Li Similarity Coefficient Research Articles

Heterogeneous nature of a 'new' pathotype of Melampsora rust on Salix revealed by AFLP.

An outbreak of rust on Salix × mollissima (S. triandra × S. viminalis) ‘Q83’, an important biomass willow, was first observed at several locations in the UK in 1992. Rust collections obtained from ‘Q83’ in 1992 at Long Ashton (south west England), Markington (Northern England) and Loughgall (Northern Ireland), were tested for pathogenicity and examined using amplified fragment length polymorphism (AFLP). All collections showed the same pathogenicity patterns on the eight willow differentials and were assigned to f.sp. larici-epitea typica of Melampsora epitea. A total of 304 AFLP markers was scored for 54 rust isolates, 20 from Long Ashton, 20 from Markington and 14 from Loughgall. Cluster analysis placed the isolates into three distinct groups according to the collection sites. Within each site, Markington isolates were least variable, Nei & Li's similarity coefficients averaging 0.996. Average similarities within isolates from Long Ashton and Loughgall were 0.899 and 0.883, respectively. Average per-locus diversity within site (Hj′), calculated using Shannon information index, was 0.014 in Markington, 0.24 in Long Ashton and 0.23 in Loughgall population. Most diversity (69.1%) was partitioned between populations. An analysis of molecular variance (AMOVA) attributed 85.8% of variance to between populations and 14.2% to the individuals within populations. The results suggest that, in 1992, this previously unknown pathotype was not spread from a common source but from separate sources. The AFLP analysis and early records on the host range of M. epitea indicate that the rust virulent to S. × mollissima may have existed in nature before 1992.

Detection of RAPD markers correlated with chloroquine resistance in Plasmodium falciparum.

We described the use of the random amplified polymorphic DNA (RAPD) technique on Plasmodium falciparum DNA to detect genetic markers for chloroquine-resistant strains. Fourteen RAPD primers were tested, three of which generated banding patterns correlated with chloroquine resistance. To measure this correlation, the RAPD profiles were analyzed using the Nei and Li similarity coefficient. Detection of distinctive RAPD bands allowed us to synthesize specific PCR primers to be used on whole-blood samples. Two primer sets were synthesized and tested on sensitive and resistant strains for their ability to amplify the DNA fragment corresponding to the RAPD marker. These results suggest that RAPD and PCR techniques can be used as powerful tools for the detection of genetic markers associated with drug resistance.

Construction of phylogenetic tree forNicotiana species based on RAPD markers

To apply random amplified polymorphic DNA for analysis of phylogenetic relationships, we used 34 synthetic oligonucleotides as primers to examine interspecific and intraspecific variations among 18 genotypes, nine species ofNicotiana. The nine species used in this study belong to sectionsTomentosae andAlatae. In addition, we attempted to clarify the taxonomic position ofN. sylvestris. A total of 354 distinct DNA fragments were obtained by polymerase chain reaction. Pair-wise comparisons of unique and shared amplification products were used to generate Jaccard's similarity coefficients and Nei and Li's similarity coefficients with the computer software of numerical taxonomy and multivariate analysis system. On the basis of the dendrogram constructed with the similarity coefficients, the 18Nicotiana genotypes were divided into two clusters. The classification analyzed by RAPD markers is in accordance with the classification of Goodspeed thatN. sylvestris is a member of sectionAlatae.