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Dive into the research topics where Edward J. Dick is active.

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Featured researches published by Edward J. Dick.


Proceedings of the National Academy of Sciences of the United States of America | 2009

Pancreatic islet amyloidosis, β-cell apoptosis, and α-cell proliferation are determinants of islet remodeling in type-2 diabetic baboons

Rodolfo Guardado-Mendoza; Alberto M. Davalli; Alberto O. Chavez; Gene B. Hubbard; Edward J. Dick; Abraham Majluf-Cruz; Carlos Enrique Tene-Pérez; Lukasz Goldschmidt; John Hart; Carla Perego; Anthony G. Comuzzie; María Elizabeth Tejero; Giovanna Finzi; Claudia Placidi; Stefano La Rosa; Carlo Capella; Glenn A. Halff; Amalia Gastaldelli; Ralph A. DeFronzo; Franco Folli

β-Cell dysfunction is an important factor in the development of hyperglycemia of type-2 diabetes mellitus, and pancreatic islet amyloidosis (IA) has been postulated to be one of the main contributors to impaired insulin secretion. The aim of this study was to evaluate the correlation of IA with metabolic parameters and its effect on islets of Langerhans remodeling and relative endocrine-cell volume in baboons. We sequenced the amylin peptide, determined the fibrillogenic propensities, and evaluated pancreatic histology, clinical and biochemical characteristics, and endocrine cell proliferation and apoptosis in 150 baboons with different metabolic status. Amylin sequence in the baboon was 92% similar to humans and showed superimposable fibrillogenic propensities. IA severity correlated with fasting plasma glucose (FPG) (r = 0.662, P < 0.001) and HbA1c (r = 0.726, P < 0.001), as well as with free fatty acid, glucagon values, decreased homeostasis model assessment (HOMA) insulin resistance, and HOMA-B. IA severity was associated with a decreased relative β-cell volume, and increased relative α-cell volume and hyperglucagonemia. These results strongly support the concept that IA and β-cell apoptosis in concert with α-cell proliferation and hypertrophy are key determinants of islets of Langerhans “dysfunctional remodeling” and hyperglycemia in the baboon, a nonhuman primate model of type-2 diabetes mellitus. The most important determinants of IA were age and FPG (R2 = 0.519, P < 0.0001), and different FPG levels were sensitive and specific to predict IA severity. Finally, a predictive model for islet amyloid severity was generated with age and FPG as required variables.


Placenta | 2009

Feto-placental adaptations to maternal obesity in the baboon.

Darren Farley; María Elizabeth Tejero; Anthony G. Comuzzie; Paul B. Higgins; Laura A. Cox; Sherry Werner; Susan L. Jenkins; Cun Li; Jaehyek Choi; Edward J. Dick; Gene B. Hubbard; Patrice A. Frost; Donald Dudley; Brandon Ballesteros; Guoyao Wu; Peter W. Nathanielsz; Natalia E. Schlabritz-Loutsevitch

Maternal obesity is present in 20-34% of pregnant women and has been associated with both intrauterine growth restriction and large-for-gestational age fetuses. While fetal and placental functions have been extensively studied in the baboon, no data are available on the effect of maternal obesity on placental structure and function in this species. We hypothesize that maternal obesity in the baboon is associated with a maternal inflammatory state and induces structural and functional changes in the placenta. The major findings of this study were: 1) decreased placental syncytiotrophoblast amplification factor, intact syncytiotrophoblast endoplasmic reticulum structure and decreased system A placental amino acid transport in obese animals; 2) fetal serum amino acid composition and mononuclear cells (PBMC) transcriptome were different in fetuses from obese compared with non-obese animals; and 3) maternal obesity in humans and baboons is similar in regard to increased placental and adipose tissue macrophage infiltration, increased CD14 expression in maternal PBMC and maternal hyperleptinemia. In summary, these data demonstrate that in obese baboons in the absence of increased fetal weight, placental and fetal phenotype are consistent with those described for large-for-gestational age human fetuses.


International Journal of Systematic and Evolutionary Microbiology | 2014

Brucella papionis sp. nov., isolated from baboons (Papio spp.)

Adrian M. Whatmore; Nicholas J Davison; Axel Cloeckaert; Sascha Al Dahouk; Michel S. Zygmunt; Simon D. Brew; Lorraine L. Perrett; Mark S. Koylass; Gilles Vergnaud; Christine Quance; Holger C. Scholz; Edward J. Dick; Gene B. Hubbard; Natalia E. Schlabritz-Loutsevitch

Two Gram-negative, non-motile, non-spore-forming coccoid bacteria (strains F8/08-60(T) and F8/08-61) isolated from clinical specimens obtained from baboons (Papio spp.) that had delivered stillborn offspring were subjected to a polyphasic taxonomic study. On the basis of 16S rRNA gene sequence similarities, both strains, which possessed identical sequences, were assigned to the genus Brucella. This placement was confirmed by extended multilocus sequence analysis (MLSA), where both strains possessed identical sequences, and whole-genome sequencing of a representative isolate. All of the above analyses suggested that the two strains represent a novel lineage within the genus Brucella. The strains also possessed a unique profile when subjected to the phenotyping approach classically used to separate species of the genus Brucella, reacting only with Brucella A monospecific antiserum, being sensitive to the dyes thionin and fuchsin, being lysed by bacteriophage Wb, Bk2 and Fi phage at routine test dilution (RTD) but only partially sensitive to bacteriophage Tb, and with no requirement for CO2 and no production of H2S but strong urease activity. Biochemical profiling revealed a pattern of enzyme activity and metabolic capabilities distinct from existing species of the genus Brucella. Molecular analysis of the omp2 locus genes showed that both strains had a novel combination of two highly similar omp2b gene copies. The two strains shared a unique fingerprint profile of the multiple-copy Brucella-specific element IS711. Like MLSA, a multilocus variable number of tandem repeat analysis (MLVA) showed that the isolates clustered together very closely, but represent a distinct group within the genus Brucella. Isolates F8/08-60(T) and F8/08-61 could be distinguished clearly from all known species of the genus Brucella and their biovars by both phenotypic and molecular properties. Therefore, by applying the species concept for the genus Brucella suggested by the ICSP Subcommittee on the Taxonomy of Brucella, they represent a novel species within the genus Brucella, for which the name Brucella papionis sp. nov. is proposed, with the type strain F8/08-60(T) ( = NCTC 13660(T) = CIRMBP 0958(T)).


Journal of Medical Primatology | 2009

A novel Brucella isolate in association with two cases of stillbirth in non-human primates - first report.

Natalia E. Schlabritz-Loutsevitch; Adrian M. Whatmore; Christine Quance; Mark Koylass; L. Bill Cummins; Edward J. Dick; Cathy L. Snider; David P. Cappelli; Jeffrey L. Ebersole; Peter W. Nathanielsz; Gene B. Hubbard

Background  Brucellosis is veterinary and human health problem.


Journal of Medical Primatology | 2009

Spontaneous heart disease in the adult chimpanzee (Pan troglodytes)

Brittany M. Seiler; Edward J. Dick; Rodolfo Guardado-Mendoza; John L. VandeBerg; Jeff T. Williams; James N. Mubiru; Gene B. Hubbard

Background  A high incidence of heart disease, especially idiopathic cardiomyopathy (IC), is seen in chimpanzees (Pan troglodytes).


Mbio | 2013

A Novel Adenovirus Species Associated with an Acute Respiratory Outbreak in a Baboon Colony and Evidence of Coincident Human Infection

Charles Y. Chiu; Shigeo Yagi; Xiaoyan Lu; Guixia Yu; Eunice C. Chen; Maria Liu; Edward J. Dick; Kenneth D. Carey; Dean D. Erdman; M. Michelle Leland; Jean L. Patterson

ABSTRACT Adenoviruses (AdVs) are DNA viruses that infect many vertebrate hosts, including humans and nonhuman primates. Here we identify a novel AdV species, provisionally named “simian adenovirus C (SAdV-C),” associated with a 1997 outbreak of acute respiratory illness in captive baboons (4 of 9) at a primate research facility in Texas. None of the six AdVs recovered from baboons (BaAdVs) during the outbreak, including the two baboons who died from pneumonia, were typeable. Since clinical samples from the two fatal cases were not available, whole-genome sequencing of nasal isolates from one sick baboon and three asymptomatic baboons during the outbreak was performed. Three AdVs were members of species SAdV-C (BaAdV-2 and BaAdV-4 were genetically identical, and BaAdV-3), while one (BaAdV-1) was a member of the recently described SAdV-B species. BaAdV-3 was the only AdV among the 4 isolated from a sick baboon, and thus was deemed to be the cause of the outbreak. Significant divergence (<58% amino acid identity) was found in one of the fiber proteins of BaAdV-3 relative to BaAdV-2 and -4, suggesting that BaAdV-3 may be a rare SAdV-C recombinant. Neutralizing antibodies to the other 3 AdVs, but not BaAdV-3, were detected in healthy baboons from 1996 to 2003 and staff personnel from 1997. These results implicate a novel adenovirus species (SAdV-C) in an acute respiratory outbreak in a baboon colony and underscore the potential for cross-species transmission of AdVs between humans and nonhuman primates. IMPORTANCE Adenoviruses (AdVs) are DNA viruses that infect many animals, including humans and monkeys. In 1997, an outbreak of acute respiratory illness from AdVs occurred in a baboon colony in Texas. Here we use whole-genome sequencing and antibody testing to investigate new AdVs in baboons (BaAdVs) during the outbreak, one of which, BaAdV-3, came from a sick animal. By sequence analysis, BaAdV-3 may be a recombinant strain that arose from a related BaAdV found in baboons nearby in the colony (who were not sick) and yet another unknown AdV. We also found antibodies to these new BaAdVs in baboons and staff personnel at the facility. Taken together, our findings of a new AdV species as the cause of an acute respiratory outbreak in a baboon colony underscore the ongoing threat from emerging viruses that may carry the potential for cross-species transmission between monkeys and humans. Adenoviruses (AdVs) are DNA viruses that infect many animals, including humans and monkeys. In 1997, an outbreak of acute respiratory illness from AdVs occurred in a baboon colony in Texas. Here we use whole-genome sequencing and antibody testing to investigate new AdVs in baboons (BaAdVs) during the outbreak, one of which, BaAdV-3, came from a sick animal. By sequence analysis, BaAdV-3 may be a recombinant strain that arose from a related BaAdV found in baboons nearby in the colony (who were not sick) and yet another unknown AdV. We also found antibodies to these new BaAdVs in baboons and staff personnel at the facility. Taken together, our findings of a new AdV species as the cause of an acute respiratory outbreak in a baboon colony underscore the ongoing threat from emerging viruses that may carry the potential for cross-species transmission between monkeys and humans.


Journal of Medical Primatology | 2007

Spontaneous neoplasia in the baboon (Papio spp.).

Rachel E. Cianciolo; Stephanie D. Butler; Jeffery S. Eggers; Edward J. Dick; M. Michelle Leland; Melissa de la Garza; Kathleen M. Brasky; Larry B. Cummins; Gene B. Hubbard

Background  There are several comprehensive reviews of spontaneous neoplasia in non‐human primates that compile individual cases or small numbers of cases, but do not provide statistical analysis of tumor incidence, demographics, or epidemiology.


Journal of Medical Primatology | 2003

Record review of baboons with histologically confirmed endometriosis in a large established colony

Edward J. Dick; Gene B. Hubbard; Lisa J. Martin; M. Michelle Leland

Abstract: Spontaneous endometriosis was diagnosed in 43 baboons over a 14‐year period. Thirty‐seven have died; five remain alive; one was sold and lost to follow‐up. The average age at diagnosis was 17.2 years; 29 (67%) were between 12 and 21 years of age. Fifteen (35%) were diagnosed by biopsy and received surgical excision of the endometriotic tissue; four of these were identified during caesarian section, confirming one prior report of endometriosis in pregnant animals. Twenty‐eight (65%) were diagnosed at or shortly preceding necropsy. When diagnosed by a palpable abdominal mass, there was a significantly greater likelihood the animal died or was killed as a result of complications of endometriosis. When diagnosis was at necropsy, there was a significantly greater likelihood that the animal died from causes unrelated to endometriosis. Early identification with surgical removal appears to provide a benefit for both survival and delivering offspring after diagnosis. In twenty‐one baboons (49%), endometriosis affected multiple sites within the peritoneal cavity. In the remaining baboons, lesions were more localized. Ovarian involvement was seen in sixteen (37%) of these baboons. This paper is the first to describe significant ovarian involvement in baboons, previously considered a limitation of the usefulness of this species as an animal model. We also describe the first reported endometriosis seeding of an abdominal surgery scar in a baboon. Many of these baboons were middle aged, had few or no offspring, or had evidence of a long duration of uninterrupted menstrual cycles, consistent with risk factors for women. Endometriosis was an incidental finding in 17 (40%) of these baboons, consistent with previous reports of minimal endometriosis as a common asymptomatic finding in baboons and in women. Overall, endometriosis in baboons presents a spontaneously occurring animal model that shares important features with the disease in women and the rhesus macaque.


Journal of Medical Primatology | 2009

Spontaneous pathology of the common marmoset (Callithrix jacchus) and tamarins (Saguinus oedipus, Saguinus mystax)

John M. David; Edward J. Dick; Gene B. Hubbard

Background  Marmosets and tamarins are increasingly used in research, but their pathology remains poorly defined compared with Old World primates.


Journal of Medical Primatology | 2009

Neoplasia in the chimpanzee (Pan spp.)

Susan L. Brown; Daniel C. Anderson; Edward J. Dick; Rodolfo Guardado-Mendoza; Anapatricia Garcia; Gene B. Hubbard

Background  Chimpanzees have over 98% genomic sequence homology with humans and may have a similar host response to malignancy. There is minimal information concerning cancer in the chimpanzee and such information would be valuable to individuals caring for and using them for research.

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Gene B. Hubbard

University of Texas Health Science Center at San Antonio

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Michael A. Owston

Texas Biomedical Research Institute

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Natalia Schlabritz-Loutsevitch

Texas Tech University Health Sciences Center

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Natalia E. Schlabritz-Loutsevitch

University of Texas Health Science Center at San Antonio

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John L. VandeBerg

Texas Biomedical Research Institute

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James N. Mubiru

Texas Biomedical Research Institute

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Rodolfo Guardado-Mendoza

University of Texas Health Science Center at San Antonio

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Shyamesh Kumar

Texas Biomedical Research Institute

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