BioProject

ABSTRACT Geobacter sulfurreducens strain KN400 was recovered in previous studies in which a culture of the DL1 strain of G. More...

ABSTRACT Geobacter sulfurreducens strain KN400 was recovered in previous studies in which a culture of the DL1 strain of G. sulfurreducens served as the inoculum in investigations on microbial current production at low (-400 mv vs Ag/AgCl) anode potentials. Differences in the genome sequences of KN400 and DL1 were too great to have arisen from adaptive evolution during growth on the anode. Previous deep sequencing (80-fold coverage) of the DL1 culture failed to detect sequences specific to KN400, suggesting that KN400 was an external contaminant inadvertently introduced into the anode culturing system. In order to evaluate this further, a portion of the gene for OmcS, a c-type cytochrome that both KN400 and DL1 possess, was amplified from the DL1 culture. HiSeq-2000 Illumina sequencing of the PCR product detected the KN400 sequence, which differs from the DL1 sequence at 14 base pairs, at a frequency of ca. 1 in 105 of the DL1 sequence. A similar low frequency of KN400 was detected with quantitative PCR of a KN400-specific gene. KN400 persisted at this frequency after intensive re-streaking of isolated colonies from the DL1 culture. However, a culture in which KN400 could no longer be detected was obtained with serial dilution-to-extinction in liquid media. The KN400-free culture could not grow on an anode poised at -400 mV. Thus, KN400 cryptically persisted in the culture dominated by DL1 for more than a decade, undetected by even deep whole-genome sequencing, and was only fortuitously uncovered by the unnatural selection pressure of growth on a low-potential electrode. Repeated streaking of isolated colonies on solidified medium remains a common strategy for obtaining pure cultures, especially for difficult to cultivate microorganisms such as strict anaerobes. The results presented here demonstrate that verifying the purity of cultures obtained in this manner may be difficult because extremely rare variants can persist, undetectable with even deep genomic DNA sequencing. The only assurance that a culture is pure is to cultivate from an initial single cell, which may be technically difficult for many environmentally significant microbes. Less...