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Dive into the research topics where Mircea Ioan Popa is active.

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Featured researches published by Mircea Ioan Popa.


BMC Microbiology | 2010

MicroDSC study of Staphylococcus epidermidis growth

Dragos Zaharia; Cezar Iancu; Alexandru T Steriade; Alexandru Muntean; Octavian Balint; Vlad Tudor Popa; Mircea Ioan Popa; Miron Bogdan

BackgroundA microcalorimetric study was carried out using a Staphylococcus epidermidis population to determine the reproducibility of bacterial growth and the variability of the results within certain experimental parameters (temperature, bacterial concentration, sample thermal history). Reproducibility tests were performed as series of experiments within the same conditions using either freshly prepared populations or samples kept in cold storage. In both cases, the samples were obtained by serial dilution from a concentrated TSB bacterial inoculum incubated overnight.ResultsThe results show that experiments are fairly reproducible and that specimens can be preserved at low temperatures (1 - 2°C) at least 4 days. The thermal signal variations at different temperatures and initial bacterial concentrations obey a set of rules that we identified.ConclusionOur study adds to the accumulating data and confirms available results of isothermal microcalorimetry applications in microbiology and can be used to standardize this method for either research or clinical setting.


Lancet Infectious Diseases | 2018

Prevalence of abdominal cystic echinococcosis in rural Bulgaria, Romania, and Turkey: a cross-sectional, ultrasound-based, population study from the HERACLES project

Francesca Tamarozzi; Okan Akhan; Carmen M. Cretu; Kamenna Vutova; Devrim Akinci; Rossitza Chipeva; Turkmen Ciftci; Corina Manuela Constantin; Massimo Fabiani; Branimir Golemanov; Denisa Janta; Patricia Mihailescu; Marin Muhtarov; Serra Orsten; Marius Petrutescu; Patrizio Pezzotti; Alexandru Cosmin Popa; Loredana Gabriela Popa; Mircea Ioan Popa; Valeri Velev; Mar Siles-Lucas; Enrico Brunetti; Adriano Casulli

BACKGROUND Cystic echinococcosis is a neglected zoonotic infection that is distributed worldwide and prioritised by WHO for control efforts. The burden of human cystic echinococcosis is poorly understood in most endemic regions, including eastern Europe. We aimed to estimate the prevalence of abdominal cystic echinococcosis in rural areas of Bulgaria, Romania, and Turkey. METHODS We did a cross-sectional ultrasound-based survey that recruited volunteers from 50 villages in rural areas of Bulgaria, Romania, and Turkey. These villages were in provinces with annual hospital incidence of cystic echinococcosis within the mid-range for the respective countries. All people who attended a session were allowed to participate if they agreed to be screened. Abdominal ultrasound screening sessions were hosted in public community structures such as community halls, primary health-care centres, schools, and mosques. Lesions were classified using an adapted WHO classification. We reported the prevalence of abdominal cystic echinococcosis adjusted by sex and age through direct standardisation, using the countrys rural population as a reference. FINDINGS From July 1, 2014, to Aug 3, 2015, 24 693 individuals presented to screening sessions and 24 687 underwent ultrasound screening. We excluded a further six indivduals due to missing data, leaving 24 681 people in our analysis. Abdominal cystic echinococcosis was detected in 31 of 8602 people screened in Bulgaria, 35 of 7461 screened in Romania, and 53 of 8618 screened in Turkey. The age and sex adjusted prevalence of abdominal cystic echinococcosis was 0·41% (95% CI 0·29-0·58) in Bulgaria, 0·41% (0·26-0·65) in Romania, and 0·59% (0·19-1·85) in Turkey. Active cysts were found in people of all ages, including children, and in all investigated provinces. INTERPRETATION Our results provide population-based estimates of the prevalence of abdominal cystic echinococcosis. These findings should be useful to support the planning of cost-effective interventions, supporting the WHO roadmap for cystic echinococcosis control. FUNDING European Union Seventh Framework Programme.


International Journal of Molecular Sciences | 2018

Nanocoatings for Chronic Wound Repair—Modulation of Microbial Colonization and Biofilm Formation

Mara Mădălina Mihai; Mădălina Preda; Iulia I. Lungu; Monica Cartelle Gestal; Mircea Ioan Popa; Alina Maria Holban

Wound healing involves a complex interaction between immunity and other natural host processes, and to succeed it requires a well-defined cascade of events. Chronic wound infections can be mono- or polymicrobial but their major characteristic is their ability to develop a biofilm. A biofilm reduces the effectiveness of treatment and increases resistance. A biofilm is an ecosystem on its own, enabling the bacteria and the host to establish different social interactions, such as competition or cooperation. With an increasing incidence of chronic wounds and, implicitly, of chronic biofilm infections, there is a need for alternative therapeutic agents. Nanotechnology shows promising openings, either by the intrinsic antimicrobial properties of nanoparticles or their function as drug carriers. Nanoparticles and nanostructured coatings can be active at low concentrations toward a large variety of infectious agents; thus, they are unlikely to elicit emergence of resistance. Nanoparticles might contribute to the modulation of microbial colonization and biofilm formation in wounds. This comprehensive review comprises the pathogenesis of chronic wounds, the role of chronic wound colonization and infection in the healing process, the conventional and alternative topical therapeutic approaches designed to combat infection and stimulate healing, as well as revolutionizing therapies such as nanotechnology-based wound healing approaches.


Journal of Microbiological Methods | 2011

Serodiagnosis of environmental mycobacterial infections.

Henriette Stavri; Irina Ulea; Dorel L. Radu; Manuela Gheorghiu Branaru; Olga Moldovan; Miron Bogdan; Cornelia Tudose; Marinela Raileanu; Dan Duiculescu; Luminita Ene; Viorel Olar; Catalin Ionita; Gabriela Loredana Popa; Mircea Ioan Popa; Patrick J. Brennan

To demonstrate the usefulness of enzyme-linked immunosorbent assay for serodiagnosis of mycobacterioses due to environmental mycobacteria we utilized a panel of glycolipid antigens selective for Mycobacterium avium-intracellulare, Mycobacterium kansasii, Mycobacterium xenopi, Mycobacterium scrofulaceum and Mycobacterium gordonae. The levels of circulating antibodies were determined against the environmental mycobacteria, and Mycobacterium tuberculosis in human immunodeficiency virus-negative and -positive patient sera. The method used immunomagnetic separation of the antigens, with covalent immobilization of antibodies to superparamagnetic amine and carboxyl terminated particles in solutions of the specific antigens. Enzyme-linked immunosorbent assay was performed on 195 patient sera: 34 with infections due to environmental mycobacteria, 114 with tuberculosis, 47 with other respiratory diseases. There were 46 human immunodeficiency virus-1 infected individuals. Among the 34 infections due to environmental mycobacteria, 9 patients were singularly infected with an environmental mycobacterium, and 25 co-infected with both M. tuberculosis and an environmental mycobacterium. Sensitivity, specificity and false positivity ranges were determined for each of the volunteer groups: tuberculosis positive, human immunodeficiency virus negative; tuberculosis positive, human immunodeficiency virus positive; those with infections due to individual environmental mycobacteria (such as M. scrofulaceum and M. kansasii); and those with other respiratory diseases. We demonstrate that such multiple assays, can be useful for the early diagnosis of diverse environmental mycobacterial infections to allow the start of treatment earlier than henceforth.


Journal of Antimicrobial Chemotherapy | 2018

Evaluation of the rapid carbapenem inactivation method (rCIM): a phenotypic screening test for carbapenemase-producing Enterobacteriaceae

Mădălina-Maria Muntean; Andrei-Alexandru Muntean; Lauraine Gauthier; Elodie Creton; Garance Cotellon; Mircea Ioan Popa; Rémy A. Bonnin; Thierry Naas

Objectives Fast and accurate diagnostic tests to identify carbapenemase-producing Enterobacteriaceae (CPE) are mandatory for proper antimicrobial therapy and implementing infection control measures. Here, we have developed a rapid Carbapenem Inactivation Method (rCIM) for CPE detection. Methods The rCIM consists of the incubation of a potential carbapenemase producer with meropenem discs and use of the resulting supernatant to challenge a susceptible indicator strain. Growth of the indicator strain is monitored using a nephelometer. The performances of the rCIM were compared with the CIM and Carba NP tests using a collection of 113 well-characterized carbapenem-resistant enterobacterial isolates, including 85 carbapenemase producers and 28 non-carbapenemase producers. In addition, rCIM was compared with the Carba NP test and PCR sequencing in a prospective analysis of 101 carbapenem-resistant enterobacterial isolates addressed to the French National Reference Center for Antimicrobial Resistance in July 2017. Results and discussion The rCIM correctly identified 84/85 carbapenemase producers and 28/28 non-carbapenemase producers, yielding a sensitivity of 99% and a specificity of 100%, slightly higher than the CIM and Carba NP test. In the prospective validation study, the rCIM showed a sensitivity and specificity of 97% and 95%, respectively. Two cephalosporinase-hyperproducing Enterobacter cloacae gave false-positive results, whereas an IMI-17-producing Enterobacter asburiae gave a false-negative result. The result was, however, positive when the isolate was grown on selective antibiotic-containing media. Conclusions The rCIM is a rapid (less than 3 h), cheap and accurate test for the detection of CPEs, which can be implemented in low-resource settings, making it a useful tool for microbiology laboratories.


Clinical & Developmental Immunology | 2018

New Insights in the Pathogenesis of HPV Infection and the Associated Carcinogenic Processes: The Role of Chronic Inflammation and Oxidative Stress

Simona Roxana Georgescu; Cristina Iulia Mitran; Madalina Irina Mitran; Constantin Caruntu; Maria Isabela Sarbu; Clara Matei; Ilinca Nicolae; Sandra Milena Tocut; Mircea Ioan Popa; Mircea Tampa

Human papillomavirus (HPV) is a small double-stranded DNA virus with tropism for epithelial cells. To this date, over 150 genotypes are known and are classified into two major groups, low-risk and high-risk strains, depending on the ability of the virus to induce malignant transformation. The hosts immunity plays a central role in the course of the infection; therefore, it may not be clinically manifest or may produce various benign or malignant lesions. The pathogenic mechanisms are complex and incompletely elucidated. Recent research suggests the role of chronic inflammation and oxidative stress (OS) in the pathogenesis of HPV infection and the associated carcinogenic processes. Chronic inflammation induces OS, which in turn promotes the perpetuation of the inflammatory process resulting in the release of numerous molecules which cause cell damage. Reactive oxygen species exert a harmful effect on proteins, lipids, and nucleic acids. Viral oncogenes E5, E6, and E7 are involved in the development of chronic inflammation through various mechanisms. In addition, HPV may interfere with redox homeostasis of host cells, inducing OS which may be involved in the persistence of the infection and play a certain role in viral integration and promotion of carcinogenesis. Knowledge regarding the interplay between chronic inflammation and OS in the pathogenesis of HPV infection and HPV-induced carcinogenesis has important consequences on the development of new therapeutic strategies.


BMC Infectious Diseases | 2014

Assessment of bacteriophage activity against local strains of Enterococcus and Pseudomonas in Romania.

Alina Cristina Neguț; Oana Săndulescu; Anca Streinu-Cercel; Zemphira Alavidze; Ioana Berciu; Veronica Ilie; Magdalena Lorena Andrei; Dana Mărculescu; Mircea Ioan Popa; Adrian Streinu-Cercel

Methods In this study we used a bacteriophage testing kit containing 4 types of Georgian products: PYO, INTESTI (Eliava BioPreparations, Tbilisi) and PHAGYO, PHAGESTI (JSC “Biochimpharm”, Tbilisi) to test the strains of Pseudomonas spp. and Enterococcus spp. isolated and stored from patients treated in the Adults II ward of the National Institute for Infectious Diseases “Prof. Dr. Matei Bals”, Romania during April 2013 – July 2014.


Current Topics in Medicinal Chemistry | 2015

Microbial Biofilms: Impact on the Pathogenesis of Periodontitis, Cystic Fibrosis, Chronic Wounds and Medical Device-Related Infections

Mara Madalina Mihai; Alina Maria Holban; Calin Giurcaneanu; Liliana Gabriela Popa; Raluca Mihaela Oanea; Veronica Lazar; Mariana Carmen Chifiriuc; Marcela Popa; Mircea Ioan Popa


BMC Microbiology | 2013

Comparative analysis of Staphylococcus aureus and Escherichia coli microcalorimetric growth

Dragos Zaharia; Alexandru Muntean; Mihnea Gabriel Popa; Alexandru Steriade; Octavian Balint; Roxana Micut; Corneliu Iftene; Ioana Tofolean; Vlad Tudor Popa; Cristian Baicus; Miron Bogdan; Mircea Ioan Popa


Indian Journal of Medical Research | 2012

Use of recombinant purified protein derivative (PPD) antigens as specific skin test for tuberculosis

Henriette Stavri; Nadia Bucurenci; Irina Ulea; Adriana Costache; Loredana Gabriela Popa; Mircea Ioan Popa

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Andrei-Alexandru Muntean

Carol Davila University of Medicine and Pharmacy

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Cristina Iulia Mitran

Carol Davila University of Medicine and Pharmacy

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Mircea Tampa

Carol Davila University of Medicine and Pharmacy

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Simona Roxana Georgescu

Carol Davila University of Medicine and Pharmacy

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Miron Bogdan

Carol Davila University of Medicine and Pharmacy

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Dragos Zaharia

Carol Davila University of Medicine and Pharmacy

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Adrian Streinu-Cercel

Carol Davila University of Medicine and Pharmacy

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