Genome of the Opportunistic Pathogen <i>Streptococcus sanguinis</i>

Ping Xu(Virginia Commonwealth University), João M. P. Alves(Virginia Commonwealth University), Todd Kitten(Virginia Commonwealth University), Arunsri Brown(Virginia Commonwealth University), Chen Zhenming(Virginia Commonwealth University), Luiz S. Ozaki(Virginia Commonwealth University), Patrício Manque(Virginia Commonwealth University), Xiuchun Ge(Virginia Commonwealth University), Myrna G. Serrano(Virginia Commonwealth University), Daniela Puiu(Virginia Commonwealth University), Stephanie Hendricks(Virginia Commonwealth University), Ying‐Ping Wang(Virginia Commonwealth University), Michael D. Chaplin(Virginia Commonwealth University), Doruk Akan(Virginia Commonwealth University), Sehmi Paik(Virginia Commonwealth University), Darrell L. Peterson(Virginia Commonwealth University), Francis L. Macrina(Virginia Commonwealth University), Gregory A. Buck(Virginia Commonwealth University)
Journal of Bacteriology
February 4, 2007
Cited by 230Open Access
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Abstract

The genome of Streptococcus sanguinis is a circular DNA molecule consisting of 2,388,435 bp and is 177 to 590 kb larger than the other 21 streptococcal genomes that have been sequenced. The G+C content of the S. sanguinis genome is 43.4%, which is considerably higher than the G+C contents of other streptococci. The genome encodes 2,274 predicted proteins, 61 tRNAs, and four rRNA operons. A 70-kb region encoding pathways for vitamin B(12) biosynthesis and degradation of ethanolamine and propanediol was apparently acquired by horizontal gene transfer. The gene complement suggests new hypotheses for the pathogenesis and virulence of S. sanguinis and differs from the gene complements of other pathogenic and nonpathogenic streptococci. In particular, S. sanguinis possesses a remarkable abundance of putative surface proteins, which may permit it to be a primary colonizer of the oral cavity and agent of streptococcal endocarditis and infection in neutropenic patients.


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