Citation: Stephen T Abedon. Bacteriophage secondary infection .VIROLOGICA SINICA, 2015, 30(1) : 3-10.

Bacteriophage secondary infection

  • Corresponding author: Stephen T Abedon,
  • Received Date: 17 November 2014
    Accepted Date: 29 December 2014
    Published Date: 13 January 2015
    Available online: 01 February 2015
  • Phages are credited with having been fi rst described in what we now, offi cially, are commemorating as the 100th. anniversary of their discovery. Those one-hundred years of phage history have not been lacking in excitement, controversy, and occasional convolution. One such complication is the concept of secondary infection, which can take on multiple forms with myriad consequences. The terms secondary infection and secondary adsorption, for example, can be used almost synonymously to describe virion interaction with already phage-infected bacteria, and which can result in what are described as superinfection exclusion or superinfection immunity. The phrase secondary infection also may be used equivalently to superinfection or coinfection, with each of these terms borrowed from medical microbiology, and can result in genetic exchange between phages, phage-on-phage parasitism, and various partial reductions in phage productivity that have been termed mutual exclusion, partial exclusion, or the depressor effect. Alternatively, and drawing from epidemiology, secondary infection has been used to describe phage population growth as that can occur during active phage therapy as well as upon phage contamination of industrial ferments. Here primary infections represent initial bacterial population exposure to phages while consequent phage replication can lead to additional, that is, secondary infections of what otherwise are not yet phage-infected bacteria. Here I explore the varying meanings and resultant ambiguity that has been associated with the term secondary infection. I suggest in particular that secondary infection, as distinctly different phenomena, can in multiple ways infl uence the success of phage-mediated biocontrol of bacteria, also known as, phage therapy.

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    1. Abedon S. 2011. Phage therapy pharmacology: calculating phage dosing. Adv Appl Microbiol. 77:10-40.

    2. Abedon ST. 1990. Selection for lysis inhibition in bacteriophage. J Theor Biol. 146:501-511.
        doi: 10.1016/S0022-5193(05)80375-3

    3. Abedon ST. 1992. Lysis of lysis inhibited bacteriophage T4-infected cells. J Bacteriol. 174:8073-8080.
        doi: 10.1128/jb.174.24.8073-8080.1992

    4. Abedon ST. 1994. Lysis and the interaction between free phages and infected cells. In: The Molecular Biology of Bacteriophage T4. Karam JD, Kutter E, Carlson K, and Guttman B (eds). Washington DC: ASM Press, pp397-405.

    5. Abedon ST. 1999. Bacteriophage T4 resistance to lysis-inhibition collapse. Genet Res, 74:1-11.
        doi: 10.1017/S0016672399003833

    6. Abedon ST. 2008. Phage population growth: constraints, games, adaptation. In: Bacteriophage Ecology. Abedon ST (ed). Cambridge: Cambridge University Press, pp64-93.

    7. Abedon ST. 2009a. Bacteriophage intraspecific cooperation and defection. In: Contemporary Trends in Bacteriophage Research.

    8. Adams HT (ed). Hauppauge: Nova Science Publishers, pp191-215.

    9. Abedon ST. 2009b. Disambiguating bacteriophage pseudolysogeny: an historical analysis of lysogeny, pseudolysogeny, and the phage carrier state. In: Contemporary Trends in Bacteriophage Research. Adams HT (ed). Hauppauge: Nova Science Publishers, pp285-307.

    10. Abedon ST. 2009c. Kinetics of phage-mediated biocontrol of bacteria. Foodborne Pathog Dis, 6:807-815.
        doi: 10.1089/fpd.2008.0242

    11. Abedon ST. 2011a. Bacteriophages and Biofilms: Ecology, Phage Therapy, Plaques. Hauppauge: Nova Science Publishers.

    12. Abedon ST. 2011b. Lysis from without. Bacteriophage. 1: 46-49.

    13. Abedon ST. 2012a. Phage therapy best practices. In: Bacteriophages in Health and Disease. Hyman P, Abedon ST (eds). Wallingford: CABI Press, pp256-272.

    14. Abedon ST. 2012b. Spatial vulnerability: bacterial arrangements, microcolonies, and biofilms as responses to low rather than high phage densities. Viruses. 4:663-687.
        doi: 10.3390/v4050663

    15. Abedon ST. 2012c. Thinking about microcolonies as phage targets. Bacteriophage. 2:200-204.
        doi: 10.4161/bact.22444

    16. Abedon ST. 2014. Bacteriophages as drugs: the pharmacology of phage therapy. In: Phage Therapy: Current Research and Applications. Borysowski J, Miedzybrodzki R, and Górski A (eds). Norfolk: Caister Academic Press, pp69-100.

    17. Abedon ST, Kuhl SJ, Blasdel BG, Kutter EM. 2011. Phage treatment of human infections. Bacteriophage. 1:66-85.
        doi: 10.4161/bact.1.2.15845

    18. Abedon ST, Thomas-Abedon C. 2010. Phage therapy pharmacology. Curr Pharm Biotechnol. 11:28-47.
        doi: 10.2174/138920110790725410

    19. Adams MH. 1959. Bacteriophages. New York: InterScience.

    20. Barron BA, Fischetti VA, Zabriskie JB. 1970. Studies of the bacteriophage kinetics of multicellular systems: a statistical model for the estimation of burst size per cell in streptococci. J Appl Bacteriol. 33:436-442.
        doi: 10.1111/jam.1970.33.issue-2

    21. Benzer S, Hudson W, Weidel W, Delbruck M, Stent GS, Weigle J J, Dulbecco R, Watson JD, Wollman EL. 1950. A syllabus on procedures, facts, and interpretations in phage. Viruses 1950. Delbruck M (ed). Pasadena: California Institute of Technology, pp100-147.

    22. Berngruber TW, Weissing FJ, Gandon S. 2010. Superinfection inhibition and the evolution of viral latency. J Virol, 84:10200-10208.
        doi: 10.1128/JVI.00865-10

    23. Bigwood T, Hudson JA, Billington C. 2009. Influence of host and bacteriophage concentrations on the inactivation of foodborne pathogenic bacteria by two phages. FEMS Microbiol Lett, 291:59-64.
        doi: 10.1111/fml.2009.291.issue-1

    24. Bull JJ, Regoes RR. 2006. Pharmacodynamics of non-replicating viruses, bacteriocins and lysins. Proc R Soc Lond B Biol Sci, 273:2703-2712.
        doi: 10.1098/rspb.2006.3640

    25. Chan BK, Abedon ST. 2012. Phage therapy pharmacology: phage cocktails. Adv Appl Microbiol, 78:1-23.
        doi: 10.1016/B978-0-12-394805-2.00001-4

    26. Chan BK, Abedon ST, Loc-Carrillo C. 2013. Phage cocktails and the future of phage therapy. Future Microbiol, 8:769-783.
        doi: 10.2217/fmb.13.47

    27. Davis BM, Kimsey HH, Chang W, Waldor MK. 1999. The Vibrio cholerae O139 Calcutta bacteriophage CTXφ is infectious and encodes a novel repressor. J Bacteriol, 181:6779-6787.

    28. Doermann AH. 1948. Lysis and lysis inhibition with Escherichia coli bacteriophage. J Bacteriol, 55:257-275.

    29. Espeland EM, Lipp EK, Huq A, Colwell RR. 2004. Polylysogeny and prophage induction by secondary infection in Vibrio cholerae. Environ Microbiol, 6:760-763.
        doi: 10.1111/emi.2004.6.issue-7

    30. Fogg PC, Allison HE, Saunders JR, McCarthy AJ. 2010. Bacteriophage lambda: a paradigm revisited. J Virol, 84:6876-6879.
        doi: 10.1128/JVI.02177-09

    31. Fogg PCM, Gossage SM, Smith DL, Saunders JR, McCarthy AJ, Allison HE. 2007. Identification of multiple integration sites for Stx-phage φ24B in the Escherichia coli genome, description of a novel integrase and evidence for a functional anti-repressor. Microbiology. 153:4098-4110.
        doi: 10.1099/mic.0.2007/011205-0

    32. French RC, Graham AF, Lesley SM, van Rooyen CE. 1952. The contribution of phosphorus from T2r+ bacteriophage to progeny. J Bacteriol. 64:597-607.

    33. Fukuda E, Kaminska KH, Bujnicki JM, Kobayashi I. 2008. Cell death upon epigenetic genome methylation: a novel function of methyl-specific deoxyribonucleases. Genome Biol. 9:R163.
        doi: 10.1186/gb-2008-9-11-r163

    34. Golshahi L, Seed KD, Dennis JJ, Finlay WH. 2008. Toward modern inhalational bacteriophage therapy: nebulization of bacteriophages of Burkholderia cepacia complex. J Aerosol Med Pulm Drug Deliv, 21:351-360.
        doi: 10.1089/jamp.2008.0701

    35. Hatfull GF, Hendrix RW. 2011. Bacteriophages and their genomes. Curr Opin Virol, 1:298-303.
        doi: 10.1016/j.coviro.2011.06.009

    36. Hendrix RW. 2008. Phage evolution. In: Bacteriophage Ecology. Abedon ST (ed). Cambridge: Cambridge University Press, pp177-194.

    37. Hendrix RW, Smith MCM, Burns RN, Ford ME, Hatfull GF. 1999. Evolutionary relationships among diverse bacteriophages and prophages: All the world's a phage. Proc Natl Acad Sci USA. 96:2192-2197.
        doi: 10.1073/pnas.96.5.2192

    38. Hudson JA, Billington C, Carey-Smith G, Greening G. 2005. Bacteriophages as biocontrol agents in food. J Food Prot, 68:426-437.
        doi: 10.4315/0362-028X-68.2.426

    39. Hughes KA, Sutherland IW, Jones MV. 1998. Biofilm susceptibility to bacteriophage attack: the role of phage-borne polysaccharide depolymerase. Microbiology. 144:3039-3047.
        doi: 10.1099/00221287-144-11-3039

    40. Hyman P, Abedon ST. 2010. Bacteriophage host range and bacterial resistance. Adv Appl Microbiol, 70:217-248.
        doi: 10.1016/S0065-2164(10)70007-1

    41. Hyman P, Abedon ST. 2012. Smaller fleas: viruses of microorganisms. Scientifica. 2012:734023.

    42. Iyer VN, James AP. 1978. Single-cell studies on the carrier state of bacteriophage IKe, a virus specific for conjugative plasmids of the N incompatibility and conjugative group. Can J Microbiol, 24:1595-1601.
        doi: 10.1139/m78-255

    43. Mann NH. 2003. Phages of the marine cyanobacterial picophytoplankton. FEMS Microbiol Rev, 27:17-34.
        doi: 10.1016/S0168-6445(03)00016-0

    44. May RM, Anderson RM. 1983. Parasite-host coevolution. In: Coevolution. Futuyma DJ, Slatkin M (eds). Sunderland: Sinauer Associates, pp186-206.

    45. Moussa SH, Kuznetsov V, Tran TA, Sacchettini JC, Young R. 2012. Protein determinants of phage T4 lysis inhibition. Protein Sci, 21:571-582.
        doi: 10.1002/pro.2042

    46. Moussa SH, Lawler JL, Young R. 2014. Genetic dissection of T4 lysis. J Bacteriol, 196:2201-2209.
        doi: 10.1128/JB.01548-14

    47. Payne RJH, Jansen VAA. 2001. Understanding bacteriophage therapy as a density-dependent kinetic process. J Theor Biol, 208:37-48.
        doi: 10.1006/jtbi.2000.2198

    48. Payne RJH, Jansen VAA. 2003. Pharmacokinetic principles of bacteriophage therapy. Clin Pharmacokinet, 42:315-325.
        doi: 10.2165/00003088-200342040-00002

    49. Payne RJH, Phil D, Jansen VAA. 2000. Phage therapy: The peculiar kinetics of self-replicating pharmaceuticals. Clin Pharmacol Ther, 68:225-230.
        doi: 10.1067/mcp.2000.109520

    50. Pratt JH. 1899. Secondary infection of the skin and subcutaneous tissues by the bacillus typhosus. J Boston Soc Med Sci, 3:170-173.

    51. Ryan EM, Gorman SP, Donnelly RF, Gilmore BF. 2011. Recent advances in bacteriophage therapy: how delivery routes, formulation, concentration and timing influence the success of phage therapy. J Pharm Pharamcol, 63:1253-1264.
        doi: 10.1111/j.2042-7158.2011.01324.x

    52. Sanders ME. 1987. Bacteriophages of industrial importance. In: Phage Ecology. Goyal SM, Gerba GP, Bitton G (eds). New York: John Wiley & Sons, pp211-244.

    53. Slavcev RA, Hayes S. 2002. Rex-centric mutualism. J Bacteriol, 184:857-858.
        doi: 10.1128/JB.184.3.857-858.2002

    54. Smith DL, Rooks DJ, Fogg PC, Darby AC, Thomson NR, McCarthy AJ, Allison HE. 2012. Comparative genomics of Shiga toxin encoding bacteriophages. BMC Genomics, 13:311.
        doi: 10.1186/1471-2164-13-311

    55. Stent GS. 1963. Molecular biology of bacterial viruses. San Francisco: WH Freeman and Co.

    56. Sturino JM, Klaenhammer TR. 2006. Engineered bacteriophage-defence systems in bioprocessing. Nat Rev Microbiol, 4:395-404.
        doi: 10.1038/nrmicro1393

    57. Tran TA, Struck DK, Young R. 2005. Periplasmic domains define holin-antiholin interactions in T4 lysis inhibition. J Bacteriol, 187:6631-6640.
        doi: 10.1128/JB.187.19.6631-6640.2005

    58. Tran TA, Struck DK, Young R. 2007. The T4 RI antiholin has an N-terminal signal anchor release domain that targets it for degradation by DegP. J Bacteriol, 189:7618-7625.
        doi: 10.1128/JB.00854-07

    59. Turner PE, Duffy S. 2008. Evolutionary ecology of multi-phage infections. In: Bacteriophage Ecology. Abedon ST (ed). Cambridge: Cambridge University Press, pp195-216.

    60. Wei W, Krone SM. 2005. Spatial invasion by a mutant pathogen. J Theor Biol, 236:335-348.
        doi: 10.1016/j.jtbi.2005.03.016

    61. Weinfeld H, Paigen K. 1964. Evidence for a new intermediate state of the viral chromosome during cooperative infection by host-modified lambda phage. Virology, 24:71-83.
        doi: 10.1016/0042-6822(64)90149-7

    62. Werner ER, Christensen JR. 1969. Infection by bacteriophage P1 and development of host-controlled restriction and modification and of lysogenic immunity. J Virol, 3:363-368.

    63. Yamada T, Kawasaki T, Nagata S, Fujiwara A, Usami S, Fujie M. 2007. New bacteriophages that infect the phytopathogen Ralstonia solanacearum. Microbiology.153:2630-2639.
        doi: 10.1099/mic.0.2006/001453-0

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    Bacteriophage secondary infection

      Corresponding author: Stephen T Abedon,
    • Department of Microbiology, the Ohio State University, Mansfield, OH 44906, USA

    Abstract: Phages are credited with having been fi rst described in what we now, offi cially, are commemorating as the 100th. anniversary of their discovery. Those one-hundred years of phage history have not been lacking in excitement, controversy, and occasional convolution. One such complication is the concept of secondary infection, which can take on multiple forms with myriad consequences. The terms secondary infection and secondary adsorption, for example, can be used almost synonymously to describe virion interaction with already phage-infected bacteria, and which can result in what are described as superinfection exclusion or superinfection immunity. The phrase secondary infection also may be used equivalently to superinfection or coinfection, with each of these terms borrowed from medical microbiology, and can result in genetic exchange between phages, phage-on-phage parasitism, and various partial reductions in phage productivity that have been termed mutual exclusion, partial exclusion, or the depressor effect. Alternatively, and drawing from epidemiology, secondary infection has been used to describe phage population growth as that can occur during active phage therapy as well as upon phage contamination of industrial ferments. Here primary infections represent initial bacterial population exposure to phages while consequent phage replication can lead to additional, that is, secondary infections of what otherwise are not yet phage-infected bacteria. Here I explore the varying meanings and resultant ambiguity that has been associated with the term secondary infection. I suggest in particular that secondary infection, as distinctly different phenomena, can in multiple ways infl uence the success of phage-mediated biocontrol of bacteria, also known as, phage therapy.

    • Phages interact with bacteria in the course of adsorption, infection, and virion release. Phage-phage interactions also can take place and may be categorized as occurring among phage virions (such as their aggregation), between phage genomes (particularly in terms of genetic recombination but also physiologically), or between virions and phage-infected bacteria. In this commentary Ⅰ initially consider the latter, which involves virion adsorption to already phage-infected bacteria—over the course of which a number of interesting phage-phage interactions can occur, e.g., (Abedon, 1994). Though these interactions all involve secondary adsorptions, they usually are referred to instead as either secondary infections or superinfections.

      Alternatively, the term secondary infection has been used in the phage literature with a distinctly different meaning, that is, to describe sequential infections that occur during phage population growth, such as in the course of phage therapy or within the context of phage contamination of industrial fermentations. Secondary infections thus can occur either in "parallel", as equivalent to secondary adsorptions or superinfections (one cell simultaneously interacting with more than one phage), or instead in "serial" as occurs during phage propagation through a bacterial culture (one phage lineage interacting sequentially with a series of cells). Here Ⅰ consider these differing uses along with their distinct impacts on the pharmacology of phage therapy.

    • The first use of the phrase "secondary infection" within the context of virion interaction with already phage-infected individual bacteria was, to my knowledge, by Doermann (1948), who was studying the then newly appreciated lysis inhibition phenomenon, and this usage is reflected in Benzer et al. (1950). Specifically, with lysis inhibition an already phage-infected bacterium– that is, a primary infection–can be induced to delay its lysis if a second phage should adsorb (Abedon, 1990; 1994; 2009a; 2012c; Moussa et al., 2012; 2014; Tran et al., 2005; 2007). In 1948, when Doermann published his lysis-inhibition study, the mechanism by which lysis inhibition was induced was little understood. Indeed, the phenomenon of superinfection exclusion had not yet been discovered (see French et al., 1952, for overview of the earliest descriptions of superinfection exclusion-related phenomena in bacteriophage); superinfection exclusion itself is a phage-expressed means by which progression from phage attachment to an already phage-infected bacterium can be prevented from progressing to coinfection of same bacterium (Abedon, 1994). There thus was little reason to distinguish between "secondary infection" and "secondary adsorption" in describing the action of subsequently adsorbing phages on already phage-infected bacteria since the secondarily adsorbing phages in the absence of superinfection exclusion could be assumed to reach the cytoplasms of their target bacteria. Indeed, Doermann employed both "secondary adsorption" and "secondary infection" in his 1948 study, seemingly interchangeably.

      The term secondary infection, as used to describe interactions between virions and phage-infected cells, subsequently has been much more frequently used than secondary adsorption. This stems, perhaps, from continuing uncertainty about the extent to which secondary adsorption in fact results in coinfection by a secondarily adsorbing phage. Alternatively, it is often the case that the terms "adsorption" and "infection" are used interchangeable, such as to describe a phage-bacterium interaction in which knowledge of successful infection also is uncertain; witness for example the use of multiplicity of infection which in many cases instead more correctly describes multiplicity of phage adsorption (Abedon, 2008; 2011a; 2012b; 2014; Abedon et al., 2010; Adams, 1959; Bigwood et al., 2009). It is possible, however, to define the concept of adsorption narrowly, that is, as a means of describing solely virion attachment, with any subsequent phage-genome uptake considered instead to represent infection. An interchange of the use of infection and adsorption, and also secondary infection vs. secondary adsorption, nonetheless is neither uncommon nor necessarily incorrect.

      The term adsorption, if defined more broadly, can describe aspects of phage-bacterium interaction that follow mere virion attachment to a bacterial cell. From this latter perspective, it thus may be possible to infer a time course of secondary phage interaction with a phage-infected bacterium, here with superinfection defined as equivalent to coinfection by a secondary phage:

      In this time course the concepts of secondary attachment and secondary adsorption, secondary adsorption and secondary infection, and also secondary infection and superinfection are assumed to not be synonymous, three assertions which are not necessarily valid. To more legitimately reflect this time course, I therefore replace arrows with the lesser-than-or-equal signs to indicate ambiguous progression by secondary phages towards successful coinfection:

      That is, secondary adsorption may or may not represent further progression ("greater than") towards secondary infection than secondary attachment, secondary infection may or may not represent further progression towards coinfection than secondary adsorption, and secondary infection may or may not be synonymous with superinfection or coinfection.

      Contrasting this lesser-than-or-equal-to progression from secondary phage attachment through coinfection we can state with much less ambiguity the following claim:

      Namely, and particularly if we define infection as beginning with phage-genome entrance into the adsorbed bacterium's cytoplasm, there is no overlap between the two extremes of virion attachment to an already phage-infected bacterium, on the one hand, and coinfection on the other. Though with less certainty, it also may be argued that the following series of inequalities might hold as well,

      where a lack of overlap is being claimed to exist between the concepts secondary adsorption and that of secondary infection. This perspective is simply a means of stating that phage infection follows phage adsorption.

      This contention of a distinction between adsorption and infection is not without precedent. The phenomenon known as lysis from without, for example, is a mechanism of phage-induced bacterial lysis that results from substantial amounts of phage adsorption but little phage infection (Abedon, 1992; 1994; 1999; 2011b). Furthermore, unless high multiplicities of adsorbing phages attach truly simultaneously to individual bacteria, then it is substantial secondary adsorption that must be inducing lysis from without rather than substantial secondary infection. Distinctions made between secondary attachment, secondary adsorption, secondary infection, and even superinfection are not necessarily consistent within the phage literature, however, nor unambiguously clear even within specific studies. Secondary infection nevertheless is a term that often has been used to mean the exposure of phage-infected bacteria to additional free phages; see Abedon (1994) for numerous older references and see also its usage by Adams (1959) and Stent (1963).

      One distinction that can be made with little ambiguity is that between infections that are productive versus infections that instead display lysogenic cycles, with both infection types at least potentially serving as primary infections, that is, infections of otherwise not phage-infected bacteria. Logically, therefore, the primary infection of a bacterial lysogen can be viewed as a secondary infection of a lysogenic infection, see for example, (Davis et al., 1999; Espeland et al., 2004; Fogg et al., 2007; Mann, 2003; Slavcev and Hayes, 2002; Smith et al., 2012; Weinfeld and Paigen, 1964; Werner and Christensen, 1969; Yamada et al., 2007). One can also describe such secondary infections within this context as superinfections (Sturino and Klaenhammer, 2006) and indeed the term "superinfection" generally appears to be more common within the phage literature than "secondary infection", including within the context of the concept of superinfection immunity as well as that of superinfection exclusion.

    • Phenomena that are directly associated with phage secondary infection or adsorption of already phage-infection bacteria include the above-noted lysis from without plus mechanisms of resistance to lysis from without (Abedon, 1994; Abedon, 1999). Both phenomena possibly play roles in the life history of certain phages, most notably the T-even phages, allowing for resistance to the premature lysis of cultures as mediated by secondary adsorption (i.e., resistance to lysis from without) along with a means of eventually assuring the lysis of those cultures, i.e., so-called lysis-inhibition collapse (Abedon, 1992; Abedon, 1999; Abedon, 2009a). Secondary infection is also seen in the parasitism of phage infections by satellite phages, such as phage P4's parasitism of phage P2 infections. See Turner and Duffy (2008) for discussion of the evolutionary ecology of phage-on-phage parasitism and Hyman and Abedon (2012) for its consideration in viral systems more generally. In addition, there is the also above-noted superinfection exclusion and superinfection immunity.

      These latter two phenomena operate by distinctly, conceptually different mechanisms (Hyman and Abedon, 2010), with superinfection exclusion a blockage as expressed by primary phages especially on the successful phage genome translocation into the adsorbed bacterium (Abedon, 1994) whereas superinfection immunity is a post genome-translocation mechanism by which subsequent secondary phage genetic contribution to infections is curtailed, though not always successfully (Fogg, et al., 2010). From the terms employed, we can view these phenomena literally as prevention (or exclusion) of secondarily adsorbing phages from superinfecting (superinfection exclusion) versus resistance (i.e., immunity) of a primary infection to the continuation of infection by secondary phages that nonetheless have successfully initiated superinfection (superinfection immunity).

      Note that Berngruber et al. (2010) collectively describe these two otherwise mechanistically distinct phenomena of blockage on successful secondary infection as superinfection inhibition. To the extent that secondary infection gives rise to some degree of coinfection then we can also consider what have been described as mutual exclusion, partial exclusion, or the depressor effect. These respectively are the prevention of replication of one of two lytically coinfecting but not closely related phages, essentially mutually exclusion but between closely related phages, and reductions in burst sizes given coinfection between phages that are not clonally related (Abedon, 1994). That is, to the extent that they act against phages that are secondarily infecting, then these mechanisms might be viewed as ones of partial or incomplete superinfection inhibition.

      In practical terms, the consequence of a failure of secondary infection is loss of the secondarily adsorbing phage. This loss occurs because the secondary phage must commit to adsorbing–that is, irreversible adsorption–prior to testing the infection status of the now adsorbed bacterium. The result inevitably is an ecological loss of phages, one which can be considered to be a potential mechanism of virion inactivation that is in addition to nucleic acid or virion-protein damage. This loss of secondary phages is of issue when phages are being employed as antibacterial agents, e.g., (Abedon et al., 2011), since phages display one-hit killing kinetics of bacteria (Bull and Regoes, 2006) and thus any more than one adsorbing phage to a single bacterium represents a loss of antibacterial agent. This loss of secondary phages as killing agents occurs regardless of whether superinfection inhibition is expressed by the primary infection since a single bacterial cell at most can only support a single phage burst. In addition, partial interference between coinfecting phages–i.e., mutual exclusion, partial exclusion, or depressor effect– can result in reductions of the productivity of resulting infections that in turn could result, for example, in less effective in situ phage amplification in numbers and/or poor phage penetration into bacterial biofilms (Abedon and Thomas-Abedon, 2010).

      Table 1.  Distinguishing among secondary infection varieties

      We would expect partial interference between coinfecting phages to occur particularly given phage therapy treatments that employ cocktails of otherwise not full coinfection-compatible phage strains. Resulting reductions in infection productivity during phage therapy, however, may be less of a concern given the formulation of infection-incompatible phages into cocktails (Chan et al., 2013; Chan and Abedon, 2012) so long as coinfection does not occur until late in phage population growth (i.e., until after most or all bacteria have already been bactericidally adsorbed), if passive rather than active treatments are employed (see below), or instead if phages are applied in multiple doses to infections rather than in just a single application (e.g., see arguments for multiple versus single dosing made in Abedon, 2012a; Abedon, 2014).

      From a non-applied perspective the superinfecting phage, even if otherwise "wasted" in terms of bacterial killing, nevertheless may still survive to some degree genetically. This survival may be measured in terms of the proportion of a burst that is associated with the secondary phage's genome (Abedon, 1994), though it remains an open question whether the associated proportional loss of primary phage genetic contribution to such bursts in fact evolutionarily selects for mechanisms of superinfection inhibition (Abedon, 1999). Of far greater relevance, however, is the contribution of secondary phage genetic survival to phage genome evolution, that is, as can result phage genomic mosaicism (Hatfull and Hendrix, 2011; Hendrix et al., 1999; Hendri et al., 2008). Whether the associated recombination between phages is a consequence of coinfection during lytic infections, the superinfection of lysogenic infections, or in some manner occurring between prophages, unless two phages have initially adsorbed simultaneously then coinfections are a consequence of secondary infections, and particularly parallel secondary infections.

    • Whether or not phage attachment, adsorption, and genome entry into a bacterium's cytoplasm occur, or indeed whether a phage contributes to an infection's burst, if the bacterium is already infected (primary infection) then these secondary phenomena can be viewed, as noted, as occurring in parallel with the primary infection. That is, they occur essentially at the same time in association with the same bacterial cell. Furthermore, and as equivalent to superinfection, this usage of secondary infection is borrowed from medical microbiology, that is, the acquisition by an already infected individual of an additional infectious agent: Two different infection processes by potentially independently originating parasites occur in association with same host at the same time, that is, in parallel.

      Within an individual host, secondary infection with a more serial connotation can refer to infections that are spatially removed from a primary focal infection, though which nonetheless are caused by the same lineages of pathogens. In a search of PubMed on "secondary infection" (in quotes), the oldest hit, dating from the late 19th Century (Pratt, 1899), appears to employ just that meaning. Here secondary can be viewed as temporally as well as spatially subsequent and therefore representing infections or at least "sub" infections that occur in serial. As the subsequent infection also occurs within the same host, the process can be viewed in addition as having tendencies towards parallel secondary infection. I described this form of secondary infection therefore as mixed parallel-serial.

      This concept of mixed parallel-serial secondary infection would not appear to be applicable to the phage infection of individual bacteria. It is also not applicable to phage penetration into clonal bacterial clumps (Abedon, 2011a; Abedon, 2012b; Abedon, 2012c; Abedon, et al., 2010), that is, unless phage spread is discontinuous such that multiple foci of phage infection (secondary infections) both become established within and are seeded by infections–focal-infection equivalents–of the same, clonal bacterial formation. Hence,

      Alternatively, Iyer and James (1978) speak of using anti-phage serum to prevent the "secondary reinfection"–and perhaps synonymously "secondary infection"– of cells that perhaps had been phage infected but in fact are no longer phage infected. These phage and bacterial hosts otherwise display what the authors describe as a carrier state (Abedon, 2009b).

      Thus, at least in principle a phage could be latently infecting a given bacterial lineage. As these bacteria replicate, at least one daughter cell could host a lytic infection while at least one other daughter cell could become spontaneously cured of its phage infection. The cured bacterium or its daughters could then become reinfected by a phage produced by the previously mentioned lytic infection. The result is secondary infection of a not-currently phage infected bacterium but where that bacterium nonetheless is a member of the same bacterial population that otherwise is still hosting the same phage population, but in a different cell/location. This is a convoluted though not necessarily unrealistic scenario and is at least suggestive that this mixed parallel-serial concept of secondary infection could be applied to more than one phage-associated circumstance. For the general scenario to hold, however, then bacteria as host organisms must in some sense be viewed as multi-celled, which provides the parallel aspect, and also some form of temporal as well as spatial discontinuity separating infection foci, infections by what otherwise is a single lineage of phages, must exist as well to supply the serial aspect.

      Secondary infections can be more purely serial by not involving subsequent infections in different locations of the same host but instead infections of entirely different hosts. Distinct from the phage literature, this usage is seen in epidemiology, e.g., (May and Anderson (1983): "R0 is the average number of secondary infections produced when one infected individual is introduced into a wholly susceptible host population" (p. 197), but comparable wording is found in the phage literature as well (Payne et al., 2000; Payne et al., 2001; Wei and Krone, 2005). This meaning, as applied to phages, appears to be equivalent to that of Sanders (1987) (p. 215), who describe how during "Cheesemaking protocols… effectively disperse phage throughout the product, encouraging secondary infections." Similarly, sequential phage infections described as "secondary infections" can be viewed as occurring within individual bacterial arrangements, e.g., such as streptococci (Barron et al, 1970), or within biofilms (Hughes et al, 1998). Equivalent usage is seen also with descriptions of the prevention of the secondary infection of clonally related bacteria as a consequence of the action of bacterial abortive infection systems (Fukuda et al, 2008).

      In short, serial secondary infections are sequential infections of different hosts, so thereby are not equivalent to parallel secondary infections which instead are of the same host. In addition, and also because infections are of different hosts, temporal and spatial discontinuities between infections occur automatically rather than requiring complicated scenarios, i.e., as was the case when considering instead mixed parallel-serial secondary infections. See Table 1 for further comparison of these varying forms of secondary infection.

    • The epidemiological or serial perspective on secondary infection has entered the phage therapy literature as a means of characterizing what has been described as "active" treatment (Payne et al, 2000; Payne and Jansen, 2001; Payne and Jansen, 2003); see also for example (Golshahi et al, 2008; Hudson et al, 2005; Ryan et al, 2011). From Payne and Jansen (2003) (p316): "It is conceptually useful to distinguish primary infection (infection of bacteria by phage from the inoculum) and secondary infection (infection of bacteria by phage that have been released by lysis of already infected cells). If the inoculated phage are numerous enough then the first round of primary infection and lysis can by itself remove significant numbers of bacteria, which we refer to as passive phage therapy. When therapy is based on secondary infection then there is an increase in phage numbers via viral self-replication, which we refer to as active phage therapy." That is, at a minimum phage-mediated biocontrol of bacteria, such as phage therapy (Abedon, 2009c), can be differentiated into that which does not require in situ phage replication (described as passive or inundative treatment) versus that which does require in situ phage population growth, i.e., active treatment (Abedon et al., 2010). With passive treatment, phages are supplied to target bacteria at high multiplicities (>>1) since bacterial eradication, for statistical reasons, requires multiple phage adsorptions of individual bacteria (Abedon, 2011).

      These multiple adsorptions, unless they all occur simultaneously, presumably involve secondary (2') infections, but of a parallel nature, that is, phage adsorption of already phage-infected bacteria:

      Payne R J H and Jansen V A A (2000) nevertheless refer to passive treatment as "by primary infection alone". They are not incorrect in this usage, however, but instead are using the term secondary infection to describe infections that occur serially rather than in parallel, i.e., in the course of phage population growth:

      Thus, initially supplied phages provide primary infections which, through phage infection and virion release, give rise to subsequent, that is, secondary infections. Indeed, the following progression more or less occurs as phage densities increase in situ in the course of phage population growth,

      with the transition between serial to parallel secondary infections, on a population-wide basis, occurring gradually rather than abruptly. Thus, the proportion of adsorptions to non-yet phage infected bacteria (serial secondary adsorption) at first predominates but then declines as the proportion of phage adsorption to already phage-infected bacteria ascends (parallel secondary adsorption). I derive this latter point further in the following section.

    • There is more to active phage therapy than simply phage population growth. Just as with passive treatment, ratios of adsorbing phages to target bacteria must substantially exceed one–due to the Poisson distribution of adsorbing phages to bacteria–if bacteria are to be eliminated (Abedon, 2011). This requirement that multiplicities ultimately exceed one leads to an interesting conflict in terms of use of the concepts of secondary infection.

      First, as noted and just as one sees with lysis from without as considered above, the "primary infections" of passive treatment, unless truly occurring simultaneously in terms of their adsorption, involve both primary and secondary infections, the latter of the parallel kind:

      For active treatment to be successful, this same end point must be reached, i.e., where phage numbers are sufficiently high that bacterial numbers are substantially reduced, a process which inherently will be associated with phage adsorption and potentially also infection of already phage-infected bacteria.

      Second, and contrasting passive treatment, with active treatment the original infections will tend to be primary in both a serial and parallel sense, with the latter due to the initially lower phage multiplicities that active treatment tends to imply. Therefore, there will be a relative lack of parallel secondary infections among these otherwise serial primary infections:

      That is, the initially added phages, which are primary infections in a serial sense, will tend to give rise to bacteria that have been adsorbed at most by only a single phage (and which as a consequence will make the majority of these serial primary infections also primary infections in a parallel sense).

      As noted, subsequent secondary infections, in an epidemiological/serial sense, ultimately must result in secondary infections in a per-target-cell/parallel sense if phage therapy is to be successful (multiple phage adsorptions of individual bacteria to assure multi-fold eradication of those target bacteria). These secondary infections that are associated with higher phage multiplicities, in other words (parallel secondary infections), represent a consequence of secondary infections that are associated with phage population growth (serial secondary infections). Thus, as presented also towards the end of the previous section,

      Secondary infection must occur for active treatment to result in substantial elimination of target bacteria. It must occur, however, as two wholly distinct phenomena: Infection of subsequent bacteria by phages produced in situ (secondary infection in a serial sense) in combination with what in most cases is a subsequent as well as staggered high multiplicity infection or adsorption of remaining target bacteria (secondary infection in a parallel sense).

    • Because of differing traditions, as well as numerous associated phenomena, the concept of secondary infection can be surprisingly complex. It is important nonethe-less to distinguish meanings, perhaps particularly as they may be employed in the phage therapy literature. To help stem confusion, for authors it can be important to define intended meanings of secondary infection upon use. In particular, parallel secondary infection, as defined here, involves at a minimum multiple, distinct phages interacting with a single bacterial cell whereas serial secondary infection involves multiple phage interactions with multiple bacterial cells.

    • The author declares that they have no competing interests. This article does not contain any study with human or animal subjects performed by any of the authors.

    Table (1) Reference (63) Relative (20)



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