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C, Wassenaar TM, Javed MA, Snipen L, Lagesen K, et al. Genomic characterization of Campylobacter jejuni strain M1. PLoS A single five: e12253. 30. Chen Y, Mukherjee S, Hoffmann M, Kotewicz ML, Young S, et al. Whole-genome sequencing of gentamicin-resistant Campylobacter coli isolated from U.S. retail meats reveals novel plasmid-mediated aminoglycoside resistance genes. Antimicrob Agents Chemother 57: 53985405. 31. Edgar RC MUSCLE: many sequence alignment with higher accuracy and high throughput. Nucleic Acids Res 32: 17921797. 32. Cost MN, Dehal PS, Arkin AP FastTree 2--approximately maximumlikelihood trees for big alignments. PLoS One particular five: e9490. 33. Snipen L, Almoy T, Ussery DW Microbial comparative pan-genomics working with binomial mixture models. Bmc Genomics 10: 385. 34. Biggs PJ, Fearnhead P, Hotter G, 1655472 Mohan V, Collins-Emerson J, et al. Whole-genome comparison of two Campylobacter jejuni isolates on the very same sequence form reveals numerous loci of diverse ancestral lineage. PLoS One particular six: e27121. 35. Rasko DA, Rosovitz MJ, Myers GS, Mongodin EF, Fricke WF, et al. The pangenome structure of Escherichia coli: comparative genomic analysis of E. coli commensal and pathogenic isolates. Journal of Bacteriology 190: 68816893. 36. Stahl M, Friis LM, Nothaft H, Liu X, Li J, et al. L-fucose utilization delivers Campylobacter jejuni with a competitive advantage. Proc Natl Acad Sci U S A 108: 71947199. 37. Sheppard SK, Dallas JF, Wilson DJ, Strachan NJ, McCarthy ND, et al. Evolution of an agriculture-associated illness causing Campylobacter coli clade: evidence from national surveillance information in Scotland. PLoS A single five: e15708. 38. Fraser C, Hanage WP, Spratt BG Recombination and the nature of bacterial speciation. Science 315: 476480. 39. Sheppard SK, Colles F, Richardson J, Cody AJ, Elson R, et al. Host association of Campylobacter genotypes transcends geographic variation. Appl INCB-3344 biological activity Environ Microbiol 76: 52695277. 40. Duncan SH, Holtrop G, Lobley GE, Calder AG, Stewart CS, et al. Contribution of acetate to butyrate formation by human faecal bacteria. Br J Nutr 91: 915923. 41. Upton AM, McKinney JD Function with the methylcitrate cycle in propionate metabolism and detoxification in Mycobacterium smegmatis. Microbiology 153: 39733982. 42. Munoz-Elias EJ, Upton AM, Cherian J, McKinney JD Part of the methylcitrate cycle in Mycobacterium tuberculosis metabolism, intracellular development, and virulence. Mol Microbiol 60: 11091122. 43. de Haan CP, Llarena AK, Revez J, Hanninen ML Association of Campylobacter jejuni metabolic traits with multilocus sequence varieties. Appl Environ Microbiol 78: 55505554. 12 ~~ ~~ Macrophages, that are derived from monocytes, are expert phagocytic cells specialized in ingesting and killing pathogens. The antimicrobial activity of Ms is due, in part, to the generation of big amounts of very toxic molecules, like reactive oxygen species, including superoxide anion, hydrogen peroxide, hydroxyl radicals and hydroxyl anion, as well as reactive nitrogen species, like nitric oxide and peroxynitrite anion. These reactive species lead to oxidative harm to a wide selection of targets, including DNA. The accumulation of DNA harm in the type of oxidation, depurination, methylation, and deamination may cause single- and double-strand breaks that impact the integrity of your whole genome; when left unrepaired, these breaks can lead to cell death,. The major DSB repair pathway in bacteria is homologous recombination, which promotes strand exchange