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  1. AU="Chien, Jung-Ting"
  2. AU="Rashidi, Muhammad Mahdi"
  3. AU="Gryton, Igal"
  4. AU="Carvajal, Zaira Y García"
  5. AU="Li, Kaixun"
  6. AU="Khuituan, Pissared"
  7. AU="L.Milano, "
  8. AU="Chandramouli, Vaishnavi"
  9. AU="Jose Luis Lavín"
  10. AU="Csályi, Kitti"
  11. AU="Orobello, Nicklas C"
  12. AU=Kim Chang H.
  13. AU="Livingston, Abel"
  14. AU="DeKoven, Mitchell P"
  15. AU="Kubota, Katsumi"

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  1. Artikel ; Online: Strain-specific quantification of root colonization by plant growth promoting rhizobacteria Bacillus firmus I-1582 and Bacillus amyloliquefaciens QST713 in non-sterile soil and field conditions.

    Mendis, Hajeewaka C / Thomas, Varghese P / Schwientek, Patrick / Salamzade, Rauf / Chien, Jung-Ting / Waidyarathne, Pramuditha / Kloepper, Joseph / De La Fuente, Leonardo

    PloS one

    2018  Band 13, Heft 2, Seite(n) e0193119

    Abstract: Bacillus amyloliquefaciens QST713 and B. firmus I-1582 are bacterial strains which are used as active ingredients of commercially-available soil application and seed treatment products Serenade® and VOTiVO®, respectively. These bacteria colonize plant ... ...

    Abstract Bacillus amyloliquefaciens QST713 and B. firmus I-1582 are bacterial strains which are used as active ingredients of commercially-available soil application and seed treatment products Serenade® and VOTiVO®, respectively. These bacteria colonize plant roots promoting plant growth and offering protection against pathogens/pests. The objective of this study was to develop a qPCR protocol to quantitate the dynamics of root colonization by these two strains under field conditions. Primers and TaqMan® probes were designed based on genome comparisons of the two strains with publicly-available and unpublished bacterial genomes of the same species. An optimized qPCR protocol was developed to quantify bacterial colonization of corn roots after seed treatment. Treated corn seeds were planted in non-sterile soil in the greenhouse and grown for 28 days. Specific detection of bacteria was quantified weekly, and showed stable colonization between ~104-105 CFU/g during the experimental period for both bacteria, and the protocol detected as low as 103 CFU/g bacteria on roots. In a separate experiment, streptomycin-resistant QST713 and rifampicin-resistant I-1582 strains were used to compare dilution-plating on TSA with the newly developed qPCR method. Results also indicated that the presence of natural microflora and another inoculated strain does not affect root colonization of either one of these strains. The same qPCR protocol was used to quantitate root colonization by QST713 and I-1582 in two corn and two soybean varieties grown in the field. Both bacteria were quantitated up to two weeks after seeds were planted in the field and there were no significant differences in root colonization in either bacteria strain among varieties. Results presented here confirm that the developed qPCR protocol can be successfully used to understand dynamics of root colonization by these bacteria in plants growing in growth chamber, greenhouse and the field.
    Mesh-Begriff(e) Bacillus amyloliquefaciens ; Bacillus firmus ; Plant Development/physiology ; Plant Roots/growth & development ; Plant Roots/microbiology ; Seeds/growth & development ; Seeds/microbiology ; Soil ; Zea mays/growth & development ; Zea mays/microbiology
    Chemische Substanzen Soil
    Sprache Englisch
    Erscheinungsdatum 2018-02-15
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0193119
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel: High-Quality Genome Assembly and Annotation for Plasmodium coatneyi, Generated Using Single-Molecule Real-Time PacBio Technology.

    Chien, Jung-Ting / Pakala, Suman B / Geraldo, Juliana A / Lapp, Stacey A / Humphrey, Jay C / Barnwell, John W / Kissinger, Jessica C / Galinski, Mary R

    Genome announcements

    2016  Band 4, Heft 5

    Abstract: Plasmodium coatneyi is a protozoan parasite species that causes simian malaria and is an excellent model for studying disease caused by the human malaria parasite, P. falciparum Here we report the complete (nontelomeric) genome sequence of P. coatneyi ... ...

    Abstract Plasmodium coatneyi is a protozoan parasite species that causes simian malaria and is an excellent model for studying disease caused by the human malaria parasite, P. falciparum Here we report the complete (nontelomeric) genome sequence of P. coatneyi Hackeri generated by the application of only Pacific Biosciences RS II (PacBio RS II) single-molecule real-time (SMRT) high-resolution sequence technology and assembly using the Hierarchical Genome Assembly Process (HGAP). This is the first Plasmodium genome sequence reported to use only PacBio technology. This approach has proven to be superior to short-read only approaches for this species.
    Sprache Englisch
    Erscheinungsdatum 2016-09-01
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2704277-7
    ISSN 2169-8287
    ISSN 2169-8287
    DOI 10.1128/genomeA.00883-16
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Multiplexed highly-accurate DNA sequencing of closely-related HIV-1 variants using continuous long reads from single molecule, real-time sequencing.

    Dilernia, Dario A / Chien, Jung-Ting / Monaco, Daniela C / Brown, Michael P S / Ende, Zachary / Deymier, Martin J / Yue, Ling / Paxinos, Ellen E / Allen, Susan / Tirado-Ramos, Alfredo / Hunter, Eric

    Nucleic acids research

    2015  Band 43, Heft 20, Seite(n) e129

    Abstract: Single Molecule, Real-Time (SMRT) Sequencing (Pacific Biosciences, Menlo Park, CA, USA) provides the longest continuous DNA sequencing reads currently available. However, the relatively high error rate in the raw read data requires novel analysis methods ...

    Abstract Single Molecule, Real-Time (SMRT) Sequencing (Pacific Biosciences, Menlo Park, CA, USA) provides the longest continuous DNA sequencing reads currently available. However, the relatively high error rate in the raw read data requires novel analysis methods to deconvolute sequences derived from complex samples. Here, we present a workflow of novel computer algorithms able to reconstruct viral variant genomes present in mixtures with an accuracy of >QV50. This approach relies exclusively on Continuous Long Reads (CLR), which are the raw reads generated during SMRT Sequencing. We successfully implement this workflow for simultaneous sequencing of mixtures containing up to forty different >9 kb HIV-1 full genomes. This was achieved using a single SMRT Cell for each mixture and desktop computing power. This novel approach opens the possibility of solving complex sequencing tasks that currently lack a solution.
    Mesh-Begriff(e) Algorithms ; Cluster Analysis ; Genetic Variation ; Genome, Viral ; HIV-1/genetics ; High-Throughput Nucleotide Sequencing/methods ; Humans ; Sequence Alignment ; Sequence Analysis, DNA/methods
    Sprache Englisch
    Erscheinungsdatum 2015-11-16
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 186809-3
    ISSN 1362-4962 ; 1362-4954 ; 0301-5610 ; 0305-1048
    ISSN (online) 1362-4962 ; 1362-4954
    ISSN 0301-5610 ; 0305-1048
    DOI 10.1093/nar/gkv630
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Distinct amino acid and lipid perturbations characterize acute versus chronic malaria.

    Cordy, Regina Joice / Patrapuvich, Rapatbhorn / Lili, Loukia N / Cabrera-Mora, Monica / Chien, Jung-Ting / Tharp, Gregory K / Khadka, Manoj / Meyer, Esmeralda Vs / Lapp, Stacey A / Joyner, Chester J / Garcia, AnaPatricia / Banton, Sophia / Tran, ViLinh / Luvira, Viravarn / Rungin, Siriwan / Saeseu, Teerawat / Rachaphaew, Nattawan / Pakala, Suman B / DeBarry, Jeremy D /
    Kissinger, Jessica C / Ortlund, Eric A / Bosinger, Steven E / Barnwell, John W / Jones, Dean P / Uppal, Karan / Li, Shuzhao / Sattabongkot, Jetsumon / Moreno, Alberto / Galinski, Mary R

    JCI insight

    2019  Band 4, Heft 9

    Abstract: Chronic malaria is a major public health problem and significant challenge for disease eradication efforts. Despite its importance, the biological factors underpinning chronic malaria are not fully understood. Recent studies have shown that host ... ...

    Abstract Chronic malaria is a major public health problem and significant challenge for disease eradication efforts. Despite its importance, the biological factors underpinning chronic malaria are not fully understood. Recent studies have shown that host metabolic state can influence malaria pathogenesis and transmission, but its role in chronicity is not known. Here, with the goal of identifying distinct modifications in the metabolite profiles of acute versus chronic malaria, metabolomics was performed on plasma from Plasmodium-infected humans and nonhuman primates with a range of parasitemias and clinical signs. In rhesus macaques infected with Plasmodium coatneyi, significant alterations in amines, carnitines, and lipids were detected during a high parasitemic acute phase and many of these reverted to baseline levels once a low parasitemic chronic phase was established. Plasmodium gene expression, studied in parallel in the macaques, revealed transcriptional changes in amine, fatty acid, lipid and energy metabolism genes, as well as variant antigen genes. Furthermore, a common set of amines, carnitines, and lipids distinguished acute from chronic malaria in plasma from human Plasmodium falciparum cases. In summary, distinct host-parasite metabolic environments have been uncovered that characterize acute versus chronic malaria, providing insights into the underlying host-parasite biology of malaria disease progression.
    Mesh-Begriff(e) Adolescent ; Adult ; Aged ; Amino Acids/blood ; Amino Acids/metabolism ; Animals ; Disease Models, Animal ; Fatty Acids/blood ; Fatty Acids/metabolism ; Female ; Gene Expression ; Glycerophospholipids/blood ; Glycerophospholipids/metabolism ; Host-Parasite Interactions/physiology ; Humans ; Lipid Metabolism ; Lipids/blood ; Macaca mulatta ; Malaria/genetics ; Malaria/metabolism ; Male ; Metabolome ; Middle Aged ; Parasitemia ; Plasmodium ; Plasmodium falciparum ; Young Adult
    Chemische Substanzen Amino Acids ; Fatty Acids ; Glycerophospholipids ; Lipids
    Sprache Englisch
    Erscheinungsdatum 2019-05-02
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ISSN 2379-3708
    ISSN (online) 2379-3708
    DOI 10.1172/jci.insight.125156
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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