Genome sequence of Avery's virulent serotype 2 strain D39 of Streptococcus pneumoniae and comparison with that of unencapsulated laboratory strain R6

被引:353
作者
Lanie, Joel A.
ng, Wai-Leu Ng
Kazmierczak, Krystyna M.
Andrzejewski, Tiffany M.
Davidsen, Tanja M.
Wayne, Kyle J.
Tettelin, Herve
Glass, John I.
Winkler, Malcolm E.
机构
[1] Indiana Univ, Dept Biol, Bloomington, IN 47405 USA
[2] Inst Genom Res, Rockville, MD 20850 USA
[3] J Craig Venter Inst, Rockville, MD 20850 USA
关键词
D O I
10.1128/JB.01148-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Streptococcus pneumoniae (pneumococcus) is a leading human respiratory pathogen that causes a variety of serious mucosal and invasive diseases. D39 is an historically important serotype 2 strain that was used in experiments by Avery and coworkers to demonstrate that DNA is the genetic material. Although isolated nearly a century ago, D39 remains extremely virulent in murine infection models and is perhaps the strain used most frequently in current studies of pneumococcal pathogenesis. To date, the complete genome sequences have been reported for only two S. pneumoniae strains: TIGR4, a recent serotype 4 clinical isolate, and laboratory strain R6, an avirulent, unencapsulated derivative of strain D39. We report here the genome sequences and new annotation of two different isolates of strain D39 and the corrected sequence of strain R6. Comparisons of these three related sequences allowed deduction of the likely sequence of the D39 progenitor and mutations that arose in each isolate. Despite its numerous repeated sequences and IS elements, the serotype 2 genome has remained remarkably stable during cultivation, and one of the D39 isolates contains only five relatively minor mutations compared to the deduced D39 progenitor. In contrast, laboratory strain R6 contains 71 single-basepair changes, six deletions, and four insertions and has lost the cryptic pDP1 plasmid compared to the D39 progenitor strain. Many of these mutations are in or affect the expression of genes that play important roles in regulation, metabolism, and virulence. The nature of the mutations that arose spontaneously in these three strains, the relative global transcription patterns determined by microarray analyses, and the implications of the D39 genome sequences to studies of pneumococcal physiology and pathogenesis are presented and discussed.
引用
收藏
页码:38 / 51
页数:14
相关论文
共 118 条
[1]   Development of competence in Streptococcus pneumoniae:: pheromone autoinduction and control of quorum sensing by the oligopeptide permease [J].
Alloing, G ;
Martin, B ;
Granadel, C ;
Claverys, JP .
MOLECULAR MICROBIOLOGY, 1998, 29 (01) :75-83
[2]   THE AMI LOCUS OF THE GRAM-POSITIVE BACTERIUM STREPTOCOCCUS-PNEUMONIAE IS SIMILAR TO BINDING PROTEIN-DEPENDENT TRANSPORT OPERONS OF GRAM-NEGATIVE BACTERIA [J].
ALLOING, G ;
TROMBE, MC ;
CLAVERYS, JP .
MOLECULAR MICROBIOLOGY, 1990, 4 (04) :633-644
[3]   STREPTOCOCCUS-PNEUMONIAE - VIRULENCE FACTORS, PATHOGENESIS, AND VACCINES [J].
ALONSODEVELASCO, E ;
VERHEUL, AFM ;
VERHOEF, J ;
SNIPPE, H .
MICROBIOLOGICAL REVIEWS, 1995, 59 (04) :591-&
[4]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[5]   2 DIFFERENT DIHYDROOROTATE DEHYDROGENASES IN LACTOCOCCUS-LACTIS [J].
ANDERSEN, PS ;
JANSEN, PJG ;
HAMMER, K .
JOURNAL OF BACTERIOLOGY, 1994, 176 (13) :3975-3982
[6]   Resistance among Streptococcus pneumoniae:: Implications for drug selection [J].
Appelbaum, PC .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (12) :1613-1620
[7]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[8]   STUDIES ON THE CHEMICAL NATURE OF THE SUBSTANCE INDUCING TRANSFORMATION OF PNEUMOCOCCAL TYPES INDUCTION OF TRANSFORMATION BY A DESOXYRIBONUCLEIC ACID FRACTION ISOLATED FROM PNEUMOCOCCUS TYPE III [J].
Avery, Oswald T. ;
MacLeod, Colin M. ;
McCarty, Maclyn .
JOURNAL OF EXPERIMENTAL MEDICINE, 1944, 79 (02) :137-158
[9]  
Barry J. M., 2005, The great influenza: The epic story of the deadliest plague in history
[10]  
Bateman A, 2002, NUCLEIC ACIDS RES, V30, P276, DOI [10.1093/nar/gkr1065, 10.1093/nar/gkp985, 10.1093/nar/gkh121]