The Phage Treaty

by Roberto

In 1938, af­ter de­vel­op­ing a keen in­ter­est in genes, Max Del­brück ar­rived at Cal­tech set to work on Dro­so­phi­la ge­net­ics with Tho­mas Mor­gan. But, as some­one trained in theo­re­ti­cal phys­ics, the pace of work­ing with fruit flies pro­ved too slow. For­tu­na­te­ly for the his­tory of mo­le­cu­lar bio­logy, Del­brück met Emo­ry El­lis who was us­ing bac­te­rio­phages in hopes of un­der­stand­ing can­cer. As a host bac­terium El­lis had cho­sen Es­cherichia coli for the sim­ple rea­son that one of Morgan's stu­dents hap­pened to have it. The El­lis and Del­brück 1939 pa­per, "The Growth of Bac­te­rio­phage," set in mo­tion the for­ma­tion of what would be­come the very fa­mil­iar Phage Group, whose mem­bers includ­ed so many of the key in­ves­ti­ga­tors of the early days of mol­e­c­u­lar bi­ol­ogy (Luria, Her­shey, Wat­son, Mesel­son, Stahl, Ben­zer and Bren­ner, among oth­ers). By 1945, Del­brück be­gan teach­ing his leg­endary sum­mer "Phage Course."

Fig­ure 1. Trans­mis­sion elec­tron micro­graph of mul­ti­ple bac­te­rio­phages at­tached to a bac­te­r­ial cell wall. Source

What is less known is the fact that in 1944 Del­brück came up with the idea of the "Phage Treaty." Not­ing that phage in­ves­ti­ga­tors from around the world each seemed to be fo­cusing on their "own" par­tic­u­lar phage, Del­brück de­creed that all mem­bers of the Phage Group, and later on all those who took the Phage Course, should agree to work exclu­sively with an E. coli B strain as host and study only the "T" phages. More­over, phage growth should be stud­ied exclu­sively at 37°C and in nu­tri­ent broth. While such rules might seem ter­ri­bly re­stric­tive (and even­tu­ally many in­ves­ti­ga­tors ven­tured else­where, wit­ness E. coli K‑12 and phage lamb­da), the fact that re­sults could be com­pared across nu­mer­ous lab­o­ra­to­ries and then eas­ily build on each other's work, proved a re­mark­able force that moved the field of mol­e­c­u­lar ge­net­ics for­wards for nearly two decades and whose legacy is still felt to­day.

Why do I bring this up now? It's in con­nec­tion to my re­cent post on the nematode's C.elegans mi­crobiome. I feel we are at a sim­i­lar junc­ture to­day. We have won­der­ful mi­cro­biome work be­ing done all over the world. But at times it seems as if al­most every­one is try­ing to find their own spe­cial mi­cro­bial com­mu­nity to study, to dif­fer­en­ti­ate them­selves from the rest. That is all fine and well. But I also think it would be ex­tremely pro­duc­tive, for ad­dress­ing some ba­sic ques­tions about mi­cro­bial com­mu­ni­ties and host in­ter­ac­tions, to have a few groups around the world fo­cus their ef­forts on a sim­ple syn­thetic com­mu­nity. I hap­pen to think that the model ne­ma­tode mi­cro­biome I pre­sented re­cently in STC is ide­ally suited for such an ef­fort. Hope­fully, a few dozen re­searchers will rally around this re­source. Per­haps there will be a ne­ma­tode mi­cro­biome sum­mer course and, who knows, some brave leader might even de­cree a ne­ma­tode mi­cro­biome treaty!

 

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