All viruses, including SARS-CoV-2, the virus that causes COVID-19, change over time. Most changes have little to no impact on the virus’s properties. However, some changes may affect the virus’s properties, such as how easily it spreads, the associated disease severity, or the performance of vaccines, therapeutic medicines, diagnostic tools, or other public health and social measures.
In June 2020, the WHO Virus Evolution Working Group was established with a specific focus on SARS-CoV-2 variants, their phenotype and their impact on countermeasures. This later became the
Technical Advisory Group on SARS-CoV-2 Virus Evolution
. In late 2020, the emergence of variants that posed an increased risk to global public health prompted WHO to characterize some as variants of interest (VOIs) and variants of concern (VOCs) in order to prioritize global monitoring and research, and to inform and adjust the COVID-19 response. From May 2021 onwards, WHO began assigning simple,
easy-to-say labels
for key variants.
Considerable progress has been made in establishing and strengthening a global system to detect signals of potential VOIs or VOCs and rapidly assess the risk posed by SARS-CoV-2 variants to public health. It remains critical that these systems are maintained, and data are shared, according to
good principles
and in a timely fashion, as SARS-CoV-2 continues to circulate at high levels around the world. While monitoring the circulation of SARS-CoV-2 globally, it also remains essential to monitor their spread in animal populations and chronically infected individuals, which are crucial aspects of the global strategy to reduce the occurrence of mutations that have negative
public health implications
. In March 2023, WHO updated its tracking system and working definitions for variants of concern, variants of interest and variants under monitoring. They can be found
here
. The previous working definitions can be found
here
.
Updated working definitions and primary actions for
SARS-CoV-2 variants
Updated working definitions and primary actions for
SARS-CoV-2 variants
|
Pango lineage
|
Nextstrain clade
|
Genetic features
|
Earliest documented samples
|
Date of designation and risk assessments
|
|
XBB.1.5
|
23A
|
Recombinant of BA.2.10.1 and BA.2.75 sublineages, i.e. BJ.1 and BM.1.1.1, with a breakpoint in S1.
XBB.1 + S:F486P (similar Spike genetic profile as XBB.1.9.1)
|
21-10-2022
|
11-01-2023
|
|
XBB.1.16
|
23B
|
Recombinant of BA.2.10.1 and BA.2.75 sublineages, i.e. BJ.1 and BM.1.1.1
XBB.1 + S:E180V, S:K478R and S:F486P
|
09-01-2023
|
17-04-2023
XBB.1.16 Initial Risk Assessment, 17 April 2023
XBB.1.16 Updated Risk Assessment, 05 June 2023
|
|
EG.5
|
Not assigned
|
XBB.1.9.2 + S:F456L
Includes EG.5.1: EG.5 + S:Q52H
|
17-02-2023
|
09-08-2023
EG.5 Initial Risk Evaluation, 09 August 2023
|
|
Pango lineage
|
Nextstrain clade
|
Genetic features
|
Earliest documented samples
|
Date of designation and risk assessments
|
|
BA.2.75
|
22D
|
BA.2 + S:K147E, S:W152R, S:F157L, S:I210V, S:G257S, S:D339H, S:G446S, S:N460K, S:Q493R reversion
|
31-12-2021
|
06-07-2022
|
|
CH.1.1
|
22D
|
BA.2.75 + S:L452R, S:F486S
|
27-07-2022
|
08-02-2023
|
|
XBB*
|
22F
|
BA.2+ S:V83A, S:Y144-, S:H146Q, S:Q183E, S:V213E, S:G252V, S:G339H, S:R346T, S:L368I, S:V445P, S:G446S, S:N460K, S:F486S, S:F490S
|
19-08-2022
|
12-10-2022
|
|
XBB.1.9.1
|
23D
|
Recombinant of BA.2.10.1 and BA.2.75 sublineages, i.e. BJ.1 and BM.1.1.1
XBB.1 + S:F486P (similar Spike genetic profile as XBB.1.5)
|
05-12-2022
|
30-03-2023
|
|
XBB.1.9.2
#
|
23D
|
Recombinant of BA.2.10.1 and BA.2.75 sublineages, i.e. BJ.1 and BM.1.1.1
XBB.1 + S:F486P, S:Q613H
|
05-12-2022
|
26-04-2023
|
|
XBB.2.3
|
23E
|
Recombinant of BA.2.10.1 and BA.2.75 sublineages, i.e. BJ.1 and BM.1.1.1
XBB + S:D253G, S:F486P, S:P521S
|
09-12-2022
|
17-05-2023
|
|
BA.2.86
(Only 3 sequences available. Added as VUM based on the large number of mutations identified)
|
Not assigned
|
Mutations relative to putative ancestor BA.2
|
24-07-2023
|
17-08-2023
|
*
Excludes XBB sublineages listed here as VOIs and VUMs
#
Excludes XBB.1.9.2 sublineages listed here as VOIs and VUMs
WHO encourages the sharing of pathogen genome
data to protect global public health. Sharing of
pathogen genome data is critical for preventing,
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