10 results on '"Bouyer, Donald H."'
Search Results
2. A biosafety level-2 dose-dependent lethal mouse model of spotted fever rickettsiosis: Rickettsia parkeri Atlantic Rainforest strain.
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Londoño, Andrés F., Mendell, Nicole L., Walker, David H., and Bouyer, Donald H.
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RICKETTSIA ,RICKETTSIAL diseases ,ANIMALS ,ANAPLASMA phagocytophilum ,RAIN forests ,FEVER ,MICE - Abstract
Background: The species of the Rickettsia genus are separated into four groups: the ancestral group, typhus group, transitional group and spotted fever group. Rickettsia parkeri, a spotted fever group Rickettsia, has been reported across the American continents as infecting several tick species and is associated with a relatively mild human disease characterized by eschar formation at the tick feeding site, regional lymphadenopathy, fever, myalgia and rash. Currently, there are several mouse models that provide good approaches to study the acute lethal disease caused by Rickettsia, but these models can only be performed in an animal biosafety level 3 laboratory. We present an alternative mouse model for acute lethal rickettsial disease, using R. parkeri Atlantic Rainforest strain and C3H/HeN mice, with the advantage that this model can be studied in an animal biosafety level 2 laboratory. Principal findings: In the C3H/HeN mouse model, we determined that infection with 1x10
6 and 1x107 viable R. parkeri Atlantic Rainforest strain organisms produced dose-dependent severity, whereas infection with 1x108 viable bacteria resulted in a lethal illness. The animals became moribund on day five or six post-infection. The lethal disease was characterized by ruffled fur, erythema, labored breathing, decreased activity, and hunched posture, which began on day three post-infection (p.i.) and coincided with the peak bacterial loads. Significant splenomegaly (on days three and five p.i.), neutrophilia (on days three and five p.i.), and thrombocytopenia (on days one, three and five p.i.) were observed. Significance: Since R. parkeri is used at biosafety level 2, the greatest advantage of this inbred mouse model is the ability to investigate immunity and pathogenesis of rickettsiosis with all the tools available at biosafety level 2. [ABSTRACT FROM AUTHOR]- Published
- 2019
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3. Type 1-skewed neuroinflammation and vascular damage associated with Orientia tsutsugamushi infection in mice.
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Soong, Lynn, Shelite, HeThomas R., Xing, Yan, Kodakandla, Harica, Liang, Yuejin, Trent, Brandon J., Horton, Paulina, Smith, Kathryn C., Zhao, Zhenyang, Sun, Jiaren, Bouyer, Donald H., and Cai, Jiyang
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TSUTSUGAMUSHI disease ,LABORATORY rats ,ENDOTHELIAL cells ,MENINGOENCEPHALITIS ,ANGIOPOIETINS ,MENINGITIS ,DIAGNOSIS - Abstract
Background: Scrub typhus is a life-threatening disease, due to infection with O. tsutsugamushi, a Gram-negative bacterium that preferentially replicates in endothelial cells and professional phagocytes. Meningoencephalitis has been reported in scrub typhus patients and experimentally-infected animals; however, the neurological manifestation and its underlying mechanisms remain poorly understood. To address this issue, we focused on Orientia tsutsugamushi Karp strain (OtK), and examined host responses in the brain during lethal versus self-healing scrub typhus disease in our newly established murine models. Principle findings: Following inoculation with a lethal dose of OtK, mice had a significant increase in brain transcripts related to pathogen-pattern recognition receptors (TLR2, TLR4, TLR9), type-1 responses (IFN-γ, TNF-α, CXCL9, CXCR3), and endothelial stress/damage such as angiopoietins, but a rapid down-regulation of Tie2. Sublethal infection displayed similar trends, implying the development of type 1-skewed proinflammatory responses in infected brains, independent of time and disease outcomes. Focal hemorrhagic lesions and meningitis were evident in both infection groups, but pathological changes were more diffuse and frequent in lethal infection. At 6–10 days of lethal infection, the cortex and cerebellum sections had increased ICAM-1-positive staining in vascular cells, as well as increased detection of CD45
+ leukocytes, CD3+ T cells, IBA1+ phagocytes, and GFAP+ astrocytes, but a marked loss of occludin-positive tight junction staining, implying progressive endothelial activation/damage and cellular recruitment in inflamed brains. Orientia were sparse in the brains, but readily detectable within lectin+ vascular and IBA-1+ phagocytic cells. These CNS alterations were consistent with type 1-skewed, IL-13-suppressed responses in lethally-infected mouse lungs. Significance: This is the first report of type 1-skewed neuroinflammation and cellular activation, accompanied with vascular activation/damage, during OtK infection in C57BL/6 mice. This study not only enhances our understanding of the pathophysiological mechanisms of scrub typhus, but also correlates the impact of immune and vascular dysfunction on disease pathogenesis. [ABSTRACT FROM AUTHOR]- Published
- 2017
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4. CD8+ T cells provide immune protection against murine disseminated endotheliotropic Orientia tsutsugamushi infection.
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Xu, Guang, Mendell, Nicole L., Liang, Yuejin, Shelite, Thomas R., Goez-Rivillas, Yenny, Soong, Lynn, Bouyer, Donald H., and Walker, David H.
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T cells ,SCURFIN (Protein) ,LYMPHOCYTES ,TSUTSUGAMUSHI disease ,MESSENGER RNA - Abstract
Scrub typhus, caused by a Gram-negative obligately intracellular coccobacillus, Orientia tsutsugamushi, is a long neglected but important tropical disease. Orientia tsutsugamushi causes illness in one million people each year, and 1 billion people are at risk. Without appropriate diagnosis and treatment, the disease can cause severe multiorgan failure with a case fatality rate of 7–15%. The current gaps in knowledge of immunity include the unknown mechanisms of host immunity to O. tsutsugamushi. Using an intravenous (i.v.) disseminated infection mouse model, we observed that more CD8
+ T cells than CD4+ T cells were present in the spleen of infected mice at 12 dpi. We also determined that Treg cells and the proportion of T cells producing IL-10 were significantly increased from 6 dpi, which correlated with the onset of illness, body weight loss, and increased bacterial loads. We further studied CD8-/- , MHC I-/- and wild type control (WT) C57BL/6J mice to determine the importance of CD8+ T cells and MHC I molecules. After infection with an ordinarily sub-lethal dose of O. tsutsugamushi, all CD8-/- and MHC I-/- mice were moribund between 12 and 15 dpi, whereas all WT mice survived. Bacterial loads in the lung, kidney, liver and spleen of CD8-/- and MHC I-/- mice were significantly greater than those in WT mice. Interferon-γ (IFN-γ) and granzyme B mRNA levels in the liver of CD8-/- and MHC I-/- mice were significantly greater than in WT mice. In addition, more severe histopathologic lesions were observed in CD8-/- mice. Finally, adoptive transfer confirmed a major role of immune CD8+ T cells as well as a less effective contribution by immune CD8 T cell-depleted splenocytes in protection against O. tsutsugamushi infection. These studies demonstrated the critical importance of CD8+ T cells in the host immune response during O. tsutsugamushi infection. [ABSTRACT FROM AUTHOR]- Published
- 2017
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5. Murine models of scrub typhus associated with host control of Orientia tsutsugamushi infection.
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Mendell, Nicole L., Bouyer, Donald H., and Walker, David H.
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INFECTION , *MICROCIRCULATION , *TSUTSUGAMUSHI disease , *LABORATORY mice , *ETIOLOGY of diseases - Abstract
Background: Scrub typhus, a febrile illness of substantial incidence and mortality, is caused by infection with the obligately intracellular bacterium Orientia tsutsugamushi. It is estimated that there are more than one million cases annually transmitted by the parasitic larval stage of trombiculid mites in the Asia-Pacific region. The antigenic and genetic diversity of the multiple strains of O. tsutsugamushi hinders the advancement of laboratory diagnosis, development of long-lasting vaccine-induced protection, and interpretation of clinical infection. Despite the life-threatening severity of the illness in hundreds of thousands of cases annually, 85–93% of patients survive, often without anti-rickettsial treatment. To more completely understand the disease caused by Orientia infection, animal models which closely correlate with the clinical manifestations, target cells, organ involvement, and histopathologic lesions of human cases of scrub typhus should be employed. Previously, our laboratory has extensively characterized two relevant C57BL/6 mouse models using O. tsutsugamushi Karp strain: a route-specific intradermal model of infection and persistence and a hematogenously disseminated dose-dependent lethal model. Principal findings: To complement the lethal model, here we illustrate a sublethal model in the same mouse strain using the O. tsutsugamushi Gilliam strain, which resulted in dose-dependent severity of illness, weight loss, and systemic dissemination to endothelial cells of the microcirculation and mononuclear phagocytic cells. Histopathologic lesions included expansion of the pulmonary interstitium by inflammatory cell infiltrates and multifocal hepatic lesions with mononuclear cellular infiltrates, renal interstitial lymphohistiocytic inflammation, mild meningoencephalitis, and characteristic typhus nodules. Significance: These models parallel characteristics of human cases of scrub typhus, and will be used in concert to understand differences in severity which lead to lethality or host control of the infection and to address the explanation for short duration of heterologous immunity in Orientia infection. [ABSTRACT FROM AUTHOR]
- Published
- 2017
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6. An Intradermal Inoculation Mouse Model for Immunological Investigations of Acute Scrub Typhus and Persistent Infection.
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Soong, Lynn, Mendell, Nicole L., Olano, Juan P., Rockx-Brouwer, Dedeke, Xu, Guang, Goez-Rivillas, Yenny, Drom, Claire, Shelite, Thomas R., Valbuena, Gustavo, Walker, David H., and Bouyer, Donald H.
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TSUTSUGAMUSHI disease ,LABORATORY mice ,ENDOTHELIAL cells ,INTRADERMAL injections ,GRAM-negative bacteria - Abstract
Scrub typhus is a neglected tropical disease, caused by Orientia tsutsugamushi, a Gram-negative bacterium that is transmitted to mammalian hosts during feeding by Leptotrombidium mites and replicates predominantly within endothelial cells. Most studies of scrub typhus in animal models have utilized either intraperitoneal or intravenous inoculation; however, there is limited information on infection by the natural route in murine model skin or its related early host responses. Here, we developed an intradermal (i.d.) inoculation model of scrub typhus and focused on the kinetics of the host responses in the blood and major infected organs. Following ear inoculation with 6 x 10
4 O. tsutsugamushi, mice developed fever at 11–12 days post-infection (dpi), followed by marked hypothermia and body weight loss at 14–19 dpi. Bacteria in blood and tissues and histopathological changes were detected around 9 dpi and peaked around 14 dpi. Serum cytokine analyses revealed a mixed Th1/Th2 response, with marked elevations of MCP-1/CCL2, MIP-1α/CCL3 and IL-10 at 9 dpi, followed by increased concentrations of pro-inflammatory markers (IL-6, IL-12, IFN-γ, G-CSF, RANTES/CCL5, KC/CCL11, IL-1α/β, IL-2, TNF-α, GM-CSF), as well as modulatory cytokines (IL-9, IL-13). Cytokine levels in lungs had similar elevation patterns, except for a marked reduction of IL-9. The Orientia 47-kDa gene and infectious bacteria were detected in several organs for up to 84 dpi, indicating persistent infection. This is the first comprehensive report of acute scrub typhus and persistent infection in i.d.-inoculated C57BL/6 mice. This is a significant improvement over current murine models for Orientia infection and will permit detailed studies of host immune responses and infection control interventions. [ABSTRACT FROM AUTHOR]- Published
- 2016
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7. IL-33-Dependent Endothelial Activation Contributes to Apoptosis and Renal Injury in Orientia tsutsugamushi-Infected Mice.
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Shelite, Thomas R., Liang, Yuejin, Wang, Hui, Mendell, Nicole L., Trent, Brandon J., Sun, Jiaren, Gong, Bin, Xu, Guang, Hu, Haitao, Bouyer, Donald H., and Soong, Lynn
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TSUTSUGAMUSHI disease ,ENDOTHELIAL cells ,APOPTOSIS ,MICE ,NITRIC-oxide synthases ,WOUNDS & injuries - Abstract
Endothelial cells (EC) are the main target for Orientia tsutsugamushi infection and EC dysfunction is a hallmark of severe scrub typhus in patients. However, the molecular basis of EC dysfunction and its impact on infection outcome are poorly understood. We found that C57BL/6 mice that received a lethal dose of O. tsutsugamushi Karp strain had a significant increase in the expression of IL-33 and its receptor ST2L in the kidneys and liver, but a rapid reduction of IL-33 in the lungs. We also found exacerbated EC stress and activation in the kidneys of infected mice, as evidenced by elevated angiopoietin (Ang) 2/Ang1 ratio, increased endothelin 1 (ET-1) and endothelial nitric oxide synthase (eNOS) expression. Such responses were significantly attenuated in the IL-33
-/- mice. Importantly, IL-33-/- mice also had markedly attenuated disease due to reduced EC stress and cellular apoptosis. To confirm the biological role of IL-33, we challenged wild-type (WT) mice with a sub-lethal dose of O. tsutsugamushi and gave mice recombinant IL-33 (rIL-33) every 2 days for 10 days. Exogenous IL-33 significantly increased disease severity and lethality, which correlated with increased EC stress and activation, increased CXCL1 and CXCL2 chemokines, but decreased anti-apoptotic gene BCL-2 in the kidneys. To further examine the role of EC stress, we infected human umbilical vein endothelial cells (HUVEC) in vitro. We found an infection dose-dependent increase in the expression of IL-33, ST2L soluble ST2 (sST2), and the Ang2/Ang1 ratio at 24 and 48 hours post-infection. This study indicates a pathogenic role of alarmin IL-33 in a murine model of scrub typhus and highlights infection-triggered EC damage and IL-33-mediated pathological changes during the course of Orientia infection. [ABSTRACT FROM AUTHOR]- Published
- 2016
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8. Rickettsia rickettsii and Other Members of the Spotted Fever Group as Potential Bioweapons.
- Author
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Anderson, Burt, Friedman, Herman, Bendinelli, Mauro, Bouyer, Donald H., and Walker, David H.
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Since the anthrax attacks in the fall of 2001, there has been an increase in the level of anxiety felt throughout society in general about the use of biological agents as weapons. Although much of the nation's and the world's attention has been focused upon anthrax, botulinum toxin, and Ebola as weapons, there are other microbes that also pose a significant threat due to their potential as bioweapons. Characteristics that are shared by each of these organisms are that they are easily obtainable in nature, difficult to detect, and highly infectious at a low dose, can be easily transmitted by aerosol, and have a short incubation period. One frequently overlooked genus of bacteria that fulfills these criteria and also poses a significant threat is the Rickettsia. Members of this genus, such as Rickettsia rickettsii, a spotted fever group (SFG) rickettsia, have long been recognized as inherently dangerous with many reports of accidental infections and even deaths because of inhalational transmission to scientists who have worked with these organisms. Rickettsia prowazekii, a member of the typhus group, not only occurs in periodic outbreaks, but also has the infamous history of having been developed as a bioweapon by both the Japanese Army during World War II and the former Soviet Union. Because of its history and reputation, many scientists suspect that R. prowazekii is the most probable Rickettsia to be utilized as a bioweapon. There is also a substantial possibility that R. rickettsii or another member of the SFG would be utilized and that we should also prepare for that scenario. R. rickettsii is the most pathogenic rickettsia, and other pathogenic members of the SFG are formidable in their own right and could have a potential devastating effect if loosed upon an unsuspecting society and an unprepared medical and public health system. [ABSTRACT FROM AUTHOR]
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- 2006
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9. Strong Type 1, but Impaired Type 2, Immune Responses Contribute to Orientia tsutsugamushi-Induced Pathology in Mice.
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Soong, Lynn, Wang, Hui, Shelite, Thomas R., Liang, Yuejin, Mendell, Nicole L., Sun, Jiaren, Gong, Bin, Valbuena, Gustavo A., Bouyer, Donald H., and Walker, David H.
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TSUTSUGAMUSHI disease ,IMMUNE response ,LABORATORY mice ,GRAM-negative bacteria ,ANGIOPOIETIN-2 ,MYELOPEROXIDASE - Abstract
Scrub typhus is a neglected, but important, tropical disease, which puts one-third of the world's population at risk. The disease is caused by Orientia tsutsugamushi, an obligately intracellular Gram-negative bacterium. Dysregulation in immune responses is known to contribute to disease pathogenesis; however, the nature and molecular basis of immune alterations are poorly defined. This study made use of a newly developed murine model of severe scrub typhus and focused on innate regulators and vascular growth factors in O. tsutsugamushi-infected liver, lungs and spleen. We found no activation or even reduction in base-line expression for multiple molecules (IL-7, IL-4, IL-13, GATA3, ROR-γt, and CXCL12) at 2, 6 and 10 days post-infection. This selective impairment in type 2-related immune responses correlated with a significant activation of the genes for IL-1β, IL-6, IL-10, TNF-α, IFN-γ, as well as CXCR3- and CXCR1-related chemokines in inflamed tissues. The elevated angiopoietin (Ang)-2 expression and Ang-2/Ang-1 ratios suggested excessive inflammation and the loss of endothelial integrity. These alterations, together with extensive recruitment of myeloperoxidase (MPO)-expressing neutrophils and the influx of CD3
+ T cells, contributed to acute tissue damage and animal death. This is the first report of selective alterations in a panel of immune regulators during early O. tsutsugamushi infection in intravenously inoculated C57BL/6 mice. Our findings shed new light on the pathogenic mechanisms associated with severe scrub typhus and suggest potential targets for therapeutic investigation. [ABSTRACT FROM AUTHOR]- Published
- 2014
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10. A Hematogenously Disseminated Orientia tsutsugamsushi-Infected Murine Model of Scrub Typhus.
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Shelite, Thomas R., Saito, Tais B., Mendell, Nicole L., Gong, Bin, Xu, Guang, Soong, Lynn, Valbuena, Gustavo, Bouyer, Donald H., and Walker, David H.
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TSUTSUGAMUSHI disease ,ETIOLOGY of diseases ,RICKETTSIAL diseases ,PARASITIC diseases ,MEDICAL parasitology - Abstract
Orientia tsutsugamushi, the etiologic agent of scrub typhus, is a mite-borne rickettsia transmitted by the parasitic larval stage of trombiculid mites. Approximately one-third of the world's population is at risk of infection with Orientia tsutsugamushi, emphasizing its importance in global health. In order to study scrub typhus, Orientia tsutsugamushi Karp strain has been used extensively in mouse studies with various inoculation strategies and little success in inducing disease progression similar to that of human scrub typhus. The objective of this project was to develop a disease model with pathology and target cells similar to those of severe human scrub typhus. This study reports an intravenous infection model of scrub typhus in C57BL/6 mice. This mouse strain was susceptible to intravenous challenge, and lethal infection occurred after intravenous inoculation of 1.25×10
6 focus (FFU) forming units. Signs of illness in lethally infected mice appeared on day 6 with death occurring ∼6 days later. Immunohistochemical staining for Orientia antigens demonstrated extensive endothelial infection, most notably in the lungs and brain. Histopathological analysis revealed cerebral perivascular, lymphohistiocytic infiltrates, focal hemorrhages, meningoencephalitis, and interstitial pneumonia. Disseminated infection of endothelial cells with Orientia in C57BL/6 mice resulted in pathology resembling that of human scrub typhus. The use of this model will allow detailed characterization of the mechanisms of immunity to and pathogenesis of O. tsutsugamushi infection. [ABSTRACT FROM AUTHOR]- Published
- 2014
- Full Text
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