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Surface display of a massively variable lipoprotein by a Legionella diversity-generating retroelement
Edited† by John J. Mekalanos, Harvard Medical School, Boston, MA, and approved April 1, 2013 (received for review January 22, 2013)

Abstract
Diversity-generating retroelements (DGRs) are a unique family of retroelements that confer selective advantages to their hosts by facilitating localized DNA sequence evolution through a specialized error-prone reverse transcription process. We characterized a DGR in Legionella pneumophila, an opportunistic human pathogen that causes Legionnaires disease. The L. pneumophila DGR is found within a horizontally acquired genomic island, and it can theoretically generate 1026 unique nucleotide sequences in its target gene, legionella determinent target A (ldtA), creating a repertoire of 1019 distinct proteins. Expression of the L. pneumophila DGR resulted in transfer of DNA sequence information from a template repeat to a variable repeat (VR) accompanied by adenine-specific mutagenesis of progeny VRs at the 3′end of ldtA. ldtA encodes a twin-arginine translocated lipoprotein that is anchored in the outer leaflet of the outer membrane, with its C-terminal variable region surface exposed. Related DGRs were identified in L. pneumophila clinical isolates that encode unique target proteins with homologous VRs, demonstrating the adaptability of DGR components. This work characterizes a DGR that diversifies a bacterial protein and confirms the hypothesis that DGR-mediated mutagenic homing occurs through a conserved mechanism. Comparative bioinformatics predicts that surface display of massively variable proteins is a defining feature of a subset of bacterial DGRs.
Footnotes
- ↵1To whom correspondence should be addressed. E-mail: jfmiller{at}ucla.edu.
Author contributions: D.A., B.A.M., H.G., P.G., and J.F.M. designed research; D.A., W.W., H.G., S.D., and P.G. performed research; M.G., E.C., and M.L. contributed new reagents/analytic tools; D.A., B.A.M., H.G., M.G., E.C., M.L., S.D., P.G., and J.F.M. analyzed data; and D.A., H.G., M.L., P.G., and J.F.M. wrote the paper.
Conflict of interest statement: J.F.M. is cofounder and chair of, and H.G. is a consultant for, the scientific advisory board of AvidBiotics Inc., a biotherapeutics company in San Francisco.
↵†This Direct Submission article had a prearranged editor.
This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1301366110/-/DCSupplemental.
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