It may have contrary effects
like inferior genotypes are rescued and maintained in population.
Complementation at high MOI leads to multiplication of defective particles.
High MOI also leads to multiple genomic copies of same gene in one infected
cell. In phage if copy number is one it will be lytic and kill the host cell
and if it exceeds one it becomes lysogenic and host cell remains alive.
The number of phage infecting
each bacterium could be calculated from Poisson equation: P(n)
= (m*n × e-m)/n! where P(n) is the probability
that the cell will be infected with exactly “n” phage and “m” is the average
number of phage per cell (that is MOI).
High MOI leads to complex
effects on genome selection Distribution of viral particles at different sites
of an infection are unknown and will affect MOI and efficiency of selection. The
population with highest fitness in the original host does not adapt well in new
hosts whereas low frequency genotypes from original host may adapt well in new host.
Different types of viruses will be affected differently by MOI.
Source: https://kb.10xgenomics.com/hc/article_attachments/360043450932/MOI.png
References
[2] A. Stern and R. Andino, “Viral Evolution: It is All About Mutations,” in Viral Pathogenesis: From Basics to Systems Biology: Third Edition, Elsevier Inc., 2016, pp. 233–240. doi:10.1016/B978-0-12-800964-2.00017-3.
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