4.6 Article

Quantifying bacterial evolution in the wild: A birthday problem for Campylobacter lineages

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PLOS GENETICS
卷 17, 期 9, 页码 -

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PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.1009829

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资金

  1. Medical Research Council [MR/L015080/1, MR/S009264/1, MR/T030062/1, MR/V001213/1]
  2. Biotechnology and Biological Sciences Research Council (BBSRC)-CASE studentship [BB/P504750/1]
  3. MRC senior research fellowship [MR/M501608/1]
  4. Shanghai Municipal Science and Technology Major Project [2019SHZDZX02]
  5. National Institute of Allergy and Infectious Diseases [1R01AI15857601]
  6. BBSRC [BB/P504750/1] Funding Source: UKRI

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This study presents a new approach to estimate the molecular clock rate in Campylobacter, drawing on the 'birthday problem'. By analyzing large genomic datasets, the synonymous rates of nucleotide change for the common pathogenic bacteria Campylobacter colt and Campylobacter jejuni were estimated. The study also inferred the number of effective lineages within the sample time frame and assessed the rate of turnover of lineages over short evolutionary timescales.
Measuring molecular evolution in bacteria typically requires estimation of the rate at which nucleotide changes accumulate in strains sampled at different times that share a common ancestor. This approach has been useful for dating ecological and evolutionary events that coincide with the emergence of important lineages, such as outbreak strains and obligate human pathogens. However, in multi-host (niche) transmission scenarios, where the pathogen is essentially an opportunistic environmental organism, sampling is often sporadic and rarely reflects the overall population, particularly when concentrated on clinical isolates. This means that approaches that assume recent common ancestry are not applicable. Here we present a new approach to estimate the molecular clock rate in Campylobacter that draws on the popular probability conundrum known as the 'birthday problem'. Using large genomic datasets and comparative genomic approaches, we use isolate pairs that share recent common ancestry to estimate the rate of nucleotide change for the population. Identifying synonymous and non-synonymous nucleotide changes, both within and outside of recombined regions of the genome, we quantify clock-like diversification to estimate synonymous rates of nucleotide change for the common pathogenic bacteria Campylobacter colt (2.4 x 10(-6) s/s/y) and Campylobacter jejuni (3.4 x 10(-6) s/s/y). Finally, using estimated total rates of nucleotide change, we infer the number of effective lineages within the sample time frame-analogous to a shared birthday-and assess the rate of turnover of lineages in our sample set over short evolutionary timescales. This provides a generalizable approach to calibrating rates in populations of environmental bacteria and shows that multiple lineages are maintained, implying that large-scale clonal sweeps may take hundreds of years or more in these species.

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