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Genotypic characterization of Enterococcus species isolated from the oral cavity and their pattern of antibiotic susceptibility

by performing specific gene uniplex polymerase chain reaction (PCR) for E. faecalis and E. faecium as previously described [ 3 ]. Identification of putative virulence genes; efaA (gene for endocarditis), gelE (gene for gelatinase), ace (gene for collagen binding antigen), asa (gene for aggregation substance), cylA (gene for cytolysin activator), and esp (gene for surface adhesin) of E. faecalis and E. faecium were performed as described previously ( Table 1 ) . Table 1 Primers used to identify species and to detect the virulence genes

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Susceptibility To Caspofungin And Fluconazole And Als1/Als3 Gene Expression In Biofilm And Dispersal Cells Of Candida Albicans / Profil Osjetljivosti Na Kaspofungin I Flukonazol I Ekspresija Gena Als1 I Als3 U Stanicama Biofilma Te Planktonskim Stanicama Vrste Candida Albicans

;26: e1000828. 15. Uppuluri P, Pierce CG, Thomas DP, Bubeck SS, Saville SP, Lopez-Ribot JL. The transcriptional regulator Nrg1p controls Candida albicans biofilm formation and dispersion. Eukaryot Cell 2010;9:1531-7. 16. Nailis H, Kucharikova S, Řičicova M, Van Dijck P, Deforce D, Nelis H, Coenye T. Real-time PCR expression profiling of genes encoding potential virulence factors in Candida albicans biofilms: identification of model-dependent and - independent gene expression. BMC Microbiol 2010;16:114. 17. Nett JE

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Assessment of Tryptophol Genotoxicity in Four Cell Lines In Vitro: A Pilot Study with Alkaline Comet Assay

USA 2004;101:5048-52. Chen H, Fink GR. Feedback control of morphogenesis in fungi by aromatic alcohols. Genes Dev 2006;20:1150-61. Enjalbert B, Whiteway M. Release from quorum-sensing molecules triggers hyphal formation during Candida albicans resumption of growth. Eukaryot Cell 2005;4:1203-10. Lo H-J, Köhler JR, DiDomenico B, Loebenberg D, Cacciapuoti A, Fink GR. Nonfilamentous C. albicans mutants are avirulent. Cell 1997;90:939-49. Ghosh S, Kebaara BW, Atkin

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Indoor Exposure to Mould Allergens

J, Pontón J. Garaizar J. Genes and molecules involved in Aspergillus fumigatus virulence. Rev Iberoam Micol 2005;22:1-23. Madan T, Priyadarsiny P, Vaid M, Kamal N, Shah A, Haq W, Bandacharya Katti S, Usha Sarma P. Use of a synthetic peptide epitope of Asp f 1, a major allergen or antigen of Aspergillus fumigatus , for improved immunodiagnosis of allergenic bronchopulmonary aspergillosis. Clin Diagn Lab Immunol 2004;11:552-8. Latgé JP. Aspergillus fumigatus and Aspergillosis. Clin Microbiol Rev 1999

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Phenotypic and Genotypic Characteristics of Enterocin Producing Enterococci against Pathogenic Bacteria

enterocin EJ97 production by Enterococcus faecalis EJ97 are located on a conjugative plasmid. Appl Environ Microbiol. 62, 1633-1641. http://dx.doi.org/10.1128/AEM.69.3.1633-1641.2003 PMCid:PMC150074 19. Vankerckhoven, V., Van Autgaerden, T., Vael, C., Lammens, C., Chapelle, S., Rossi, R., Jabes, D., Goossens, H. (2004). Development of a multiplex PCR for the detection of asa1, gelE, cylA, esp and hyl genes in enterococci and survey for virulence determinants among European hospital isolates of Enterococcus faecium. J Clin Microbiol. 42, 4473-4479. http

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Identification of Periopathogenes from Dental Plaque in Periodontal Patients with PCR Technique and Their Association with Composite Interleukin-1 Genotype

Kameswara Subrahmanya Lakkakula B, Venugopal P, Paul SF, Rao SR.Polymorphic regions in the interleukin-1 gene and susceptibility to chronic periodontitis: a genetic association study. Genet Test Mol Bio-markers. 2015 Apr; 19(4): 175–81. doi: 10.1089/gtmb.2014.0275. Epub 2015 Feb 24. 7. Puri K, Chhokra M, Dodwad V, Puri N. Association of interleukin-1 α (-889) gene polymorphism in patients with generalized aggressive and chronic periodontitis.Dent Res J (Isfahan). 2015 Jan-Feb; 12(1): 76–82. 8. Paster BJ, Boches SK, Galvin JL, Ericson RE, Lau CN, Levanos VA

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in PRILOZI
Brief communication (Original). Differentially expressed genes of Naegleria fowleri during exposure to human neuroblastma cells

, Lin J, et al. Comparing gene discovery from Affymetrix GeneChip microarrays and Clontech PCR-select cDNA subtraction: a case study. BMC Genomics. 2004; 5: 26. 10. Lacrue AN, Jamus AA, Beerntsen BT. The novel Plasmodium gallinaceum sporozoite protein, Pg93, is preferentially expressed in the nucleus of oocyst sporozoites. Am J Trop Med Hyg. 2005; 73:634-43. 11. Florent I, Porcel BM, Guillaume E, Silva CD, Artiguenave F, Maréchal E, et al. A Plasmodium falciparum FcB1-schizont-EST collection providing clues to schizont specific gene

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Original article. Electron micrographs of human and avian influenza viruses with high and low pathogenicity

Abstract

Background: An outbreak of highly pathogenic avian influenza (HPAI) H5N1 virus in Thailand was first reported in 2004. To date, electron micrographs demonstrating the morphology of HPAI H5N1 virus particle are quite limited.

Objective: To demonstrate the morphology of HPAI H5N1 virus particles, avian influenza viruses with low pathogenicity, seasonal influenza viruses, and H5N1 structural components in infected cells. The M amino acid residues that might affect the viral morphology were also analyzed.

Methods: Electron micrographs of negatively-stained virus particles and positively-stained thin sections of the HPAI H5N1 virus infected cells were visualized under a transmission electron microscope. M amino acid sequences of the study viruses were retrieved from the GenBank database and aligned with those of reference strains with known morphology and residues that are unique for the morphological type of the virus particles.

Results: Morphologically, three forms of influenza virus particles, spherical, regular, and irregular rods, and long filamentous particles, were demonstrated. However, the spherical form was the most predominant morphological type and accounted for more than 80% of the virus populations examined. In addition, the viral entry and exit steps including incomplete particles in infected Madin-Darby canine kidney cells were visualized. Our analyses did not find any M amino acid residues that might influence the viral morphology.

Conclusion: Of all virus isolates studied, we demonstrated that the spherical particles were the major population observed regardless of virus subtype, host of origin, virus virulence, or passage history. Our study suggested that the morphology of influenza virus particles released, might not be strongly influenced by M gene polymorphism.

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Sensitivity enhancement of nucleic acid detection by lateral flow strip test using UV crosslink method

detection of infectious spleen and kidney necrosis virus by loop-mediated isothermal amplification combined with a lateral flow dipstick. Archives of Virology. 2010; 155:385-9. 7. Odenthal KJ, Gooding JJ. An introduction to electrochemical DNAbiosensors. Analyst. 2007; 132: 603-10. 8. Noguera P, Posthuma-Trumpie G, van Tuil M, van der Wal F, de Boer A, Moers A, et al. Carbon nanoparticles in lateral flow methods to detect genes encoding virulence factors of Shiga toxin-producing Escherichia coli. Analytical and Bioanalytical Chemistry. 2011

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A step forward into respiratory genetics: overview contribution of genetics in respiratory diseases

. Novel CFTR mutations in a Korean infant with cystic fibrosis and pancreatic insufficiency. J Korean Med Sci. 2010; 25:163-5. 6. Collins F. Genetics terminology for respiratory physicians. Paediatr Respir Rev. 2009; 10:124-33. 7. Fu J, Festen EA, Wijmenga C. Multi-ethnic studies in complex traits. Hum Mol Genet. 2011; 20:R206-13. 8. Ober C, Hoffjan S. Asthma genetics 2006: the long and winding road to gene discovery. Genes Immun. 2006; 7:95-100. 9. Moffatt MF, Kabesch M, Liang L, Dixon AL, Strachan D

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