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. 2011 May 11;6(5):e19688. doi: 10.1371/journal.pone.0019688

Table 2. African isolates of C. neoformans var. grubii are more diverse than the global population: comparison of the diversity indices and neutrality tests at each locus.

Locus Populationa No. of isolatesb Gene diversity Nucleotide diversity Mean pairwise difference Tajima's
(h) (π) (d) TD c
GPD1 African 99 0.86 0.005 2.3 −0.67
Global 57 0.35 0.001 0.51 −1.8
TEF1 African 99 0.84 0.003 2.01 1.07
Global 57 0.72 0.002 1.29 −1.62
CAP59 African 97 0.6 0.002 0.97 −0.38
Global 47 0.61 0.002 1.01 −1.6
PLB1 African 80 0.77 0.003 1.89 −1.12
Global 57 0.68 0.002 0.94 −0.89
IGS1 African 93 0.81 0.01 7.02 −1.7
Global 41 0.23 0.0008 0.57 −1.7
SOD1 African 94 0.6 0.009 5.17 0.4
Global 57 0.03 0.0005 0.28 −2.1
LAC1 African 88 0.82 0.006 2.67 0.45
Global 49 0.73 0.004 1.3 1.02
URA5 African 92 0.75 0.007 4.7 0.24
Global 47 0.6 0.001 1 −1.59
a

The diversity of clinical and environmental strains of C. neoformans var. grubii from Botswana and South Africa was compared with that of a selection of the most genetically diverse global isolates available [10]. The “African” population included all clinical and avian isolates of C. neoformans var. grubii (85 strains) as well as 14 isolates from African trees; that is, we analyzed only one isolate per tree because multiple isolates from the same tree and surrounding soil were clonal. The “Global” sample was comprised of a larger sample of 57 previously genotyped, non-arboreal strains from 14 different countries (excluding Botswana and South Africa), and they included multiple isolates of each unique MLST or AFLP genotype [10]. Except for the CAP59 locus, this purposely enlarged and intentionally diversified global sample revealed less variation (i.e., lower h, π and d values) than the sample of African isolates.

b

We excluded strains with recombinant haplotypes at a locus.

c

Values of Tajima's TD for which the null hypothesis of neutrality was rejected are bolded.