Alan Kleinman
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- Feb 14, 2021
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Even if you are starting with a single founder bacterium, the population very rapidly diversifies. For example, in the Kishony experiment, he uses e coli. Assume the genome length is 5e6. When that founder and descendants have done 200 replications, there will have been 1e9 base replications. For a mutation rate of 1e-9, that means on average there will be one variant with a mutation somewhere in the genome and 199 clones of the original founder. As the population grows (more replications) another variant with a mutation somewhere in the genome will occur every 200 replications. With a billion replications, you will have on average 1 member in that population with a mutation at each site in the genome. You will have 5E6 variants and (1E9-5E6) exact clones of the original founder (on average). Lenski's founders were far from being exact clones. And you are correct, you have to sum over generations the number of replications in each generation to get the total number of replications of a given variant in an evolutionary lineage. But you don't sum all variants because a mutation that might be beneficial for one variant in a population might be neutral or detrimental to a different variant in that population.Alan Kleinman said: said:But the Kishony and Lenski experiments are credible evidence and these experiments show that it takes a billion or more replications for each evolutionary adaptive step.Well, you are starting with clonal isolates. Most populations already start with significant diversity. Wouldn't replications = population x #number of generations more accurately reflect a general case? Yet you refer only to a list of population sizes in a different post above.
Kishony's team has to limit the concentration of antibiotics such that only a single beneficial mutation gives improved fitness. If the concentration is too large (requiring more than a single mutation to give improved fitness, his experiment doesn't have the carrying capacity to give the population size needed to give those two or more mutations. His population would run out of nutrients in the drug-free region before the drug-resistant variant ever appears.Alan Kleinman said: said:If a particular population doesn't have sufficient numbers and then is subject to selection pressure, those populations often go extinct.sesquiterpene said: said:Your examples also use rather extreme selective agents. it might take many generations for a population to go extinct for more typical pressures, say "it's a bit colder than usual this winter". And indeed, most populations do go extinct.
As I pointed out in post #354, Lenski published a paper where his founder bacteria showed drug-resistance to numerous antibiotics even though his bacteria were never exposed to antibiotics. Variants occur simply occur because mutations occur. The larger the carrying capacity of the environment, the larger the population size, and the larger the population size, the greater the diversity of the population. Lenski's founders were grown in a much larger carrying capacity environment than used in his experiment. That's why these drug-resistant variants appeared even though these populations were never exposed to antibiotics.
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