Lineage B.1.617 is a lineage ofSARS-CoV-2, the virus that causesCOVID-19.[1] It first came to international attention in late March 2021 after the newly establishedINSACOG performed genome sequencing on positive samples throughout variousIndian states. Analysis of samples fromMaharashtra had revealed that compared to December 2020, there was an increase in the fraction of samples with the E484Q andL452R mutations.[2] Lineage B.1.617 later came to be dubbed adouble mutant by news media.[3]
Lineage B.1.617 has three sublineages according to thePANGO nomenclature:
B.1.617.1 (Kappa variant), first detected in India in December 2020
B.1.617.2 (Delta variant), first detected in India in late 2020
Here are some of the common mutations present in thespike protein of lineage B.1.617. Not all sublineages of B.1.617 share the same mutations:
L452R. The substitution at position 452, aleucine-to-arginine substitution, confer stronger affinity of the spike protein for theACE2 receptor and decreased recognition capability of the immune system.[5][6] These mutations, when taken individually, are not unique to the variant; rather, their simultaneous occurrence is.[5][7] This mutation is present in all three sublineages of B.1.617.
T478K. The substitution at position 478, athreonine-to-lysine substitution,[8] is only found in lineage B.1.617.2.[9]
E484Q. The substitution at position 484, aglutamic acid-to-glutamine substitution, confers lineage B.1.617 stronger binding potential to the humanACE2 receptor, as well as better ability to evade hosts' immune systems in comparison to other variants. This mutation is not present in the B.1.617.2 genome.[10]
P681R. The substitution at position 681, aproline-to-arginine substitution, which, according toWilliam A. Haseltine, may boost cell-level infectivity of the variant "by facilitating cleavage of the S precursor protein to the active S1/S2 configuration".[10] This mutation is present in all three sublineages of B.1.617.
The first B.1.617 genome sequence was submitted toGISAID in fall 2020 according to one source.[12] The team at PANGO behind manually curating thephylogenetic tree of SARS-CoV-2 noted the earliest sequence was from 7 December 2020. They proposed a new designation for the variant containing the mutations at the spike protein including G142D, L452R, E484Q, D614G, P681R among others and this variant went to be assigned PANGO lineage B.1.617 on 1 April 2021.[13] They revised the phylogenetic tree to include three sublineages of B.1.617 on 21 April 2021 after noticing that not all genome sequences being assigned by the PANGOLIN tool contained the same set of mutations.[14]
Up until mid-April 2021, India submitted the most B.1.617 genomes, followed in frequency by UK and the US. Based on genome information, lineage B.1.617 was first detected in the UK on 22 February 2021, and in the US on 23 February 2021.[12]
After detecting 77 cases of lineage B.1.617 in the UK in mid-April 2021,Public Health England designated the lineage as a variant under investigation.[15] In less than two months, the Delta variant would go on to become the dominant variant in the UK with researchers stating early evidence suggested there may be an increased risk of hospitalization for Delta compared to the previously dominant Alpha variant.[16]
^Koshy, Jacob (8 April 2021)."Coronavirus | Indian 'double mutant' strain named B.1.617".The Hindu. Retrieved19 April 2021.Though these mutations have individually been found in several other coronavirus variants, the presence of both these mutations together have been first found in some coronavirus genomes from India.
^Greenwood, Michael (30 March 2021)."SARS-CoV-2 mutation T478K spreading at alarming speed in Mexico".Medical News. Retrieved6 September 2021.The T478K mutation constitutes the exchange of the non-charged amino acid threonine with the positively charged lysine at position 478...
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This article incorporates text published under the BritishOpen Government Licence v3.0: