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Keywords = genome integrity

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31 pages, 1754 KiB  
Review
Current Trends and Future Prospects in Controlling the Citrus Nematode: Tylenchulus semipenetrans
by Anil Baniya, Omar Zayed, Jiranun Ardpairin, Danelle Seymour and Adler R. Dillman
Agronomy 2025, 15(2), 383; https://doi.org/10.3390/agronomy15020383 (registering DOI) - 31 Jan 2025
Abstract
Citrus nematode (Tylenchulus semipenetrans) is one of the dominant plant-parasitic nematodes in citrus-growing regions, resulting in an average yield loss between 10 and 30%. Tylenchulus semipenetrans is a sedentary semi-endoparasitic nematode that infects the roots of citrus trees, causing stunted growth, [...] Read more.
Citrus nematode (Tylenchulus semipenetrans) is one of the dominant plant-parasitic nematodes in citrus-growing regions, resulting in an average yield loss between 10 and 30%. Tylenchulus semipenetrans is a sedentary semi-endoparasitic nematode that infects the roots of citrus trees, causing stunted growth, reduced fruit yield, and poor fruit quality; collectively this pathology and thus the disease caused is referred to as the slow decline of citrus. Despite its huge importance, the citrus nematode is regarded as a neglected parasite, and most research focuses on biological control and integrated pest management. Advancements in understanding the molecular mechanisms of other plant-parasitic nematodes, such as sedentary endoparasites with biological similarities to citrus nematodes, can be leveraged to gain deeper insights into the molecular mechanisms of citrus nematodes. In this review, we examine the biology, and integrated pest management of citrus nematodes, and explore future research directions toward understanding the role of genomics, gene-editing tools, and the molecular mechanisms of host-seeking and effectors used by other plant-parasitic nematodes to cause infection, which can serve as a foundation for future work in citrus nematode management. Full article
(This article belongs to the Special Issue Nematode Diseases and Their Management in Crop Plants)
17 pages, 3036 KiB  
Article
Nodal Injection of Agrobacterium tumefaciens for Gene Functional Analysis in Peanut: An Appraisal
by Malizukiswe Vincent Vacu, Chunjiao Jiang, Haojie Sun, Guangdi Yuan, Jing Yu, Jun Zhang and Chuantang Wang
Agronomy 2025, 15(2), 384; https://doi.org/10.3390/agronomy15020384 - 31 Jan 2025
Viewed by 45
Abstract
Peanut is a key cash crop worldwide, yet the limited availability of functional genes and markers for breeding hinders further progress, largely due to the lack of an efficient and user-friendly transformation system. This study aimed to comprehensively evaluate the effectiveness of nodal [...] Read more.
Peanut is a key cash crop worldwide, yet the limited availability of functional genes and markers for breeding hinders further progress, largely due to the lack of an efficient and user-friendly transformation system. This study aimed to comprehensively evaluate the effectiveness of nodal agroinjection, a novel transformation technique we developed for peanut, by introducing the soybean cold-tolerance gene SCTF-1. Putative transgenic seeds and seedlings were screened using genomic DNA PCR, while transgene expression was analyzed via qRT-PCR and phenotypic assessments. Southern blotting confirmed the stable integration of SCTF-1. The transgenic seedlings displayed enhanced chilling tolerance, characterized by increased proline accumulation, reduced malondialdehyde (MDA), and elevated peroxidase (POD) activity. These findings demonstrate that nodal agroinjection is an efficient and reliable approach for generating transgenic peanut and analyzing gene function. This method offers a promising alternative to conventional tissue culture-based transformation strategies. Full article
(This article belongs to the Section Crop Breeding and Genetics)
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<p>Partial map of plant expression vector pCPB-SCTF-1, showing the region between right and left borders [<a href="#B17-agronomy-15-00384" class="html-bibr">17</a>].</p>
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<p>DNA PCR identification of <span class="html-italic">A. tumefaciens</span> transformants carrying the pCPB-SCTF-1 construct, along with putative transgenic seeds derived from 6 landraces and seedlings derived from 4 landraces, with the lengths of PCR-amplified products (bp) specified. M: 2000 bp DNA marker; P: positive control; N: untransformed negative control. The numbers above the lanes represented individual colonies, seeds, and seedlings. A single primer pair (SCTF-1F/R) was used for <span class="html-italic">A. tumefaciens</span> and seeds, whereas three primer pairs (BarF/BarR, NOSF/NOSR, and SCTF-1F/R) were used for seedlings.</p>
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<p>RT-PCR analysis of transgenic peanut seedlings using <span class="html-italic">SCTF-1</span> gene specific primers. M: 2000 bp DNA marker; P: positive control; N: untransformed negative control; 1–14: putative transgenic seedlings derived from ZH1160, ZH1105, ZH1059 and ZH1085.</p>
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<p>Comparison of chromatograms: partial sequences from direct sequencing of RT-PCR products from seedlings (1–4) aligned with the corresponding <span class="html-italic">SCTF-1</span> gene sequence region in the vector (V).</p>
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<p>Relative expression of <span class="html-italic">SCTF-1</span> at mRNA level as determined by qRT-PCR in RT-PCR positive seedlings at normal temperature and at low temperature (5 °C for 95 h), with error bars indicating the standard error of the mean.</p>
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<p>Southern blot analysis of putative transgenic peanut seedlings. M: DIG DNA marker; P: positive control (plasmid DNA uncut); N: untransformed negative control; 1–4 representing ZH1160, ZH1105, ZH1059, and ZH1085 derived genomic DNA PCR positive seedlings, respectively.</p>
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<p>Phenotypes of transgenic peanut seedlings immediately and five days after chilling stress treatment. Landraces labeled with <span class="html-italic">SCTF-1</span> represent transgenic seedlings, while those labeled with CK represent untransformed controls.</p>
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17 pages, 3837 KiB  
Article
Dynamic Immune Response Landscapes of Avian Peripheral Blood Post-Vaccination Against Infectious Bronchitis Virus Infection
by Xuefeng Li, Yumeng Liang, Yu Zhang, Zheyi Liu, Lu Cui, Miaomiao Xi, Shufeng Feng, Xiaoxiao Liu, Yongxin Zhu, Shengwang Liu and Hai Li
Vaccines 2025, 13(2), 146; https://doi.org/10.3390/vaccines13020146 - 30 Jan 2025
Viewed by 328
Abstract
Background/Objectives: Despite decades of extensive vaccinations against avian infectious bronchitis virus (IBV) infection, outbreaks caused by constantly emerging variants due to genome recombination between different viral strains, including vaccine strains, occur annually worldwide. The development of novel vaccines with favorable safety and [...] Read more.
Background/Objectives: Despite decades of extensive vaccinations against avian infectious bronchitis virus (IBV) infection, outbreaks caused by constantly emerging variants due to genome recombination between different viral strains, including vaccine strains, occur annually worldwide. The development of novel vaccines with favorable safety and effectiveness is required but is hindered by a limited understanding of vaccination against IBV. Methods: Here, we performed a comprehensive analysis of the in vivo dynamics of peripheral blood mononuclear cells (PBMCs) in specific pathogen-free chickens inoculated with the widely used live attenuated IBV vaccine strain H120 at single-cell level, using high-throughput single-cell transcriptome sequencing (scRNA-seq). Results: High-quality sequencing dataset for four scRNA-seq data containing the transcriptomes of 29,846 individual chicken PBMCs were obtained, defining 22 populations and 7 cell types based on distinct molecular signatures and known markers. Further integrative analysis constructed the time series dynamic cell transition and immune response landscapes within the two weeks post-prime vaccination against IBV. Enhanced crosstalk between antigen-presenting cells and T lymphocytes was revealed as early as four days post-vaccination. The specific immune cell populations and their comprehensive cellular and molecular networks involved in the initiation phase of antiviral adaptive immune responses were elucidated in details. Conclusions: Our study provides a comprehensive view of the dynamic initiation of immune responses in chickens against IBV infection at the cellular and molecular levels, which provides theoretical support and potential solutions for the future rational design of safe and effective vaccines, the augmentation of the efficacy of current vaccines, and the optimization of immune programs. Full article
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<p>Constructing the dynamic transcriptomic landscape of chicken PBMCs upon IBV vaccination. (<b>A</b>) Illustration of the experimental workflow. (<b>B</b>) Detection of antibodies targeting viral N protein. <span class="html-italic">n</span> = 6. (<b>C</b>) Detection of serum-neutralizing antibody. <span class="html-italic">n</span> = 6. (<b>D</b>) Uniform manifold approximation and projection (UMAP) clustering of chicken PBMCs. Cells of each cluster are labelled by different colors. (<b>E</b>) Dot plots of the expression of chicken immune cell markers. scRNA-seq: Single-cell RNA sequencing, dpv: days post-vaccination, ***: <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Dynamic PBMC landscapes and overview of cell–cell communication network upon vaccination. (<b>A</b>) Transition of chicken PBMC composition upon vaccination. (<b>B</b>) The dynamic cell–cell communication network upon vaccination was inferred using CellChat (version 1.4.0). Circle plots presenting the network centrality analysis of the signaling pathways transduced among PBMCs within two weeks post-vaccination. Different colors represent different cell types, and edge width is proportional to the communication probability. Arrows and edge color indicate direction (source: target). (<b>C</b>) The numbers of inferred interactions at indicated days post-vaccination were summarized. (<b>D</b>) Comparison of the cell–cell communication of PBMCs post-vaccination with those at the onset of vaccination is presented with circle plots. Different colors represent different cell types, and edge width is proportional to the communication probability. Arrows indicate direction (source: target). Edge color: red indicates promotion, and blue indicates reduction. (<b>E</b>) Signaling in red font indicates more enrichment in the mock group, while signaling in blue font indicates more enrichment in the vaccination group. Signaling equally enriched in both groups is colored black. dpv: days post-vaccination.</p>
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<p>Identification of major signaling changed at 4 days post-vaccination. (<b>A</b>) Significant ligand–receptor pairs between PBMCs before and after vaccination. The communication probabilities were reflected with the color of dot color, and the computed <span class="html-italic">p</span>-values were reflected with the size of dot. The communication probability of zero was presented as empty space. One-sided permutation test was used to compute <span class="html-italic">p</span>-values. (<b>B</b>,<b>C</b>) Comparison of these significant ligand–receptor pairs between each cell type, presented in a heatmap (<b>B</b>) and dot plot (<b>C</b>), respectively.</p>
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<p>Global intercellular communication of major APCs during the initiation of antiviral adaptive immune response. (<b>A</b>) t-distributed stochastic neighbor embedding (t-SNE) clustering of chicken monocytes. Each subcluster of monocytes is labelled by different colors. (<b>B</b>) t-SNE clustering of chicken dendritic cells. Each subcluster of dendritic cells is labelled by different colors. (<b>C</b>) Circle plots presenting the overall cell–cell communication network among each subcluster of APCs and other PBMCs. Different colors represent different cell types, and edge width is proportional to the communication probability. Arrows and edge color indicate direction (source: target). (<b>D</b>) The deduced communication patterns of secreting cells and the reception patterns of target cells illustrate the relationship between the inferred latent patterns and cell groups, along with the signaling pathways. The flow’s thickness represents the extent of contribution from each cell group or signaling pathway to the latent pattern.</p>
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<p>Dynamic transition of the global intercellular communication of major APCs at 4 days post-vaccination. (<b>A</b>,<b>B</b>) Heatmaps presenting the coordination of cells and signaling based on outgoing communication patterns of secreting cells (<b>A</b>) and incoming communication patterns of target cells (<b>B</b>). (<b>C</b>) Heatmap presenting the comparison of significant signaling between each cell type. (<b>D</b>) Circle plots presenting the inferred MHC class II signaling network centrality analysis of the signaling pathways transduced among PBMCs at 4 days post-vaccination. Different colors represent different cell types. Arrows and edge color indicate direction (source: target).</p>
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<p>Global intercellular communication of T lymphocytes during the initiation of antiviral adaptive immune response. (<b>A</b>) t-distributed stochastic neighbor embedding (t-SNE) clustering of chicken T lymphocytes. Each subcluster of T lymphocytes is labeled with different colors. (<b>B</b>) Dot plots showing the expression of chicken T lymphocyte and natural killer cell markers. (<b>C</b>) Circle plots presenting the overall cell–cell communication network among each subcluster of APCs and T lymphocytes. Different colors represent different cell types, and edge width is proportional to the communication probability. Arrows and edge color indicate direction (source: target). (<b>D</b>) Heatmap presenting the comparison of significant signaling between each cell type. (<b>E</b>) Circle plots presenting the inferred MHC class II signaling network and CD80 signaling network centrality analysis of the signaling pathways transduced among PBMCs at 4 days post-vaccination. Different colors represent different cell types. Arrows and edge color indicate direction (source: target).</p>
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13 pages, 2000 KiB  
Article
Design and Expression of Fasciola hepatica Multiepitope Constructs Using mRNA Vaccine Technology
by Javier Sánchez-Montejo, Tania Strilets, Raúl Manzano-Román, Julio López-Abán, Mariano A. García-Blanco, Belén Vicente and Antonio Muro
Int. J. Mol. Sci. 2025, 26(3), 1190; https://doi.org/10.3390/ijms26031190 - 30 Jan 2025
Viewed by 234
Abstract
Fasciola hepatica is a parasitic trematode responsible for fascioliasis, a significant zoonotic disease affecting livestock worldwide, as well as humans. This study identifies peptides with potential for use in vaccines against Fasciola hepatica and validates multi-epitope constructs from those peptides in vitro. Putative [...] Read more.
Fasciola hepatica is a parasitic trematode responsible for fascioliasis, a significant zoonotic disease affecting livestock worldwide, as well as humans. This study identifies peptides with potential for use in vaccines against Fasciola hepatica and validates multi-epitope constructs from those peptides in vitro. Putative protein sequences derived from the genome of F. hepatica were integrated with phase-specific transcriptomic data to prioritize highly expressed proteins. Among these, extracellular proteins were selected using DeepLoc 2.0 and strong binding affinities across diverse human and murine alleles were predicted with the IEDB MHC II tool. Peptides were further selected based on their toxicity, immunogenicity, and allergenicity. Finally, 55 high-priority candidates were obtained. To express these candidates, mRNA constructs encoding various combinations of these peptides were designed, synthesized using in vitro transcription with T7 or SP6 RNA polymerases, and transfected into cells for expression analysis. SP6 polymerase produced proper capping using CleanCapAG and was far superior in transcribing peptide constructs. Peptides fused in frame with eGFP were expressed efficiently, particularly when peptides were positioned at the 3′ terminus, opening a new field of peptide vaccines created using mRNA technology. Full article
(This article belongs to the Special Issue RNA Vaccines and Therapeutics: Challenges and Opportunities)
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<p>Pipeline to select 55 peptides that putatively bind seven human alleles and one murine allele of class II MHC and have high immunogenic potential against <span class="html-italic">Fasciola hepatica</span>.</p>
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<p>Schematic of the prediction of AlphaFold structures and in vitro transcription of multi-peptides constructs using the GPGPG, KK, and AAY linkers (<b>A</b>). Schematic representation of a construct of 3 peptides (Px, Pz, Py) fused by one of the linker combinations (GPGPG/KK/AAY) and ending in a 6xHis tag. (<b>B</b>). AlphaFold predictions of secondary structures of the 15-peptide constructs with different linkers. (<b>C</b>). T7-transcribed mRNAs from 15-peptide constructs with each combination of linkers, resolved in 2% agarose gels. (<b>D</b>). SP6-transcribed mRNAs from 15-peptide constructs with each combination of linkers, resolved in 2% agarose gel electrophoresis.</p>
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<p>Multi-peptide constructs associated with a carrier molecule. (<b>A</b>). Schematic of the triple-peptide fusion constructs with eGFP on either the N- or C-terminus (3P-GFP and GFP-3P, respectively) (<b>B</b>). T7-transcribed mRNAs with standard reaction conditions resolved on a 2% agarose gel. (<b>C</b>). WB results of HEK293T cells 24 h post-transfection with the 3P-GFP or GFP-3P mRNA constructs. Tags were detected using an anti-GFP antibody, anti-FLAG antibody, or anti-6x histidine antibody.</p>
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<p>Design of the expression vector for mRNA vaccination. (<b>A</b>). Sequence of the T7 promotor adapted for use with CleanCap AG. (<b>B</b>). Sequence of the in-house SP6 promotor adapted for use with CleanCap AG. (<b>C</b>). Visual representation of the expression vector used in this study.</p>
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16 pages, 2992 KiB  
Article
Resequencing Composite Kazakh Whiteheaded Cattle: Insights into Ancestral Breed Contributions, Selection Signatures, and Candidate Genetic Variants
by Aigerim K. Khamzina, Alexander V. Igoshin, Zhadyra U. Muslimova, Asset A. Turgumbekov, Damir M. Khussainov, Nikolay S. Yudin, Yessengali S. Ussenbekov and Denis M. Larkin
Animals 2025, 15(3), 385; https://doi.org/10.3390/ani15030385 - 29 Jan 2025
Viewed by 300
Abstract
This study investigates the genetic architecture of the Kazakh Whiteheaded (KWH) cattle, applying population genetics approaches to resequenced genomes. FST analysis of 66 cattle breeds identified breeds for admixture analysis. At K = 19, the composite KWH breed showed contributions from Hereford, [...] Read more.
This study investigates the genetic architecture of the Kazakh Whiteheaded (KWH) cattle, applying population genetics approaches to resequenced genomes. FST analysis of 66 cattle breeds identified breeds for admixture analysis. At K = 19, the composite KWH breed showed contributions from Hereford, Altai, and Kalmyk cattle. Principal component analysis and ancestry inference confirmed these patterns, with KWH genomes comprising 45% Hereford, 30% Altai, and 25% Kalmyk ancestries. Haplotype analysis revealed 73 regions under putative selection in KWH, some shared with Hereford (e.g., with the gene DCUN1D4) and some KWH-specific (e.g., with the gene SCMH1). FST analysis identified 105 putative intervals under selection, with key genes (KITLG, SLC9C1, and SCMH1) involved in coat colour and physiological adaptations. Functional enrichment using The Database for Annotation, Visualization, and Integrated Discovery (DAVID) in selected regions highlighted clusters associated with developmental processes, ubiquitination, and fatty acid metabolism. Point FST identified 42 missense variants in genes enriched in functions related to economically important traits. Local ancestry inference revealed genomic intervals with predominantly non-Hereford ancestry, including high Altai (e.g., SCAPER) and Kalmyk (e.g., SRD5A2) contributions, while Hereford-dominated regions included genes ENO1 and RERE. This work elucidates the genomic contributions and adaptive signatures of selection shaping the KWH breed, providing candidate genetic variants for breeding program improvement and enhanced genome predictions. Full article
(This article belongs to the Special Issue Genomic Prediction in Livestock)
14 pages, 955 KiB  
Review
Perspectives of Genome Editing Mediated Haploid Inducer Systems in Legumes
by Yiqian Liu, Musazade Elshan, Geng Li, Xiao Han, Xiao Chen and Xianzhong Feng
Int. J. Mol. Sci. 2025, 26(3), 1154; https://doi.org/10.3390/ijms26031154 - 29 Jan 2025
Viewed by 361
Abstract
Genome editing-mediated haploid inducer systems (HISs) present a promising strategy for enhancing breeding efficiency in legume crops, which are vital for sustainable agriculture due to their nutritional benefits and ability to fix nitrogen. Traditional legume breeding is often slow and complicated by the [...] Read more.
Genome editing-mediated haploid inducer systems (HISs) present a promising strategy for enhancing breeding efficiency in legume crops, which are vital for sustainable agriculture due to their nutritional benefits and ability to fix nitrogen. Traditional legume breeding is often slow and complicated by the complexity of legumes’ genomes and the challenges associated with tissue culture. Recent advancements have broadened the applicability of HISs in legume crops, facilitating a reduction in the duration of the breeding cycle. By integrating genome editing technology with haploid breeding systems, researchers can achieve precise genetic modifications and rapidly produce homozygous lines, thereby significantly accelerating the development of desired traits. This review explores the current status and future prospects of genome editing-mediated HISs in legumes, emphasizing the mechanisms of haploid induction; recent breakthroughs; and existing technical challenges. Furthermore, we highlight the necessity for additional research to optimize these systems across various legume species, which has the potential to greatly enhance breeding efficiency and contribute to the sustainability of legume production. Full article
(This article belongs to the Special Issue Crop Genome Editing : 2nd Edition)
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<p>Overview of haploid induction methods in plants. Haploid induction can be divided into in vitro (gynogenesis and androgenesis) and in vivo methods (spontaneous induction, HILs, and interspecific hybridization). Microtubule-blocking agents disrupt spindle fiber formation during cell division, leading to whole-genome duplication. This process converts haploid cells into DH plants by preventing chromosome segregation, resulting in diploid cells.</p>
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<p>Potential application of candidate <span class="html-italic">DMP</span> genes for haploid induction in legumes. CRISPR/Cas9-mediated candidate <span class="html-italic">DMP</span> genes (e.g., <span class="html-italic">GmDMP</span> and <span class="html-italic">MtDMP</span>) are used in HILs to enable chromosome elimination, producing haploids that undergo chromosome doubling to form DHs. These transgene-free, gene-edited plants serve as valuable tools for legume breeding programs.</p>
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14 pages, 8059 KiB  
Article
New Mitogenomes of the Harnischia Generic Complex (Diptera: Chironomidae) and Their Implication in Phylogenetics
by Wenbin Liu, Yaning Tang, Jiaxin Nie, Haoran Yan, Wentao Liang, Yanfei Zhang and Chuncai Yan
Diversity 2025, 17(2), 96; https://doi.org/10.3390/d17020096 - 29 Jan 2025
Viewed by 249
Abstract
The Harnischia generic complex, a significant assemblage within the tribe Chi-ronomini, extensive global sampling and the integration of multi-characteristic data for comprehensive analysis are essential to elucidate the phylogenetic relationships within the Harnischia generic complex. We sequenced, assembled, and annotated the mitochondrial genomes [...] Read more.
The Harnischia generic complex, a significant assemblage within the tribe Chi-ronomini, extensive global sampling and the integration of multi-characteristic data for comprehensive analysis are essential to elucidate the phylogenetic relationships within the Harnischia generic complex. We sequenced, assembled, and annotated the mitochondrial genomes of a single species each from the genera Parachironomus Lenz, Robackia Saether and Saetheria Jackson. Additionally, we incorporated 26 previously published mitogenomes into our analysis to delve deeper into the characteristics of these mitogenomes. Our findings indicate the close affinity between (Cryptochironomus + Demicryptochironomus) and (Harnischia + Microchironomus), aligning consistently with previous research outcomes showing that the Harnischia generic complex and Chironomus are phylogenetically close, and their clade forms a sister group with the Polypedilum generic complex. Based on mitochondrial genome data, Robackia is identified as the basal taxon being relatively primitive, with Parachironomus and Saetheria also appearing as primitive within the complex. Full article
(This article belongs to the Special Issue Freshwater Zoobenthos Biodiversity, Evolution and Ecology)
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<p>The mitogenome map delineates the distinct mitochondrial genome characteristics of various representative species across three genera within the <span class="html-italic">Harnischia</span> generic complex. The map uses arrows to denote gene transcription direction and employs standard abbreviations for PCGs and rRNAs, along with simplified tRNA notations, for clarity. The second circle displays GC content, revealing nucleotide composition, while the third circle shows GC-skew, highlighting structural asymmetry. The innermost circle summarizes mitogenome length, offering a holistic view of its attributes.</p>
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<p>Evolution rate of 13 PCGs of the subfamily Chironominae in mitogenomes, (<b>a</b>): <span class="html-italic">Harnischia</span> generic complex, (<b>b</b>): other genera within Chironominae. Ka and Ks represent non-synonymous and synonymous nucleotide substitutions, respectively, with their ratio, Ka/Ks, indicating the selection pressure on protein-coding genes (PCGs). The plot’s x-axis shows 13 PCGs, and the y-axis shows Ka/Ks values.</p>
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<p>The assessment of the heterogeneity among the mitogenomes of 29 species belonging to the Chironomidae. This figure highlights the sequence similarities among Protein-Coding Genes (PCGs), amino acid sequences, and ribosomal RNAs (rRNAs) through a visually striking color-coded block representation. Utilizing the AliGROOVE scoring system, we assigned colors from −1 (red, denoting high heterogeneity) to +1 (blue, denoting low heterogeneity). The color scheme is such that lighter shades represent increased genetic variability, and deeper tones suggest reduced heterogeneity.</p>
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<p>Phylogenetic tree of Chironominae, ML tree based on analysis cds_rRNA in Partition.</p>
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38 pages, 1061 KiB  
Review
Can Wastewater Surveillance Enhance Genomic Tracking of Climate-Driven Pathogens?
by Laura A. E. Van Poelvoorde, Erik A. Karlsson, Myrielle Dupont-Rouzeyrol and Nancy H. C. J. Roosens
Microorganisms 2025, 13(2), 294; https://doi.org/10.3390/microorganisms13020294 - 28 Jan 2025
Viewed by 416
Abstract
Climate change heightens the threat of infectious diseases in Europe, necessitating innovative surveillance methods. Based on 390 scientific papers, for the first time, this review associates climate-related pathogens, data related to their presence in wastewater, and associated available genomic detection methods. This deep [...] Read more.
Climate change heightens the threat of infectious diseases in Europe, necessitating innovative surveillance methods. Based on 390 scientific papers, for the first time, this review associates climate-related pathogens, data related to their presence in wastewater, and associated available genomic detection methods. This deep analysis reveals a wide range of pathogens that can be tracked through methods such as quantitative and digital PCR, as well as genomic pathogen enrichment in combination with sequencing and metagenomics. Nevertheless, significant gaps remain in the development of methods, particularly for vector-borne pathogens, and in their general harmonization relating to performance criteria. By offering an overview of recent advancements while identifying critical gaps, we advocate for collaborative research and validation to integrate detection techniques into surveillance frameworks. This will enhance public health resilience against emerging infectious diseases driven by climate change. Full article
(This article belongs to the Section Environmental Microbiology)
19 pages, 4489 KiB  
Article
Genomic Prediction and Genome-Wide Association Study for Growth-Related Traits in Taiwan Country Chicken
by Tsung-Che Tu, Chen-Jyuan Lin, Ming-Che Liu, Zhi-Ting Hsu and Chih-Feng Chen
Animals 2025, 15(3), 376; https://doi.org/10.3390/ani15030376 - 28 Jan 2025
Viewed by 393
Abstract
Taiwan Country chickens are integral to Taiwanese culture and the poultry industry. By establishing a crossbreeding system, breeders must consider the growth-related traits of the dam line to achieve acceptable traits in commercial meat-type chickens. This study compared the accuracy of genomic estimated [...] Read more.
Taiwan Country chickens are integral to Taiwanese culture and the poultry industry. By establishing a crossbreeding system, breeders must consider the growth-related traits of the dam line to achieve acceptable traits in commercial meat-type chickens. This study compared the accuracy of genomic estimated breeding values (GEBVs) predicted using the pedigree-based best linear unbiased prediction (PBLUP) model and the single-step genomic BLUP (ssGBLUP) model. Additionally, we conducted a genome-wide association study (GWAS) to identify single-nucleotide polymorphisms (SNPs) associated with growth, shank, and body conformation traits to support marker-assisted selection (MAS). The results showed that the ssGBLUP model achieved 4.3% to 16.4% higher prediction accuracy than the PBLUP model. GWAS identified four missense SNPs and four significant SNPs associated with body weight, shank length, and shank width at 12 weeks. These findings highlight the potential of integrating the ssGBLUP model with identified SNPs to improve genetic gain and breeding efficiency and provide preliminary results to assess the feasibility of genomic prediction and MAS in Taiwan Country chicken breeding programs. Further research is necessary to validate these findings and explore their mechanisms and broader application across different breeding programs, particularly for the NCHU-G101 breed of Taiwan Country chickens. Full article
(This article belongs to the Section Animal Genetics and Genomics)
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<p>Average genomic inflation factor (<math display="inline"><semantics> <mrow> <mover accent="true"> <mrow> <mi>λ</mi> </mrow> <mo>¯</mo> </mover> </mrow> </semantics></math>) when varying numbers of principal components (PCs) are used as covariates in the genome-wide association study (GWAS) for different traits. Growth traits include body weight at 8 and 12 weeks of age; shank traits include shank length and width; and body conformation traits include back length and width.</p>
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<p>Manhattan (<b>left</b>) and QQ (<b>right</b>) plots of genome-wide association study (GWAS) results obtained using GEMMA software for body weight at 8 weeks (BW8), body weight at 12 weeks (BW12), shank length (SL), shank width (SW), back length (BBL), and back width (BBW). The red solid line represents the threshold for 5% Bonferroni genome-wide significance (<span class="html-italic">p</span> = 2.00 × 10<sup>−6</sup> for BW8 and BW12; <span class="html-italic">p</span> = 2.00 × 10<sup>−6</sup> for SL, SW, BBL, and BBW). The blue dotted line represents the suggestive threshold (<span class="html-italic">p</span> = 4.00 × 10<sup>−5</sup> for BW8 and BW12; <span class="html-italic">p</span> = 4.01 × 10<sup>−5</sup> for SL, SW, BBL, and BBW).</p>
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<p>Boxplots of phenotypes for body weight at 12 weeks (BW12), shank length (SL), and shank width (SW) by alleles of missense SNP markers. The boxes show the first, median, and third quartile, with whiskers extending 1.5 times the interquartile range. ** above the bars indicates significant differences (<span class="html-italic">p</span> &lt; 0.05) between genotypes within each SNP, while “ns” indicates no significant difference, based on Tukey’s HSD test. Numbers in parentheses next to the genotypes represent the sample size for each group, with the total sample size possibly being lower because of missing genotyped data for some individuals.</p>
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<p>Boxplots of phenotypes for shank length (SL) and shank width (SW) by genotypes of SNP markers with 5% Bonferroni genome-wide significance. The boxes represent the first, median, and third quartiles, with whiskers extending up to 1.5 times the interquartile range. ** above the bars indicates significant differences (<span class="html-italic">p</span> &lt; 0.05) based on Tukey’s HSD test. Numbers in parentheses next to the genotypes indicate the sample size for each group. The total sample size was reduced in some cases because of missing genotyped data for certain individuals.</p>
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16 pages, 2388 KiB  
Article
Polo-like Kinase 1 Inhibitors Demonstrate In Vitro and In Vivo Efficacy in Preclinical Models of Small Cell Lung Cancer
by Guojing Zhang, Abbe Pannucci, Andrey A. Ivanov, Jeffrey Switchenko, Shi-Yong Sun, Gabriel L. Sica, Zhentao Liu, Yufei Huang, John C. Schmitz and Taofeek K. Owonikoko
Cancers 2025, 17(3), 446; https://doi.org/10.3390/cancers17030446 - 28 Jan 2025
Viewed by 386
Abstract
Objective: To investigate the preclinical efficacy and identify predictive biomarkers of polo-like kinase 1 (PLK1) inhibitors in small cell lung cancer (SCLC) models. Methods: We tested the cytotoxicity of selective PLK1 inhibitors (rigosertib, volasertib, and onvansertib) in a panel of SCLC cell lines. [...] Read more.
Objective: To investigate the preclinical efficacy and identify predictive biomarkers of polo-like kinase 1 (PLK1) inhibitors in small cell lung cancer (SCLC) models. Methods: We tested the cytotoxicity of selective PLK1 inhibitors (rigosertib, volasertib, and onvansertib) in a panel of SCLC cell lines. We confirmed the therapeutic efficacy of subcutaneous xenografts of representative cell lines and in four patient-derived xenograft models generated from patients with platinum-sensitive and platinum-resistant SCLC. We employed an integrated analysis of genomic and transcriptomic sequencing data to identify potential biomarkers of the activity and mechanisms of resistance in laboratory-derived resistance models. Results: Volasertib, rigosertib, and onvansertib showed strong in vitro cytotoxicity at nanomolar concentrations in human SCLC cell lines. Rigosertib, volasertib, and onvansertib showed equivalent efficacy to that of standard care agents (irinotecan and cisplatin) in vivo with significant growth inhibition superior to cisplatin in PDX models of platinum-sensitive and platinum-resistant SCLC. There was an association between YAP1 expression and disruptive or inactivation TP53 gene mutations, with greater efficacy of PLK1 inhibitors. Comparison of lab-derived onvansertib-resistant H526 cells to parental cells revealed differential gene expression with upregulation of NAP1L3, CYP7B1, AKAP7, and FOXG1 and downregulation of RPS4Y1, KDM5D, USP9Y, and EIF1AY highlighting the potential mechanisms of resistance in the clinical setting. Conclusions: We established the efficacy of PLK1 inhibitors in vitro and in vivo using PDX models of platinum-sensitive and resistant relapsed SCLC. An ongoing phase II trial is currently testing the efficacy of onvansertib in patients with SCLC (NCT05450965). Full article
(This article belongs to the Section Molecular Cancer Biology)
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<p>Assessment of in vitro antiproliferative activity of targeted agents in a panel of SCLC cell lines (<b>a</b>); effect of volasertib (<b>b</b>) and onvansertib (<b>c</b>) on proliferation of SCLC cell lines. Cells were treated for 72 h with indicated agents. Cell proliferation was determined using colorimetric or luminescent assays depending on the degree of clustering of SCLC cell lines in culture. Values represent the mean ± S.D. from a minimum of 3 independent experiments. Blue and orange curves define cell lines with non-disruptive and disruptive p53 mutations, respectively. Basal protein expression in SCLC cell lines (<b>d</b>). SCLC subtype based on expression are indicated after each cell line: ASCL1 (A), POU2F3 (P), YAP1 (Y).</p>
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<p>In vivo efficacy of PLK1 inhibitors in SCLC. Mice bearing H526 xenografts were i.p. administered volasertib (20 mg/kg), irinotecan (25 mg/kg), or cisplatin (3 mg/kg) weekly. Tumor volumes represent the mean ± SEM from groups of 6 mice. *** <span class="html-italic">p</span> ≤ 0.001.</p>
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<p>Antitumor efficacy of PLK1 inhibitors in SCLC PDXs. Mice bearing platinum-resistant PDXs TKO-002 and TKO-008 (<b>a</b>,<b>b</b>) and platinum-sensitive PDXs TKO-005 and TKO-010 (<b>c</b>,<b>d</b>) were administered cisplatin (3 mg/kg; i.p. weekly), rigosertib (250 mg/kg; i.p. daily), and onvansertib (60 mg/kg; oral × 10 days, 4 days off). Tumor volumes represent the mean ± S.D. from groups of 6 mice per group. *: significant and ns: not significant versus control group. * <span class="html-italic">p</span> ≤ 0.05, ** <span class="html-italic">p</span> ≤ 0.01.</p>
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<p>Correlative analysis between <span class="html-italic">TP53</span>, <span class="html-italic">PLK1</span>, and <span class="html-italic">MYC</span> expression (NCBI public database Gene Expression Omnibus GSE55830 [<a href="#B30-cancers-17-00446" class="html-bibr">30</a>]) and cell line sensitivity to PLK1 inhibition (<b>a</b>); YAP1 expression in SCLC-Y cell lines versus other subtypes (<b>b</b>); volcano plot of differentially expressed genes between SCLC-Y and not SCLC-Y cell lines (<b>c</b>); analysis of therapeutic vulnerability based on differential sensitivity of YAP1-positive cell lines showing PLK1 inhibitor as a potential candidate (<b>d</b>); Reactome analysis of active cellular function based on DEG between SCLC-Y and not SCLC-Y lines identified major differences in immune regulation and muscle contraction (<b>e</b>); KEGG analysis of differentially activated signaling pathways between the 2 groups (<b>f</b>).</p>
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<p>Effect of <span class="html-italic">TP53</span> mutational status on PLK1 inhibitor sensitivity. Comparison of mean IC<sub>50</sub> to <span class="html-italic">TP53</span> gene mutation status (<b>a</b>). <span class="html-italic">TP53</span> gene status in 166 tumor samples in cbioportal.org (<b>b</b>) and 50 SCLC cell lines from publicly available CCLE data (<b>c</b>). Activity of PLK1 inhibitor onvansertib in parental and resistant H526 cells (IC<sub>50</sub> concentration in the resistant vs. parent: 447 nM vs. 51 nM) (<b>d</b>). Gene expression profiles of matched parental and PLK1 inhibitor resistant H526 cells from 3 separate samples (<b>e</b>). Heatmap shows the top differential gene expression (<span class="html-italic">p</span>-adj &lt; 0.5; logFC &gt; 4 cut-off) with red indicating high and blue indicating low natural log-transformed expression.</p>
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19 pages, 5197 KiB  
Article
Genome-Wide Association Studies for Lactation Performance in Buffaloes
by Wangchang Li, Henggang Li, Chunyan Yang, Haiying Zheng, Anqin Duan, Liqing Huang, Chao Feng, Xiaogan Yang and Jianghua Shang
Genes 2025, 16(2), 163; https://doi.org/10.3390/genes16020163 - 27 Jan 2025
Viewed by 313
Abstract
Background: Buffaloes are considered an indispensable genetic resource for dairy production. However, improvements in lactation performance have been relatively limited. Advances in sequencing technology, combined with genome-wide association studies, have facilitated the breeding of high-quality buffalo. Methods: We conducted an integrated [...] Read more.
Background: Buffaloes are considered an indispensable genetic resource for dairy production. However, improvements in lactation performance have been relatively limited. Advances in sequencing technology, combined with genome-wide association studies, have facilitated the breeding of high-quality buffalo. Methods: We conducted an integrated analysis of genomic sequencing data from 120 water buffalo, the high-quality water buffalo genome assembly designated as UOA_WB_1, and milk production traits, including 305-day milk yield (MY), peak milk yield (PM), total protein yield (PY), protein percentage (PP), fat percentage (FP), and total milk fat yield (FY). Results: The results identified 56 significant SNPs, and based on these markers, 54 candidate genes were selected. These candidate genes were significantly enriched in lactation-related pathways, such as the cAMP signaling pathway (ABCC4), TGF-β signaling pathway (LEFTY2), Wnt signaling pathway (CAMK2D), and metabolic pathways (DGAT1). Conclusions: These candidate genes (e.g., ABCC4, LEFTY2, CAMK2D, DGAT1) provide a substantial theoretical foundation for molecular breeding to enhance milk production in buffaloes. Full article
(This article belongs to the Section Animal Genetics and Genomics)
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<p>Correlation analysis of various lactation traits. MY, milk yield; PM, peak milk yield; PY, protein yield; FY, fat yield; PP, protein percentage; FP, fat percentage.</p>
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<p>The sample clustering obtained from PCA through three two-dimensional scatter plots, namely scatter (<b>A</b>), scatter (<b>B</b>), and scatter (<b>C</b>); scree plot (<b>D</b>). The percentage of variance explained by each PC is noted in parentheses. In the scatter plots, colored circles represent four different groups: DB, MB, NB, and ZB correspond to 1 DB, 42 MBs, 31 NBs, and 46 ZBs, respectively.</p>
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<p>The line graph illustrating the cross-validation error rate is depicted, with the number of sample clusters delineated along the <span class="html-italic">x</span>-axis and the corresponding cross-validation error rate indicated on the <span class="html-italic">y</span>-axis.</p>
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<p>Genetic bar chart illustration for K-means clustering with varying numbers of clusters (K = 2 to 9).</p>
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<p>Association analysis with milk production-related traits in water buffalo was conducted using the GLM-Q approach. The traits investigated include MY (<b>A</b>), PM (<b>B</b>), PY (<b>C</b>), FY (<b>D</b>), PP (<b>E</b>), and FP (<b>F</b>). The Manhattan plot on the left, created using the qqman package, illustrates the <span class="html-italic">p</span>-values for SNP markers across 25 chromosomes (comprising 24 autosomes and 1 X chromosome). The blue line delineating the Manhattan plot signifies the significance threshold, determined by 0.05/N (number of SNP). Markers that surpass this threshold are deemed significant. The plot on the right is a Q-Q plot, where the <span class="html-italic">x</span>-axis denotes the observed values of the markers, and the <span class="html-italic">y</span>-axis represents the expected values, which have been transformed into the −10 log scale.</p>
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<p>GO and KEGG analysis of candidate genes. (<b>A</b>) GO bar plot diagram showing the top 20 enriched GO terms. GO categories, including cellular component, biological process, and molecular function. (<b>B</b>) The enrichment circle diagram shows the KEGG analysis of the top 20 pathways. Four circles from the outside to the inside. First circle: the classification of enrichment; outside the circle is the scale of the number of genes. Different colors represent different categories. Second circle: number and <span class="html-italic">p</span>-values of the classification in the background genes. The more genes, the longer the bars; the smaller the value, the redder the color. Third circle: bar chart of the total number of candidate genes. Fourth circle: rich factor value of each classification (number of candidate genes in this classification divided by the number of background genes). Each cell of the background helper line represents 0.1, and the color coding signifies the statistical significance of the corresponding enrichment.</p>
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33 pages, 935 KiB  
Review
Pharmaco-Multiomics: A New Frontier in Precision Psychiatry
by Dhoha Dhieb and Kholoud Bastaki
Int. J. Mol. Sci. 2025, 26(3), 1082; https://doi.org/10.3390/ijms26031082 - 26 Jan 2025
Viewed by 973
Abstract
The landscape of psychiatric care is poised for transformation through the integration of pharmaco-multiomics, encompassing genomics, proteomics, metabolomics, transcriptomics, epigenomics, and microbiomics. This review discusses how these approaches can revolutionize personalized treatment strategies in psychiatry by providing a nuanced understanding of the molecular [...] Read more.
The landscape of psychiatric care is poised for transformation through the integration of pharmaco-multiomics, encompassing genomics, proteomics, metabolomics, transcriptomics, epigenomics, and microbiomics. This review discusses how these approaches can revolutionize personalized treatment strategies in psychiatry by providing a nuanced understanding of the molecular bases of psychiatric disorders and individual pharmacotherapy responses. With nearly one billion affected individuals globally, the shortcomings of traditional treatments, characterized by inconsistent efficacy and frequent adverse effects, are increasingly evident. Advanced computational technologies such as artificial intelligence (AI) and machine learning (ML) play crucial roles in processing and integrating complex omics data, enhancing predictive accuracy, and creating tailored therapeutic strategies. To effectively harness the potential of pharmaco-multiomics approaches in psychiatry, it is crucial to address challenges such as high costs, technological demands, and disparate healthcare systems. Additionally, navigating stringent ethical considerations, including data security, potential discrimination, and ensuring equitable access, is essential for the full realization of this approach. This process requires ongoing validation and comprehensive integration efforts. By analyzing recent advances and elucidating how different omic dimensions contribute to therapeutic customization, this review aims to highlight the promising role of pharmaco-multiomics in enhancing patient outcomes and shifting psychiatric treatments from a one-size-fits-all approach towards a more precise and patient-centered model of care. Full article
(This article belongs to the Special Issue Innovative Therapeutic Approaches in Neuropsychiatric Disorders)
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<p>Navigating the path to precision psychiatry. This figure outlines a novel approach in personalized psychiatry, predicated on the integration of diverse datasets and encompassing pharmaco-multiomics. Utilizing advanced AI and ML technologies, these integrated data are leveraged to yield precise insights that enable the formulation of tailored therapeutic interventions and dynamic management strategies. This methodology distinctly addresses the intricate needs of psychiatric care and emphasizes patient-centered care.</p>
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11 pages, 1291 KiB  
Article
Accuracy of Genomic Predictions for Resistance to Gastrointestinal Parasites in Australian Merino Sheep
by Brenda Vera, Elly A. Navajas, Elize Van Lier, Beatriz Carracelas, Pablo Peraza and Gabriel Ciappesoni
Genes 2025, 16(2), 159; https://doi.org/10.3390/genes16020159 - 26 Jan 2025
Viewed by 653
Abstract
Infection by gastrointestinal nematodes (GINs) in sheep is a significant health issue that affects animal welfare and leads to economic losses in the production sector. Genetic selection for parasite resistance has shown promise in improving animal health and productivity. This study aimed to [...] Read more.
Infection by gastrointestinal nematodes (GINs) in sheep is a significant health issue that affects animal welfare and leads to economic losses in the production sector. Genetic selection for parasite resistance has shown promise in improving animal health and productivity. This study aimed to determine if incorporating genomic data into genetic prediction models currently used in Uruguay could improve the accuracy of breeding value estimations for GIN resistance in the Australian Merino breed. This study compared the accuracy of breeding value predictions using the BLUP (Best Linear Unbiased Prediction) and ssGBLUP (single-step genomic BLUP) models on partial and complete data sets, including 32,713 phenotyped and 3238 genotyped animals. The quality of predictions was evaluated using a linear regression method, focusing on 145 rams. The inclusion of genomic data increased the average individual accuracies by 4% for genotyped and phenotyped animals. For animals with genomic and non-phenotyped data, the accuracy improvement reached 8%. Of these, one group of animals that benefited from an ssGBLUP evaluation came from a facility with a strong connection to the informative nucleus and showed an average increase of 20% in their individual accuracy. Additionally, ssGBLUP slightly outperformed BLUP in terms of prediction quality. These findings demonstrate the potential of genomic information to improve the accuracy of breeding value predictions for parasite resistance in sheep. The integration of genomic data, particularly in non-phenotyped animals, offers a promising tool for enhancing genetic selection in Australian Merino sheep to improve resistance to gastrointestinal parasites. Full article
(This article belongs to the Special Issue Genetics and Genomics of Sheep and Goat)
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<p>Workflow for comparing individual accuracies and quality estimators between BLUP and ssGBLUP models.</p>
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<p>(G)EBV accuracies in validation population (<b>A</b>) without and (<b>C</b>) with FEC phenotype. Boxplot diagrams for accuracy increase using ssGBLUP compared to BLUP in evaluations (<b>B</b>) without phenotype and (<b>D</b>) with phenotype.</p>
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25 pages, 2730 KiB  
Review
Red-Leafed Lettuces: Genetic Variation or Epigenetic Photomorphogenesis?
by Natalya V. Smirnova, Ivan A. Timofeenko and Konstantin V. Krutovsky
Plants 2025, 14(3), 363; https://doi.org/10.3390/plants14030363 - 25 Jan 2025
Viewed by 345
Abstract
Red-leaf lettuces, rich in bioactive compounds like anthocyanins and flavonoids, offer health benefits by reducing oxidative stress and boosting immunity. This article provides an extensive review of the genetic, epigenetic, environmental, and technological factors influencing anthocyanin biosynthesis and leaf coloration in red-leaf lettuce, [...] Read more.
Red-leaf lettuces, rich in bioactive compounds like anthocyanins and flavonoids, offer health benefits by reducing oxidative stress and boosting immunity. This article provides an extensive review of the genetic, epigenetic, environmental, and technological factors influencing anthocyanin biosynthesis and leaf coloration in red-leaf lettuce, emphasizing its significance in agriculture and nutrition. The genetics of anthocyanin biosynthesis, environmental influences, practical applications, agronomic insights, and future directions are the main areas covered. Anthocyanin accumulation is regulated by structural, regulatory, and transporter genes, as well as the MYB-bHLH-WD40 (MBW) complex. Mutations in these genes impact coloration and stress responses. Advances in genomic studies, such as GWAS and QTL mapping, have identified key genes and pathways involved in anthocyanin biosynthesis, aiding breeding programs for desirable traits. In addition, light intensity, stress conditions (e.g., drought, temperature), and phytohormones affect anthocyanin levels and photomorphogenesis in general. Controlled environments, like vertical farms, optimize these conditions to enhance pigmentation and phytochemical content. LED lighting and tailored cultivation techniques improve color intensity, antioxidant capacity, and yield in controlled settings. Sustainable production technologies for red-leaf lettuce in vertical farms are being developed to meet consumer demand and promote functional foods, integrating genetic, epigenetic, and environmental research into agronomy. This review highlights red-leaf lettuce’s aesthetic, nutritional, and functional value, advocating for innovative cultivation methods to enhance its market and health potential. Full article
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<p>Basic structure of anthocyanidins and anthocyanins with carbon atom numbering (modified from Figure 1 in [<a href="#B16-plants-14-00363" class="html-bibr">16</a>]).</p>
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<p>The diagram demonstrates the relationship between environmental conditions and the individual characteristics of a plant at all stages of its development: the individual development of each crop of a certain variety or species is determined by the genetic characteristics of the individual, which are manifested in the activity of the main biological processes: respiration, photosynthesis, transpiration, metabolic processes, and the accumulation of nutrients in tissues and different parts of the plant. In addition, all processes are also under the influence of abiotic and biotic factors that determine the speed and rate of the growth and development of plants, changes in phenophases, the rate of seed maturation, and the quality of plant raw materials for various purposes.</p>
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<p>Light-sensitive system of red-leaf lettuce, providing different productivity and product quality.</p>
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<p>Conversion of anthocyanins into interchangeable forms at different pH levels (adapted from Figure 4 in [<a href="#B71-plants-14-00363" class="html-bibr">71</a>]).</p>
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14 pages, 1950 KiB  
Article
The Complete Mitochondrial Genome of the Korean Endemic Polychaete Phyllodoce koreana (Lee & Jae, 1985) from Jindong Bay, Korea, with Additional Morphological and Ecological Features
by Dae-Hun Kim, So Jin Ryu, Jong Rae Kim, Seong-il Eyun and Man-Ki Jeong
J. Mar. Sci. Eng. 2025, 13(2), 223; https://doi.org/10.3390/jmse13020223 - 25 Jan 2025
Viewed by 575
Abstract
Phyllodoce koreana was first described in 1985 in Gwangyang Bay, a semi-enclosed bay in Korea affected by significant organic input from the Seomjin River and dredging activities near the Gwangyang Port. Since then, this Korean endemic species has received limited attention in taxonomic [...] Read more.
Phyllodoce koreana was first described in 1985 in Gwangyang Bay, a semi-enclosed bay in Korea affected by significant organic input from the Seomjin River and dredging activities near the Gwangyang Port. Since then, this Korean endemic species has received limited attention in taxonomic and ecological studies. Phyllodoce koreana is known for its resilience to mild disturbances but is vulnerable to severe environmental changes. In this study, P. koreana specimens were collected from organically polluted Asian stalked tunicate aquaculture farms at eight sites in Jindong Bay, a location with environmental conditions similar to those of Gwangyang Bay, over the course of five sampling events from March to November. Both bays experience benthic hypoxia in summer due to elevated water temperatures and organic matter accumulation. Phyllodocid specimens were primarily collected in March and November 2023, non-hypoxic periods, suggesting potential seasonal adaptations to environmental fluctuations. The morphological features of the collected specimens were consistent with the original description of P. koreana, confirming their identification. Additionally, we reported previously overlooked morphological details, contributing to a more comprehensive taxonomic understanding of the species. We also present, for the first time, the complete mitochondrial genome of this species, comprising 15,559 bp, which provides essential genetic data for future taxonomic and phylogenetic studies. The phylogenetic analysis of protein-coding genes shows that, among 17 related polychaete species, P. koreana (family Phyllodocidae) is closely related to the family Goniadidae. Future research should expand our knowledge of polychaete taxonomy by integrating additional mitochondrial genomes and investigating the role of conserved gene synteny within Polychaeta. Full article
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<p>A map of the study area in Jindong Bay on the southern coast of Korea. The circles represent collection sites, with red circles indicating where phyllodocid specimens were collected. The green dotted line indicates the boundary of Asian stalked tunicate aquaculture.</p>
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<p><span class="html-italic">P. koreana</span>: (<b>A</b>) dorsal view; (<b>B</b>) prostomium, dorsal view; (<b>C</b>) anterior segment, ventral view; (<b>D</b>) composite chaetae (PR: prostomium; PER: peristomium; AT: antennae; TC: tentacular cirrus; DC: dorsal cirri; VC: ventral cirri; NEPL: neuropodial lobe of 4th segment; SG: segment).</p>
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<p>The mitochondrial genome map of <span class="html-italic">P. koreana</span> inhabiting Asian stalked tunicate aquaculture farms in Jindong Bay. The innermost ring is a blue bar plot representing the GC content. The middle purple ring shows the sequencing depth. The outermost ring depicts the genes in order according to color: red for COX genes, violet for ATP synthase, green for COB, and navy for ND genes. The two rRNA genes are shown in gray, and the 22 tRNA genes are shown in yellow.</p>
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<p>Two species in the family Syllidae were used as the outgroup. Bootstrap support values &gt; 60% based on the maximum likelihood (ML) and Bayesian Inference (BI) methods (ML/BI) are included at each node. The background colors at the right delineate different families. The scale bar represents the relative substitution rates per site. The synteny of the 13 mitochondrial protein-coding genes is shown to the right of the tree.</p>
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