Extent and pattern of genetic differentiation within and between phenotypic populations of Leymus chinensis (Poaceae) revealed by AFLP analysis

2007 ◽  
Vol 85 (9) ◽  
pp. 813-821 ◽  
Author(s):  
Lei Gong ◽  
Xinxin Song ◽  
Mu Li ◽  
Wanli Guo ◽  
Lanjuan Hu ◽  
...  
Keyword(s):  
Genetic Differentiation ◽  
Fragment Length Polymorphism ◽  
Green Leaf ◽  
Leymus Chinensis ◽  
Aflp Analysis ◽  
Natural Habitats ◽  
Aflp Data ◽  
Original Population ◽  
Naturally Occurring ◽  
Mantel’S Test

The extent and pattern of genetic differentiation between two naturally occurring phenotypes, grey–green leaf (GGL) and yellow–green leaf (YGL), of Leymus chinensis (Trin.) Tzvel., which colonize distinct habitats in the Songnen Prairie in northeast China, were investigated by amplified fragment length polymorphism (AFLP) analysis. Twelve selected AFLP primer pairs amplified 593 reproducible bands, of which 148 (24.96%) were polymorphic among 69 individuals taken from three populations: two natural ones (YGL and GGL1) and one transplanted (GGL2). Cluster analysis based on the AFLP data categorized the plants into distinct groups that are in line with their phenotypes and population origins, thus denoting clear genetic differentiation between the two phenotypes. This, together with their adaptation to contrasting natural habitats, suggests that the two phenotypes probably represent stabilized ecotypes. The grouping was supported by multiple statistical analyses including Mantel’s test, principal coordinate analysis (PCOORDA), and analysis of molecular variance (AMOVA). The GGL phenotype harbors a higher level of within-population genetic diversity than YGL, possibly reflecting selection by habitat heterogeneity. Although GGL2 is largely similar to its original population (GGL1), further diversification since transplantation was evident. Sequence analysis of a subset of phenotype-specific or phenotype-enriched AFLP bands implicated diverse biological functions being involved in ecological adaptation and formation of the two phenotypes.

Genetic Variability in the Potato Pathogen Colletotrichum coccodes as Determined by Amplified Fragment Length Polymorphism and Vegetative Compatibility Group Analyses

2006 ◽  
Vol 96 (10) ◽  
pp. 1097-1107 ◽  
Author(s):  
Larry J. Heilmann ◽  
Nadav Nitzan ◽  
Dennis A. Johnson ◽  
Julie S. Pasche ◽  
Curt Doetkott ◽  
...  
Keyword(s):  
Length Polymorphism ◽  
Fragment Length ◽  
Fragment Length Polymorphism ◽  
Amplified Fragment Length Polymorphism ◽  
Vegetative Compatibility ◽  
Colletotrichum Coccodes ◽  
Aflp Analysis ◽  
Aflp Data ◽  
Bootstrap Analysis ◽  
Nit Mutants

Amplified fragment length polymorphism (AFLP) using three primer sets was used to characterize 211 Colletotrichum coccodes isolates from North America, 112 of which were assigned to six vegetative compatibility groups (VCGs) using nitrate nonutilizing (nit) mutants. These isolates clustered into five corresponding groups by unweighted pairgroup method with arithmetic means-based cluster analysis of AFLP banding patterns. Isolates of C. coccodes belonging to NA-VCG1 and NA-VCG3 were closely related, as were isolates belonging to NA-VCG2 and NA-VCG5. Based on bootstrap analysis of AFLP data, the two isolates originally assigned to NA-VCG4 clustered with isolates belonging to NA-VCG2 and NA-VCG5. C. coccodes isolates that clustered with two isolates belonging to NA-VCG6 were the most diverged from other groups, including seven isolates collected from hosts other than potato. As opposed to the bootstrap analysis, a quadratic discriminant analysis (QDA) of AFLP data correctly categorized the two isolates of NA-VCG4. Furthermore, in isolates where VCG determinations had been made, this model correctly classified isolates of all VCGs. QDA classifications were identical to those made by the bootstrap analysis, with the exception of VCG4. Overall, classifications made by the QDA model were strongly correlated (r = 0.970, P < 0.001) to the VCGs assigned by traditional methods. All 99 C. coccodes isolates evaluated only by AFLP also were subjected to QDA, leading to the assignment of a presumptive VCG for each isolate. No isolates of VCG4 or VCG6 were identified by QDA within this population. Symptoms of black dot developed in plants inoculated with isolates collected from both potato and non-potato hosts. However, total yield was not significantly reduced by infection with non-potato isolates. The lack of any additional groups identified by AFLP analysis may be an indicator of a limited level of genetic variation among North American C. coccodes isolates. AFLP is a much more efficient technique for subspecific characterization in C. coccodes than VCG analysis utilizing nit mutants and will provide an effective means by which the population biology of this pathogen can be further investigated worldwide.

Genetic structure of the Anthyllis vulneraria L. s. l. species complex in Estonia based on AFLPs

2008 ◽  
Vol 3 (4) ◽  
pp. 442-450 ◽  
Author(s):  
Egle Köster ◽  
Elena Bitocchi ◽  
Roberto Papa ◽  
Silvia Pihu
Keyword(s):  
Species Complex ◽  
Fragment Length Polymorphism ◽  
Aflp Analysis ◽  
Data Sets ◽  
Geographic Scale ◽  
Aflp Data ◽  
Anthyllis Vulneraria ◽  
Directional Variation ◽  
Intraspecific Structure ◽  
Cryptic Taxa

AbstractAnthyllis vulneraria L. (Fabaceae) s. lato includes many cryptic taxa, ranging from 25 to 60 subspecies according to different authors. The delimitation of intraspecific taxa of A. vulneraria s. lato has always been complicated and inconsistent. Different data sets (multivariate analyses of morphological variation, allozymes, chloroplast SSRs and ITS) have not resolved the existing problem with distinguishing some subspecies. We used the amplified fragment length polymorphism (AFLP) analysis to describe the differentiation in this species complex and to characterize variation on a geographic scale. Some correlation was found between genetic variability and geographic distribution (western-eastern directional variation), but AFLP data analysis did not reveal clear intraspecific structure of the seven analysed taxa. The analysed specimens did not comprise groups correlated with the subspecies.

scholarly journals Characterization of Verticillium albo-atrum Field Isolates Using Pathogenicity Data and AFLP Analysis

Plant Disease ◽  
2003 ◽  
Vol 87 (6) ◽  
pp. 633-638 ◽  
Author(s):  
Sebastjan Radišek ◽  
Jernej Jakše ◽  
Andrej Simončič ◽  
Branka Javornik
Keyword(s):  
Fragment Length Polymorphism ◽  
Economic Losses ◽  
Aflp Analysis ◽  
Mild Form ◽  
Aflp Data ◽  
Green Pepper ◽  
Clear Separation ◽  
Pathogenicity Tests ◽  
Verticillium Albo Atrum

Since 1997, hop wilt induced by a virulent pathotype of Verticillium albo-atrum has caused considerable economic losses in hop fields in Slovenia. In all, 20 isolates of V. albo-atrum, including 12 from plants affected with the lethal form (PG2) of hop wilt, 6 from plants with the mild form (PG1), 1 from cucumber, and 1 from petunia, as well as 1 isolate of V. dahliae each from hop and green pepper, were analyzed by amplified fragment length polymorphism (AFLP). Differences in the virulence of hop isolates were confirmed by pathogenicity tests on hop cultivars. The AFLP method was optimized for analysis of these fungi and 7 of 39 primer combinations tested were used for the analysis of polymorphism among isolates. Cluster analysis of AFLP data divided the isolates into two, well-separated V. albo-atrum and V. dahliae clusters, confirming that the two species are genetically distinct. Within the V. albo-atrum cluster, isolates were further separated into two distinct groups: the A1 group contained PG1 hop pathotype and cucumber and petunia isolates, and the A2 group all hop isolates of the PG2 pathotype. Minor genetic variation was detected within pathotype-associated AFLP groups, but the clear separation of V. albo-atrum hop isolates according to their level of virulence shows genetic differentiation among hop V. albo-atrum pathotypes.

scholarly journals Molecular and Morphological Investigation of Ornamental Liriopogons

2003 ◽  
Vol 128 (4) ◽  
pp. 575-577 ◽  
Author(s):  
Mwamburi Mcharo ◽  
Edward Bush ◽  
Don La Bonte ◽  
Catherine Broussard ◽  
Lowell Urbatsch
Keyword(s):  
Genetic Variability ◽  
Genetic Differentiation ◽  
Fragment Length Polymorphism ◽  
Morphological Investigation ◽  
Dice Coefficient ◽  
Floral Structure ◽  
Aflp Data ◽  
Grouping Strategies ◽  
Morphological Assessment ◽  
Group Effects

Eighteen commercial taxa in genera Liriope and Ophiopogon were evaluated genetically and morphologically. Three hundred and forty-four Amplified Fragment Length Polymorphism (AFLP) markers were identified and used in the analysis. Relatedness among taxa was estimated by analyzing the AFLP data using the Dice coefficient of similarity and UPGMA methods. The molecular analysis revealed relatively no genetic differentiation among the taxa ascribed to their respective genera, Liriope and Ophiopogon, based on morphological assessment of floral structure. Greater than 95% of the total genetic variability present was attributed to within group effects using various grouping strategies among the taxa. Among group effects were correspondingly low and not significant (P ≤ 0.05). Results suggest an indistinguishable genetic relationship may exist in the tribe Ophiopogonae between what is currently ascribed as two distinct genera.

scholarly journals Genotypic Analysis of Escherichia coli Strains from Poultry Carcasses and Their Susceptibilities to Antimicrobial Agents

2001 ◽  
Vol 67 (4) ◽  
pp. 1940-1944 ◽  
Author(s):  
Ifigenia Geornaras ◽  
John W. Hastings ◽  
Alexander von Holy
Keyword(s):  
Escherichia Coli ◽  
South African ◽  
Length Polymorphism ◽  
Antimicrobial Agents ◽  
Susceptibility Testing ◽  
Fragment Length Polymorphism ◽  
Aflp Analysis ◽  
Aflp Data ◽  
Genotypic Analysis ◽  
Plasmid Profiling

ABSTRACT Plasmid profiling and amplified fragment length polymorphism (AFLP) analysis were used to genotype 50 Escherichia coli strains from poultry carcasses. Thirty different plasmid profiles were evident, and clustering of the AFLP data showed that they were a distinctly heterogeneous group of strains. Susceptibility testing against five antimicrobial agents used in the South African poultry industry showed all strains to be susceptible to danofloxacin and colistin, while the majority (96%) were resistant to two tetracyclines.

scholarly journals Fourier Transform Infrared and Raman Spectroscopy for Characterization of Listeria monocytogenes Strains

2006 ◽  
Vol 72 (1) ◽  
pp. 228-232 ◽  
Author(s):  
Astrid Oust ◽  
Trond Møretrø ◽  
Kristine Naterstad ◽  
Ganesh D. Sockalingum ◽  
Isabelle Adt ◽  
...  
Keyword(s):  
Fatty Acids ◽  
Raman Spectroscopy ◽  
Fourier Transform ◽  
Listeria Monocytogenes ◽  
Fragment Length Polymorphism ◽  
Fourier Transform Infrared ◽  
Aflp Analysis ◽  
Aflp Data ◽  
Infrared And Raman Spectroscopy

ABSTRACT The purpose of this study was to characterize the variation in biochemical composition of 89 strains of Listeria monocytogenes with different susceptibilities towards sakacin P, using Fourier transform infrared (FTIR) spectroscopy and Raman spectroscopy. The strains were also analyzed using amplified fragment length polymorphism (AFLP) analysis. Based on their susceptibilities to sakacin P, the 89 strains have previously been divided into two groups. Using the FTIR spectra and AFLP data, the strains were basically differentiated into the same two groups. Analyses of the FTIR and Raman spectra revealed that the strains in the two groups contained differences in the compositions of carbohydrates and fatty acids. The relevance of the variation in the composition of carbohydrates with respect to the variation in the susceptibility towards sakacin P for the L. monocytogenes strains is discussed.

scholarly journals Genetic Diversity of Rhubarb Cultivars

2008 ◽  
Vol 133 (4) ◽  
pp. 587-592 ◽  
Author(s):  
Joseph C. Kuhl ◽  
Veronica L. DeBoer
Keyword(s):  
Genetic Diversity ◽  
Central Asia ◽  
Length Polymorphism ◽  
Genetic Relationship ◽  
Fragment Length ◽  
Fragment Length Polymorphism ◽  
18Th Century ◽  
Pedigree Information ◽  
Aflp Analysis ◽  
Fingerprint Analysis

The genus Rheum L., commonly known as rhubarb, is composed of ≈60 species, primarily distributed throughout northern and central Asia. Rhubarb species have been used for medicinal purposes for thousands of years; however, it was not until the 18th century that the culinary use of petioles was first reported. Although the origin(s) of culinary rhubarb is not clear, it is thought that they originated from hybridization of rhubarb species originally brought to Europe for medicinal purposes. Most rhubarb cultivars lack pedigree information, and the genetic relationship among cultivars is largely unknown. Amplified fragment length polymorphism (AFLP) markers were generated for fingerprint analysis of 37 cultivars and four putative Rheum species accessions. Ten EcoRI and MseI primer combinations were analyzed for a total of 1400 scored polymorphisms, with an average of 140 polymorphisms per primer combination. Results show at least two clusters of related cultivars, as well as distantly related accessions. This study provides an estimate of rhubarb cultivar genetic diversity using AFLP analysis.

scholarly journals Genomic Relatedness of ChlamydiaIsolates Determined by Amplified Fragment Length Polymorphism Analysis

1999 ◽  
Vol 181 (15) ◽  
pp. 4469-4475 ◽  
Author(s):  
Adam Meijer ◽  
Servaas A. Morré ◽  
Adriaan J. C. Van Den Brule ◽  
Paul H. M. Savelkoul ◽  
Jacobus M. Ossewaarde
Keyword(s):  
Cluster Analysis ◽  
Length Polymorphism ◽  
Fragment Length ◽  
Fragment Length Polymorphism ◽  
Amplified Fragment Length Polymorphism ◽  
Chlamydia Psittaci ◽  
Rrna Genes ◽  
Aflp Analysis ◽  
Polymorphism Analysis ◽  
Genomic Relatedness

ABSTRACT The genomic relatedness of 19 Chlamydia pneumoniaeisolates (17 from respiratory origin and 2 from atherosclerotic origin), 21 Chlamydia trachomatis isolates (all serovars from the human biovar, an isolate from the mouse biovar, and a porcine isolate), 6 Chlamydia psittaci isolates (5 avian isolates and 1 feline isolate), and 1 Chlamydia pecorum isolate was studied by analyzing genomic amplified fragment length polymorphism (AFLP) fingerprints. The AFLP procedure was adapted from a previously developed method for characterization of clinical C. trachomatis isolates. The fingerprints of all C. pneumoniae isolates were nearly identical, clustering together at a Dice similarity of 92.6% (± 1.6% standard deviation). The fingerprints of the C. trachomatis isolates of human, mouse, and swine origin were clearly distinct from each other. The fingerprints of the isolates from the human biovar could be divided into at least 12 different types when the presence or absence of specific bands was taken into account. The C. psittacifingerprints could be divided into a parakeet, a pigeon, and a feline type. The fingerprint of C. pecorum was clearly distinct from all others. Cluster analysis of selected isolates from all species revealed groups other than those based on sequence data from single genes (in particular, omp1 and rRNA genes) but was in agreement with available DNA-DNA hybridization data. In conclusion, cluster analysis of AFLP fingerprints of representatives of all species provided suggestions for a grouping of chlamydiae based on the analysis of the whole genome. Furthermore, genomic AFLP analysis showed that the genome of C. pneumoniae is highly conserved and that no differences exist between isolates of respiratory and atherosclerotic origins.

Comparative Fingerprinting Analysis ofCampylobacter jejuni subsp. jejuni Strains by Amplified-Fragment Length Polymorphism Genotyping

2000 ◽  
Vol 38 (9) ◽  
pp. 3379-3387 ◽  
Author(s):  
Bjørn-Arne Lindstedt ◽  
Even Heir ◽  
Traute Vardund ◽  
Kjetil K. Melby ◽  
Georg Kapperud
Keyword(s):  
Length Polymorphism ◽  
Fragment Length ◽  
Fragment Length Polymorphism ◽  
Amplified Fragment Length Polymorphism ◽  
Epidemiological Surveillance ◽  
Aflp Analysis ◽  
Polymorphism Analysis ◽  
Pcr Rflp ◽  
Pcr Products ◽  
Ofcampylobacter Jejuni

Amplified-fragment length polymorphism (AFLP) analysis with the endonucleases BglII and MfeI was used to genotype 91 Campylobacter jejuni subsp. jejunistrains from outbreaks and sporadic cases. AFLP-generated fragments were labeled with fluorescent dye and separated by capillary electrophoresis. The software packages GeneScan and GelCompar II were used to calculate AFLP pattern similarities and to investigate phylogenetic relationships among the genotyped strains. The AFLP method was compared with two additional DNA-based typing methods, pulsed-field gel electrophoresis (PFGE) using SmaI and restriction fragment length polymorphism analysis on PCR products (PCR-RFLP) of theflaA and flaB genes. We found that AFLP analysis of C. jejuni strains is a rapid method that offers better discriminatory power than do both PFGE and PCR-RFLP. AFLP and, to a lesser extent, PCR-RFLP could differentiate strains within the same PFGE profiles, which also makes PCR-RFLP an alternative to PFGE. We were able to clearly distinguish 9 of 10 recognized outbreaks by AFLP and to identify similarities among outbreak and sporadic strains. Therefore, AFLP is suitable for epidemiological surveillance ofC. jejuni and will be an excellent tool for source identification in outbreak situations.

scholarly journals Relationships among Morphological Characters, Isozymes Polymorphism and DNA Variability – the Impact on Lactuca Germplasm Taxonomy

2011 ◽  
Vol 39 (No. 2) ◽  
pp. 59-67 ◽  
Author(s):  
I. Doležalová ◽  
A. Lebeda ◽  
M. Dziechciarková ◽  
E. Křístková ◽  
D. Astley ◽  
...  
Keyword(s):  
Dna Content ◽  
Fragment Length Polymorphism ◽  
Morphological Variability ◽  
Morphological Characters ◽  
Aflp Analysis ◽  
Dapi Staining ◽  
Lactuca Species ◽  
Relative Dna Content ◽  
The Impact

Fifty one accessions of nineteen Lactuca species, the hybrid L. serriola &times; L. sativa and the related species Mycelis muralis were evaluated for morphological variability, esterase (EST) polymorphism, Amplified Fragment Length Polymorphism (AFLP) and relative DNA content. Sixteen Lactuca accessions were classified taxonomically on the basis of morphology, isozyme analysis and AFLP. Twenty-eight bands (isoforms) of EST were recorded allowing 82% of accessions to be distinguished. The relative DNA content, measured using flow-cytometry (DAPI staining), ranged from 2.02 pg in L. capensis to 17.96 pg in L. canadensis. The results from AFLP analysis and the relative DNA content measurement corresponded well with recent taxonomic classification of the genus Lactuca. &nbsp;

Sign in / Sign up

Export Citation Format

Share Document