohm, in comparison to 300 mg/L at 1000 ohm. The results show that the response of the MFC can potentially be tuned by adjusting the external load. Our preliminary study suggests that Shewanella baltica strain 20 may be used for online monitoring of BOD (biological oxygen demand) in wastewater.},
	keywords = {SYSTEMS; biosensors; Biosensor; wastewater; Microbial fuel cell; Biological oxygen demand (BOD)},
	year = {2024},
	eissn = {1532-236X}
}

@{MTMT:34823736,
	title = {Antimikróbás kezelés},
	url = {https://m2.mtmt.hu/api/publication/34823736},
	author = {Bátai, István and Kerényi, Mónika},
	booktitle = {Súlyos baleseti agysérültek ellátása},
	unique-id = {34823736},
	year = {2024},
	pages = {190-191},
	orcid-numbers = {Kerényi, Mónika/0000-0002-5767-9662}
}

@CONFERENCE{MTMT:34814487,
	title = {A gesztenyeméz biofilm képződést gátló hatása},
	url = {https://m2.mtmt.hu/api/publication/34814487},
	author = {Koloh, Regina and Farkas, Ágnes and Balázs, Viktória Lilla and Kocsis, Béla},
	booktitle = {Absztraktkötet: XII. Interdiszciplináris Doktorandusz Konferencia = Book of Abstract: XII. Interdisciplinary Doctoral Conference},
	unique-id = {34814487},
	year = {2024},
	pages = {87-87},
	orcid-numbers = {Farkas, Ágnes/0000-0002-8590-3203}
}

@CONFERENCE{MTMT:34814458,
	title = {Mi az evidenciaalapú megközelítés alapján megítélt összefüggés a Pseudomonas aeruginosa baktérium és a kakukkfű illóolaj között?},
	url = {https://m2.mtmt.hu/api/publication/34814458},
	author = {Nagy, Anett and Ormai, Edit and Horváth, Györgyi and Kocsis, Béla and Balázs, Viktória Lilla},
	booktitle = {Absztraktkötet: XII. Interdiszciplináris Doktorandusz Konferencia = Book of Abstract: XII. Interdisciplinary Doctoral Conference},
	unique-id = {34814458},
	year = {2024},
	pages = {86-86},
	orcid-numbers = {Horváth, Györgyi/0000-0001-5344-0294}
}

@CONFERENCE{MTMT:34814440,
	title = {Hársméz, levendula illóolaj és kombinációjuk antibakteriális aktivitása},
	url = {https://m2.mtmt.hu/api/publication/34814440},
	author = {Ángyán, Virág Diána and Farkas, Ágnes and Kocsis, Béla and Radványi, Lilla},
	booktitle = {Absztraktkötet: XII. Interdiszciplináris Doktorandusz Konferencia = Book of Abstract: XII. Interdisciplinary Doctoral Conference},
	unique-id = {34814440},
	year = {2024},
	pages = {85-85},
	orcid-numbers = {Farkas, Ágnes/0000-0002-8590-3203}
}

@CONFERENCE{MTMT:34814410,
	title = {Nozokomiális patogének és a szegfűszeg illóolaj kapcsolatának bemutatása evidenciaalapú megközelítésben},
	url = {https://m2.mtmt.hu/api/publication/34814410},
	author = {Ormai, Edit and Kocsis, Béla and Böszörményi, Andrea and Horváth, Györgyi and Balázs, Viktória Lilla},
	booktitle = {Absztraktkötet: XII. Interdiszciplináris Doktorandusz Konferencia = Book of Abstract: XII. Interdisciplinary Doctoral Conference},
	unique-id = {34814410},
	year = {2024},
	pages = {83-83},
	orcid-numbers = {Horváth, Györgyi/0000-0001-5344-0294}
}

@article{MTMT:34796888,
	title = {Decidual γδT cells of early human pregnancy produce angiogenic and immunomodulatory proteins while also possessing cytotoxic potential},
	url = {https://m2.mtmt.hu/api/publication/34796888},
	author = {Nörenberg, Jasper Maximilian and Vida, P. and Bösmeier, I. and Forró, B. and Nörenberg, A. and Buda, Á. and Simon, Diána and Erdő-Bonyár, Szabina and Jáksó, Pál and Kovács, Kálmán András and Mikó, Éva and Berki, Tímea and Mezősi, Emese and Barakonyi, Alíz},
	doi = {10.3389/fimmu.2024.1382424},
	journal-iso = {FRONT IMMUNOL},
	journal = {FRONTIERS IN IMMUNOLOGY},
	volume = {15},
	unique-id = {34796888},
	issn = {1664-3224},
	year = {2024},
	eissn = {1664-3224},
	orcid-numbers = {Berki, Tímea/0000-0002-0134-8127; Mezősi, Emese/0000-0001-9367-3877}
}

@article{MTMT:34796272,
	title = {Detection and complete genome characterization of a genogroup X (GX) sapovirus (family Caliciviridae) from a golden jackal (Canis aureus) in Hungary},
	url = {https://m2.mtmt.hu/api/publication/34796272},
	author = {Balázs, Benigna and Boros, Ákos and Pankovics, Péter and Nagy, Gábor and Szekeres, Sándor and Urbán, Péter and Reuter, Gábor},
	doi = {10.1007/s00705-024-06034-2},
	journal-iso = {ARCH VIROL},
	journal = {ARCHIVES OF VIROLOGY},
	volume = {169},
	unique-id = {34796272},
	issn = {0304-8608},
	abstract = {In this study, a novel genotype of genogroup X (GX) sapovirus (family Caliciviridae ) was detected in the small intestinal contents of a golden jackal ( Canis aureus ) in Hungary and characterised by viral metagenomics and next-generation sequencing techniques. The complete genome of the detected strain, GX/Dömsöd/DOCA-11/2020/HUN (PP105600), is 7,128 nt in length. The ORF1- and ORF2-encoded viral proteins (NSP, VP1, and VP2) have 98%, 95%, and 88% amino acid sequence identity to the corresponding proteins of genogroup GX sapoviruses from domestic pigs, but the nucleic acid sequence identity values for their genes are significantly lower (83%, 77%, and 68%). During an RT-PCR-based epidemiological investigation of additional jackal and swine samples, no other GX strains were detected, but a GXI sapovirus strain, GXI/Tótfalu/WBTF-10/2012/HUN (PP105601), was identified in a faecal sample from a wild boar ( Sus scrofa ). We report the detection of members of two likely underdiagnosed groups of sapoviruses (GX and GXI) in a golden jackal and, serendipitously, in a wild boar in Europe.},
	year = {2024},
	eissn = {1432-8798},
	orcid-numbers = {Boros, Ákos/0000-0001-5843-4360; Nagy, Gábor/0000-0002-4924-6322; Szekeres, Sándor/0000-0002-6150-8356; Reuter, Gábor/0000-0002-5857-4934}
}

@article{MTMT:34757150,
	title = {Co-infecting viruses of species Bovine rhinitis B virus (Picornaviridae) and Bovine nidovirus 1 (Tobaniviridae) identified for the first time from a post-mortem respiratory sample of a sheep (Ovis aries) in Hungary},
	url = {https://m2.mtmt.hu/api/publication/34757150},
	author = {Tóth, Fruzsina and Gáspár, Gábor and Pankovics, Péter and Urbán, Péter and Herczeg, Róbert and Albert, Mihály and Reuter, Gábor and Boros, Ákos},
	doi = {10.1016/j.meegid.2024.105585},
	journal-iso = {INFECT GENET EVOL},
	journal = {INFECTION GENETICS AND EVOLUTION},
	volume = {120},
	unique-id = {34757150},
	issn = {1567-1348},
	abstract = {In this study, a picornavirus and a nidovirus were identified from a single available nasopharyngeal swab (NPS) sample of a freshly deceased sheep, as the only vertebrate viruses found with viral metagenomics and next-generation sequencing methods. The sample was originated from a mixed feedlot farm in Hungary where sheep and cattle were held together but in separate stalls. Most of the sheep had respiratory signs (coughing and increased respiratory effort) at the time of sampling. Other NPS were not, but additional enteric samples were collected from sheep (n = 27) and cattle (n = 11) of the same farm at that time. The complete/nearly complete genomes of the identified viruses were determined using RT-PCR and Nanopore (MinION-Flonge) / Dye-terminator sequencing techniques. The results of detailed genomic and phylogenetic analyses indicate that the identified picornavirus most likely belongs to a type 4 genotype of species Bovine rhinitis B virus (BRBV-4, OR885914) of genus Aphthovirus, family Picornaviridae while the ovine nidovirus (OvNV, OR885915) - as a novel variant - could belong to the recently created Bovine nidovirus 1 (BoNV) species of genus Bostovirus, family Tobaniviridae. None of the identified viruses were detectable in the enteric samples using RT-PCR and generic screening primer pairs. Both viruses are well-known respiratory pathogens of cattle, but their presence was not demonstrated before in other animals, like sheep. Furthermore, neither BRBV-4 nor BoNVs were investigated in European cattle and/or sheep flocks, therefore it cannot be determined whether the presence of these viruses in sheep was a result of a single host species switch/spillover event or these viruses are circulating in not just cattle but sheep populations as well. Further studies required to investigate the spread of these viruses in Hungarian and European sheep and cattle populations and to identify their pathogenic potential in sheep.},
	keywords = {SHEEP; Respiratory disease; Picornavirus; Co-infection; Spillover; nidovirus; Bovine rhinitis B virus},
	year = {2024},
	eissn = {1567-7257},
	orcid-numbers = {Herczeg, Róbert/0000-0002-5903-0082; Reuter, Gábor/0000-0002-5857-4934; Boros, Ákos/0000-0001-5843-4360}
}

@article{MTMT:34753258,
	title = {Gram-negative rough mutants used as test bacteria can increase sensitivity of direct bioautography},
	url = {https://m2.mtmt.hu/api/publication/34753258},
	author = {Balázs, Viktória Lilla and Böszörményi, Andrea and Kocsis, Béla and Horváth, Györgyi},
	doi = {10.1007/s00764-024-00293-0},
	journal-iso = {J PLANAR CHROMATOGR MOD TLC},
	journal = {JPC - JOURNAL OF PLANAR CHROMATOGRAPHY - MODERN TLC},
	unique-id = {34753258},
	issn = {0933-4173},
	abstract = {Currently, the antimicrobial activity of essential oils (EOs) is an outstanding research field due to antibiotic resistance of microorganisms. Thin-layer chromatography‒direct bioautography (TLC‒DB) is an effective, fast method to find components with antimicrobial activity in a mixture of plant compounds, e.g., in EOs. The volatility and hydrophobic characters of EOs require special experimental conditions, and disc diffusion assay is not appropriate to explore the antimicrobial activity of them. The aim of this study was to use “R” mutants, which are more sensitive to synthetic antimicrobial drugs, in DB to increase the sensitivity of this method. Our hypothesis was that these mutants show sensitivity to some EOs (thyme, clove, and peppermint) as well. The chemical composition of our tested EOs was measured with gas chromatography‒mass spectrometry (GC‒MS). The main compounds (39.8% thymol, 78.8% eugenol, and 50.4% menthol) of EOs showed notable antibacterial activity in TLC‒DB. Based on our results, we suggest to use Salmonella minnesota Re595 rough strain as test bacterium in bioautography, because it showed the highest sensitivity to the tested antibiotics (gentamicin and cephalexin) and EOs. Furthermore, this rough mutant could make TLC‒DB more faster, because only 4 h incubation time was enough to detect the inhibition zones of the active compounds used in this study.},
	year = {2024},
	eissn = {1789-0993},
	orcid-numbers = {Böszörményi, Andrea/0000-0003-3982-7059; Horváth, Györgyi/0000-0001-5344-0294}
}