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Table 1 Reassortant geographical and temporal distributions and time of the most recent common ancestor (TMRCA)

From: Frequency of influenza H3N2 intra-subtype reassortment: attributes and implications of reassortant spread

Reassortant lineage

Genomes (N)a

Sampling year

TMRCA (95% HPDb)

Lineage persistencec (CI)

Existence since TMRCAd(CI)

Sampling lagg

Global

High Local

Low Local

I (Baby Blue)

4

2012

2011.8 (2011.5-2011.9)

0.5 (0-1)*

0.7 (0.1-1.5)

0.2

  

N America

II (Dark Blue)e

20

2013-2014

2012.5 (2012.2-2012.8)

0.7 (0.53-0.87)

1.7 (1.23-2.17)

1

 

M Easte

 

III (Light Blue)

103

2010-2013

2009.7 (2009.6-2009.8)

3 (2.64-3.36)

3.8 (3.34-4.26)

0.8

Yes

  

IV (BlueD)

25

2011

2010.3

0.5 (0-1)*

1.2 (0.7-1.7)

0.7

 

Asia

 

V (GreenD)

11

2012

2011.5 (2011.2-2011.7)

0.5 (0-1)*

1 (0.3-1.8)

0.5

  

N America

VI (GreenL)

5

2012

2011.3 (2011-2011.7)

0.47 (0.27-0.67)

1.2 (0.6-1.7)

0.7

 

Australia

 

VII (Green)

85

2010-2011

2009.2 (2009-2009.3)

1 (0.5-1.5)

2.3 (1.7-3)

1.3

 

SC America

 

VIII (Dark Green)

8

2010

2009.7 (2009.4-2009.8)

0.5 (0-1)*

0.8 (0.2-1.6)

0.3

  

SC America

IX (Salmon)

13

2010

2009.3 (2009-2009.5)

0.5 (0-1)*

1.2 (0.5-2)

0.7

  

SC America

X (Red)

351

2010-2012

2008.8 (2008.3-2009.1)

2 (1.54-2.46)

3.7 (2.94-4.66)

1.7

Yes

  

XI (Maroon)

46

2012-2013

2011.1 (2010.9-2011.3)

1 (0.5-1.5)

2.4 (1.7-3.1)

1.4

 

N America

 

XII (Dark Red)

14

2011-2013

2010.9 (2010.6-2011.4)

2 (1.57-2.43)

2.6 (1.67-3.33)

0.6

Yes

  

XIII (Orange)

15

2010-2011

2009.1 (2009-2009.2)

1 (0.5-1.5)

2.4 (1.8-3)

1.4

 

Asia

 

XIV (Purple)

40

2009

2007.8 (2007.4-2008.1)

0.5 (0-1)*

1.7 (0.9-2.6)

1.2

 

N America

 

XV (Lavender)

5

2009

2008.6 (2008.3-2008.9)

0.5 (0-1)*

0.9 (0.1-1.7)

0.4

  

N America

XVI (Pink)

3

2009

2008.9 (2008.7-2009)

0.5 (0-1)*

0.6 (0-1.3)

0.1

  

N America

Yellow (single unique)f

53 + 4

2008-2013

       

Total

805

        
  1. aThe 7 recurring reassortant vaccine genomes (see Methods) were not counted
  2. b HPD highest posterior density intervals
  3. cRefers to the period of time when the lineage was observed in the human population
  4. dRefers to the total lifespan of the reassortant variant in question
  5. eAlthough assigned High Local by the criteria, it cannot with certainty be regarded as such due to low regional and temporal sampling
  6. f4 genomes were identical to 4 of the unique reassortants
  7. gSampling lag is defined in the “Between-lineage and vaccine clade reassortment despite limited reassortant lifespan” subsection of Results
  8. *All genomes were sampled in the same year with no exact dates. Thus, the persistence was given a value of 0.5, given the sampling uncertainty of 6 months