The automated sequencing of purified DNA fragments by spin column

The automated sequencing of purified DNA fragments by spin columns (Qiagen, Chatsworth, Calif.) was performed by the cycle-sequencing dye terminator method. The Big Dye Terminator Cycle Sequencing Ready Reaction Kit (ABIPRISM 100, Applied Biosystems, Foster City, CA) was chosen for sequencing. The RG-7388 manufacturer sequences obtained were deposited in the GenBank database (AF856321-AF856328; AF856341-AF856350). Phylogenetic and Recombination studies TrN93 substitution

model was used to make the phylogenetic analysis since this model showed to be the best to analyze DENV sequences by using “”Model Selection”" implemented in “”DataMonkey”" [28, 29] The DENV-2 sequences of partial C91-prM-E-NS12400 genome (90) or E gene (180) were aligned using Clustal W [49]; keeping the more representative sequences (17 and 16 respectively) to obtain plots and phylogenies trees to evaluate recombination in our isolates and clones. The accession number of sequences selleck screening library are as follow: VEN_2_87 (AF100465), MEX_131-92(AF100469), THNH_P36_93 (AF022441), TH_CO390_99 (AF100462), BANGKOK_74 (AJ487271), NGC_44 (D00346), CHINA_43_89 (AF204178), CHINA_FJ_10_00 (AF276619), INDI_GWL102_01 (DQ448233), INDO_BA05i_05 (AY858035), INDO_ 98900666_04 (AB189124), BR_64022_02 Dichloromethane dehalogenase (AF489932),

JAM_N1409_83 (M20558), CHINA_04_85 (AF119661), DR_23_01 (AB122020), MART_703_98 (AF208496), CUBA_13_97 (AY702034), MEX_95 (DQ364562). The aligned sequences were analyzed by Recombinant Detection Program version 3 (RDP3) [50] using default parameters (window of 200nt, step of 20nt, Jin and Nei, 1990 [51] substitution models and 1000 bootstrap) and by the

genetic algorithm for recombination detection (GARD) [52, 29]. Acknowledgements Maria Guadalupe Aguilar Gonzalez (Nucleic Acids Unity of CINVESTAV-IPN) and Eduardo Carrillo Tapia (Sequencer Unity of Genomic Sciences Program from UACM) are gratefully acknowledged for their assistance with the automated sequencing. This work was supported by the CONACYT grant CB-2005-01-50603. References 1. Gubler DJ, Meltzer M: Impact of dengue/dengue haemorrhagic fever on the developing world. Adv Virus Res 1999, 53:35–70.CrossRefPubMed 2. Thu HM, Lowry K, Myint TT, Shwe TN, Han AM, Khin KK, Thant KZ, Thein S, Aaskov JG: Myanmar dengue outbreak associated with displacement of serotypes 2, 3 and 4 by dengue 1. Emerg Infect Dis 2004, 10:593–597.PubMed 3. Wang WK, Chao DY, Lin SR, King CC, Chang SC: Concurrent infections by two dengue virus serotypes among dengue patients in Taiwan. J Microbiol Immunol Infect 2003, 36:89–95.PubMed 4.

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