Cyanophage N-1

In this article, we will explore the most relevant aspects about Cyanophage N-1, a topic that has aroused great interest in contemporary society. Over the years, Cyanophage N-1 has represented a point of discussion and reflection in various areas, both academic and in daily life. From its origins to its current impact, Cyanophage N-1 has been the subject of numerous investigations, debates and controversies, becoming a topic of enormous relevance today. Through this analysis, we seek to offer a comprehensive and updated vision of Cyanophage N-1, providing the reader with a complete and detailed overview that allows us to understand its importance and implications in today's society.

Cyanophage N-1
Virus classification
Group:
Group I (dsDNA)
Order:
Caudovirales
Family:
Myoviridae
Genus:
Cyanomyovirus (proposed)
Species:
Cyanophage N-1

Cyanophage N-1 is a myovirus bacteriophage that infects freshwater filamentous cyanobacteria of the Nostoc genus. The virus was first isolated by Kenneth Adolph and Robert Haselkorn in 1971 in the US, from the nitrogen-fixing cyanobacterium, Nostoc muscorum. N-1 is closely related to cyanophage A-1, but only distantly to other cyanophages of freshwater or marine origin.

Structure

The virus has a polyhedral head with a diameter of around 61 nm. The contractile tail is 100 nm long, and is attached to the head via a tail capital. The neck region bears fibres. The mature virus particle contains at least 19 proteins.

Genome

The linear, double-stranded DNA genome is 64,960 base pairs in length – only half the size of most phages with contractile tails, which typically fall in the range 161–231 kb. It has a GC-content of 35.4%. Of the 91 open reading frames (ORFs), only 33 show similarity to other known sequences. Remarkably, the genome of Cyanophage N1 encodes a functional CRISPR array, which has been suggested to protect the host against infection by competing viruses.

Life cycle and interaction with the host

The optimal pH for viral adsorption to N. muscorum is 7.6–8.1. The rate of adsorption is reduced with increasing age of the host cells. The viral latent period is 7 hours, which is similar to cyanophages of the LPP-1 group. The burst size is 100 plaque-forming units per cell.

Host photosynthesis is required for the virus to replicate, with photosynthesis being required throughout the life cycle, rather than at any particular point. Viral replication is powered by cyclic photophosphorylation and the use of carbohydrate stores; photosystem II activity is not required. Cyanophage N-1 infection of N. muscorum is associated with several changes in the host's carbon and nitrogen metabolism, including an increase in glucose-6-phosphate dehydrogenase enzyme concentration and a decrease in glutamine synthetase activity.

References

  1. ^ a b c Chénard C, Wirth JF, Suttle CA (2016), "Viruses Infecting a freshwater filamentous cyanobacterium (Nostoc sp.) encode a functional CRISPR array and a proteobacterial DNA polymerase B", mBio, 7 (3): e00667-16, doi:10.1128/mBio.00667-16, PMC 4916379, PMID 27302758
  2. ^ a b Adolph KW, Haselkorn R (1971), "Isolation and characterization of a virus infecting the blue-green alga Nostoc muscorum", Virology, 46 (2): 200–208, doi:10.1016/0042-6822(71)90023-7, PMID 4108613
  3. ^ Sarma 2012, pp. 420, 423
  4. ^ Sarma 2012, p. 423
  5. ^ Adolph KW, Haselkorn R (1973), "Blue-green algal virus N-1: Physical properties and disassembly into structural parts", Virology, 53 (2): 427–40, doi:10.1016/0042-6822(73)90222-5, PMID 4268208
  6. ^ Sarma 2012, pp. 427, 429
  7. ^ Sarma 2012, p. 430
  8. ^ Calendar 2006, p. 524
  9. ^ Sarma 2012, p. 433

Sources

Wikious
Boobota
Sagapedia