population structure

人口结构
  • 文章类型: Journal Article
    多亲本高级世代交叉(MAGIC)种群的特征是在数量性状基因座(QTL)作图的能力和分辨率方面具有巨大潜力,但是基于单核苷酸多态性(SNP)的GWAS并未完全发挥其潜力。在这项研究中,从五个水稻亚组的四个西安和四个庚品种中开发了1021个品系的MAGIC种群。共有44.000个基因在8个父母中显示出功能多态性,包括移码变异或过早终止密码子变异,这提供了绘制几乎所有MAGIC群体基因的潜力。主成分分析结果表明,MAGIC种群具有较弱的种群结构。构建了24.414箱的高密度箱图。分离畸变发生在具有遗传不相容性和配子发育基础基因的区域中。基于SNP的关联分析和基于bin的连锁分析确定了抽穗日期的25个显著基因座和47个QTL,包括14个已知的标题日期基因.基因的作图分辨率取决于遗传效应,主要效应基因的偏移距离<55kb,中等效应基因的偏移距离<123kb。四个因果变异和非编码结构变异被鉴定为与标题日期相关。三到四种类型的等位基因具有很强的,中间,弱,没有发现八位父母的遗传效应,为水稻抽穗期的改良提供了灵活性。在大多数情况下,粳稻携带弱等位基因,和印度水稻携带强等位基因和非功能性等位基因。这些结果证实,MAGIC群体提供了检测QTL的特殊机会,鼓励将其用于定位基因和挖掘有利的等位基因以进行育种。
    The multiparent advanced generation intercross (MAGIC) population is characterized with great potentials in power and resolution of quantitative trait locus (QTL) mapping, but single nucleotide polymorphism (SNP)-based GWAS does not fully reach its potential. In this study, a MAGIC population of 1021 lines was developed from four Xian and four Geng varieties from five subgroups of rice. A total of 44 000 genes showed functional polymorphisms among eight parents, including frameshift variations or premature stop codon variations, which provides the potential to map almost all genes of the MAGIC population. Principal component analysis results showed that the MAGIC population had a weak population structure. A high-density bin map of 24 414 bins was constructed. Segregation distortion occurred in the regions possessing the genes underlying genetic incompatibility and gamete development. SNP-based association analysis and bin-based linkage analysis identified 25 significant loci and 47 QTLs for heading date, including 14 known heading date genes. The mapping resolution of genes is dependent on genetic effects with offset distances of <55 kb for major effect genes and <123 kb for moderate effect genes. Four causal variants and noncoding structure variants were identified to be associated with heading date. Three to four types of alleles with strong, intermediate, weak, and no genetic effects were identified from eight parents, providing flexibility for the improvement of rice heading date. In most cases, japonica rice carries weak alleles, and indica rice carries strong alleles and nonfunctional alleles. These results confirm that the MAGIC population provides the exceptional opportunity to detect QTLs, and its use is encouraged for mapping genes and mining favorable alleles for breeding.
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  • 文章类型: Journal Article
    全基因组关联研究(GWAS)被广泛用于表征与收获前发芽和种子休眠相关的基因或数量性状基因座(QTL)。GWAS可以在不同的遗传小组中识别先前发现的和新的QTL。高通量SNP阵列或下一代测序技术促进了许多遗传标记的鉴定,从而显著提高GWAS的分辨率。尽管已经开发了各种方法,这些技术的基本原理保持不变。这里,我们提供了一个基本的技术流程来进行种子休眠测定,其次是使用人口结构控制的GWAS,并将其与以前鉴定的QTL和基因进行比较。
    Genome-wide association study (GWAS) is widely used to characterize genes or quantitative trait loci (QTLs) associated with preharvest sprouting and seed dormancy. GWAS can identify both previously discovered and novel QTLs across diverse genetic panels. The high-throughput SNP arrays or next-generation sequencing technologies have facilitated the identification of numerous genetic markers, thereby significantly enhancing the resolution of GWAS. Although various methods have been developed, the fundamental principles underlying these techniques remain constant. Here, we provide a basic technological flow to perform seed dormancy assay, followed by GWAS using population structure control, and compared it with previous identified QTLs and genes.
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  • 文章类型: Journal Article
    结论:美国proso小米的中试规模全基因组关联研究确定了五个形态农艺性状的20个标记-性状关联,确定了未来研究的基因组区域(例如分子育种和基于图谱的克隆)。Proso小米(PanicummiliaceumL.)是一种古老的谷物,以其出色的水分利用效率和短的生长季节而闻名。它是美国高平原地区以冬小麦为基础的旱地种植系统中不可或缺的一部分。它的谷物具有很高的营养和促进健康的特性,使其在全球市场上越来越受欢迎的健康谷物。谷子中缺乏基因组资源来开发分子工具以补充常规育种以开发高产品种。全基因组关联研究(GWAS)是一种广泛使用的方法来剖析复杂性状的遗传学。在这项美国proso小米有史以来第一个GWAS的试点研究中,在内布拉斯加州西部的两个地点,评估了109个美国proso小米核心收藏的71个全球不同基因型的五个主要形态农艺性状,并进行GWAS以鉴定与这些性状相关的单核苷酸多态性(SNP)。方差分析表明,各基因型之间存在显著差异,并且还发现所有五个性状彼此高度相关。来自通过测序进行基因分型(GBS)的序列读段用于鉴定11,147个高质量双等位基因SNP。使用这些SNP的群体结构分析显示核心集合内的分层。GWAS鉴定了这5个性状的20个标记-性状关联(MTA)。还鉴定了29个与这5个性状相关的推定候选基因。这些基因组区域可用于开发遗传标记,用于谷子育种中的标记辅助选择。
    CONCLUSIONS: The pilot-scale genome-wide association study in the US proso millet identified twenty marker-trait associations for five morpho-agronomic traits identifying genomic regions for future studies (e.g. molecular breeding and map-based cloning). Proso millet (Panicum miliaceum L.) is an ancient grain recognized for its excellent water-use efficiency and short growing season. It is an indispensable part of the winter wheat-based dryland cropping system in the High Plains of the USA. Its grains are endowed with high nutritional and health-promoting properties, making it increasingly popular in the global market for healthy grains. There is a dearth of genomic resources in proso millet for developing molecular tools to complement conventional breeding for developing high-yielding varieties. Genome-wide association study (GWAS) is a widely used method to dissect the genetics of complex traits. In this pilot study of the first-ever GWAS in the US proso millet, 71 globally diverse genotypes of 109 the US proso millet core collection were evaluated for five major morpho-agronomic traits at two locations in western Nebraska, and GWAS was conducted to identify single nucleotide polymorphisms (SNPs) associated with these traits. Analysis of variance showed that there was a significant difference among the genotypes, and all five traits were also found to be highly correlated with each other. Sequence reads from genotyping-by-sequencing (GBS) were used to identify 11,147 high-quality bi-allelic SNPs. Population structure analysis with those SNPs showed stratification within the core collection. The GWAS identified twenty marker-trait associations (MTAs) for the five traits. Twenty-nine putative candidate genes associated with the five traits were also identified. These genomic regions can be used to develop genetic markers for marker-assisted selection in proso millet breeding.
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  • 文章类型: Journal Article
    背景:猕猴桃(Actinidiaceae家族)是中国和新西兰经济上重要的果树。这是一种典型的雌雄异株植物,经过频繁的自然杂交,以及猕猴桃属的染色体倍性多样性,导致种间和种内性状之间更高的遗传差异和园艺多样性。这种多样性为育种提供了丰富的遗传基础。中国不仅是猕猴桃属物种的原始中心,也是其分布中心,居住最驯化的物种:A.chinensisvar。中国,A.中国变种。deliciosa,A.阿古塔,和一夫多妻制。然而,关于猕猴桃植物DNA标记的应用和遗传基础的研究相对较少。通过结合来自叶绿体特异性SNP和核SCoT(nSCoT)标记的信息,我们可以发现遗传变异的互补方面,人口结构,和进化关系。在这项研究中,从9个cpDNA候选对中选择一个叶绿体DNA(cpDNA)标记对。选择了20个nSCoT标记,并用于评估55种猕猴桃植物(猕猴桃)的种群结构和叶绿体特异性DNA单倍型多样性,包括20个中国A.中国,22个A.chinensisvar样品。deliciosa,11个阿古塔的样本,和两个多边形的样本,根据从中国收集的形态学观察。
    结果:对于叶绿体特异性SNP标记,55个样品之间的平均遗传距离为0.26,对于nSCoT标记为0.57。Mantel检验显示出非常小的相关性(r=0.21)。使用贝叶斯分析将55个样本分为不同的亚群,带算术平均值的未加权对组方法(UPGMA),和主成分分析(PCA)方法,分别。基于对205个可变位点的分析,共观察到15种叶绿体特异性DNA单倍型,有助于更高水平的多态性,Hd为0.78。大多数叶绿体特异性DNA单倍型多样性分布在种群中,但在种群内也观察到显著的多样性。H1由24个样本共享,其中包括12个中国的变种。中国和12个中国的变种。deliciosa,表明H1是55个叶绿体特异性序列中的一种古老的显性单倍型。H2可能没有进一步演化。其余的单倍型是罕见和独特的,其中一些似乎是特定品种的专属,并且经常在单个个体中检测到。例如,H15单倍型仅在多利马A中发现。
    结论:叶绿体特异性SNP标记解释的群体遗传变异比nSCoTs解释的具有更大的功效,叶绿体特异性DNA单倍型是最有效的。A.chinensisvar之间的基因流似乎更为明显。中国和A.chinensisvar。deliciosa,因为它们共享叶绿体特异性DNA单倍型,相比之下,A.arguta和A.polygama拥有自己的特征单倍型,源自A.chinensisvar的单倍型。中国。与A.chinensis相比,A.arguta和A.polygama显示出更好的分组。筛选出来似乎也至关重要,对于每种类型的分子标记,尤其是单倍型,猕猴桃属的核心标记。
    BACKGROUND: Kiwifruit (Actinidiaceae family) is an economically important fruit tree in China and New Zealand. It is a typical dioecious plant that has undergone frequent natural hybridization, along with chromosomal ploidy diversity within the genus Actinidia, resulting in higher genetic differences and horticultural diversity between interspecific and intraspecific traits. This diversity provides a rich genetic base for breeding. China is not only the original center of speciation for the Actinidia genus but also its distribution center, housing the most domesticated species: A. chinensis var. chinensis, A. chinensis var. deliciosa, A. arguta, and A. polygama. However, there have been relatively few studies on the application of DNA markers and the genetic basis of kiwifruit plants. By combining information from chloroplast-specific SNPs and nuclear SCoT (nSCoT) markers, we can uncover complementary aspects of genetic variation, population structure, and evolutionary relationships. In this study, one chloroplast DNA (cpDNA) marker pair was selected out of nine cpDNA candidate pairs. Twenty nSCoT markers were selected and used to assess the population structure and chloroplast-specific DNA haplotype diversity in 55 kiwifruit plants (Actinidia), including 20 samples of A. chinensis var. chinensis, 22 samples of A. chinensis var. deliciosa, 11 samples of A. arguta, and two samples of A. polygama, based on morphological observations collected from China.
    RESULTS: The average genetic distance among the 55 samples was 0.26 with chloroplast-specific SNP markers and 0.57 with nSCoT markers. The Mantel test revealed a very small correlation (r = 0.21). The 55 samples were categorized into different sub-populations using Bayesian analysis, the Unweighted Pair Group Method with the Arithmetic Mean (UPGMA), and the Principal Component Analysis (PCA) method, respectively. Based on the analysis of 205 variable sites, a total of 15 chloroplast-specific DNA haplotypes were observed, contributing to a higher level of polymorphism with an Hd of 0.78. Most of the chloroplast-specific DNA haplotype diversity was distributed among populations, but significant diversity was also observed within populations. H1 was shared by 24 samples, including 12 of A. chinensis var. chinensis and 12 of A. chinensis var. deliciosa, indicating that H1 is an ancient and dominant haplotype among the 55 chloroplast-specific sequences. H2 may not have evolved further.The remaining haplotypes were rare and unique, with some appearing to be exclusive to a particular variety and often detected in single individuals. For example, the H15 haplotype was found exclusively in A. polygama.
    CONCLUSIONS: The population genetic variation explained by chloroplast-specific SNP markers has greater power than that explained by nSCoTs, with chloroplast-specific DNA haplotypes being the most efficient. Gene flow appears to be more evident between A. chinensis var. chinensis and A. chinensis var. deliciosa, as they share chloroplast-specific DNA haplotypes, In contrast, A.arguta and A. polygama possess their own characteristic haplotypes, derived from the haplotype of A. chinensis var. chinensis. Compared with A. chinensis, the A.arguta and A. polygama showed better grouping. It also seems crucial to screen out, for each type of molecular marker, especially haplotypes, the core markers of the Actinidia genus.
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  • 文章类型: Journal Article
    产量是提高作物产量最复杂的性状,确定高产的遗传决定因素是新品种育种的主要问题。在蚕豆(ViciafabaL.)中,数量性状基因座(QTL)先前已在双亲定位种群的研究中检测到,但是控制主要性状成分的基因在很大程度上仍然未知。在这项研究中,我们首次研究了六个蚕豆产量相关性状的遗传控制:破碎(SH),每株豆荚(PP),每个豆荚的种子(SP),每株植物种子(SPL),100-种子重量(HSW),和地块产量(PY),使用全基因组关联研究(GWAS)对全球352个纯合蚕豆种质进行了研究,目的是鉴定与它们相关的标记。在三个地点的田间试验中进行了表型鉴定(西班牙,英国,和塞尔维亚)超过2年。用AffymetrixfababeanSNP芯片对蚕豆面板进行基因分型,产生22,867个SNP标记。GWAS分析确定了97个候选基因中的112个标记-性状关联(MTA),分布在六个蚕豆染色体上。在至少两个环境中检测到八个MTA,五个与多个性状相关。下一步将是在不同遗传背景下验证这些候选物,为蚕豆产量的标记辅助育种提供资源。
    Yield is the most complex trait to improve crop production, and identifying the genetic determinants for high yield is a major issue in breeding new varieties. In faba bean (Vicia faba L.), quantitative trait loci (QTLs) have previously been detected in studies of biparental mapping populations, but the genes controlling the main trait components remain largely unknown. In this study, we investigated for the first time the genetic control of six faba bean yield-related traits: shattering (SH), pods per plant (PP), seeds per pod (SP), seeds per plant (SPL), 100-seed weight (HSW), and plot yield (PY), using a genome-wide association study (GWAS) on a worldwide collection of 352 homozygous faba bean accessions with the aim of identifying markers associated with them. Phenotyping was carried out in field trials at three locations (Spain, United Kingdom, and Serbia) over 2 years. The faba bean panel was genotyped with the Affymetrix faba bean SNP-chip yielding 22,867 SNP markers. The GWAS analysis identified 112 marker-trait associations (MTAs) in 97 candidate genes, distributed over the six faba bean chromosomes. Eight MTAs were detected in at least two environments, and five were associated with multiple traits. The next step will be to validate these candidates in different genetic backgrounds to provide resources for marker-assisted breeding of faba bean yield.
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  • 文章类型: Journal Article
    背景:贵州高原,作为茶树的原始中心之一,具有深厚的多民族文化底蕴和丰富的茶树种质资源。然而,土著社区因素对遗传多样性的影响,茶树的种群结构和地理分布尚不清楚。
    结果:使用基因分型测序(GBS)方法,我们从研究地点收集了415种茶树,估计遗传多样性,开发了一个核心集合,并基于99,363个高质量的单核苷酸多态性(SNP)进行了全基因组关联研究(GWAS)。共有415个茶树种被分为六个种群(GP01,GP02,GP03,GP04,GP05和GP06),结果表明,GP04和GP05具有最高和最低的遗传多样性(Pi=0.214和Pi=0.145)。此外,选择了136个茶种质(33%)来构建可以代表整个种质遗传多样性的核心集。通过分析与一芽两叶萌发期(OTL)和一芽三叶萌发期(OtL)等性状相关的7个显著SNP标记,确定了四个可能与OTL和OtL相关的候选基因。
    结论:这项研究揭示了土著社区对415种茶叶种群结构的影响,指出文化实践对保护和利用茶树遗传资源的重要性。还鉴定了与茶树的OTL和OtL相关的四个潜在候选基因,这将促进基因研究,种质保护,和繁殖。
    BACKGROUND: Guizhou Plateau, as one of the original centers of tea plant, has a profound multi-ethnic cultural heritage and abundant tea germplasm resources. However, the impact of indigenous community factors on the genetic diversity, population structure and geographical distribution of tea plant is still unclear.
    RESULTS: Using the genotyping-by-sequencing (GBS) approach, we collected 415 tea plant accessions from the study sites, estimated genetic diversity, developed a core collection, and conducted a genome-wide association study (GWAS) based on 99,363 high-quality single-nucleotide polymorphisms (SNPs). A total of 415 tea accessions were clustered into six populations (GP01, GP02, GP03, GP04, GP05 and GP06), and the results showed that GP04 and GP05 had the highest and lowest genetic diversity (Pi = 0.214 and Pi = 0.145, respectively). Moreover, 136 tea accessions (33%) were selected to construct the core set that can represent the genetic diversity of the whole collection. By analyzing seven significant SNP markers associated with the traits such as the germination period of one bud and two leaves (OTL) and the germination period of one bud and three leaves (OtL), four candidate genes possibly related to OTL and OtL were identified.
    CONCLUSIONS: This study revealed the impact of indigenous communities on the population structure of 415 tea accessions, indicating the importance of cultural practices for protection and utilization of tea plant genetic resources. Four potential candidate genes associated with the OTL and OtL of tea plant were also identified, which will facilitate genetic research, germplasm conservation, and breeding.
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  • 文章类型: Journal Article
    小麦是世界许多地区的主食。在20世纪,育种者和科学家能够大大提高小麦产量。然而,产量高原已经成为一个令人担忧的问题,并威胁到粮食安全。对尖端技术的投资,包括基因组学和精确物候测量,可以提供有价值的工具来推动作物改良。这项研究的目的是(i)调查一组冬小麦品系的遗传多样性,(ii)表征它们在不同春化和光周期条件下的物候响应,和(iii)鉴定与物候性状相关的有效标记。使用35KAxiom®小麦育种者阵列对总共249种不同地理来源的适应基因型进行了基因分型。总共11,476个SNP用于遗传分析。该集合显示平均多态性信息含量为0.37,遗传多样性为0.43。人口结构分析揭示了三个不同的亚种群,主要与其地理起源有关(欧洲,北美,和西亚)。CGIAR起源的品系显示出最大的多样性,与所有其他亚群的遗传距离最低。在受控条件下,使用长(19小时光照)和短光周期(13小时光照)和长春化(在5°C下49天)和无春化的四种组合研究了该组的物候。有了这个,物候特征,如早期本身(Eps),对春化的相对反应(RRV),并计算了对光周期的相对响应(RRP)。在所有物候组合中,生长度日的表型变异显着。RRV范围为0至0.56,而RRP较高,总体平均值为0.25。GWAS分析检测到与5个物候性状相关的30个标记性状关联。在染色体2D上检测到最高显著标记,值-log10(p)=11.69。只有四个已知调节开花的基因座超过-log10(p)>5.1的Bonferroni校正阈值。这些结果为解决全球粮食安全奠定了坚实的基础,并为推进作物改良战略提供了巨大的机会。
    Wheat is a staple food in many areas around the World. In the 20th century, breeders and scientists were able to boost wheat yield considerably. However, a yield plateau has become a concern and is threatening food security. Investments in cutting-edge technologies, including genomics and precision phenology measurements, can provide valuable tools to drive crop improvement. The objectives of this study were to (i) investigate the genetic diversity in a set of winter wheat lines, (ii) characterize their phenological response under different vernalization and photoperiod conditions, and (iii) identify effective markers associated with the phenological traits. A total of 249 adapted genotypes of different geographical origin were genotyped using the 35K Axiom® Wheat Breeder\'s Array. A total of 11,476 SNPs were used for genetic analysis. The set showed an average polymorphism information content of 0.37 and a genetic diversity of 0.43. A population structure analysis revealed three distinct subpopulations mainly related to their geographical origin (Europe, North America, and Western Asia). The lines of CGIAR origin showed the largest diversity and the lowest genetic distance to all other subpopulations. The phenology of the set was studied under controlled conditions using four combinations of long (19 h light) and short photoperiod (13 h light) and long vernalization (49 days at 5 °C) and no vernalization. With this, phenological traits such as earliness per se (Eps), relative response to vernalization (RRV), and relative response to photoperiod (RRP) were calculated. The phenotypic variation of growing degree days was significant in all phenology combinations. RRV ranged from 0 to 0.56, while RRP was higher with an overall average of 0.25. The GWAS analysis detected 30 marker-trait associations linked to five phenological traits. The highest significant marker was detected on chromosome 2D with a value of -log10(p) = 11.69. Only four loci known to regulate flowering exceeded the Bonferroni correction threshold of -log10(p) > 5.1. These results outline a solid foundation to address global food security and offer tremendous opportunities for advancing crop improvement strategies.
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  • 文章类型: Journal Article
    鼠李糖乳杆菌(L.鼠李糖)被广泛认为是一种益生菌,它存在于各种环境中,包括宿主肠道和乳制品。这项工作旨在对384个鼠李糖乳杆菌基因组进行大规模比较基因组学分析(来自肠道相关分离株的257个全序列或宏基因组组装的基因组[122和135从UHGG和NCBI数据库检索,分别]和127个来自乳制品分离株的基因组[34个来自NCBI数据库;93个从奶酪样品中分离并在此处测序])。我们的结果表明,鼠李糖乳杆菌具有大而开放的泛基因组(从所有384个基因组中鉴定出15,253个泛基因;如果排除了93个奶酪来源的分离株,则为15,028个泛基因)。由384个鼠李糖乳杆菌基因组构建的核心基因系统发育树包括五个系统发育分支,乳制品和肠道相关分离株/基因组在整个树上随机分布。在乳制品和肠道相关基因组之间的代谢相关基因的总体概况中没有发现显着差异;但是,特别是,肠道相关菌株/分离株含有更多编码特定代谢途径和碳水化合物活性酶的基因,例如,乳-N-生物糖苷酶(EC3.2.1.140;GT20)和乳-N-二糖磷酸化酶/半乳糖-N-二糖磷酸化酶(EC2.4.1.211;GH112)。Further,我们发现93个奶酪来源的鼠李糖乳杆菌分离株具有明显的种内多样性,形成三个进化枝(进化枝A,B,和C)在重建的核心基因系统发育树中。在这三个进化枝上有许多单核苷酸变异(超过10,000)。此外,不同进化枝的代谢相关基因含量差异显著(p<0.05,Adonis检验),其特征在于在进化枝C中富含糖苷水解酶并且在每个进化枝中拥有独特的代谢途径。这些结果涉及鼠李糖乳杆菌在单一食物基质中的基因组学/功能多样化,以及来自乳制品和宿主肠道相关来源的分离物的生态位驱动的适应性进化。我们的研究为食品工业应用的候选菌株的选择提供了见解。
    Lacticaseibacillus rhamnosus (L. rhamnosus) is widely recognized as a probiotic species, and it exists in a variety of environments including host gut and dairy products. This work aimed at conducting a large-scale comparative genomics analysis of 384 L. rhamnosus genomes (257 whole-sequence or metagenomic-assembled genomes from gut-associated isolates [122 and 135 retrieved from the UHGG and NCBI databases, respectively] and 127 genomes from dairy isolates [34 from the NCBI database; 93 isolated from a cheese sample and sequenced here]). Our results showed that L. rhamnosus had a large and open pan-genome (15,253 pan-genes identified from all 384 genomes; 15,028 pan-genes if the 93 cheese-originated isolates were excluded). The core-gene phylogenetic tree constructed from the 384 L. rhamnosus genomes comprised five phylogenetic branches, with a random distribution of dairy and gut-associated isolates/genomes across the tree. No significant difference was identified in the overall profile of metabolism-related genes between dairy and gut-associated genomes; however, notably, the gut-associated strains/isolates contained more genes coding for specific metabolic pathways and carbohydrate-active enzymes, e.g., lacto-N-biosidase (EC 3.2.1.140; GT20) and lacto-N-biose phosphorylase/galacto-N-biose phosphorylase (EC 2.4.1.211; GH112). Further, we found that there was obvious intra-species diversification of the 93 cheese-originated L. rhamnosus isolates, forming three clades (Clades A, B, and C) in the reconstructed core-gene phylogenetic tree. There were numerous single nucleotide variations (over 10,000) across the three clades. Moreover, significant differences were observed in the content of metabolism-related genes across clades (p < 0.05, Adonis test), characterized by the enrichment in glycoside hydrolases in Clade C and the possession of unique metabolic pathways in each clade. These results implicated genomics/functional diversification of L. rhamnosus in a single food matrix and niche-driven adaptive evolution of isolates from dairy and host gut-associated origins. Our study shed insights into the selection of candidate strains for food industry applications.
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  • 文章类型: Randomized Controlled Trial
    背景:撒哈拉以南非洲的许多地理区域,尤其是在农村地区,缺乏完整和最新的人口统计数据,对公共卫生干预措施的实施和评估以及开展大规模卫生研究构成了挑战。在Mopeia地区完成了人口调查,位于莫桑比克赞比西亚省,告知BroadOne健康Endectocide为基础的非洲疟疾干预(BOHEMIA)集群随机临床试验,测试了伊维菌素对人类和/或牲畜的大规模药物施用,作为减少疟疾传播的潜在新策略。
    方法:人口调查是一项前瞻性描述性研究,收集了该地区所有接受参与的家庭的数据。家庭通过地理位置进行映射,并用唯一的标识号进行标识。收集家庭成员的基本人口统计数据,每个人都获得了研究的永久识别号。
    结果:对25,550户家庭进行了人口调查,该区共有131,818人登记。平均家庭人数为5名成员,有76.9%的家庭确定了男性户主。住房条件往往不符合标准,获得改善的供水系统和电力的机会很少。据报告,室内残留喷洒的疟疾干预措施覆盖率为71.1%,长效杀虫蚊帐普遍覆盖率为54.1%。人口的中位年龄为15岁。据报道,在过去的12个月中,有910人死亡,5岁以下儿童占43.9%。
    结论:研究表明,该地区对疟疾病媒控制工具的覆盖率很高,但生活条件欠佳,获得基本服务的机会较差。大多数家庭由男性领导,MopeiaSede/Cuacua是该地区人口最多的地区。Mopeia人口年轻(<15岁),儿童死亡率很高。这项调查的结果至关重要,因为它们提供了家庭和人口概况,并允许设计和实施整群随机临床试验。试验注册NCT04966702。
    BACKGROUND: Many geographical areas of sub-Saharan Africa, especially in rural settings, lack complete and up-to-date demographic data, posing a challenge for implementation and evaluation of public health interventions and carrying out large-scale health research. A demographic survey was completed in Mopeia district, located in the Zambezia province in Mozambique, to inform the Broad One Health Endectocide-based Malaria Intervention in Africa (BOHEMIA) cluster randomized clinical trial, which tested ivermectin mass drug administration to humans and/or livestock as a potential novel strategy to decrease malaria transmission.
    METHODS: The demographic survey was a prospective descriptive study, which collected data of all the households in the district that accepted to participate. Households were mapped through geolocation and identified with a unique identification number. Basic demographic data of the household members was collected and each person received a permanent identification number for the study.
    RESULTS: 25,550 households were mapped and underwent the demographic survey, and 131,818 individuals were registered in the district. The average household size was 5 members and 76.9% of households identified a male household head. Housing conditions are often substandard with low access to improved water systems and electricity. The reported coverage of malaria interventions was 71.1% for indoor residual spraying and 54.1% for universal coverage of long-lasting insecticidal nets. The median age of the population was 15 years old. There were 910 deaths in the previous 12 months reported, and 43.9% were of children less than 5 years of age.
    CONCLUSIONS: The study showed that the district had good coverage of vector control tools against malaria but sub-optimal living conditions and poor access to basic services. The majority of households are led by males and Mopeia Sede/Cuacua is the most populated locality in the district. The population of Mopeia is young (< 15 years) and there is a high childhood mortality. The results of this survey were crucial as they provided the household and population profiles and allowed the design and implementation of the cluster randomized clinical trial. Trial registration NCT04966702.
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  • 文章类型: Journal Article
    UNASSIGNED: Oat (Avena sativa L.) is an important cereal crop grown worldwide for grain and forage, owing to its high adaptability to diverse environments. However, the genetic and genomics research of oat is lagging behind that of other staple cereal crops.
    UNASSIGNED: In this study, a collection of 288 oat lines originating worldwide was evaluated using 2,213 single nucleotide polymorphism (SNP) markers obtained from an oat iSelect 6K-beadchip array to study its genetic diversity, population structure, and linkage disequilibrium (LD) as well as the genotype-phenotype association for hullessness and lemma color.
    UNASSIGNED: The average gene diversity and polymorphic information content (PIC) were 0.324 and 0.262, respectively. The first three principal components (PCs) accounted for 30.33% of the genetic variation, indicating that the population structure of this panel of oat lines was stronger than that reported in most previous studies. In addition, accessions could be classified into two subpopulations using a Bayesian clustering approach, and the clustering pattern of accessions was closely associated with their region of origin. Additionally, evaluation of LD decay using 2,143 mapped markers revealed that the intrachromosomal whole-genome LD decayed rapidly to a critical r2 value of 0.156 for marker pairs separated by a genetic distance of 1.41 cM. Genome-wide association study (GWAS) detected six significant associations with the hullessness trait. Four of these six markers were located on the Mrg21 linkage group between 194.0 and 205.7 cM, while the other two significant markers mapped to Mrg05 and Mrg09. Three significant SNPs, showing strong association with lemma color, were located on linkage groups Mrg17, Mrg18, and Mrg20.
    UNASSIGNED: Our results discerned relevant patterns of genetic diversity, population structure, and LD among members of a worldwide collection of oat landraces and cultivars proposed to be \'typical\' of the Qinghai-Tibetan Plateau. These results have important implications for further studies on association mapping and practical breeding in high-altitude oat.
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