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Dive into the research topics where Kymberlie Hallsworth-Pepin is active.

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Featured researches published by Kymberlie Hallsworth-Pepin.


PLOS ONE | 2010

Genome sequence of Cronobacter sakazakii BAA-894 and comparative genomic hybridization analysis with other Cronobacter species.

Eva Kucerova; Sandra W. Clifton; Xiao-Qin Xia; Fred Long; Steffen Porwollik; Lucinda Fulton; Catrina C. Fronick; Patrick Minx; Kim Kyung; Wesley C. Warren; Robert S. Fulton; Dongyan Feng; Aye Wollam; Neha Shah; Veena Bhonagiri; William E. Nash; Kymberlie Hallsworth-Pepin; Richard Wilson; Michael McClelland; Stephen J. Forsythe

Background The genus Cronobacter (formerly called Enterobacter sakazakii) is composed of five species; C. sakazakii, C. malonaticus, C. turicensis, C. muytjensii, and C. dublinensis. The genus includes opportunistic human pathogens, and the first three species have been associated with neonatal infections. The most severe diseases are caused in neonates and include fatal necrotizing enterocolitis and meningitis. The genetic basis of the diversity within the genus is unknown, and few virulence traits have been identified. Methodology/Principal Findings We report here the first sequence of a member of this genus, C. sakazakii strain BAA-894. The genome of Cronobacter sakazakii strain BAA-894 comprises a 4.4 Mb chromosome (57% GC content) and two plasmids; 31 kb (51% GC) and 131 kb (56% GC). The genome was used to construct a 387,000 probe oligonucleotide tiling DNA microarray covering the whole genome. Comparative genomic hybridization (CGH) was undertaken on five other C. sakazakii strains, and representatives of the four other Cronobacter species. Among 4,382 annotated genes inspected in this study, about 55% of genes were common to all C. sakazakii strains and 43% were common to all Cronobacter strains, with 10–17% absence of genes. Conclusions/Significance CGH highlighted 15 clusters of genes in C. sakazakii BAA-894 that were divergent or absent in more than half of the tested strains; six of these are of probable prophage origin. Putative virulence factors were identified in these prophage and in other variable regions. A number of genes unique to Cronobacter species associated with neonatal infections (C. sakazakii, C. malonaticus and C. turicensis) were identified. These included a copper and silver resistance system known to be linked to invasion of the blood-brain barrier by neonatal meningitic strains of Escherichia coli. In addition, genes encoding for multidrug efflux pumps and adhesins were identified that were unique to C. sakazakii strains from outbreaks in neonatal intensive care units.


Nature Genetics | 2014

Genome of the human hookworm Necator americanus

Yat T. Tang; Xin Gao; Bruce A. Rosa; Sahar Abubucker; Kymberlie Hallsworth-Pepin; John Martin; Rahul Tyagi; Esley Heizer; Xu Zhang; Veena Bhonagiri-Palsikar; Patrick Minx; Wesley C. Warren; Qi Wang; Bin Zhan; Peter J. Hotez; Paul W. Sternberg; Annette Dougall; Soraya Gaze; Jason Mulvenna; Javier Sotillo; Shoba Ranganathan; Élida Mara Leite Rabelo; Richard Wilson; Philip L. Felgner; Jeffrey M. Bethony; John M. Hawdon; Robin B. Gasser; Alex Loukas; Makedonka Mitreva

The hookworm Necator americanus is the predominant soil-transmitted human parasite. Adult worms feed on blood in the small intestine, causing iron-deficiency anemia, malnutrition, growth and development stunting in children, and severe morbidity and mortality during pregnancy in women. We report sequencing and assembly of the N. americanus genome (244 Mb, 19,151 genes). Characterization of this first hookworm genome sequence identified genes orchestrating the hookworms invasion of the human host, genes involved in blood feeding and development, and genes encoding proteins that represent new potential drug targets against hookworms. N. americanus has undergone a considerable and unique expansion of immunomodulator proteins, some of which we highlight as potential treatments against inflammatory diseases. We also used a protein microarray to demonstrate a postgenomic application of the hookworm genome sequence. This genome provides an invaluable resource to boost ongoing efforts toward fundamental and applied postgenomic research, including the development of new methods to control hookworm and human immunological diseases.


Nucleic Acids Research | 2015

Helminth.net: expansions to Nematode.net and an introduction to Trematode.net

John Martin; Bruce A. Rosa; Philip Ozersky; Kymberlie Hallsworth-Pepin; Xu Zhang; Veena Bhonagiri-Palsikar; Rahul Tyagi; Qi Wang; Young-Jun Choi; Xin Gao; Samantha N. McNulty; Paul J. Brindley; Makedonka Mitreva

Helminth.net (http://www.helminth.net) is the new moniker for a collection of databases: Nematode.net and Trematode.net. Within this collection we provide services and resources for parasitic roundworms (nematodes) and flatworms (trematodes), collectively known as helminths. For over a decade we have provided resources for studying nematodes via our veteran site Nematode.net (http://nematode.net). In this article, (i) we provide an update on the expansions of Nematode.net that hosts omics data from 84 species and provides advanced search tools to the broad scientific community so that data can be mined in a useful and user-friendly manner and (ii) we introduce Trematode.net, a site dedicated to the dissemination of data from flukes, flatworm parasites of the class Trematoda, phylum Platyhelminthes. Trematode.net is an independent component of Helminth.net and currently hosts data from 16 species, with information ranging from genomic, functional genomic data, enzymatic pathway utilization to microbiome changes associated with helminth infections. The databases’ interface, with a sophisticated query engine as a backbone, is intended to allow users to search for multi-factorial combinations of species’ omics properties. This report describes updates to Nematode.net since its last description in NAR, 2012, and also introduces and presents its new sibling site, Trematode.net.


PLOS Genetics | 2017

Genomes of Fasciola hepatica from the Americas Reveal Colonization with Neorickettsia Endobacteria Related to the Agents of Potomac Horse and Human Sennetsu Fevers.

Samantha N. McNulty; José F. Tort; Gabriel Rinaldi; Kerstin Fischer; Bruce A. Rosa; Pablo Smircich; Santiago Fontenla; Young-Jun Choi; Rahul Tyagi; Kymberlie Hallsworth-Pepin; Victoria H. Mann; Lakshmi Kammili; Patricia S. Latham; Nicolás Dell’Oca; Fernanda Dominguez; Carlos Carmona; Peter U. Fischer; Paul J. Brindley; Makedonka Mitreva

Food borne trematodes (FBTs) are an assemblage of platyhelminth parasites transmitted through the food chain, four of which are recognized as neglected tropical diseases (NTDs). Fascioliasis stands out among the other NTDs due to its broad and significant impact on both human and animal health, as Fasciola sp., are also considered major pathogens of domesticated ruminants. Here we present a reference genome sequence of the common liver fluke, Fasciola hepatica isolated from sheep, complementing previously reported isolate from cattle. A total of 14,642 genes were predicted from the 1.14 GB genome of the liver fluke. Comparative genomics indicated that F. hepatica Oregon and related food-borne trematodes are metabolically less constrained than schistosomes and cestodes, taking advantage of the richer millieux offered by the hepatobiliary organs. Protease families differentially expanded between diverse trematodes may facilitate migration and survival within the heterogeneous environments and niches within the mammalian host. Surprisingly, the sequencing of Oregon and Uruguay F. hepatica isolates led to the first discovery of an endobacteria in this species. Two contigs from the F. hepatica Oregon assembly were joined to complete the 859,205 bp genome of a novel Neorickettsia endobacterium (nFh) closely related to the etiological agents of human Sennetsu and Potomac horse fevers. Immunohistochemical studies targeting a Neorickettsia surface protein found nFh in specific organs and tissues of the adult trematode including the female reproductive tract, eggs, the Mehlis’ gland, seminal vesicle, and oral suckers, suggesting putative routes for fluke-to-fluke and fluke-to-host transmission. The genomes of F. hepatica and nFh will serve as a resource for further exploration of the biology of F. hepatica, and specifically its newly discovered trans-kingdom interaction with nFh and the impact of both species on disease in ruminants and humans.


Genome Announcements | 2015

Extreme Sensory Complexity Encoded in the 10-Megabase Draft Genome Sequence of the Chromatically Acclimating Cyanobacterium Tolypothrix sp. PCC 7601

Shaila Yerrapragada; Animesh Shukla; Kymberlie Hallsworth-Pepin; Kwangmin Choi; Aye Wollam; Sandra W. Clifton; Xiang Qin; Donna M. Muzny; Sriram Raghuraman; Haleh Ashki; Akif Uzman; Sarah K. Highlander; Bartlomiej G. Fryszczyn; George E. Fox; Madhan R. Tirumalai; Yamei Liu; Sun Kim; David M. Kehoe; George M. Weinstock

ABSTRACT Tolypothrix sp. PCC 7601 is a freshwater filamentous cyanobacterium with complex responses to environmental conditions. Here, we present its 9.96-Mbp draft genome sequence, containing 10,065 putative protein-coding sequences, including 305 predicted two-component system proteins and 27 putative phytochrome-class photoreceptors, the most such proteins in any sequenced genome.


Nature microbiology | 2017

Genomic diversity in Onchocerca volvulus and its Wolbachia endosymbiont.

Young-Jun Choi; Rahul Tyagi; Samantha N. McNulty; Bruce A. Rosa; Philip Ozersky; John Martin; Kymberlie Hallsworth-Pepin; Thomas R. Unnasch; Carmelle T. Norice; Thomas B. Nutman; Gary J. Weil; Peter U. Fischer; Makedonka Mitreva

Ongoing elimination efforts have altered the global distribution of Onchocerca volvulus, the agent of river blindness, and further population restructuring is expected as efforts continue. Therefore, a better understanding of population genetic processes and their effect on biogeography is needed to support elimination goals. We describe O. volvulus genome variation in 27 isolates from the early 1990s (before widespread mass treatment) from four distinct locales: Ecuador, Uganda, the West African forest and the West African savanna. We observed genetic substructuring between Ecuador and West Africa and between the West African forest and savanna bioclimes, with evidence of unidirectional gene flow from savanna to forest strains. We identified forest:savanna-discriminatory genomic regions and report a set of ancestry informative loci that can be used to differentiate between forest, savanna and admixed isolates, which has not previously been possible. We observed mito-nuclear discordance possibly stemming from incomplete lineage sorting. The catalogue of the nuclear, mitochondrial and endosymbiont DNA variants generated in this study will support future basic and translational onchocerciasis research, with particular relevance for ongoing control programmes, and boost efforts to characterize drug, vaccine and diagnostic targets.


Biotechnology Advances | 2015

Cracking the nodule worm code advances knowledge of parasite biology and biotechnology to tackle major diseases of livestock

Rahul Tyagi; Anja Joachim; Bärbel Ruttkowski; Bruce A. Rosa; John Martin; Kymberlie Hallsworth-Pepin; Xu Zhang; Philip Ozersky; Richard Wilson; Shoba Ranganathan; Paul W. Sternberg; Robin B. Gasser; Makedonka Mitreva

Many infectious diseases caused by eukaryotic pathogens have a devastating, long-term impact on animal health and welfare. Hundreds of millions of animals are affected by parasitic nematodes of the order Strongylida. Unlocking the molecular biology of representatives of this order, and understanding nematode-host interactions, drug resistance and disease using advanced technologies could lead to entirely new ways of controlling the diseases that they cause. Oesophagostomum dentatum (nodule worm; superfamily Strongyloidea) is an economically important strongylid nematode parasite of swine worldwide. The present article reports recent advances made in biology and animal biotechnology through the draft genome and developmental transcriptome of O. dentatum, in order to support biological research of this and related parasitic nematodes as well as the search for new and improved interventions. This first genome of any member of the Strongyloidea is 443 Mb in size and predicted to encode 25,291 protein-coding genes. Here, we review the dynamics of transcription throughout the life cycle of O. dentatum, describe double-stranded RNA interference (RNAi) machinery and infer molecules involved in development and reproduction, and in inducing or modulating immune responses or disease. The secretome predicted for O. dentatum is particularly rich in peptidases linked to interactions with host tissues and/or feeding activity, and a diverse array of molecules likely involved in immune responses. This research progress provides an important resource for future comparative genomic and molecular biological investigations as well as for biotechnological research toward new anthelmintics, vaccines and diagnostic tests.


PLOS Genetics | 2017

Genomic introgression mapping of field-derived multiple-anthelmintic resistance in Teladorsagia circumcincta.

Young-Jun Choi; S.A. Bisset; Stephen R. Doyle; Kymberlie Hallsworth-Pepin; John Martin; Warwick N. Grant; Makedonka Mitreva

Preventive chemotherapy has long been practiced against nematode parasites of livestock, leading to widespread drug resistance, and is increasingly being adopted for eradication of human parasitic nematodes even though it is similarly likely to lead to drug resistance. Given that the genetic architecture of resistance is poorly understood for any nematode, we have analyzed multidrug resistant Teladorsagia circumcincta, a major parasite of sheep, as a model for analysis of resistance selection. We introgressed a field-derived multiresistant genotype into a partially inbred susceptible genetic background (through repeated backcrossing and drug selection) and performed genome-wide scans in the backcross progeny and drug-selected F2 populations to identify the major genes responsible for the multidrug resistance. We identified variation linking candidate resistance genes to each drug class. Putative mechanisms included target site polymorphism, changes in likely regulatory regions and copy number variation in efflux transporters. This work elucidates the genetic architecture of multiple anthelmintic resistance in a parasitic nematode for the first time and establishes a framework for future studies of anthelmintic resistance in nematode parasites of humans.


Genome Announcements | 2017

Genome Sequence of Christensenella minuta DSM 22607T

Bruce A. Rosa; Kymberlie Hallsworth-Pepin; John Martin; Aye Wollam; Makedonka Mitreva

ABSTRACT Obesity influences and is influenced by the human gut microbiome. Here, we present the genome of Christensenella minuta, a highly heritable bacterial species which has been found to be strongly associated with obesity through an unknown biological mechanism. This novel genome provides a valuable resource for future obesity therapeutic studies.


Genome Announcements | 2016

Genome Sequences of 11 Human Vaginal Actinobacteria Strains.

Amanda L. Lewis; Grace E. Deitzler; Maria J. Ruiz; Cory Weimer; SoEun Park; Lloyd S. Robinson; Kymberlie Hallsworth-Pepin; Aye Wollam; Makedonka Mitreva; Warren G. Lewis

ABSTRACT The composition of the vaginal microbiota is an important health determinant. Several members of the phylum Actinobacteria have been implicated in bacterial vaginosis, a condition associated with many negative health outcomes. Here, we present 11 strains of vaginal Actinobacteria (now available through BEI Resources) along with draft genome sequences.

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Makedonka Mitreva

Washington University in St. Louis

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Aye Wollam

Washington University in St. Louis

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Bruce A. Rosa

Washington University in St. Louis

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John Martin

Washington University in St. Louis

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Amanda L. Lewis

Washington University in St. Louis

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Cory Weimer

Washington University in St. Louis

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Grace E. Deitzler

Washington University in St. Louis

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Lloyd S. Robinson

Washington University in St. Louis

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SoEun Park

Washington University in St. Louis

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Warren G. Lewis

Washington University in St. Louis

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