Virus. ...sim­ply a piece of bad news wrapped up in pro­tein, re­ally ?

by Christoph

In my prior post, I an­swered the ques­tion "are viruses alive?" with a firm: no. That was the short an­swer, but there is also a long an­swer... and it's long be­cause it's com­pli­cated.

For all bi­ol­o­gists, life oc­curs in the con­text of cells. This has been the case since the mid­dle of the 19th cen­tury when the mantra of cell the­ory, Om­nis cel­lula e cel­lula (all cells come from cells), was pinned on the door of all bi­ol­ogy lab­o­ra­to­ries. Bi­ol­ogy went through rad­i­cal trans­for­ma­tions at the time with the re­jec­tion of spon­ta­neous gen­er­a­tion, and the ush­er­ing in of the 'Dar­win­ian revolu­tion', and Mendelian in­her­i­tance. The lat­ter two the­o­ries did evolve (!) con­sid­er­ably over the last hun­dred years − think mod­ern syn­the­sis − but cell the­ory was never chal­lenged.

Fig­ure 1. SEM of B. sub­tilis (LAS72, RecA-YFP) spo­res (cov­ered with ex­ospo­ria) sprayed on glass cov­er­slips af­ter low-pres­sure plasma treat­ment. Source

In the con­text of cell the­ory, we can en­ter the dis­cus­sion of viruses be­ing alive or not by com­par­ing and contrast­ing them to spores. Dor­mant en­dospores, from Bacil­lus sub­tilis for ex­am­ple, are not alive when sim­ply sus­pend­ed in buffer. But they kick back to life if given the right nudge. Present them with L‑valine, which they sense through a re­cep­tor pro­tein and ger­mi­na­tion en­sues, fol­lowed by veg­e­ta­tive growth if the nec­es­sary nu­tri­ents are avail­able. When nu­tri­ents be­come lim­it­ing sporu­la­tion can oc­cur once again. Sin­gle spores form within 'mother cells' as al­most 'vit­ri­fied' ver­sions of a veg­e­ta­tive cell. They con­tain a com­plete, con­densed chro­mo­some − co­pied from the 'mother chro­mo­some' and im­ported into the form­ing spore − and a re­duced set of tran­scrip­tion and trans­la­tion fac­tors along with a few me­tabolic en­zymes. The spore mem­brane is pop­u­lated by nu­mer­ous re­cep­tors, me­tab­o­lism brought to close-to-zero, and the en­tire spore wrapped in a thick opaque coat that is highly resis­tant to phys­i­cal dam­age. The mother cell un­der­goes ly­sis af­ter com­ple­tion of spore for­ma­tion, set­ting the dor­mant spore free (cov­ered by a pro­tec­tive pro­tein coat, the ex­ospo­rium (Fig­ure 1).) Avoid­ing a de­ci­sion of whether spores are alive or not, bi­ol­o­gists pre­fer to call this state crypto­biosis, or, al­most po­et­i­cally, 'sus­pended an­i­ma­tion.' Case solved.

Fig­ure 2. SEM of E. coli bac­te­rio­phage T4 virion. Source

Now con­trast spore for­ma­tion to the life cy­cle of phage T4, and note the sim­i­lar­i­ties. T4 viri­ons, the meta­bol­i­cally in­ac­tive 'trans­port ve­hi­cle' of the phage chro­mo­some (Fig­ure 2) are not alive when re­sus­pended in buffer or cell-free nu­tri­ent medium. But they kick back to life upon en­coun­ter­ing E. coli host cells in nu­tri­ent medium. They at­tach and bind to lipopolysac­cha­ride (LPS) and the ma­jor outer mem­brane pro­tein, OmpC, by means of their tail fibers. The at­tach­ment trig­gers the con­trac­tion of the virion's tail sheath, which lit­er­ally lets the tail drill a hole through both cell mem­branes and the pep­ti­do­gly­can layer by me­chan­i­cal force, en­forced by the en­zy­matic mu­rein hy­dro­lase ac­tiv­ity of a base­plate pro­tein. Once the tail has drilled through the in­ner mem­brane the phage genome is in­jected through the tail's in­ner chan­nel into the cell's cy­to­plasm. Re­mark­ably, both processes, tail sheath con­trac­tion and DNA de­liv­ery into the host cell cy­to­plasm do not re­quire en­ergy in­put. The en­ergy re­quired for both processes was in­vested in the virion com­po­nents as a con­for­ma­tion dur­ing the as­sem­bly of the virion, anal­o­gous to a coiled spring that re­leases the stored me­chan­i­cal en­ergy when let­ting go. In­side the cell, the T4 chro­mo­some (ds­DNA) is tran­scribed by host RNA poly­merase and trans­lated by host ri­bo­somes. Once phage-en­coded pro­teins are made, phage repli­ca­tion and recom­bination dom­i­nate the cell, ul­ti­mately yield­ing ~100 prog­eny T4 chro­mo­somes. Phage pro­teins di­rect the in­tra­cel­lu­lar for­ma­tion of phage cap­sids and pack­ag­ing of the chro­mo­somes into the pre-as­sem­bled phage heads. The tail sheath, col­lar, whiskers, base­plate, and tail fibers, along with DNA-filled head form the phage T4 virion. Seven dif­fer­ent phage en­coded pro­teins in­duce ly­sis of the host cell, which re­leases the viri­ons into the en­vi­ron­ment. Clearly, the process of mak­ing pro­geny phage is very much a "liv­ing sys­tem."

Woll­man & Ja­cob (1961) do not at­tach much im­por­tance to the ques­tion of whether viruses/pha­ges are alive, rather they see dif­fer­ent states: "...a virus may ex­ist in three states; the only thing com­mon to the virus in the three states is that it car­ries at all times much the same ge­netic infor­mation en­coded in DNA. In the ex­tra­cel­lu­lar in­fec­tious state the nu­cleic acid is en­closed in a pro­tective, re­sis­tant shell. The virus then re­mains in­ert like the spore of a bac­terium... In the vege­ta­tive state of au­tonomous repli­ca­tion the ge­netic ma­te­r­ial is free of its shell, over­rides the regu­la­tory mech­a­nism of the host and im­poses its own com­mands on the syn­thetic ma­chin­ery of the cell. The vi­ral genes are fully ac­tive." In today's ter­mi­nol­ogy, the "ex­tra­cel­lu­lar in­fec­tious state" of a virus/phage is called a virion, or virus par­ti­cle. The sec­ond state, "the veg­e­ta­tive state of autono­mous repli­ca­tion," is con­cep­tu­ally equiv­a­lent to the veg­e­ta­tive growth phase of bac­te­ria, and I will come to the third state, the "provi­ral state," in a mo­ment.

Fig­ure 3. ©2020 Janie Kim

Raoult & Forterre en­tered the fray of the virus alive or not de­bate by propos­ing, in 2008, "...to di­vide bi­o­log­i­cal en­ti­ties into two groups of or­gan­isms: ri­bo­some-en­­cod­ing or­gan­isms, which in­clude eu­kary­otic, ar­chaeal and bac­te­r­ial or­gan­isms, and cap­sid-en­cod­ing or­gan­isms, which in­clude vi­rus­es." With­out out­right stat­ing it, they seem to cat­e­go­rize viruses as "alive" since they put them on the same level as eu­kary­otic, ar­chaeal and bac­te­r­ial or­gan­isms, en­ti­ties that em­body the proper­ties of life. Our own Elio and his co-au­thor Roland Wolkow­icz joined the dis­cus­sion through a com­ment to the Raoult & For­ter­re pa­per where they "pro­pose that the defin­ing at­tri­bute of all viruses is their dis­in­te­gration and recon­sti­tu­tion... Im­por­tantly, dis­in­te­gra­tion and re­con­sti­tu­tion are to­tal­ly in­de­pen­dent of time, with re­con­sti­tu­tion oc­cur­ring min­utes, days, years or cen­turies af­ter dis­in­te­gration." With this pro­posal, Schaechter & Wolkow­icz had to cre­ate a new, sep­a­rate cat­e­gory for the cap­sid-less state, join­ing it to the gen­eral group­ing of vi­roids. All four au­thors at­tach im­por­tance to the cap­sids of the virus­es as defin­ing struc­tural el­e­ments, the "ex­tra­cel­lu­lar in­fec­tious state" ac­cord­ing to Woll­man & Ja­cob. But only Schaechter & Wolkow­icz men­tion the "veg­e­ta­tive state" al­beit not speci­fi­cal­ly, on­ly in a rather in­di­rect for­mu­la­tion ad­dress­ing its time span as be­ing "min­utes, days, years or cen­tu­ries af­ter dis­in­te­gra­tion" of the virion.

Per­haps be­cause it does not af­fect all phages but only the so-called tem­per­ate or lyso­genic pha­ges, nei­ther Raoult & Forterre nor Schaechter & Wolkow­icz ad­dress in their pa­pers the third vi­ral state de­scribed by Woll­man & Ja­cob: "in the provi­ral state the ge­netic ma­te­r­ial of the virus has be­come sub­ject to the reg­u­la­tory sys­tem of the host and repli­cates as if it were part of the bac­te­r­ial chro­mo­some. A spe­cific sys­tem of sig­nals pre­vents the genes of the virus from ex­press­ing them­selves; com­plete virus par­ti­cles are there­fore not man­u­fac­tured." This de­scrip­tion of the "third state" of a vi­ral genome as a largely silent com­po­nent of the host genome can no longer be con­si­dered com­pletely ac­cu­rate to­day. We have am­ple ev­i­dence that genes of lytic and lyso­genic pha­ges that do not only en­code repli­ca­tion or im­mu­nity func­tions but rather con­tribute to the pheno­type of their host cell. One clas­sic ex­am­ple is a vir­u­lence fac­tor of path­o­genic Vib­rio cholerae strains, cholera toxin (CTX), which is ex­pressed from the CTXϕ prophage. The nu­mer­ous ex­am­ples of phage genes ex­pressed in the lyso­genic state prompted Patrick Forterre to re­fine his con­cept, and he now states: "The liv­ing form of the virus is the meta­bol­i­cally ac­tive 'veg­e­ta­tive state of au­to­nomous repli­ca­tion', that is, its in­tra­cel­lu­lar form." And ac­knowl­edg­ing that both the geno­type and phe­no­type of a cell in­fected by a lytic or lyso­genic phage clearly dif­fers from those of the un­in­fect­ed cell he pro­poses: "The vi­ro­cell, be­ing a cel­lu­lar or­gan­ism, cor­re­sponds to the 'liv­ing form' of the virus, whereas viri­ons are in fact the equiv­a­lent of seeds or spores for mul­ti­cel­lu­lar or­gan­isms." So, ac­cord­ing to Forterre, viruses/phages can be con­sid­ered alive, and not just "bad news." In fact, for bi­ol­ogy as a whole, viruses in­deed bring with them a lot of "good news" be­cause be­ing some of the ma­jor agents of hor­i­zon­tal gene trans­fer, they lay the foun­da­tion for many of the pos­si­ble di­rec­tions of evo­lu­tion.

You re­ally don't have to be wor­ried that af­ter this tour de force I will also de­vote my­self to the grander ques­tion "what is life?" I hap­pily leave that to Er­win Schrödinger and George Har­ri­son, in equal shares.

Fi­nally, not a con­clu­sion

I bor­rowed the ti­tle of this piece from Carl Zim­mer, the re­known sci­ence jour­nal­ist, who cites Jean and Pe­ter Medawar in the NYT with their quote "[A virus is] sim­ply a piece of bad news wrapped up in pro­tein." Yet, as it of­ten goes with quotes, it is dif­fi­cult to ac­cu­rately trace their ori­gin, and over time, they of­ten loose or gain words, not un­like viruses lose and gain genes. Such seems to be the case here. Prob­a­bly the Medawars' drew heav­ily from the sen­tence "A virus can there­fore be con­sid­ered a ge­netic el­e­ment en­closed in a pro­tein coat" in the re­view pa­per by Elie Woll­man and François Ja­cob from 1961. You find the quote as "A virus is a piece of bad news wrapped in pro­tein" in Wikipedia, which gives Pe­ter Medawar as au­thor yet ig­nores the coau­thor, Jean Meda­war, Peter's spouse and life­long col­lab­o­ra­tor (Wikipedia has been re­peat­edly crit­i­cized for its gen­der bias to­wards male sci­en­tists, not the least by Jess Wade). As a third ver­sion, Michael Old­stone gives it as "[viruses are] a piece of bad news wrapped in a pro­tein coat." The 'pro­tein coat' smells of Woll­man & Ja­cob, but is Old­stone trust­wor­thy? Not so much, as he gives in his (peer-re­viewed) jour­nal ar­ti­cle as ref­er­ence the book by Pe­ter and Jean Medawar with the ti­tle "Aris­to­tle to Zeus, a philo­soph­i­cal dic­tio­nary of bi­ol­ogy" (Cam­bridge, Mass, Har­vard Uni­ver­sity Press, 1983, page 275) while Har­vard Uni­ver­sity Press lists ex­actly this book un­der the ti­tle "Aris­to­tle to Zoos. A Philo­so­phical Dic­tio­nary of Bi­ol­ogy" (1985). Hey, that's more than a neg­li­gi­ble typo, it's a shift to­wards the meta-phys­i­cal! But be­fore I go on nag­ging − or even dare to list here all the other vari­ants you find by googling, be­ware! − I sim­ply stop with an­other quote from said book of the Medawars: "It is a pop­u­lar fal­lacy that chew­ing gum re­gains its fla­vor if re­moved from the mouth and parked, say, un­der a chair."

 

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