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Monitoring of Selected Genes in Campylobacter Jejuni and Campylobacter Coli Isolates from Domestic Animals

References 1. Andrzejewska M., Klawe J.J., Szczepańska B., Śpica D.: Occurrence of virulence genes among Campylobacter jejuni and Campylobacter coli isolates from domestic animals and children. Pol J Vet Sci 2011, 2 , 207-211. 2. Bang D.D., Scheutz F., Ahrens P., Pedersen K., Blom J., Madsen M.: Prevalence of cytolethal distending toxin (cdt) genes and CDT production in Campylobacter spp. isolated from Danish broilers. J Med Microbiol 2001, 50 , 1087-1094. 3. Carvalho A.C., Ruiz-Palacios G

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Varying abundance and dispersal of the two-spotted spider mite (Tetranychus urticae Koch, 1836, Acari: Prostigmata: Tetranychidae) on Mi-tomato plants differing in allelic combination

behavior of two potato aphid clones with differing levels of virulence. Entomol. Exp. Appl. 135: 295-307. Rossi M., Goggin F. L., Milligan S. B., Kaloshian I., Ullman D. E., Williamson V. M. 1998. The nematode resistance gene Mi of tomato confers resistance against the potato aphid. Proc. Natl. Acad. Sci. USA 95: 9750-9754. Simmons A. T., Gurr G. M. 2005. Trichomes of Lycopersicon species and their hybrids: effects on pests and natural enemies. Agric. For. Entomol. 7: 265-276. Smith C. M

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Epidemiological and Clinical Characteristics of 28 Cases of Cholera

References 1. Huang YL. Clinical Infectious Diseases. Beijing: People’s Medical Publishing House, 1990:246-253. 2. Peng WW. Epidemiology fifth edition. Beijing: People’s Health Publishing House, 2002:156-157. 3. Harris JB, LaRocque RC, Qadri F, Ryan ET, Calderwood SB. Cholera. Lancet 2012;379(9835):2466-2476. 4. Jiang LJ, Wang R, Qiao Y, Wang BR. O1 group O139 and non-O1 Vibrio cholerae virulence comparative study. Adv Microbial Immunol 1995; 23:1-11. 5. Duan YQ, Yang B, Cui JD

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Histopathological and cytopathological findings in minipigs infected with Streptococcus suis serotype 2

to increase susceptibility of piglets to challenge by Streptococcus suis type II. J Virol 2001, 75, 4889-4895. 6. Fittipaldi N., Sekizaki T., Takamatsu D., de la Cruz Domínguez- Punaro M., Harel J., Bui N.K., Vollmer W., Gottschalk M.: Significant contribution of the pgdA gene to the virulence of Streptococcus suis. Mol Microbiol 2008, 70, 1120-1135. 7. Glass-Kaastra S.K., Pearl D.L., Reid-Smith R., McEwen B., Slavic D., Fairles J., McEwen S.A.: Multiple-class antimicrobial resistance surveillance in swine Escherichia coli F4

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Genetic changes in pigeon paramyxovirus type-1 induced by serial passages in chickens and microscopic lesions caused by the virus in various avian hosts

Haas N., Braber M., Römer-Oberdörfer A., van den Elzen P., van der Marel P.: Newcastle disease virus (NDV) marker vaccine: an immunodominant epitope on the nucleoprotein gene of NDV can be deleted or replaced by a foreign epitope. J Virol 2002, 76, 10138–10146. 23. Meng C., Qiu X., Yu S., Li C., Sun Y., Chen Z., Liu K., Zhang X., Tan L., Song C., Liu G., Ding C.: Evolution of Newcastle disease virus quasispecies diversity and enhanced virulence after passage through chicken air sacs. J Virol 2015, 90, 2052–2063. 24. Meulemans G., van den Berg T

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Siderophore production by Gram-negative rods isolated from human polymicrobial infections

. Scand. 2: 450-454. Dean C. R., Poole K. 1993. Cloning and characterization of the ferric enterobactin receptor gene ( pfeA ) of Pseudomonas aeruginosa . J. Bacteriol. 175: 317-324. Dorsey C. W., Tomaras A. P., Connerly P. L., Tolmasky M. E., Crosa J. H., Actis L. A. 2004. The siderophore-mediated iron acquisition systems of Acinetobacter baumannii ATCC 19606 and Vibrio anguillarum 775 are structurally and functionally related. Microbiology 150: 3657-3667. Faraldo-Gómez J. D., Sansom M

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Proteus sp. – an opportunistic bacterial pathogen – classification, swarming growth, clinical significance and virulence factors

-7181. BELAS, R., MANOS, J., SUVANASUTHI, R. 2004. Proteus mirabilis ZapA metalloprotease degrades a broad spectrum of substrates, including antimicrobial peptides. Infect. Immun.72: 5159-5167. BELAS, R., SUVANASUTHI, R. 2005. The ability of Proteus mirabilis to sense surfaces and regulate virulence gene expression involves FliL, a flagellar basal body protein. J. Bacteriol. 187: 6789-6803. BERLICKI, L., BOCHNO, M., GRABOWIECKA, A., BIAŁAS, A., KOSIKOWSKA, P., KAFARSKI, P. 2011. N-substituted aminomethanephosphonic and aminomethane- P

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Genotypic Markers of Yersinia Enterocolitica O:9 Isolated from Cows Positive in Serological Examination for Bovine Brucellosis

by immunomagnetic separation, nested polymerase chain reactions and colorimetric detection of amplified DNA. Appl Environ Microbiol 1993, 59 , 2938-2944. 9. Kot B., Piechota M., Jakubczak A.: Analysis of occurrence of virulence genes among Yersinia enterocolitica isolates belonging to different biotypes and serotypes. Pol J Vet Sci 2010, 13 , 13-19. 10. Kot B.: Chromosomally and plasmid-encoded virulence determinants of Y. enterocolitica. Medycyna Wet 2010, 66, 294-298. 11. Lubeck P.S., Skurnik M., Akrens

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Response of Lithuanian Winter Wheat Advanced Lines to Common Bunt (Tilletia tritici (BJERK.) WINT)

References Anonymous (2006). Bundesssortenamt. Beschreibende Sortenliste 2006. Hannover GmbH. 271 p. Blažkova, V., Bartoš, P. (2002). Virulence pattern of European bunt samples ( Tilletia tritici and T. leavis ) and sources of resistance. Cereal Res. Commun.,   30 (3/4), 335--342. Bonman, J.M., Bockelman, H.E., Goates, B.J., Don Obert, E., McGuire, P.E., Qualset, C.O., Hijmans, R.J. (2006). Geographic distribution of common and dwarf bunt resistance in landraces of Triticum

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Phenotypic and Genotypic Antimicrobial Resistance of Lactococcus Sp. Strains Isolated from Rainbow Trout (Oncorhynchus Mykiss)

PFGE analysis. Lett Appl Microbiol 2011, 53, 614-619. 27. Turker H, Yildirim A.B, Karakas F.P.: Sensitivity of bacteria isolated from fish to some medicinal plants. Turk J Fish Aquat Sc 2009, 9, 181-186. 28. Van T.T.H, Chin J, Chapman T, Tran L.T, Coloe P.J.: Safety of raw meat and shellfish in Vietnam: an analysis of Escherichia coli isolations for antibiotic resistance and virulence genes. Int J Food Microbiol 2008, 124, 217-223. 29. Vendrell D, Balcázar J.L, Ruiz-Zarzuela I, Gironés O, Múzquiz J.L.: Lactococcus garvieae in fish: A review. Comp Immunol

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