TY - JOUR
T1 - Identifying Genetic Determinants Needed to Establish a Human Gut Symbiont in Its Habitat
AU - Goodman, Andrew L.
AU - McNulty, Nathan P.
AU - Zhao, Yue
AU - Leip, Douglas
AU - Mitra, Robi D.
AU - Lozupone, Catherine A.
AU - Knight, Rob
AU - Gordon, Jeffrey I.
N1 - Funding Information:
We thank David O'Donnell, Maria Karlsson, Sabrina Wagoner, Nicole Koropatkin, Daniel Peterson, Pankaj Pal, Laura Langton, Jessica Hoisington-López, Xuhua Chen, Laura Kyro, and James Dover for assistance, plus Gary Stormo, Jay Shendure, Ryan Kennedy, and the Gordon laboratory for helpful suggestions. This work was supported by National Institutes of Health grants DK30292 and 1F32AI078628-01 (to A.G.).
PY - 2009/9/17
Y1 - 2009/9/17
N2 - The human gut microbiota is a metabolic organ whose cellular composition is determined by a dynamic process of selection and competition. To identify microbial genes required for establishment of human symbionts in the gut, we developed an approach (insertion sequencing, or INSeq) based on a mutagenic transposon that allows capture of adjacent chromosomal DNA to define its genomic location. We used massively parallel sequencing to monitor the relative abundance of tens of thousands of transposon mutants of a saccharolytic human gut bacterium, Bacteroides thetaiotaomicron, as they established themselves in wild-type and immunodeficient gnotobiotic mice, in the presence or absence of other human gut commensals. In vivo selection transforms this population, revealing functions necessary for survival in the gut: we show how this selection is influenced by community composition and competition for nutrients (vitamin B12). INSeq provides a broadly applicable platform to explore microbial adaptation to the gut and other ecosystems.
AB - The human gut microbiota is a metabolic organ whose cellular composition is determined by a dynamic process of selection and competition. To identify microbial genes required for establishment of human symbionts in the gut, we developed an approach (insertion sequencing, or INSeq) based on a mutagenic transposon that allows capture of adjacent chromosomal DNA to define its genomic location. We used massively parallel sequencing to monitor the relative abundance of tens of thousands of transposon mutants of a saccharolytic human gut bacterium, Bacteroides thetaiotaomicron, as they established themselves in wild-type and immunodeficient gnotobiotic mice, in the presence or absence of other human gut commensals. In vivo selection transforms this population, revealing functions necessary for survival in the gut: we show how this selection is influenced by community composition and competition for nutrients (vitamin B12). INSeq provides a broadly applicable platform to explore microbial adaptation to the gut and other ecosystems.
KW - MICROBIO
UR - http://www.scopus.com/inward/record.url?scp=69949123813&partnerID=8YFLogxK
U2 - 10.1016/j.chom.2009.08.003
DO - 10.1016/j.chom.2009.08.003
M3 - Article
C2 - 19748469
AN - SCOPUS:69949123813
SN - 1931-3128
VL - 6
SP - 279
EP - 289
JO - Cell Host and Microbe
JF - Cell Host and Microbe
IS - 3
ER -