TY - JOUR
T1 - Elevating fitness after a horizontal gene exchange in bacteriophage φX174
AU - Doore, Sarah M.
AU - Schweers, Nicholas J.
AU - Fane, Bentley A.
N1 - Funding Information:
The authors acknowledge the support of the National Science Foundation ( MCB1408217 to B.A.F).
Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2017/1/15
Y1 - 2017/1/15
N2 - In an earlier study, protein-based barriers to horizontal gene transfer were investigated by placing the bacteriophage G4 G gene, encoding the major spike protein, into the φX174 genome. The foreign G protein promoted off-pathway assembly reactions, resulting in a lethal phenotype. After three targeted genetic selections, one of two foreign spike proteins was productively integrated into the φX174 system: the complete G4 or a recombinant G4/φX174 protein (94% G4:6% φX174). However, strain fitness was very low. In this study, the chimeras were characterized and experimentally evolved. Inefficient assembly was the primary contributor to low fitness: accordingly, mutations affecting assembly restored fitness. The spike protein preference of the ancestral and evolved strains was determined in competition experiments between the foreign and φX174 G proteins. Before adaptation, both G proteins were incorporated into virions; afterwards, the foreign proteins were strongly preferred. Thus, a previously inhibitory protein became the preferred substrate during assembly.
AB - In an earlier study, protein-based barriers to horizontal gene transfer were investigated by placing the bacteriophage G4 G gene, encoding the major spike protein, into the φX174 genome. The foreign G protein promoted off-pathway assembly reactions, resulting in a lethal phenotype. After three targeted genetic selections, one of two foreign spike proteins was productively integrated into the φX174 system: the complete G4 or a recombinant G4/φX174 protein (94% G4:6% φX174). However, strain fitness was very low. In this study, the chimeras were characterized and experimentally evolved. Inefficient assembly was the primary contributor to low fitness: accordingly, mutations affecting assembly restored fitness. The spike protein preference of the ancestral and evolved strains was determined in competition experiments between the foreign and φX174 G proteins. Before adaptation, both G proteins were incorporated into virions; afterwards, the foreign proteins were strongly preferred. Thus, a previously inhibitory protein became the preferred substrate during assembly.
KW - Experimental evolution
KW - Microviridae
KW - Microvirus
KW - Virus assembly
KW - φX174
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U2 - 10.1016/j.virol.2016.10.029
DO - 10.1016/j.virol.2016.10.029
M3 - Article
C2 - 27855283
AN - SCOPUS:84995545595
SN - 0042-6822
VL - 501
SP - 25
EP - 34
JO - Virology
JF - Virology
ER -