I have mapped the polymorphisms for this strains in the h1n1 sequences - I believe it's more appropriate in this thread.
I used NewYork/06 as an (arbitrary) consensus sequence.
I included each sequence that shares at least one SNP with HK/2369 that is not "widespread" (ie. that doesn't have more than 6 individuals in my bank).
Code:
HA NA
006 220 229 239 240 314 391 470 106 158 248 275 291
consensus GTA ACA CCG GAT CAA CCG GAG TTA ATA CTA GAT CAC GTG
marker (Syn, Widespread) S W SW SW SW W S W S
-------------------------------------------------------------------------------------
A/Hong Kong/2369/2009(H1N1) GTG GAA TCG TAC GTA
A/New Jersey/01/2009(H1N1) GAA GTA
A/Paris/2591/2009(H1N1) TCA GAA TTA
A/Oklahoma/03/2009(H1N1) TCA CCT GAA CTA GTA AAT GTA
A/Finland/553/2009(H1N1) GTG CGA
x3
Of the five HK/2369 specific markers, three can be found in other sequences whose correspondence cannot be explained by direct lineage.
I then expanded Finland/553 in a similar fashion to unroll its (non-widespread) 240CGA SNP :
Code:
HA NA
006 073 169 220 229 239 240 314 391 470 565 106 158 248 275 291
consensus GTA AAC GTT ACA CCG GAT CAA CCG GAG TTA TGT ATA CTA GAT CAC GTG
marker (Syn, Widespread) S S S W SW SW SW S W S W S
-------------------------------------------------------------------------------------------------
A/Hong Kong/2369/2009(H1N1) GTG GAA TCG TAC GTA
A/New Jersey/01/2009(H1N1) GAA GTA
A/Paris/2591/2009(H1N1) TCA GAA TTA
A/Oklahoma/03/2009(H1N1) TCA CCT GAA CTA GTA AAT GTA
A/Finland/553/2009(H1N1) GTG CGA
A/Mexico/InDRE4487/2009(H1N1) TCA CGA CTA GTA AAT
A/Texas/17/2009(H1N1) AAT GTC TCA CGA CTA TGC GTA AAT
A/Texas/37/2009(H1N1) AAT GTC TCA CTA TGC GTA AAT
This SNP (240CGA) appears in three individuals on which the marker presence cannot be explained by simple direct lineage.
I have 391 individuals in my bank for HA and 367 for NA (I only use sequences with full coding regions).
Whatever the reason - codon bias, recombination...; something not random is going on here - or it's some very low-entropy kind of random.