Measles morbillivirus

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Measles virus
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Measles morbillivirus
"Measles morbillivirus" electron micrograph
Measles morbillivirus
electron micrograph
Virus classification Edit this classification
(unranked): Virus
Realm: Riboviria
Kingdom: Orthornavirae
Phylum:
Negarnaviricota
Class: Monjiviricetes
Order: Mononegavirales
Family: Paramyxoviridae
Genus: Morbillivirus
Species:
Measles morbillivirus
Synonyms[1]

Measles virus

Measles morbillivirus (MeV), also called measles virus (MV), is a

single-stranded, negative-sense, enveloped, non-segmented RNA virus of the genus Morbillivirus within the family Paramyxoviridae. It is the cause of measles
. Humans are the natural hosts of the virus; no animal reservoirs are known to exist.

Disease

The virus causes

erythematous rash and a pathognomonic Koplik spot seen on buccal mucosa opposite to lower 1st and 2nd molars. The virus is spread by coughing and sneezing via close personal contact or direct contact with secretions.[2]

Replication cycle

Measles morbillivirus cell entry receptors.
Measles morbillivirus genome structure

Entry

The measles virus has two envelope

signaling lymphocyte activation molecule (SLAMF1) and the cell adhesion molecule Nectin-4.[3] For wild type and vaccine strains, extracellular domains of CD150 (SLAM or SLAMF1)[4][5] and/or of nectin-4 (also called Poliovirus-Receptor-Like 4 (PVRL4))[6][7] mainly work as cell entry receptors. A minor fraction of wild type virus strains and all modern vaccine strains derived from the Edmonston strain also use CD46.[8][9]

Genome replication and viral assembly

Once the virus has entered a host cell, its strand of negative sense ssRNA is used as a template to create a positive sense copy using the RNA-dependent RNA polymerase that's included in the virion. Then this copy is used to create a new negative copy, and so on, to create many copies of the ssRNA. The positive sense ssRNA is then mass translated by host ribosomes, producing all viral proteins. The viruses are then assembled from their proteins and negative sense ssRNA, and the cell will lyse, discharging the new viral particles and restarting the cycle.[10]

Measles morbillivirus virion structure
Measles morbillivirus life cycle

Genome and virion structure

The RNA genome of the virus codes 6 main proteins Nucleoprotein (N), Phosphoprotein (P), Matrix protein (M), Fusion protein (F), Hemagglutinin (H), and Large Protein (L),[11] which represents RNA dependent RNA polymerase (RdRp). The viral genome also codes two non-structural proteins C and V. These non-structural proteins are innate immunity antagonists; they help the virus to escape host immune response. Inside the virion genomic RNA is forming complex with N, L and P proteins. N, P and M proteins regulate RNA synthesis by RdRp. The virus is enveloped by a lipid membrane and glycoproteins H and F are virion surface proteins that are associated with this lipid membrane.[citation needed]

Artist's impression of a cross-section through a measles virus

Evolution

The measles virus evolved from the now eradicated rinderpest virus which infected cattle.[12] Sequence analysis has suggested that the two viruses most probably diverged in the 11th and 12th centuries, though the periods as early as the 5th century fall within the 95% confidence interval of these calculations.[12]

Other analysis has suggested that the divergence may be even older because of the technique's tendency to underestimate ages when strong

purifying selection is in action.[13] There is some linguistic evidence for an earlier origin within the seventh century.[11][14] The current epidemic strain evolved at the beginning of the 20th century—most probably between 1908 and 1943.[15]

Genotypes

The measles virus genome is typically 15,894 nucleotides long and encodes eight proteins.

clades of measles (A–H). Subtypes are designed with numerals—A1, D2 etc. Currently, 23 subtypes are recognised. The 450 nucleotides that code for the C‐terminal 150 amino acids of N are the minimum amount of sequence data required for genotyping a measles virus isolate. The genotyping scheme was introduced in 1998 and extended in 2002 and 2003.[citation needed
]

Despite the variety of measles genotypes, there is only one measles serotype. Antibodies to measles bind to the hemagglutinin protein. Thus, antibodies against one genotype (such as the vaccine strain) protect against all other genotypes.[17]

The major genotypes differ between countries and the status of measles circulation within that country or region. Endemic transmission of measles virus was interrupted in the United States and Australia by 2000 and the Americas by 2002.[18]

Infection

In the early stages of infection, the measles virus via

T lymphocytes[23] also via SLAMF1 receptor.  In addition, it infects epithelial cells located in the airways. These cells become infected via nectin-4 receptor and by cell to cell contacts with infected immune cells. The infection of epithelial cells allows the virus to be released via the airstream.[24][25]

References

  1. ^ "ICTV Taxonomy history: Measles morbillivirus". International Committee on Taxonomy of Viruses (ICTV). Retrieved 15 January 2019.
  2. ^ CDC (5 November 2020). "Measles is Easily Transmitted". Centers for Disease Control and Prevention. Retrieved 28 December 2023.
  3. PMID 23631113
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  6. OCLC 806252697.{{cite book}}: CS1 maint: multiple names: authors list (link
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  17. ^ "Measles". Biologicals — Vaccine Standardization. World Health Organization. 11 March 2013. Archived from the original on 1 May 2014.
  18. ^ "No endemic transmission of measles in the Americas since 2002". Pan American Health Organization. 14 February 2017. Retrieved 11 September 2017.
  19. PMID 20042501
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External links