by Rob Phillips and Ron Milo
Figure 1. Source
Viruses proliferate by infecting cells and hijacking their replication and protein synthesis machinery. After new viral proteins are synthesized and assembled, bursts of viruses are released from the infected (and usually soon to be dead) cells, starting the process all over again. The "viral burst size" – the number of viruses released from each infected cell – alludes to the fact that often virus emission leads to either cell lysis (bacteriophage) or cell death (HIV infection of T-cells). The emission of new viruses from an infected cell hence occurs as a burst of a characteristic numbers of viruses, on time scales lasting from minutes to days, depending upon the kind of virus and host. Burst sizes for different viruses have a large range corresponding in turn with the range of different sizes of the host cells. For example, SIV, a cousin and model for the HIV virus, is released from infected T cells with a burst size of ≈50,000 (BNID 102377) whereas cyanobacterial viruses have characteristic burst sizes of ≈40−80 (BNID 103247, 104841, 104842) and phage lambda and other phages (such as T4, T5 and T7) attacking bacteria have burst sizes of ≈100−300. (BNID 105025, 105870).
(click to enlarge) Figure 2. Source
One interesting way to garner an impression of the impact of a viral infection on the host metabolism is by thinking about the volume taken up by the newly synthesized viruses in comparison with the size of the host cell. In particular, we ask what fraction of the host cell volume is occupied by all the viruses making up a viral burst? These volumes can be thought of as a proxy for biomass and thus reflect on the cell’s resources that were seized. An SIV virion is roughly 100 nm in diameter and the host cell has a corresponding diameter of about 10 μm. Given these numbers, 50,000 virions thus represent about 5% of the cell’s volume. In the case of bacteria and the viruses that infect them, a T-phage with ≈50 nm diameter (BNID 105870) shows burst sizes of ≈200 in an E. coli cell, representing ≈2% of the volume. Therefore, the characteristic volume fraction taken up by the viruses in these two very distinct cell types shows a much smaller range (100-fold). This may reflect limits to how much biomass viruses can extract from infected cells. In the marine environment, which is often depleted in phosphorus that is mostly required for nucleotides, it was suggested that the DNA sizes of the virus and host govern the virion burst size as the virus utilizes the host DNA building blocks (C. M. Brown et al., J. Mar. Bio. Ass. U.K., 86:491, 2006). The measurements and estimates throughout this vignette raise the very interesting question of what governs the overall burst size, as well as what fraction of the synthesized viral DNA and proteins actually make it into infectious viruses.
From Cell Biology by the Numbers, found here.
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