Search Results (115)

Background: Common bean (Phaseolus vulgaris L.) is an important grain legume crop of nutritional and economic value across Africa. Genetic improvements of the crop to enhance productivity and resilience depend on understanding the diversity within the African germplasm. Methods: Following PRISMA guidelines, the genetic diversity and population structure of common bean in Africa were reviewed systematically based on existing research. A protocol for conducting the systematic review was developed registered in OSF. Twenty-nine studies met the inclusion criteria after a comprehensive search in ScienceDirect, PubMed, Google Scholar, PubMed, AGRICOLA, Taylor & Francis, and SpringerLink. Data on molecular markers and diversity metrics, thus PIC, He, and AMOVA, were extracted and synthesized qualitatively. Results: Despite substantial heterogeneity in panel sizes, reporting completeness, and marker systems (SSR, SNP, POX, ISSR), consistent patterns emerged. Studies revealed moderate to high levels of genetic diversity. Population-structure analyses recovered the canonical Andean and Mesoamerican gene pools with extensive admixture and high gene flow. AMOVA results indicated that a substantial proportion of total genetic variation was attributed to within-population components. Conclusions: The results are consistent with previous studies, but the sample size and types of markers make direct comparisons impossible. More future studies should use standardized genotyping approaches to increase data consistency. These insights are useful for yield improvement under both non-stress and stress conditions and for developing Africa’s diverse environments. Full article

Rivomarginella morrisoni (Gastropoda: Marginellidae) is a narrowly distributed freshwater snail inhabiting drainage basins of central and southern Thailand. To clarify patterns of genetic differentiation across its range, 45 individuals from 11 sites across eight river basins were analyzed using two dominant molecular markers: sequence-related amplified polymorphism (SRAP) and inter-simple sequence repeats (ISSR). SRAP primers produced higher polymorphic information content (PIC) values than ISSR primers (0.35 vs. 0.27). Analysis of molecular variance (AMOVA) revealed strong population structure, with 80.29% of the genetic variation occurring among populations and 19.71% within populations Population differentiation statistic (PhiPT) = 0.803, p < 0.001). Unweighted Pair Group Method with Arithmetic mean (UPGMA) and principal coordinate analysis (PCoA) consistently separated central and southern populations, and STRUCTURE supported K = 2 as the most likely number of clusters. Similarly, principal component analysis (PCA) of morphological traits also distinguished specimens into two groups corresponding to these geographic regions, confirming region-specific divergence. Overall, the genetic and morphological patterns indicate restricted gene flow among basins and a clear separation between central and southern lineages of R. morrisoni. This study provides the first molecular evidence of population structure in this species and offers important baseline information for future taxonomic, ecological, and conservation research on freshwater marginellid snails. Full article

Breakdown of cold-chain integrity drives the persistence of foodborne pathogens in poultry supply chains in warm, mountainous climates. This study used Al-Mandaq (Saudi Arabia) as a model to assess genetic diversity and contamination in bacteria from poultry storage units using 16S rRNA sequencing, VITEK 2, selective culturing, and ISSR/RAPD fingerprinting on 150 swabs. The Salmonella enterica complex comprised 15/29 isolates (51.7%), followed by Escherichia spp. 6/29 (20.7%) and Bacillus spp. 3/29 (10.3%). Five Salmonella serovars were identified: Enteritidis (8), Waycross (3), Minnesota (2), Typhimurium (1), and Dublin (1). S. Enteritidis accounted for 8/29 isolates (27.6%) and predominated among Salmonella in supermarket retail samples in Al-Mandaq. Combined ISSR and RAPD cluster analysis revealed highly clonal S. Enteritidis groupings, consistent with cross-contamination and prolonged survival in refrigeration equipment. In resource-limited settings, the combined ISSR and RAPD approach enhanced identification and differentiation of bacterial contamination sources within refrigeration equipment, providing superior strain-level discrimination compared to single-marker systems and improving epidemiological traceability of cross-contamination events. These results highlight the risk of clonal pathogen persistence in poultry cold-chain environments and the value of integrated molecular fingerprinting for surveillance in challenging climates. Full article

Major historic olive tree cultivars around the Mediterranean originate from the Jordan area and possess a proven abiotic stress tolerance; however, they were unexplored from the diversity perspective. Therefore, historic olive tree accessions from three northern regions—Irbid (i), Jerash (J), and Ajloun (A)—were analyzed using DNA molecular markers to identify and study their genetic relationships and genetic structure. DNA molecular markers of inter-simple sequence repeats (ISSR) were used. A total of 3150 data entries (859 present and 2291 absent) were generated with fragment sizes ranging from 350 to 2000 bp. Data entries were evaluated with UPGMA and population genetic structure analysis. The results showed that similarity among the investigated sixty-three accessions ranged from 9% between J14 and i20 up to 100% between ‘J11’ and ‘J12’ and between A8 and A9. The discriminating power values for ISSR_807, ISSR_810, and ISSR_825 were 0.70, 0.61, and 0.83, respectively. A generated dendrogram showed ten major clades, while the genetic structure could resolve four unique genetic pools: one for Irbid, one for Jerash, and two for Ajloun. In addition, analysis of 19 phenotypic parameters covering leaf, fruit, stone, and flesh was able to confirm the molecular data. Phenotypic and ISSR data were analyzed using PCA, cluster, and Mantel tests. ISSR markers showed clear genetic differentiation among groups, whereas phenotypic traits displayed lower variation but a significant correlation with molecular diversity. Promising accessions with either pure or admixture genetic makeup were identified. The resolved genetic structure of the investigated historic olive accessions would open new frontiers for olive breeding and utilization, helping to overcome current production challenges and climate change limitations. Full article

This study evaluated the genetic diversity of 33 Coffea canephora genotypes through morphophysiological and molecular analyses, aiming to identify promising genotypes for pre-breeding purposes in the southern region of Espírito Santo, Brazil. Cutting-propagated seedlings were evaluated 120 days after planting, considering height, stem and crown diameter, number of leaves, fresh and dry shoot and root weight, chlorophyll content, and root characteristics. Molecular analysis was performed on 32 genotypes; one was excluded due to absent DNA, and 18 ISSR markers were used. Morphological data were analyzed by ANOVA, Scott–Knott’s mean test, principal component analysis, and cluster analysis. The results revealed significant diversity among genotypes. The first two principal components explained 75.5% of the total variability. Genotypes 2, 3, 4, 5, 6, 10, 32, and 33 stood out as those that produced the most vigorous seedlings. Molecular analysis also revealed genetic diversity among genotypes, with the formation of 16 groups, while the morphophysiological analysis revealed four groups. The Mantel test demonstrated a small but significant positive difference (r = 0.228; p = 0.018) between the genetic and morphophysiological distances of the genotypes. This diversity indicates that the genotypes evaluated are promising for use in C. canephora breeding programs. Full article

The Chinese holly (Ilex chinensis Sims.), an evergreen tree species native to China, is distributed mainly in regions south of the Qinling Mountains and Huai River. This research aimed to characterize the molecular profiles and genetic relationships of 40 Chinese holly genotypes via inter-simple sequence repeat (ISSR) and start codon targeted (SCoT) polymorphism markers. Genetic diversity analysis revealed that the ISSR markers detected 111 polymorphic bands from 13 primers, with a polymorphism rate of 88.10%. The analysis generated parameters such as the observed allele number (Na = 1.876), effective allele number (Ne = 1.461), Shannon’s information index (I = 0.271), and expected heterozygosity (H = 0.411). In comparison, the SCoT markers produced 65 polymorphic bands from the 6 primers, resulting in a 100% polymorphism rate, with Na = 2.000, Ne = 1.695, I = 0.393, and H = 0.575. Cluster analysis classified the 40 genotypes into two main clusters with genetic similarity coefficients of 0.69 (ISSR) and 0.55 (SCoT). The ISSR markers presented the greatest similarity between the ZSS and ZLS genotypes, whereas the ZZDH and ZWW genotypes presented lower similarity. Conversely, the SCoT markers identified ZZP and ZJDS as the most similar, with ZLJ and ZHX showing less similarity. These results provide a theoretical basis for hybrid breeding, germplasm innovation, and conservation strategies of Chinese holly in China. Full article

Callicarpa peichieniana is an important traditional Chinese medicinal plant with pharmacological benefits for digestive system diseases and wounds, as well as high ornamental value. The goal of this study is to establish an effective in vitro regeneration system in order to satisfy the expanding market demand. Extracts from algae can enhance the proliferation and rooting effect of adventitious buds and can improve the survival rate of transplantation. This study developed an in vitro regeneration system using apical bud explants of C. peichieniana associated with Chlorella sorokiniana (an alga species). Inter simple sequence repeat (ISSR) molecular markers confirmed the genetic fidelity of the regenerated plantlets. The highest number of adventitious buds (5.00 buds) was induced from the apical buds with 0.5 mg/L 6-BA in a Murashige and Skoog (MS) medium, and the highest proliferation coefficient (5.83) was achieved with 2.0 mg/L 6-BA. A rooting rate of 100% was achieved by using 0.1 mg/L NAA, MS with 50% macroelements, and 20 g/L sucrose, averaging 6.36 roots per explant and a root length of 1.32 cm. In all micropropagation stages, C. sorokiniana coexisted and proliferated alongside C. peichieniana materials. ISSR showed that the genetic fidelity of C. peichieniana regenerated plants was 95.45%. Coconut coir/perlite = 1∶1 (v/v) was identified as the optimal transplantation substrate, achieving a 100% survival rate. The “C. peichieniana–C. sorokiniana association” in vitro regeneration system established in this study not only enables the mass production of high-quality regenerated plantlets but provides new ideas and demonstrations for culturing multiple species in the same in vitro system. Full article

This study presents an integrated approach combining molecular, phytochemical, and biological analyses to characterize a newly discovered Zizania specimen from the northern Nile Delta, Egypt. Genetic fingerprinting using RAPD and ISSR markers revealed 85% band-sharing similarity with Zizania texana (Z. texana), though distinct morphological and genetic traits suggested potential intraspecific variation. Phytochemical profiling identified high concentrations of bioactive compounds, including quercetin (42.1 µg/mL), β-caryophyllene (11.21%), and gallic acid (23.4 µg/mL), which are pertinent and correlated with robust biological activities. The ethanolic leaf extract exhibited significant antioxidant capacity (IC₅₀ = 38.6 µg/mL in DPPH assay), potent antimicrobial effects against Candida albicans (C. albicans) (IC₅₀ = 4.9 ± 0.6 µg/mL), and dose-dependent cytotoxicity against cancer cell lines. MCF-7 has the lowest IC₅₀ (28.3 ± 1.5 µg/mL), indicating the highest potency among the tested cell lines. In contrast, HepG2 demonstrates moderate sensitivity (IC₅₀ = 31.4 ± 1.8 µg/mL), while A549 shows the highest IC₅₀ value (36.9 ± 2.0 µg/mL), indicating greater resistance. These findings underscore the taxonomic novelty of the specimen and its potential as a source of natural antioxidants, antimicrobials, and anticancer agents. The study highlights the importance of interdisciplinary approaches in resolving taxonomic uncertainties and unlocking the medicinal value of understudied aquatic plants. Full article

The nopal cactus, a plant from the Cactaceae family, holds significant economic and nutritional value for Mexico. This study aimed to enhance the genetic diversity and morphological traits of Opuntia velutina, a species cultivated as a vegetable nopal. A total of 1050 in vitro O. velutina explants were exposed to 15 different doses of gamma radiation from ⁶⁰Co gamma, ranging from 5 to 125 Gy. The lethal dose was above 50 Gy, with an LD₅₀ of 22.8 Gy for stimulating in vitro shoot growth. Shoots derived from doses between 5 and 50 Gy were subjected to in vitro shoot proliferation across four consecutive generations to stabilize morphological traits. Cluster analysis categorized the 178 irradiated shoots into 13 distinct morphological groups (CG1–CG13). Twenty-seven shoots exhibiting significant morphological improvements, such as a 50–100% increase in cladode length, up to a six-fold increase in shoot number, and up to a seven-fold increase in root number, were selected for molecular analysis of genetic diversity. Six primers were used with the Inter Simple Sequence Repeat (ISSR) molecular markers to examine genetic uniformity, yielding 54.5% polymorphic bands, indicating a high level of genetic variation. Both a UPGMA dendrogram and STRUCTURE-based Bayesian analysis confirmed the genetic divergence among the selected mutant lines. Overall, gamma irradiation effectively enhanced both phenotypic and genotypic diversity in O. velutina. This study corroborates that in vitro mutagenesis through gamma radiation is a viable strategy for generating novel genotypes with breeding potential within the Opuntia genus. Full article

Melina (Gmelina arborea Roxb.) is a tree native to Asia, whose timber is not utilized in that region for a variety of reasons. However, the tree’s fast growth and extensive range of applications have increased its acceptance in other world’regions. G. arborea was introduced to Mexico in 1971, and it is currently the fifth most utilized forest species in commercial forest plantations (CFPs). However, its genetic diversity has not been evaluated in Mexico. The objective of this research was to investigate the genetic variability of Melina in Mexico using molecular markers. This investigation was undertaken to acquire valuable insights for the implementation of effective improvement strategies. A total of 85 Melina samples were collected from various locations in southeastern Mexico between 2017 and 2022. Genetic fingerprints were obtained using ten simple primer amplification reactions (SPARs): five Directed Amplification of Minisatellite DNA regions (DAMD), and five Inter-Simple Sequence Repeats (ISSRs). The polymorphic information content (PIC) was 0.940 and 0.950 for the DAMD and ISSR, respectively, and the similarity coefficients ranged from 0.12 to 0.88, indicating a high degree of polymorphism in the species under investigation. This is the first attempt to ascertain the genetic variability of Gmelina arborea in Mexico. Full article

Efficient extraction of high-quality DNA from plants is a critical challenge in molecular research, especially in species such as Gossypium barbadense L., native to Peru, due to the presence of inhibitors such as polysaccharides and phenolic compounds. This study presents a modified CTAB-based protocol with silica columns that is designed to overcome these limitations without the need for liquid nitrogen or expensive reagents. Native cotton samples were collected in Lambayeque, Peru, and processed using a simplified procedure that optimizes the purity and concentration of the extracted DNA. Eight cultivars of G. barbadense L. with colored fibers (cream, fifo, light brown, dark brown, orange-brown, reddish, fine reddish, and white) were evaluated, yielding DNA with A260/A280 ratios between 2.14 and 2.19 and A260/A230 ratios between 1.8 and 3.14; these values are higher than those obtained with the classical CTAB method. DNA quality was validated by PCR amplification using ISSR and RAPD molecular markers, which yielded clear and well-defined banding patterns. Furthermore, the extracted DNA was suitable for advanced applications, such as Sanger sequencing, by which high-quality electropherograms were obtained. The results demonstrate that the proposed protocol is an efficient, economical, and adaptable alternative for laboratories with limited resources, allowing the extraction of high-quality DNA from Gossypium barbadense L. and other plant species. This simplified approach facilitates the development of genetic and biotechnological research, contributing to the knowledge and valorization of the genetic resources of Peruvian native cotton. Full article

Garlic (Allium sativum L.) is the second most significant species within the Allium genus worldwide, widely used in cooking and both traditional and modern medicine due to its beneficial biological and therapeutic properties. In Italy, diverse pedo-climatic conditions and historical–cultural fragmentation have led to the development of various garlic landraces, prized for their unique organoleptic qualities and cultural importance. This study aimed to assess the intra-varietal diversity and uniqueness of two red garlic landraces from the Lazio region in central Italy, “Aglio Rosso di Castelliri” and “Aglio Rosso di Proceno”, using SSR and ISSR molecular markers, along with evaluations of bulb morphological traits, total phenolic content, and antioxidant properties. The molecular analysis included 11 accessions of “Aglio Rosso di Castelliri”, nine of “Aglio Rosso di Proceno”, and 15 control accessions, comprising eight Italian red-type garlic landraces, four Spanish red garlic commercial varieties, two white garlic accessions, and an accession of A. ampeloprasum var. holmense used as an outgroup. SSR and ISSR markers revealed moderate genetic diversity within the collection, with mean PIC values of 0.41 and 0.17, respectively. The molecular data identified four distinct genetic clusters, with the two Lazio landraces forming separate groups, indicating their genetic distinctiveness. The results from the STRUCTURE analysis support the hypothesis that these landraces may have originated from the widely cultivated “Aglio Rosso di Sulmona” or a common ancestral population once prevalent in central Italy. The study also revealed significant intra-population genetic diversity within the two garlic landraces, underscoring the need for in situ conservation and clonal selection. Phenotypic evaluations confirmed the distinctiveness of the two landraces, with “Aglio Rosso di Castelliri” characterized by smaller bulbs and cloves with higher dry matter content and distinct color profiles. Additionally, significant variation in total phenolic content and antioxidant activity was observed by analyzing 13 selected accessions from the two landraces (six from “Aglio Rosso di Proceno” and seven from “Aglio Rosso di Castelliri”) and five red garlic control accessions, with the two Lazio landraces exhibiting higher levels than the control group. This study highlights the importance of integrating molecular, phenotypic, and chemical analyses to understand garlic landrace diversity, with significant implications for their conservation and protection of local agro-food products. Full article

Alternaria includes endophytes, saprophytes, and pathogens affecting both plants and animals, with a global distribution across various hosts and substrates. It is categorized into 29 sections, each defined by a type species and six monophyletic lineages. The Alternaria section Nimbya comprises 10 species primarily associated with the families Juncaceae and Cyperaceae, functioning as either saprophytes or plant pathogens. In this study, 189 fungal strains were collected from multiple locations across six provinces in Iran. The isolates were initially classified based on morphological characteristics and ISSR-PCR molecular marker banding patterns. Multi-gene phylogenetic analyses of 38 selected strains, using ITS–rDNA, GAPDH, TEF1, RPB2, and Alt a 1 gene sequences, combined with morphological data, led to the identification of 13 species, including eight new species, namely Alternaria caricifolia, A. cyperi, A. juncigena, A. junci-inflexi, A. persica, A. schoenoplecti, A. salkadehensis, and A. urmiana. In addition, this work identified new host associations (matrix nova) for three previously known species: A. caricicola on Cyperus sp., A. cypericola on Eleocharis sp., and A. junci-acuti on Carex sp. The study provides detailed morphological descriptions and illustrations of all identified species, discusses their habitats, distribution, and phylogenetic relationships within section Nimbya, and presents a key for species identification within this section in Iran. Furthermore, these findings highlight the significance of studying fungal biodiversity in Iran and contribute to a better understanding of species distribution and host range within the Alternaria section Nimbya. Full article

In this study, we present the first-ever comparison of the effectiveness of SRAP and ISSR markers on three Allium species. In addition, to visualize the results of each dataset in a simpler way, the Fruchterman–Reingold algorithm was used to generate a link graph and neighbor-joining methods were used to obtain a phylogenetic tree. The genetic similarity matrices were compared using the Mantel test. Primers generated 59 ISSR and 72 SRAP fragments. There was no statistically significant difference between the polymorphism information content of the marker sets. In terms of the effective multiplex ratio, SRAP markers were higher than ISSR markers, with values of 6.700 for garlic, 6.400 for onion, and 5.800 for leek (3.490, 4.316, and 2.573, respectively). Similarly, the marker index was calculated as 2.820, 3.056, and 2.505 for SRAP and 1.903, 1.523, and 1.050 for ISSR in onion, garlic, and leek species, respectively. The highest value regarding cophenetic correlation coefficients was obtained from the Jaccard method. According to the neighbor-joining method, the tree drawn using SRAP and ISSR data together shows a more distinct hierarchical structure of genotypes. The results obtained proved that SRAPs have higher values in terms of sign efficiency criteria, but they are not sufficient for the homogeneous grouping of different Allium species. Full article

The semi-deciduous Brazilian Atlantic Forest has faced intense fragmentation, impacting Metrodorea nigra St. Hill., a fly-pollinated and autochorous tree. We investigated population structure, inbreeding, and spatial genetic structure (SGS) across adult (Adu) and juvenile (Juv) generations in three fragmented populations of M. nigra in Ribeirão Preto, São Paulo, Brazil. We tested whether the magnitude of these effects could result from its mating system, seed dispersal, anthropogenic disturbances, matrix, and fragment size. Populations affected by selective logging, fire, and trail openings include M13-Rib (84 ha) and FAC-Crav (8 ha), both surrounded by sugar cane and BSQ-Rib (3 ha) in an urban matrix. We evaluated phenological events and germination rates in the BSQ-Rib fragment. We sampled leaves and amplified their DNA using ISSR (UBC 1, 2, 820, 834, 851, 858, 860, 886) and SSR (Mtn 1, 3, 13, 16, 19, 87, 95) molecular markers. Fst, PCoA, and AMOVA values suggest a lack of generational isolation, with most variance within generations. Inbreeding values were significant in all populations (Fis and Fit, p = 0.001), probably intensified by natural seed dispersal and pollinator behavior favoring geitonogamy. However, fragmentation, anthropogenic disturbances, and the surrounding matrix influenced SGS. The urban BSQ-Rib fragment recorded the highest SGS values (26 m Juv, 24 m Adu [ISSR]; 7 m Juv, 9 m Adu [SSR]), which may result in low fruit and seed production and germination rates. Despite being the largest fragment, M13-Rib shows SGS in the first distance class (19 m Juv, 24 m Adu [ISSR]; 0 m Juv, and 10 m Adu [SSR]), possibly due to selective logging and fire. FAC-Crav, a more conserved fragment, showed no SGS in adults but punctual SGS in juveniles (27 m [ISSR] and 8 m [SSR]), pointing to it as a promising source for seed collections for reforestation purposes. In summary, inbreeding in M. nigra, influenced by pollinator behavior and seed dispersal, along with fragmentation, anthropogenic disturbances, and the surrounding matrix, are critical in shaping SGS. These factors potentially impact the reproductive success of M. nigra and their long-term survival in the face of climate change. Full article