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processes in a large number of species ( Kassen and Rainey, 2004 ; Mes, 2008 ).
Until recently, however, population genetics studies have mostly employed a
very limited number of loci due to sequencing and labor expenses ( Butlin, 2010 ).
With the present flood of new data unleashed by the arrival of affordable,
rapid, high-quality sequencing technologies, the focus is rapidly shifting from the
mechanics of generating sequence data to the problems of analyzing it. This cre-
ates an urgent need for better ways to compare and visualize genomic data ( Field
et al., 2006 ). By analogy with the application of the Human Variome Database
( Ring et al., 2006 ), an important aim of microbial pathogenomics would be devel-
opment of a Microbial Variome Database ( Chattopadhyay et al., 2013 ). Such a
database would constitute a species-specific genomic resource. The information
about all the changes in sequence, origin of isolation of the strains where such
changes accumulated and their potential adaptive values will bring bacterial evo-
lutionary genomics to a new level, both quantitatively and qualitatively, offering
broad applicability of population genomics tools to experimental research, clini-
cal diagnostics, epidemiology, and environmental control of pathogens. Similar
to the case with the human genome, such a database would be extremely helpful
to associate genetic variation in bacteria (such as gene presence/absence or muta-
tion) with the bacterial ability to cause disease and, thus, greatly contribute to
understanding virulence evolution. It would provide genome-wide information on
potential targets for vaccines, antibiotics, and other therapeutics development on
one hand, while on the other it would offer a global surveillance system to enable
rapid determination of newly emerging pathogenic clones and genetic mecha-
nisms behind the emergence.
REFERENCES
Al-Hasani, K., Henderson, I.R., Sakellaris, H., et al., 2000. The sigA gene which is borne on the she
pathogenicity island of Shigella lexneri 2a encodes an exported cytopathic protease involved
in intestinal luid accumulation. Infect. Immun. 68 (5), 2457-2463 .
Allen, S.J., Martinez, E.G., Gregorio, G.V., Dans, L.F., 2010. Probiotics for treating acute infectious
diarrhoea. [Meta-Analysis Review]. Cochrane Database Syst. Rev. (11) CD003048 .
Ambrozic, J., Ostroversnik, A., Starcic, M., Kuhar, I., Grabnar, M., Zgur-Bertok, D., 1998.
Escherichia coli CoIV plasmid pRK100: genetic organization, stability and conjugal transfer.
Microbiology 144 (Pt 2), 343-352 .
Andersson, S.G., Zomorodipour, A., Andersson, J.O., et al., 1998. The genome sequence of Rickett-
sia prowazekii and the origin of mitochondria. Nature 396 (6707), 133-140 .
Asadulghani, M., Ogura, Y., Ooka, T., et al., 2009. The defective prophage pool of Escherichia coli
O157 prophage-prophage interactions potentiate horizontal transfer of virulence determinants.
PLoS Pathog. 5 (5), e1000408 .
Asakura, M., Hinenoya, A., Alam, M.S., et al., 2007. An inducible lambdoid prophage encoding
cytolethal distending toxin (Cdt-I) and a type III effector protein in enteropathogenic Esch-
erichia coli . Proc. Natl. Acad. Sci. USA 104 (36), 14483-14488 .
Baur, B., Hanselmann, K., Schlimme, W., Jenni, B., 1996. Genetic transformation in freshwater:
Escherichia coli is able to develop natural competence. Appl. Environ. Microbiol. 62 (10),
3673-3678 .
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