Miklos Gyuranecz
@vmri.hu
Zoonotic Bacteriology and Mycoplasmology
Veterinary Medical Research Institute
I am a DVM, PhD, DSc, habil, Dipl. ECVM, head of a 15-member research group and the vice director of the Veterinary Medical Research Institute, an honorary professor at the University of Veterinary Medicine, Budapest, Hungary and the director of the Mycoplasma diagnostic & biotech company, MolliScience Ltd. I am the author of more than 130 peer-reviewed scientific papers and three book chapters. My laboratory served as an OIE reference laboratory between 2015 and 2018. Currently I am the supervisor of six graduated and three active PhD students.
EDUCATION
2021 De facto Diplomate, European College of Veterinary Microbiology
2021 DSc (Doctor of Science), Hungarian Academy of Sciences, Hungary
2019 Habilitation, University of Veterinary Medicine, Hungary
2011 PhD (Summa cum laude), Faculty of Veterinary Science, Szent István University, Hungary
2007 DVM and BSc in wildlife management, Faculty of Veterinary Science, Szent István University, Hungary
RESEARCH INTERESTS
I am keenly interested in infectious diseases, particularly bacterial pathogens. My current work is primarily on mycoplasmosis but I also work with a variety of other diseases, including tularemia, brucellosis and Q fever.
FUTURE PROJECTS
National Laboratory of Infectious Animal Diseases, Antimicrobial Resistance, Veterinary Public Health and Food Chain Safety
The establishment of the laboratory is of key importance for the national economy, since the rapid recognition of infectious diseases, along with effective prevention and treatment are especially important due to the large number of farm animals in Hungary and the annual increase in revenue they generate. Also playing an important role in the project is the study of the increasingly alarming spread of antimicrobial resistance, especially with regard to the possibility of its transfer from animals to humans. The laboratory's innovative competences and modern infrastructural capacity not only further the nation's human and animal health, they also increase the international competitiveness of domestic livestock breeding.
Applications Invited
PhD students, post-docs
Development of diagnostic and control procedures for infectious diseases of domestic and wild bird species with high economic and public health risk
Most of VMRI's research groups are involved in the research project. The project’s main objectives were generated by the animal health problems caused by viruses, bacteria and parasites that threaten the competitiveness of poultry industry, and that could lead to market improvements for the sector. Research directions have been identified that can effectively help to address the current challenges in poultry nutrition, food chain safety and zoonoses.
Applications Invited
PhD students, post-docs
National Laboratory of Health Safety
The aim of the Health Safety National Laboratory is to create a scientific basis for decision-making in Hungary based on data and analysis in the areas of health care, epidemic prevention and ecological systems. The project encompasses research carried out in the fields of epidemic mathematics, epidemic ecology, invasion biology and data-driven health care, among other topics. The laboratory unites and coordinates the research groups operating in this area in Hungary in an insular fashion along the "One Health" concept, thereby supporting networking and the creation of an effectively collaborative and internationally competitive research community.
Applications Invited
PhD students, post-docs
Scopus Publications
Scholar Citations
Scholar h-index
Scholar i10-index
Scopus Publications
Anna Sawicka-Durkalec, Zsuzsa Kreizinger, Dénes Grózner, Olimpia Kursa, Grzegorz Tomczyk, and Miklós Gyuranecz
Springer Science and Business Media LLC
Abstract Background Mycoplasma anserisalpingitidis is an emerging waterfowl pathogen associated with reproductive tract infections, embryo mortality, and reduced egg production. While direct and vertical transmission routes have been described, its environmental persistence remains poorly understood. In waterfowl production systems, open water sources can be used for drinking and bathing, potentially facilitating indirect transmission. Prolonged survival in such environments may extend the period during which birds are exposed to the pathogen. Understanding the ability of M. anserisalpingitidis to survive outside the host, particularly under environmental stress, is essential for assessing transmission risks. Results This study evaluated the survival of two M. anserisalpingitidis strains in water at environmental temperatures of 0 °C, 4 °C, and 22 °C. To our knowledge, this is the first study to compare environmental survival between two strains of an avian mycoplasma species. Survival was found to be both temperature-dependent and strain-specific. Strain A remained viable for up to 12 days at 0 °C and 8 days at 4 °C, while strain B survived for the entire 28-day experiment at both temperatures. At 22 °C, strain A lost viability within 24 h, while strain B persisted for 3 days. qPCR analysis of DNA concentrations confirmed these survival patterns, indicating better recovery of strain B under low-temperature conditions. Conclusions These findings demonstrate the capacity of M. anserisalpingitidis to persist in cold water and highlight the potential role of water sources as environmental reservoirs contributing to indirect transmission in waterfowl farming. The results emphasize the importance of considering water systems as potential environmental reservoirs when designing biosecurity and disease control strategies.
Eszter Zsófia Nagy, Dorottya Földi, Fruzsina Madzig, Enikő Wehmann, Adél Orosz, András Kempf, László Buza, János Mátyus, László Búza, Dénes Grózner,et al.
Springer Science and Business Media LLC
Abstract Background Mycoplasma (M.) hyopharyngis, M. hyopneumoniae, M. hyorhinis, and M. hyosynoviae can all be transiently present in the swine tonsils without causing any clinical signs or lesions. M. hyopharyngis is considered a commensal bacterium, however, our knowledge about its prevalence and pathogenic capabilities is lacking. M. hyopneumoniae, M. hyorhinis and M. hyosynoviae are widespread pathogens, responsible for significant economic losses. M. hyopneumoniae is known as the causative agent of porcine enzootic pneumonia, while M. hyorhinis and M. hyosynoviae are associated with arthritis and polyserositis. The objective of this study was to evaluate the detection rates of these mycoplasmas in Central-Eastern Europe (Croatia, the Czech Republic, Hungary, and Slovakia) through a cross-sectional investigation. In parallel, a novel quantitative polymerase chain reaction (qPCR) assay was designed targeting M. hyopharyngis to facilitate the identification of this bacterium. Results Tonsils of 15 animals per herd were sampled from six-month-old fattening pigs, and a total of 150 herds were examined. Tonsils form each herd were divided into three pools, each comprising five tonsils. The samples were submitted for species-specific TaqMan assay and isolation. M. hyopharyngis was identified in 92.67% (139/150, 95% confidence interval: 87.35–95.86%) of the stocks, with successful isolation from 20 herds. Besides, M. hyopneumoniae was detected in 51.33% (77/150, 95% confidence interval: 43.40-59.19%) of the stocks. Additionally, M. hyorhinis was identified in all herds (100.00%; 150/150, 95% confidence interval: 97.50–100.00%) by qPCR examination and was successfully isolated from 107 stocks. Regarding the occurrence of M. hyosynoviae, 88.00% (132/150, 95% confidence interval: 81.83–92.27) of the herds showed positive PCR results, and the pathogen was successfully isolated in 122 cases. Moreover, the newly developed M. hyopharyngis qPCR assay proved to be a reliable and sensitive method. Conclusions This study determined the detection rates of several porcine mycoplasmas (M. hyopharyngis, M. hyopneumoniae, M. hyorhinis, and M. hyosynoviae) in fattening pigs in Central-Eastern Europe. Additionally, the developed M. hyopharyngis qPCR assay may facilitate future prevalence studies and diagnostic procedures concerning this neglected bacterium.
Ulrich Klein, Dorottya Földi, Eszter Zsófia Nagy, Lilla Tóth, Nikolett Belecz, Karola Költő, E. Wehmann, S. Marton, Marianna Merenda, M. Gastaldelli,et al.
Eszter Zsófia Nagy, Dorottya Földi, Fruzsina Madzig, Enikő Wehmann, Adél Orosz, András Kempf, László Buza, János Mátyus, László Búza, Dénes Grózner,et al.
Herman Otto Intezet Nonprofit Kft.
Vizsgálataik során a szerzők négy sertéspatogén Mycoplasma faj (Mycoplasma (M.) hyopharyngis, M. hyopneumoniae, M. hyorhinis, és M. hyosynoviae) előfordulási arányát határozták meg 150 közép-európai hízósertés-állományból származó mandulamintából. A M. hyopharyngis-t az állományok 92,67%-ában (139/150), a M. hyopneumoniae-t 51,33%-ában (77/150), a M. hyorhinis-t 100%-ában (150/150), a M. hyosynoviae-t pedig 88%-ában (132/150) tudták kimutatni PCR-tesztekkel. A vizsgált telepek 13,33%-ából (20/150) M. hyopharyngis-t, 71,33%-ából (107/150) M. hyorhinis-t és 81,33%-ából (122/150) pedig M. hyosynoviae-t sikerült kitenyészteniük.
Eszter Zsófia Nagy, Levente Szeredi, Hiromi Muramatsu, Noémi Nagy, Dénes Grózner, Zsuzsa Kreizinger, Kinga M. Sulyok, Bandana Pangabam, Lilla Tóth, Rachel H.J. Jun,et al.
Elsevier BV
Anneke Feberwee, Naola Ferguson-Noel, Salvatore Catania, Marco Bottinelli, Nadeeka Wawagema, Miklos Gyuranecz, Anne V. Gautier-Bouchardon, Inna Lysnyansky, Jeanine Wiegel, Franca Möller Palau-Ribes,et al.
Informa UK Limited
Mycoplasma gallisepticum (Mg) and Mycoplasma synoviae (Ms) are regarded as the most important avian mycoplasma species for today's chicken and turkey farming industry from a clinical and economical perspective. Control strategies for Mg and Ms have become more efficient due to investments in mycoplasma research over the last 70 years. These investments have contributed to the further implementation of serological and molecular testing, the development of vaccines, and the improvement of antimicrobial treatment strategies. However the increasing spotlight on welfare, the pressure on prudent use of antimicrobials and the expected global increase in poultry production, are expected to have an impact on the future control of avian mycoplasmas in commercial poultry. In this paper a group of avian mycoplasma experts discuss the future challenges in mycoplasma control considering the background of these expected changes and the relevance for future avian mycoplasma research.
Barbara M. Binney, Edna Gias, Jonathan Foxwell, Alvey Little, Patrick J. Biggs, Nigel French, Callum Lambert, Hye Jeong Ha, Glen P. Carter, Miklós Gyuranecz,et al.
Frontiers Media SA
In 2017 an outbreak of Mycoplasma bovis (M. bovis), an infectious agent of cattle, was identified in Aotearoa New Zealand. This study characterizes the genomic population structure of the outbreak in New Zealand and compares it with the known global population structure using multilocus sequence typing (MLST) and genomic analysis. The New Zealand outbreak strain was MLST genotyped as ST21. A comprehensive collection of 840 genomes from the New Zealand outbreak showed a pattern of clonal expansion when characterized by MLST, core genome MLST (cgMLST) and whole genome MLST (wgMLST). A lineage of genomes was found with no in silico identifiable pta2 locus, a housekeeping gene used in the MLST scheme. We compared a sample set of 40 New Zealand genomes to 47 genomes from other countries. This group had 79 ST21 genomes and eight genomes that were single nucleotide polymorphism (SNP) variants within the MLST loci of ST21. Two of the 47 international genomes showed signs of extensive unique recombination. Unique alleles in six genes were identified as present only in the New Zealand genomes. These novel variants were in the genes; haeIIIM encoding for cytosine-specific methyltransferase, cysC encoding for cysteinyl tRNA synthetase, era encoding for GTPase Era, metK encoding for S-adenosylmethionine synthase, parE encoding for DNA topoisomerase, and hisS encoding for histidine-tRNA ligase. This finding could be due to a population bottleneck, genetic drift, or positive selection. The same sample set of 40 New Zealand genomes were compared using MLST to 404 genomes from 15 other countries and 11 genomes without a known country. A FastBAPS analysis of 455 genomes showed a global population structure with 11 clusters. Some countries, such as Canada, Denmark and Australia contained both internally closely related genomes and some genomes that were more closely related to genomes found in other countries. Our results support the need for Whole Genome Sequencing (WGS) as well as MLST genotyping in M. bovis outbreaks. They also support the importance of understanding the national and international movement patterns of cattle and their genetic material, as possible routes of transmission, when managing the spread of M. bovis.
Dorottya Földi, Eszter Zsófia Nagy, Gergely Tóth, László Makrai, László Gombos, Zsuzsa Kreizinger, and Miklós Gyuranecz
Akademiai Kiado Zrt.
AbstractBackgroundMycoplasma hyopharyngis is a commensal bacterium in the upper respiratory tract of swine. As it is recognized to be apathogenic, examinations regarding this species are scarce, compared to other swine mycoplasmas. However, in a few cases, M. hyopharyngis was detected in lesions of different organs. This report presents a case study in which M. hyopharyngis (along with other bacteria) was isolated from the joint of a pig showing lameness.Case presentationA Hungarian farm was repopulated with 250 gilts and 1,700 finishers after undergoing a complete depopulation and disinfection. Two days later, cases of diarrhoea and septicaemia caused by Salmonella enterica serovar typhimurium were seen in the finishers. At the same time, following the first farrowing, swollen joints were observed in 21–25 days old piglets. Joint samples were collected, and isolation of Mycoplasma sp. and other bacteria was attempted. Analysis of the joint samples revealed the presence of Staphylococcus haemolyticus, Staphylococcus hyicus, Aerococcus viridans, Trueperella pyogenes, Streptococcus agalactiae and M. hyopharyngis.ConclusionsThis is the second isolation of M. hyopharyngis from joints, which highlights the necessity of a better understanding the biology of this often-overlooked species, and its role in the progress of arthritis or other lesions.
Árisz Ziszisz, Márton Hoitsy, Viktória Sós-Koroknai, Endre Sós, Anna Linda Nógrádi, Zsuzsa Kreizinger, Miklós Gyuranecz, and János Gál
Herman Otto Intezet Nonprofit Kft.
A szerzők egy megfelelő tartási körülmények között, de hibásan takarmányozott, rovar-monodiétán tartott, kifejlett szakállas agámában állapítottak meg heveny, légzőszervi tünetekkel járó, mind a légutakat, mind a tüdőt érintő gyulladásos folyamatokat. A légcsőben hámhyperplasia, a tüdőben nagy mennyiségű nyúlós-nyálkás tartalom felhalmozódása volt látható. A felső légutakból kinyert váladék PCR-vizsgálata során a vizsgált szakaszon a Mycoplasma iguanae-val 76%-os átfedést mutató Mycoplasma baktériumokat sikerült izolálni. Hazánkban elsőként mutattunk ki szakállas agámában klinikai tünetekben megnyilvánuló és elhullást okozó mycoplasmosist.
Dénes Grózner, Zsuzsa Kreizinger, Alexa Mitter, Katinka Bekő, Dominika Buni, Áron B. Kovács, Enikő Wehmann, Eszter Zsófia Nagy, Ádám Dobos, Ádám Dán,et al.
Informa UK Limited
AbstractThe aim of the present study was to monitor the dynamics and to measure the safety and efficacy of a live, attenuated, thermosensitive Mycoplasma anserisalpingitidis vaccine candidate, namely MA271, in geese breeder flocks under field condition. Two rearing flocks were vaccinated with MA271 at four-week of age and boosted at 24 weeks of age by cloaca inoculation (1 ml) and eye-dropping (60 µl). The geese then were transported to multi-aged breeding farms. Two breeding flocks served as controls. Colonisation of the cloaca by MA271 showed 75% maximum prevalence between 4 and 6 weeks after the first vaccination. Then the prevalence decreased to 25% until the cooler, humid fall months which coincided with the booster vaccination. Boostering raised cloacal colonisation to 100%. No clinical signs were observed in the vaccinated birds. After transportation to five multi-aged breeding farms, the wild-type strain appeared beside MA271 in three flocks. In one flock the wild-type strain completely displaced MA271, while in one flock only MA271 was detected. Only wild-type strains were detected in the control flocks, however, due to a HPAI outbreak both flocks were exterminated before the end of the study. Based on the available data the median percentage of infertile eggs were 3.7-5.1% in the MA271 vaccinated flocks, while 7.7% in the non-vaccinated flock. In conclusion MA271 is able to colonise the cloaca of geese under field condition. MA271 proved to be safe and presumably provides protection against M. anserisalpingitidis induced reproduction losses.
Lisa Käbisch, Anne-Kathrin Schink, Doris Hoeltig, Jutta Verspohl, Miklós Gyuranecz, Joachim Spergser, Corinna Kehrenberg, and Stefan Schwarz
MDPI AG
Organizations like the Clinical and Laboratory Standards Institute (CLSI) or the European Committee of Antimicrobial Susceptibility Testing (EUCAST) provide standardized methodologies for antimicrobial susceptibility testing of a wide range of nonfastidious and fastidious bacteria, but so far not for Mycoplasma spp. of animal origin. Recently, a proposed method for the standardized broth microdilution testing of Mycoplasma hyorhinis using commercial Sensititre microtiter plates was presented. In this study, we evaluated this broth microdilution method with 37 field isolates and tested their susceptibility toward the following antimicrobial agents: doxycycline, enrofloxacin, erythromycin, florfenicol, gentamicin, marbofloxacin, tetracycline, tiamulin, tilmicosin, tulathromycin, and tylosin. The isolates originated from different countries, isolation sites, and years. The broth microdilution method was carried out using a modified Friis broth as the culture and test medium. For macrolides and lincosamides, a bimodal distribution with elevated MIC values could be observed for almost half of the tested field isolates, deducing reduced susceptibility toward these substances. With a recently published protocol, we were able to test a variety of field isolates, and consistent data could be obtained. Using this method, monitoring studies of Mycoplasma hyorhinis isolates can be carried out in a comparable manner, and the observed susceptibility profiles can be screened for possible changes in MIC values in the future.
Sándor Hornok, Jenő Kontschán, Nóra Takács, Heloise Heyne, Áron Botond Kovács, Olivier Plantard, Gergő Keve, Denis Fedorov, Miklós Gyuranecz, and Ali Halajian
Springer Science and Business Media LLC
Abstract Background Among hard ticks (Acari: Ixodidae), the genus Ixodes comprises the highest number of species, which in turn are most numerous in the Afrotropical zoogeographic region. In South Africa extensive morphological studies have been performed on Ixodes species but only few reports included molecular analyses. Methods In this study, 58 Ixodes spp. ticks, collected from ten mammalian and eight avian host species in South Africa, were molecularly and phylogenetically analyzed. In addition, a newly collected sample of the Palearctic Ixodes trianguliceps was included in the analyses. Results Among the ticks from South Africa, 11 species were identified morphologically. The majority of ticks from mammals represented the Ixodes pilosus group with two species (n = 20), followed by ticks resembling Ixodes rubicundus (n = 18) and Ixodes alluaudi (n = 3). In addition, single specimens of Ixodes rhabdomysae, Ixodes ugandanus, Ixodes nairobiensis and Ixodes simplex were also found. Considering bird-infesting ticks, Ixodes theilerae (n = 7), Ixodes uriae (n = 4) and ticks most similar to Ixodes daveyi (provisionally named I. cf. daveyi, n = 2) were identified. Molecular analyses confirmed two species in the I. pilosus group and a new species (I. cf. rubicundus) closely related to I. rubicundus sensu stricto. Phylogenetic trees based on concatenated mitochondrial or mitochondrial and nuclear gene sequences indicated that the subgenus Afrixodes forms a monophyletic clade with bird-associated exophilic ticks (subgenus Trichotoixodes). Ixodes trianguliceps clustered separately whereas I. alluaudi with their morphologically assigned subgenus, Exopalpiger. Conclusions Phylogenetic analyses shed new lights on the relationships of Ixodes subgenera when including multiple sequences from subgenus Afrixodes and African as well as Palearctic species of subgenera Trichotoixodes and Exopalpiger. Subgenera Afrixodes and bird-associated Trichotoixodes share common ancestry, suggesting that the latter might have also originated in Africa. Regarding the subgenus Exopalpiger, I. alluaudi is properly assigned as it clusters among different Australian Ixodes, whereas I. trianguliceps should be excluded. Graphical Abstract
Dominika Buni, Áron Botond Kovács, Dorottya Földi, Krisztián Bányai, Krisztina Bali, Marianna Domán, Enikő Wehmann, Janet Bradbury, Marco Bottinelli, Salvatore Catania,et al.
Elsevier BV
Áron Botond Kovács, Zsuzsa Kreizinger, Barbara Forró, Dénes Grózner, Alexa Mitter, Szilvia Marton, Krisztina Bali, Anna Sawicka, Grzegorz Tomczyk, Krisztián Bányai,et al.
Herman Otto Intezet Nonprofit Kft.
A Mycoplasma anserisalpingitidis jelentős anyagi károkat okozó vízibaromfi-patogén baktérium. A vizsgálatukban a szerzők fajra jellemző, alapgénkészletre („mag” genomra) hoztak létre egy multilókusz szekvenciatipizáló sémát, amely elősegíti a M. anserisalpingitidis változatosságának pontosabb diagnosztizálását. A séma fejlesztése során 110 M. anserisalpingitidis törzset vizsgáltak, ezek elsősorban Európából származtak, de kínai és vietnámi mintákat is elemeztek. Az általuk fejlesztett tipizáló módszer segítségével sikeresen azonosítottak egy állattenyésztési integrációból származó mintákat, ill. egy állományból, vagy egy állatból származó mintákat is.
Edina Nemesházi, Enikő Wehmann, Dénes Grózner, Dorottya Sára Nagy, Áron Botond Kovács, Dorottya Földi, Zsuzsa Kreizinger, and Miklós Gyuranecz
Public Library of Science (PLoS)
Waterfowl-specific mycoplasmas cause significant economic losses worldwide. However, only limited resources are available for the specific detection of three such bacteria, Mycoplasma anatis, M. anseris and M. cloacale. We developed species-specific TaqMan assays and tested their reliability across 20 strains of the respective target species as well as 84 non-target avian bacterial strains. Furthermore, we analysed 32 clinical DNA samples and compared the results with those of previously published conventional PCRs. The TaqMan assays showed 100% specificity and very high sensitivity, enabling the detection of target DNA as low as either 10 or 100 copies/μl concentration, depending on the assay. Importantly, we found that while the here developed TaqMan assays are reliable for species-specific detection of M. anatis, the previously published conventional PCR assay may give false positive results. In conclusion, the new assays are reliable, sensitive and suitable for clinical diagnostics of the target species.
Áron B. Kovács, Enikő Wehmann, Dénes Grózner, Krisztina Bali, Edina Nemesházi, Veronika Hrivnák, Chris J. Morrow, Krisztián Bányai, Zsuzsa Kreizinger, and Miklós Gyuranecz
Elsevier BV
István Filipsz, Ervin Albert, Imre Biksi, Dorottya Földi, Miklós Gyuranecz, Zsolt György, and József Földi
Herman Otto Intezet Nonprofit Kft.
A szerzők hízósertéseken, nagyüzemi körülmények között vizsgálták 10 mg/ttkg, ivóvízben, 5 napon át adagolt tilvalozin (TVN) hatékonyságát Mycoplasma hyopneumoniae okozta légzőszervi betegség gyógy- és metafilaktikus kezelésére. A gyógyulási arány 91,7% volt a TVN, 86,7% a referens kontrollcsoportban, ami szignifikáns egyenértékűséget jelent. Az új megbetegedés aránya szignifikánsan kisebb volt (0,9% szemben a 4,5%-kal), valamint a légzőszervi tünetek enyhébb formában jelentek meg a TVN (átlag pontszám: 0,09, ill. 0,26), mint a kezeletlen kontrollcsoportban. Az eredmények alátámasztják a tilvalozin hatékonyságát a sertések Mycoplasma-pneumoniájának gyógy- és metafilaktikus kezelésére
Eszter Zsófia Nagy, Áron Botond Kovács, Enikő Wehmann, Katinka Bekő, Dorottya Földi, Krisztián Bányai, Zsuzsa Kreizinger, and Miklós Gyuranecz
Frontiers Media SA
IntroductionMycoplasma anserisalpingitidis is one of the most important waterfowl-pathogenic mycoplasmas. Due to inadequate antibiotic treatment, many strains with high minimal inhibitory concentration (MIC) values for multiple drugs have been isolated lately. Decreased antibiotic susceptibility in several Mycoplasma species are known to be associated with mutations in topoisomerase and ribosomal genes, but other strategies such as active efflux pump mechanisms were also described. The scope of this study was the phenotypic and genetic characterization of the active efflux mechanism in M. anserisalpingitidisMethodsWe measured the MIC values in the presence and absence of different efflux pump inhibitors (EPIs), such as carbonyl cyanide m-chlorophenylhydrazine (CCCP), orthovanadate (OV), and reserpine (RSP). Moreover, bioinformatic tools were utilized to detect putative regulatory sequences of membrane transport proteins coding genes, while comparative genome analysis was performed to reveal potential markers of antibiotic resistance.ResultsOut of the three examined EPIs, CCCP decreased the MICs at least two-fold below the original MICs (in 23 cases out of 36 strains). In the presence of OV or RSP, MIC value differences could be seen only if modified dilution series (10% decrease steps were used instead of two-fold dilutions) were applied (in 24/36 cases with OV and 9/36 with RSP). During comparative genome analysis, non-synonymous single nucleotide polymorphisms (nsSNPs) were identified in genes encoding ABC membrane transport proteins, which were displayed in higher percentages in M. anserisalpingitidis strains with increased MICs. In terms of other genes, a nsSNP was identified in DNA gyrase subunit A (gyrA) gene which can be related to decreased susceptibility to enrofloxacin. The present study is the first to highlight the importance of efflux pump mechanisms in M. anserisalpingitidis.DiscussionConsidering the observed effects of the EPI CCCP against this bacterium, it can be assumed, that the use of EPIs would increase the efficiency of targeted antibiotic therapy in the future control of this pathogen. However, further research is required to obtain a more comprehensive understanding of efflux pump mechanism in this bacterium.
Dorottya Földi, Zsófia Eszter Nagy, Nikolett Belecz, Levente Szeredi, József Földi, Anna Kollár, Miklós Tenk, Zsuzsa Kreizinger, and Miklós Gyuranecz
Frontiers Media SA
IntroductionMycoplasma hyorhinis is an emerging swine pathogen with high prevalence worldwide. The main lesions caused are arthritis and polyserositis, and the clinical manifestation of the disease may result in significant economic losses due to decreased weight gain and enhanced medical costs. We aimed to compare two challenge routes to induce M. hyorhinis infection using the same clinical isolate.MethodsFive-week-old, Choice hybrid pigs were inoculated on 2 consecutive days by intravenous route (Group IV-IV) or by intravenous and intraperitoneal routes (Group IV-IP). Mock-infected animals were used as control (control group). After the challenge, the clinical signs were recorded for 28 days, after which the animals were euthanized. Gross pathological and histopathological examinations, PCR detection, isolation, and genotyping of the re-isolated Mycoplasma sp. and culture of bacteria other than Mycoplasma sp. were carried out. The ELISA test was used to detect anti-M. hyorhinis immunoglobulins in the sera of all animals.ResultsPericarditis and polyarthritis were observed in both challenge groups; however, the serositis was more severe in Group IV-IV. Statistically significant differences were detected between the challenged groups and the control group regarding the average daily weight gain, pathological scores, and ELISA titers. Additionally, histopathological scores in Group IV-IV differed significantly from the scores in the control group. All re-isolated strains were the same or a close genetic variant of the original challenge strain.DiscussionOur results indicate that both challenge routes are suitable for modeling the disease. However, due to the evoked more severe pathological lesions and the application being similar to the hypothesized natural route of infection in Group IV-IV, the two-dose intravenous challenge is recommended by the authors to induce serositis and arthritis associated with M. hyorhinis infection.
Sara M. Klose, Olusola M. Olaogun, Jillian F. Disint, Pollob Shil, Miklós Gyuranecz, Zsuzsa Kreizinger, Dorottya Földi, Salvatore Catania, Marco Bottinelli, Arianna Dall'Ora,et al.
American Society for Microbiology
Preventative measures, such as vaccination, are commonly used for the control of mycoplasmal infections in poultry. A live attenuated vaccine strain (Vaxsafe MS; MS-H; Bioproperties Pty.
Tamara Szentiványi, Sándor Hornok, Áron B. Kovács, Nóra Takács, Miklós Gyuranecz, Wanda Markotter, Philippe Christe, and Olivier Glaizot
Wiley
Katinka Bekő, Eszter Zsófia Nagy, Dénes Grózner, Zsuzsa Kreizinger, and Miklós Gyuranecz
Akademiai Kiado Zrt.
Abstract Several Mycoplasma species can form biofilm, facilitating their survival in the environment, and shielding them from therapeutic agents. The aim of this study was to examine the biofilm-forming ability and its potential effects on environmental survival and antibiotic resistance in Mycoplasma anserisalpingitidis, the clinically and economically most important waterfowl Mycoplasma species. The biofilm-forming ability of 32 M. anserisalpingitidis strains was examined by crystal violet assay. Biofilms and planktonic cultures of the selected strains were exposed to a temperature of 50 °C (20 and 30 min), to desiccation at room temperature (16 and 24 h), or to various concentrations of eight different antibiotics. Crystal violet staining revealed great diversity in the biofilm-forming ability of the 32 tested M. anserisalpingitidis strains, with positive staining in more than half of them. Biofilms were found to be more resistant to heat and desiccation than planktonic cultures, while no correlation was shown between biofilm formation and antibiotic susceptibility. Our results indicate that M. anserisalpingitidis biofilms may contribute to the persistence of the organisms in the environment, which should be taken into account for proper management. Antibiotic susceptibility was not affected by biofilm formation; however, it is important to note that correlations were examined only in vitro.
Ulrich Klein, Dorottya Földi, Nikolett Belecz, Veronika Hrivnák, Zoltán Somogyi, Michele Gastaldelli, Marianna Merenda, Salvatore Catania, Arkadiusz Dors, Ute Siesenop,et al.
Public Library of Science (PLoS)
Mycoplasma hyorhinis is an emerging swine pathogen bacterium causing polyserositis and polyarthritis in weaners and finishers. The pathogen is distributed world-wide, generating significant economic losses. No commercially available vaccine is available in Europe. Therefore, besides improving the housing conditions for prevention, antimicrobial therapy of the diseased animals is the only option to control the infection. Our aim was to determine the minimal inhibitory concentrations (MIC) of ten antimicrobials potentially used against M. hyorhinis infection. The antibiotic susceptibility of 76 M. hyorhinis isolates from Belgium, Germany, Hungary, Italy and Poland collected between 2019 and 2021 was determined by broth micro-dilution method and mismatch amplification mutation assay (MAMA). Low concentrations of tiamulin (MIC90 0.312 μg/ml), doxycycline (MIC90 0.078 μg/ml), oxytetracycline (MIC90 0.25 μg/ml), florfenicol (MIC90 2 μg/ml) and moderate concentrations of enrofloxacin (MIC90 1.25 μg/ml) inhibited the growth of the isolates. For the tested macrolides and lincomycin, a bimodal MIC pattern was observed (MIC90 >64 μg/ml for lincomycin, tulathromycin, tylosin and tilmicosin and 5 μg/ml for tylvalosin). The results of the MAMA assay were in line with the conventional method with three exceptions. Based on our statistical analyses, significant differences in MIC values of tiamulin and doxycycline were observed between certain countries. Our results show various levels of antimicrobial susceptibility among M. hyorhinis isolates to the tested antibiotics. The data underline the importance of susceptibility monitoring on pan-European level and provides essential information for proper antibiotic choice in therapy.
Sándor Hornok, Sándor Szekeres, Gábor Horváth, Nóra Takács, Katinka Bekő, Jenő Kontschán, Miklós Gyuranecz, Barnabás Tóth, Attila D. Sándor, Alexandra Juhász,et al.
Elsevier BV
RECENT SCHOLAR PUBLICATIONS
MOST CITED SCHOLAR PUBLICATIONS
GRANT DETAILS
2022-2027 Lendület II (Momentum) program
2022-2026 National Laboratory of Infectious Animal Diseases, Antimicrobial Resistance, Veterinary Public Health and Food Chain Safety
2022-2026 National Laboratory of Health Safety
2022-2025 Improving the diagnostics and control of production and zoonotic diseases of poultry and wild birds
2021-2023 Antimicrobial resistance in animal production
2021-2025 Characterization of Mycoplasma iowae strains and improving the therapy of infection
2019-2023 Novel strategies in Mycoplasma control
2019-2021 Pan-European resistance monitoring program of M. hyorhinis
2018-2020 Mycopath III: Pan-European resistance monitoring program of M. bovis, M. hypneumoniae, M. gallisepticum and M. synoviae
2017-2021 Studying the virulence mechanisms of Mycoplasma gallisepticum and M. synoviae
2016-2020 Improving the control of Mycoplasma synoviae infection
2015-2016 Mycopath II: Pan-European resistance monitoring program of M. bovis, M. hypneumoniae, M. gallisepticum and M. synoviae
2013-2016 EU FP7-HEALTH-2013-INNOVATION-1:
2012-2017 Lendület I (Momentum) program
2012 National Institute of Health – USA (NIH) travel grant
2012 Hungarian Academy of Sciences Junior Travel Award
2010-2012 Mycopath I: Pan-European resistance monitoring program of M. bovis, M. hypneumoniae, M. gallisepticum and M. synoviae
2009-2012 Comparative characterization of Francisella tularensis strains
RESEARCH OUTPUTS (PATENTS, SOFTWARE, PUBLICATIONS, PRODUCTS)
- P 21 00357: Live, attenuated Mycoplasma anserisalpingitidis vaccine candidate
- Beside fundamental research we provide diagnostic, contract and training services globally.
- We produce In Vitro Diagnostics (IVD) under our own brand and sell know-how under royalty agreement to different producers.
- We are proud that BioChek B.V. (The Netherlands), the global market leader company in the field of poultry diagnostics, has bought under a royalty agreement our DIVA tests which differentiate Mycoplasma gallisepticum and M. synoviae wild-type and vaccine strains.
CONSULTANCY
My team collaborate with farmers, veterinarians, contract sponsors and academic institutions. Our multidisciplinary team is qualified and experienced in conducting a wide range of studies from laboratory related research and development projects, via animal facility based experiments to field studies.
We also provide diagnostic services globally. During our servicies we help to design the sampling to be the most appropriate and cost-effective for each special case. We help to interpret the results and give personal advice, such as what additional diagnostic tests can be performed. We are also able to suggest treatment options as well as eradication and control measures such as vaccination or monitoring plan.
Industry, Institute, or Organisation Collaboration
We collaborate with several research institutions, like:
- University of Veterinary Medicine and Pharmacy, Slovakia
- University of Pennsylvania, USA
- Royal GD, the Netherlands
- Istituto Zooprofilattico Sperimentale della Venezie, Italy
- Kimron Veterinary Institute, Israel
- The University of Melbourne, Australia
- ANSES, France
We have several industry partners, like:
- Bioproperties Pty LtD., Australia
- Huvepharma NV, Belgium
- CEVA Sante Animale, France
- BioChek BV, the Netherlands
- FarmPharma, Sweden
STARTUP
We opened MolliScience Ltd., our Startup company specialised on Mycoplasma diagnostic & biotech services. We turn our know-how and fundamental research results into application. We develop In Vitro Diagnostics (IVD) under our own brand and we run vaccine invention research projects.