scholarly journals Comparative and phylogenomic analyses of mitochondrial genomes in Coccinellidae (Coleoptera: Coccinelloidea)

PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e12169
Author(s):  
Xinghao Li ◽  
Nan Song ◽  
Heng Zhang
Keyword(s):  
Phylogenetic Relationships ◽  
Phylogenetic Analyses ◽  
Phylogenetic Reconstruction ◽  
Intergenic Spacer ◽  
Ribosomal Subunits ◽  
Intergenic Spacer Region ◽  
Economic Significance ◽  
Multispecies Coalescent ◽  
Phylogenomic Analyses ◽  
Generation Sequencing

The Coccinellidae are one of the most familiar beetle families, the ladybirds. Despite the great ecological and economic significance, the phylogenetic relationships of Coccinellidae remain poorly understood. One of the reasons is that the sequenced mitogenomes available for this family are very limited. We sequenced complete or nearly complete mitogenomes from seven species of the tribe Coccinellini with next-generation sequencing. All species have the same gene content and gene order as the putatively ancestral insect mitogenome. A large intergenic spacer region (> 890 bp) was found located between trnI and trnQ. The potential for using secondary structures of the large and small ribosomal subunits for phylogenetic reconstruction was predicted. The phylogenetic relationships were explored through comparative analyses across more than 30 coccinellid species. We performed phylogenetic analyses with both concatenation methods (Maximum Likelihood and Bayesian Inference) and multispecies coalescent method (ASTRAL). Phylogenetic results strongly supported the monophyly of Coccinellidae. Within Coccinellidae, the Epilachnini and the Coccinellini including Halyziini were monophyletic, while the Scymnini and Coccidulini were non-monophyletic.

Description and phylogenetic analyses of ribosomal transcription units from species of Fasciolidae (Platyhelminthes: Digenea)

2020 ◽  
Vol 94 ◽  
Author(s):  
T.H. Le ◽  
K.L.T. Pham ◽  
H.T.T. Doan ◽  
T.K. Xuyen Le ◽  
K.T. Nguyen ◽  
...  
Keyword(s):  
Fasciola Hepatica ◽  
Phylogenetic Analyses ◽  
Intergenic Spacer ◽  
Transcription Unit ◽  
Rrna Genes ◽  
28S Rrna ◽  
Intergenic Spacer Region ◽  
Repeat Units ◽  
Complete Sequences ◽  
Fasciolopsis Buski

Abstract Many members of Fasciolidae are common trematodes in cattle, buffaloes, sheep, elephants, pigs, with some capable of infecting humans also. In this study, the complete or near-complete sequences of ribosomal transcription unit (rTU or rDNA), each of Fasciola hepatica (Australia), Fascioloides jacksoni (Sri Lanka), Fasciolopsis buski (Vietnam) and three isolates of F. gigantica (Vietnam), were obtained and characterized. The full length of rDNA for each F. hepatica, ‘hybrid’ Fasciola sp., Fas. jacksoni and Fa. Buski, was 7657 bp, 7966 bp, 7781 bp and 8361 bp, with the complete intergenic spacer region (IGS) (862 bp, 1170 bp, 987 bp and 561 bp), respectively. The rDNA of two ‘pure’ F. gigantica isolates from Vietnam was 6794 bp with unsequenced IGS. For 28S rRNA genes the Fasciola spp. are equal, 1958 bp for 18S, 160 bp for 5.8S, 3863 bp and 454 bp for ITS1 but ITS2 differ by one nucleotide (Thymine) (359 or 360 bp). The ITS1 of the sensu lato Fa. buski has some distinguishable features, 286 bp for ITS2, 3862 bp for 28S and four repeat units of 356–361 bp each found in ITS1. The 28S rDNA analysis showed the lowest level of divergence (0–0.57%) between F. hepatica and F. gigantica and higher (2.23–2.62%) and highest (6–6.42%) for Fas. jacksoni and Fasciolopsis, respectively. The tree of 43 strains/species clearly produced a well-supported phylogeny, where 18 fasciolids consistently grouped, forming a discrete Fasciolidae clade, distinct from Philophthalmidae, Echinostomatidae and Echinochasmidae in Echinostomatoidea. Fascioloides jacksoni is outside Fasciola spp.: basal with Fas. magna, as previously demonstrated.

scholarly journals Phylogeny of Porphyromonas gingivalis by Ribosomal Intergenic Spacer Region Analysis

2000 ◽  
Vol 38 (5) ◽  
pp. 1807-1810 ◽  
Author(s):  
Robert W. Rumpf ◽  
Ann L. Griffen ◽  
Eugene J. Leys
Keyword(s):  
Porphyromonas Gingivalis ◽  
Random Amplified Polymorphic Dna ◽  
Bacterial Species ◽  
Phylogenetic Reconstruction ◽  
Intergenic Spacer ◽  
Variable Region ◽  
Ribosomal Gene ◽  
Heteroduplex Analysis ◽  
Enzyme Electrophoresis ◽  
Intergenic Spacer Region

Periodontitis has been associated with the presence ofPorphyromonas gingivalis, and previous studies have shown phenotypic differences in the pathogenicities of strains of P. gingivalis. An accurate and comprehensive phylogeny of strains ofP. gingivalis would be useful in determining if there is an evolutionary basis to pathogenicity in this species. Previous phylogenies of P. gingivalis strains based on random amplified polymorphic DNA (RAPD) analysis and multilocus enzyme electrophoresis (MLEE) show little agreement. While the 16S ribosomal gene is the standard for phylogenetic reconstruction among bacterial species, it is insufficiently variable for this purpose. In the present study, the phylogeny of P. gingivalis was constructed on the basis of the sequence of the most variable region of the ribosomal operon, the intergenic spacer region (ISR). Heteroduplex analysis of the ISR has been used to study the variability of P. gingivalis strains in periodontitis. In the present study, typing by heteroduplex analysis was compared to ISR sequence-based phylogeny and close agreement was observed. The two strains of P. gingivalis whose heteroduplex types are strongly associated with periodontitis were found to be closely related and were well separated from strains whose heteroduplex types are less strongly associated with disease, suggesting a relationship between pathogenicity and phylogeny.

scholarly journals Molecular Diversity of The Tidal Swamp Rice (Oryza sativa L.) Germplasm of The South Kalimantan, Indonesia

2018 ◽  
Author(s):  
Dindin H. Mursyidin ◽  
Purnomo Purnomo ◽  
Issirep Sumardi ◽  
Budi S. Daryono
Keyword(s):  
Genetic Diversity ◽  
Phylogenetic Trees ◽  
Phylogenetic Reconstruction ◽  
Intergenic Spacer ◽  
The South ◽  
Abiotic And Biotic Stresses ◽  
Intergenic Spacer Region ◽  
Biotic Stresses ◽  
Tidal Swamp ◽  
Wide Range

Tidal swamp rice has long been cultivated by the local people of the South Kalimantan, Indonesia. This germplasm possess some important traits for adapted to a wide range of abiotic and biotic stresses. In this study, a total of sixteen cultivars of this germplasm, consisting of fifteen of the South Kalimantan Province and one of Sumatera Island, Indonesia (an outgroup) were analyzed, phylogenetically based on the chloroplast trnL-F and nuclear intergenic spacer region (IGS). The results showed that this germplasm has a relatively more extraordinary genetic diversity than other local rice germplasm. In a nucleotide level, this germplasm showed a genetic diversity of 0.61 for nuclear IGS and 0.58 for trnL-F. The phylogenetic reconstruction also exhibited that this germplasm has the unique illustration of phylogenetic trees, particularly for the combined sequence datasets. Thus, the results of our study would provide useful information for further understanding of evolutionary relationships of this germplasm and facilitate the efficient utilization of valuable genes for genetic improvement, particularly in the tidal swamp areas.

scholarly journals The complete mitochondrial genome of stag beetle Lucanus cervus (Coleoptera: Lucanidae) and phylogenetic analysis

PeerJ ◽  
2019 ◽  
Vol 7 ◽  
pp. e8274 ◽  
Author(s):  
Dan Chen ◽  
Jing Liu ◽  
Luca Bartolozzi ◽  
Xia Wan
Keyword(s):  
Mitochondrial Genome ◽  
Bayesian Methods ◽  
Phylogenetic Relationships ◽  
Phylogenetic Analyses ◽  
Complete Mitochondrial Genome ◽  
Illumina Platform ◽  
Protein Coding ◽  
Protein Coding Genes ◽  
Rna Genes ◽  
Generation Sequencing

Background The stag beetle Lucanus cervus (Coleoptera: Lucanidae) is widely distributed in Europe. Habitat loss and fragmentation has led to significant reductions in numbers of this species. In this study, we sequenced the complete mitochondrial genome of L. cervus and reconstructed phylogenetic relationships among Lucanidae using complete mitochondrial genome sequences. Methods Raw data sequences were generated by the next generation sequencing using Illumina platform from genomic DNA of L. cervus. The mitochondrial genome was assembled by IDBA and annotated by MITOS. The aligned sequences of mitochondrial genes were partitioned using PartitionFinder 2. Phylogenetic relationships among 19 stag beetle species were constructed using Maximum Likelihood (ML) method implemented in IQ-TREE web server and Bayesian method implemented in PhyloBayes MPI 1.5a. Three scarab beetles were used as outgroups. Results The complete mitochondrial genome of L. cervus is 20,109 bp in length, comprising 13 protein-coding genes, 22 transfer RNA genes, two ribosomal RNAs and a control region. The A + T content is 69.93% for the majority strand. All protein-coding genes start with the typical ATN initiation codons except for cox1, which uses AAT. Phylogenetic analyses based on ML and Bayesian methods shown consistent topologies among Lucanidae.

scholarly journals Complex Molecular Relationship Between Vegetative Compatibility Groups (VCGs) in Verticillium dahliae: VCGs Do Not Always Align with Clonal Lineages

2014 ◽  
Vol 104 (6) ◽  
pp. 650-659 ◽  
Author(s):  
María del Mar Jiménez-Gasco ◽  
Glenna M. Malcolm ◽  
Mónica Berbegal ◽  
Josep Armengol ◽  
Rafael M. Jiménez-Díaz
Keyword(s):  
Verticillium Dahliae ◽  
Phylogenetic Analyses ◽  
Evolutionary Relationship ◽  
Intergenic Spacer ◽  
Vegetative Compatibility ◽  
Data Sets ◽  
Nucleotide Polymorphisms ◽  
Vegetative Compatibility Groups ◽  
Intergenic Spacer Region ◽  
Phylogenetic Lineages

Verticillium wilts caused by the soilborne fungus Verticillium dahliae are among the most challenging diseases to control. Populations of this pathogen have been traditionally studied by means of vegetative compatibility groups (VCGs) under the assumption that VCGs comprise genetically related isolates that correlate with clonal lineages. We aimed to resolve the phylogenetic relationships among VCGs and their subgroups based on sequences of the intergenic spacer region (IGS) of the ribosomal DNA and six anonymous polymorphic sequences containing single-nucleotide polymorphisms (VdSNPs). A collection of 68 V. dahliae isolates representing the main VCGs and subgroups (VCGs 1A, 1B, 2A, 2B, 3, 4A, 4B, and 6) from different geographic origins and hosts was analyzed using the seven DNA regions. Maximum parsimony (MP) phylogenies inferred from IGS and VdSNP sequences showed five and six distinct clades, respectively. Phylogenetic analyses of individual and combined data sets indicated that certain VCG subgroups (e.g., VCGs 1A and 1B) are closely related and share a common ancestor; however, other subgroups (e.g., VCG 4B) are more closely related to members of a different VCG (e.g., VCG 2A) than to subgroups of the same VCG (VCG 4B). Furthermore, MP analyses indicated that VCG 2B is polyphyletic, with isolates placed in at least three distinct phylogenetic lineages based on IGS sequences and two lineages based on VdSNP sequences. Results from our study suggest the existence of main VCG lineages that contain VCGs 1A and 1B; VCGs 2A and 4B; and VCG 4A, for which both phylogenies agree; and the existence of other VCGs or VCG subgroups that seem to be genetically heterogeneous or show discrepancies in their phylogenetic placement: VCG 2B, VCG 3, and VCG 6. These results raise important caveats regarding the interpretation of VCG analyses: genetic homogeneity and close evolutionary relationship between members of a VCG should not be assumed.

scholarly journals Maize (Zea mays L.): A New Host for Ligustrum witches’ Broom Phytoplasma

Pathogens ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 723
Author(s):  
Behçet Kemal Çağlar ◽  
Serkan Pehlivan ◽  
Ekrem Atakan ◽  
Toufic Elbeaino
Keyword(s):  
Phylogenetic Analyses ◽  
Intergenic Spacer ◽  
23S Rrna ◽  
Rrna Gene ◽  
Universal Primer ◽  
New Host ◽  
Intergenic Spacer Region ◽  
Distant Relationship ◽  
Molecular Information ◽  
Corn Plants

In the 2019–2020 growing season, two corn fields located in İmamoğlu town (Adana Province, Turkey) were surveyed following the appearance of phytoplasma-like symptoms on maize plants. A total of 40 samples were collected and tested in first-round and nested PCR using universal primer pairs P1/P7 and R16F2n/R16R2, respectively. All maize-diseased plants reacted positively, whilst no PCR amplifications were obtained from asymptomatic plants. Blast sequence analysis of R16F2n/R16R2-primed amplicons from different maize isolates showed 99.2% to 100% of identity with the 16S rRNA gene of Ligustrum witches’ broom phytoplasma (LiWBP). To gain additional molecular information on the 16S ribosomal RNA and 23S rRNA intergenic spacer region of LiWBP, not identified previously, the P1/P7-primed amplicons were also sequenced and analyzed. The results show that maize isolates from Turkey share 99.6% to 100% of identity among them, whereas the highest identity found (91%) was with members of groups 16SrII and 16SrXXV (peanut and tea witches’ broom groups, respectively). This distant relationship between LiWBP and members of 16SrII and XXV was also confirmed by RFLP and phylogenetic analyses. This is the first finding of LiWBP on maize in nature, where it was found responsible for phyllody disease of corn plants in Turkey. The additional molecular information acquired in this study on the 16S–23S rRNA intergenic spacer region of LiWBP further corroborates its distant relationship to any other phytoplasma groups.

scholarly journals Phylogenomic analyses support traditional relationships within Cnidaria

2015 ◽  
Author(s):  
Felipe Zapata ◽  
Freya E Goetz ◽  
Stephen A Smith ◽  
Mark Howison ◽  
Stefan Siebert ◽  
...  
Keyword(s):  
Molecular Evolution ◽  
Phylogenetic Relationships ◽  
Phylogenetic Analyses ◽  
Sister Group ◽  
Diverse Group ◽  
Transcriptome Data ◽  
Evolutionary Processes ◽  
Phylogenetic Hypotheses ◽  
Phylogenomic Analyses

Cnidaria, the sister group to Bilateria, is a highly diverse group of animals in terms of morphology, lifecycles, ecology, and development. How this diversity originated and evolved is not well understood because phylogenetic relationships among major cnidarian lineages are unclear, and recent studies present contrasting phylogenetic hypotheses. Here, we use transcriptome data from 15 newly-sequenced species in combination with 26 publicly available genomes and transcriptomes to assess phylogenetic relationships among major cnidarian lineages. Phylogenetic analyses using different partition schemes and models of molecular evolution, as well as topology tests for alternative phylogenetic relationships, support the monophyly of Medusozoa, Anthozoa, Octocorallia, Hydrozoa, and a clade consisting of Staurozoa, Cubozoa, and Scyphozoa. Support for the monophyly of Hexacorallia is weak due to the equivocal position of Ceriantharia. Taken together, these results further resolve deep cnidarian relationships, largely support traditional phylogenetic views on relationships, and provide a historical framework for studying the evolutionary processes involved in one of the most ancient animal radiations.

scholarly journals Multispecies coalescent analysis unravels the non-monophyly and controversial relationships of Hexapoda

2017 ◽  
Author(s):  
Lucas A. Freitas ◽  
Beatriz Mello ◽  
Carlos G. Schrago
Keyword(s):  
Phylogenetic Relationships ◽  
Gene Tree ◽  
Genomic Data ◽  
Population Level ◽  
Phylogenetic Inference ◽  
Evolutionary Relationships ◽  
Effective Population ◽  
Multispecies Coalescent ◽  
Population Sizes ◽  
Phylogenomic Analyses

AbstractWith the increase in the availability of genomic data, sequences from different loci are usually concatenated in a supermatrix for phylogenetic inference. However, as an alternative to the supermatrix approach, several implementations of the multispecies coalescent (MSC) have been increasingly used in phylogenomic analyses due to their advantages in accommodating gene tree topological heterogeneity by taking account population-level processes. Moreover, the development of faster algorithms under the MSC is enabling the analysis of thousands of loci/taxa. Here, we explored the MSC approach for a phylogenomic dataset of Insecta. Even with the challenges posed by insects, due to large effective population sizes coupled with short deep internal branches, our MSC analysis could recover several orders and evolutionary relationships in agreement with current insect systematics. However, some phylogenetic relationships were not recovered by MSC methods. Most noticeable, a remiped crustacean was positioned within the Insecta. Additionally, the interordinal relationships within Polyneoptera and Neuropteroidea contradicted recent works, by suggesting the non-monophyly of Neuroptera. We notice, however, that these phylogenetic arrangements were also poorly supported by previous analyses and that they were sensitive to gene sampling.

scholarly journals Isolation of Bartonella species from rodents in Taiwan including a strain closely related to ‘Bartonella rochalimae’ from Rattus norvegicus

2008 ◽  
Vol 57 (12) ◽  
pp. 1496-1501 ◽  
Author(s):  
Jen-Wei Lin ◽  
Chun-Yu Chen ◽  
Wan-Ching Chen ◽  
Bruno B. Chomel ◽  
Chao-Chin Chang
Keyword(s):  
Rattus Norvegicus ◽  
Phylogenetic Analyses ◽  
Intergenic Spacer ◽  
Rflp Analysis ◽  
23S Rrna ◽  
Human Pathogens ◽  
Bartonella Species ◽  
Intergenic Spacer Region ◽  
Pcr Rflp ◽  
Rodent Populations

An increasing number of Bartonella species originally isolated from small mammals have been identified as emerging human pathogens. During an investigation of Bartonella infection in rodent populations carried out in Taiwan in 2006, a total of 58 rodents were tested. It was determined that 10.3 % (6/58) of the animals were Bartonella bacteraemic. After PCR/RFLP analysis, four isolates were identified as Bartonella elizabethae and one isolate as Bartonella tribocorum. However, there was one specific isolate with an unrecognized PCR/RFLP pattern. After further sequence and phylogenetic analyses of the gltA, ftsZ and rpoB genes, and the 16S–23S rRNA intergenic spacer region, the results indicated that this specific isolate from Rattus norvegicus was closely related to human pathogenic ‘Bartonella rochalimae’. Further studies need to be conducted to evaluate whether this rodent species could be a reservoir for ‘B. rochalimae’.

scholarly journals Soybean SDS in South Africa is Caused by Fusarium brasiliense and a Novel Undescribed Fusarium sp.

Plant Disease ◽  
2017 ◽  
Vol 101 (1) ◽  
pp. 150-157 ◽  
Author(s):  
Yared T. Tewoldemedhin ◽  
Sandra C. Lamprecht ◽  
Martha M. Vaughan ◽  
Gail Doehring ◽  
Kerry O’Donnell
Keyword(s):  
South Africa ◽  
Phylogenetic Analyses ◽  
Elongation Factor ◽  
Intergenic Spacer ◽  
The United States ◽  
Positive Control ◽  
Primary Objective ◽  
Intergenic Spacer Region ◽  
Soybean Cultivars ◽  
Fusarium Sp

Soybean sudden death syndrome (SDS) was detected in South Africa for the first time during pathogen surveys conducted in 2013 to 2014. The primary objective of this study was to characterize the 16 slow-growing Fusarium strains that were isolated from the roots of symptomatic plants. Molecular phylogenetic analyses of a portion of translation elongation factor 1-α (TEF1) and the nuclear ribosomal intergenic spacer region (IGS rDNA) indicated that the etiological agents were Fusarium brasiliense and a novel, undescribed Fusarium sp. This is the first report of F. brasiliense outside of Brazil and Argentina and the novel Fusarium sp. causing soybean SDS. Koch’s postulates were completed for both fusaria on seven soybean cultivars that are commercially available in South Africa. Results of the pathogenicity experiment revealed that the strains of F. brasiliense and Fusarium sp. differed in aggressiveness to soybean, as reflected in differences in foliar symptoms, root rot, and reduction in shoot length. Cell-free culture filtrates of the two soybean SDS pathogens from South Africa and two positive control strains of F. virguliforme from the United States induced typical SDS symptoms on susceptible soybean cultivars in a whole-seedling assay, indicating that they contained phytotoxins.

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