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. Author manuscript; available in PMC: 2010 Apr 5.
Published in final edited form as: Parasitology. 2009 Jul 27;136(10):1097–1105. doi: 10.1017/S0031182009990539

Table 2.

Proportions of mixed-clone infections, mean number of microsatellite alleles per locus, genetic diversity (virtual heterozygosity [HE]), and linkage disequilibrium (standardized index of association [IS A]) in malaria parasite populations from rural Amazonia

ISA by infection typed
Parasite species Multiple-clone infections (%) Alleles per locus, mean±S.E. (range) HE mean±S.E. (range) All Those with unique haplotypes
P. falciparuma 13·9 2·8±0·4 (2–4) 0·43±0·06 (0·09–0·67) 0·088 (n=44) 0·032 (n=31)
P. falciparumb 21·8 3·3±0·4 (2–5) 0·46±0·04 (0·20–0·68) 0·070 (n=55) 0·028 (n=40)
P. vivaxc 49·0 6·9±0·8 (3–14) 0·71±0·04 (0·34–0·88) 0·202 (n=49) 0·119 (n=39)
a

44 samples collected in Granada between 2004 and 2006.

b

44 samples collected in Granada between 2004 and 2006 and 11 samples collected in Plácido de Castro in 2008.

c

49 samples collected in Granada between 2004 and 2005 and genotyped with 14 microsatellites (Ferreira et al. 2007).

d

All IS A values were significantly larger than zero (P = 0·001), denoting significant multilocus linkage disequilibrium.