TY - JOUR
T1 - Genomic islands from five strains of Burkholderia pseudomallei
AU - Tuanyok, Apichai
AU - Leadem, Benjamin R.
AU - Auerbach, Raymond K.
AU - Beckstrom-Sternberg, Stephen M.
AU - Beckstrom-Sternberg, James S.
AU - Mayo, Mark
AU - Wuthiekanun, Vanaporn
AU - Brettin, Thomas S.
AU - Nierman, William C.
AU - Peacock, Sharon J.
AU - Currie, Bart J.
AU - Wagner, David M.
AU - Keim, Paul
N1 - Funding Information:
AT holds a Career Development Award (May 2007–April 2009) from the NIH Pacific Southwest Regional Center of Excellence. This work was funded by NIH-NIAID grants U54 AI-065359 and U01AI-075568.
PY - 2008/11/27
Y1 - 2008/11/27
N2 - Background: Burkholderia pseudomallei is the etiologic agent of melioidosis, a significant cause of morbidity and mortality where this infection is endemic. Genomic differences among strains of B. pseudomallei are predicted to be one of the major causes of the diverse clinical manifestations observed among patients with melioidosis. The purpose of this study was to examine the role of genomic islands (GIs) as sources of genomic diversity in this species. Results: We found that genomic islands (GIs) vary greatly among B. pseudomallei strains. We identified 71 distinct GIs from the genome sequences of five reference strains of B. pseudomallei: K96243, 1710b, 1106a, MSHR668, and MSHR305. The genomic positions of these GIs are not random, as many of them are associated with tRNA gene loci. In particular, the 3′ end sequences of tRNA genes are predicted to be involved in the integration of GIs. We propose the term "tRNA-mediated site-specific recombination" (tRNA-SSR) for this mechanism. In addition, we provide a GI nomenclature that is based upon integration hotspots identified here or previously described. Conclusion: Our data suggest that acquisition of GIs is one of the major sources of genomic diversity within B. pseudomallei and the molecular mechanisms that facilitate horizontally-acquired GIs are common across multiple strains of B. pseudomallei. The differential presence of the 71 GIs across multiple strains demonstrates the importance of these mobile elements for shaping the genetic composition of individual strains and populations within this bacterial species.
AB - Background: Burkholderia pseudomallei is the etiologic agent of melioidosis, a significant cause of morbidity and mortality where this infection is endemic. Genomic differences among strains of B. pseudomallei are predicted to be one of the major causes of the diverse clinical manifestations observed among patients with melioidosis. The purpose of this study was to examine the role of genomic islands (GIs) as sources of genomic diversity in this species. Results: We found that genomic islands (GIs) vary greatly among B. pseudomallei strains. We identified 71 distinct GIs from the genome sequences of five reference strains of B. pseudomallei: K96243, 1710b, 1106a, MSHR668, and MSHR305. The genomic positions of these GIs are not random, as many of them are associated with tRNA gene loci. In particular, the 3′ end sequences of tRNA genes are predicted to be involved in the integration of GIs. We propose the term "tRNA-mediated site-specific recombination" (tRNA-SSR) for this mechanism. In addition, we provide a GI nomenclature that is based upon integration hotspots identified here or previously described. Conclusion: Our data suggest that acquisition of GIs is one of the major sources of genomic diversity within B. pseudomallei and the molecular mechanisms that facilitate horizontally-acquired GIs are common across multiple strains of B. pseudomallei. The differential presence of the 71 GIs across multiple strains demonstrates the importance of these mobile elements for shaping the genetic composition of individual strains and populations within this bacterial species.
UR - http://www.scopus.com/inward/record.url?scp=58149313638&partnerID=8YFLogxK
U2 - 10.1186/1471-2164-9-566
DO - 10.1186/1471-2164-9-566
M3 - Article
C2 - 19038032
AN - SCOPUS:58149313638
SN - 1471-2164
VL - 9
JO - BMC Genomics
JF - BMC Genomics
M1 - 566
ER -