0.9.0. Reference sequences were downloaded from GenBank and the software program GARLI [Genetic Algorithm for Rapid Likelihood Inference] was used to generate the maximum likelihood (ML) tree [14]. Development of ISSR Fingerprinting Method The ISSR primers were designed to flank di-, tri- and tetra-nucleotide repeats.

A total of ten repeat primers were synthesized: two di-nuclotide [DDB(nn)8], five trinucleotide [DDB(nnn)5], and three tetranuclotide [DDB(nnnn)4] (capital letters denote degenerate sites: B denotes nucleotides c, g, or t; D denotes a, g, or t; subscripts indicate the number of repeats) and 5′ labeled with 6-carboxyfluorescein dye (6-FAM) at the Centers for Disease Control and Prevention Biotechnology Core Facility (VX-689 ic50 Atlanta, CA-4948 chemical structure GA) (Table 1). Table 1 ISSR primers designed for this study Primer Sequence Repeat Type ISSR_7 DDB(agg) 5 Trinucleotide ISSR_8 DDB(cag)5 Trinucleotide ISSR_9 DDB(gag)5 Trinucleotide ISSR_10 DDB(ctc) 5 Trinucleotide ISSR_11 DDB(gtg)5 Trinucleotide ISSR_12 DDB(aacg)4 Tetranucleotide ISSR_13 DDB(cgca) 4 Tetranucleotide ISSR_14 DDB(gcca)4 Tetranucleotide ISSR_15

DDB(ct)8 Dinucleotide ISSR_16 DDB(ca)8 Dinucleotide Capital letters in ISSR primer sequences denote degenerate sites: B denotes nucleotides c, g, or t; D denotes a, g, or t. Subscripts indicate the number of repeats. Bold lettering indicates the primers used for fingerprinting. Initially, ten ISSR primers were tested for their ability to generate reproducible, complex fingerprinting patterns on a panel of 40 A. terreus isolates randomly selected AZD1390 price from the global isolate collection. For PCR amplification, 3-5 μl of genomic DNA was used as the template in a final reaction volume of 25 μl consisting of PCR buffer (10 mM Tris-HCl, 1.5 mM MgCl2, 50 mM KCl, pH 8.3); 0.2 mM each of dATP, dGTP, dCTP, and dTTP; 2 pmol of a single primer; and 1.3 U of Taq DNA polymerase (Roche Applied Science, Mannheim, Germany). Amplification

was performed in a GeneAmp PCR system 9700 thermocycler (Applied Biosystems, Carlsbad, CA). Initial denaturation at 95°C for 5 min was followed by 36 cycles of 95°C for 30 s, 50°C for 45 s, and 72°C for 2 Protein kinase N1 min. The last cycle was followed by a final extension at 72°C for 7 min. Fluorescently labeled PCR products were separated by capillary electrophoresis on an ABI 3130 DNA analyzer (Applied Biosystems, Carlsbad, CA). Briefly, 0.5 μl of a 1:10 dilution of PCR product was added to 0.25 μl GeneScanTM 1200 LIZ internal size standard and 9.25 μl Hi-Di formamide (Applied Biosystems, Carlsbad, CA). The 10 μl samples were denatured by heating to 95°C for 3 min., cooled and run on a 50 cm array in the POP-7 polymer matrix using the 1200LIZ run module. Four of the ten primers tested produced complex, reproducible, banding patterns over multiple PCR reactions and a series of DNA concentrations, and these four ISSR primers were therefore selected for the analysis of the remaining sequence-confirmed A. terreus isolates.