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  1. Article ; Online: Cytomegalovirus infection disrupts the influence of short-chain fatty acid producers on Treg/Th17 balance.

    Chin, Ning / Narayan, Nicole R / Méndez-Lagares, Gema / Ardeshir, Amir / Chang, W L William / Deere, Jesse D / Fontaine, Justin H / Chen, Connie / Kieu, Hung T / Lu, Wenze / Barry, Peter A / Sparger, Ellen E / Hartigan-O'Connor, Dennis J

    Microbiome

    2022  Volume 10, Issue 1, Page(s) 168

    Abstract: Background: Both the gut microbiota and chronic viral infections have profound effects on host immunity, but interactions between these influences have been only superficially explored. Cytomegalovirus (CMV), for example, infects approximately 80% of ... ...

    Abstract Background: Both the gut microbiota and chronic viral infections have profound effects on host immunity, but interactions between these influences have been only superficially explored. Cytomegalovirus (CMV), for example, infects approximately 80% of people globally and drives significant changes in immune cells. Similarly, certain gut-resident bacteria affect T-cell development in mice and nonhuman primates. It is unknown if changes imposed by CMV on the intestinal microbiome contribute to immunologic effects of the infection.
    Results: We show that rhesus cytomegalovirus (RhCMV) infection is associated with specific differences in gut microbiota composition, including decreased abundance of Firmicutes, and that the extent of microbial change was associated with immunologic changes including the proliferation, differentiation, and cytokine production of CD8
    Conclusions: Gut microbes have an important influence on health and disease. Diet is known to shape the microbiota, but the influence of concomitant chronic viral infections is unclear. We found that CMV influences gut microbiota composition to an extent that is correlated with immunologic changes in the host. Additionally, pre-existing correlations between immunophenotypes and gut microbes can be subverted by CMV infection. Immunologic effects of CMV infection on the host may therefore be mediated by two different mechanisms involving gut microbiota. Video Abstract.
    MeSH term(s) Animals ; CD8-Positive T-Lymphocytes ; Cytokines ; Cytomegalovirus/genetics ; Cytomegalovirus Infections ; Fatty Acids, Volatile ; Macaca mulatta ; Mice ; T-Lymphocytes, Regulatory
    Chemical Substances Cytokines ; Fatty Acids, Volatile
    Language English
    Publishing date 2022-10-10
    Publishing country England
    Document type Journal Article ; Video-Audio Media ; Research Support, N.I.H., Extramural
    ZDB-ID 2697425-3
    ISSN 2049-2618 ; 2049-2618
    ISSN (online) 2049-2618
    ISSN 2049-2618
    DOI 10.1186/s40168-022-01355-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: SIV clearance from neonatal macaques following transient CCR5 depletion.

    Deere, Jesse D / Merriam, David / Leggat, Kawthar Machmach / Chang, Wen-Lan William / Méndez-Lagares, Gema / Kieu, Hung / Dutra, Joseph / Fontaine, Justin / Lu, Wenze / Chin, Ning / Chen, Connie / Tran, Bryant Chi-Thien / Salinas, Jessica / Miller, Corey N / Deeks, Steven G / Lifson, Jeffrey D / Engelman, Kathleen / Magnani, Diogo / Reimann, Keith /
    Stevenson, Mario / Hartigan-O'Connor, Dennis J

    bioRxiv : the preprint server for biology

    2023  

    Abstract: Treatment of people with HIV (PWH) with antiretroviral therapy (ART) results in sustained suppression of viremia, but HIV persists indefinitely as integrated provirus in CD4-expressing cells. Intact persistent provirus, the "rebound competent viral ... ...

    Abstract Treatment of people with HIV (PWH) with antiretroviral therapy (ART) results in sustained suppression of viremia, but HIV persists indefinitely as integrated provirus in CD4-expressing cells. Intact persistent provirus, the "rebound competent viral reservoir" (RCVR), is the primary obstacle to achieving a cure. Most variants of HIV enter CD4
    Language English
    Publishing date 2023-05-01
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.05.01.533682
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Early Life Wildfire Smoke Exposure Is Associated with Immune Dysregulation and Lung Function Decrements in Adolescence.

    Black, Carolyn / Gerriets, Joan E / Fontaine, Justin H / Harper, Richart W / Kenyon, Nicholas J / Tablin, Fern / Schelegle, Edward S / Miller, Lisa A

    American journal of respiratory cell and molecular biology

    2017  Volume 56, Issue 5, Page(s) 657–666

    Abstract: The long-term health effects of wildfire smoke exposure in pediatric populations are not known. The objectives of this study were to determine if early life exposure to wildfire smoke can affect parameters of immunity and airway physiology that are ... ...

    Abstract The long-term health effects of wildfire smoke exposure in pediatric populations are not known. The objectives of this study were to determine if early life exposure to wildfire smoke can affect parameters of immunity and airway physiology that are detectable with maturity. We studied a mixed-sex cohort of rhesus macaque monkeys that were exposed as infants to ambient wood smoke from a series of Northern California wildfires in the summer of 2008. Peripheral blood mononuclear cells (PBMCs) and pulmonary function measures were obtained when animals were approximately 3 years of age. PBMCs were cultured with either LPS or flagellin, followed by measurement of secreted IL-8 and IL-6 protein. PBMCs from a subset of female animals were also evaluated by Toll-like receptor (TLR) pathway mRNA analysis. Induction of IL-8 protein synthesis with either LPS or flagellin was significantly reduced in PBMC cultures from wildfire smoke-exposed female monkeys. In contrast, LPS- or flagellin-induced IL-6 protein synthesis was significantly reduced in PBMC cultures from wildfire smoke-exposed male monkeys. Baseline and TLR ligand-induced expression of the transcription factor, RelB, was globally modulated in PBMCs from wildfire smoke-exposed monkeys, with additional TLR pathway genes affected in a ligand-dependent manner. Wildfire smoke-exposed monkeys displayed significantly reduced inspiratory capacity, residual volume, vital capacity, functional residual capacity, and total lung capacity per unit of body weight relative to control animals. Our findings suggest that ambient wildfire smoke exposure during infancy results in sex-dependent attenuation of systemic TLR responses and reduced lung volume in adolescence.
    MeSH term(s) Aging/physiology ; Air Pollution/analysis ; Animals ; Body Weight ; California ; Environmental Exposure ; Female ; Fires ; Leukocytes, Mononuclear/metabolism ; Ligands ; Linear Models ; Lung/immunology ; Lung/physiopathology ; Macaca mulatta ; Male ; NF-kappa B/metabolism ; Particle Size ; Particulate Matter/analysis ; Respiratory Function Tests ; Smoke ; Toll-Like Receptors/metabolism
    Chemical Substances Ligands ; NF-kappa B ; Particulate Matter ; Smoke ; Toll-Like Receptors
    Language English
    Publishing date 2017-05
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1025960-0
    ISSN 1535-4989 ; 1044-1549
    ISSN (online) 1535-4989
    ISSN 1044-1549
    DOI 10.1165/rcmb.2016-0380OC
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Early life allergen and air pollutant exposures alter longitudinal blood immune profiles in infant rhesus monkeys.

    Crowley, Candace M / Fontaine, Justin H / Gerriets, Joan E / Schelegle, Edward S / Hyde, Dallas M / Miller, Lisa A

    Toxicology and applied pharmacology

    2017  Volume 328, Page(s) 60–69

    Abstract: Early life is a critical period for the progressive establishment of immunity in response to environmental stimuli; the impact of airborne challenges on this process is not well defined. In a longitudinal fashion, we determined the effect of episodic ... ...

    Abstract Early life is a critical period for the progressive establishment of immunity in response to environmental stimuli; the impact of airborne challenges on this process is not well defined. In a longitudinal fashion, we determined the effect of episodic house dust mite (HDM) aerosol and ozone inhalation, both separately and combined, on peripheral blood immune cell phenotypes and cytokine expression from 4 to 25weeks of age in an infant rhesus monkey model of childhood development. Immune profiles in peripheral blood were compared with lung lavage at 25weeks of age. Independent of exposure, peripheral blood cell counts fluctuated with chronologic age of animals, while IFNγ and IL-4 mRNA levels increased over time in a linear fashion. At 12weeks of age, total WBC, lymphocyte numbers, FoxP3 mRNA and IL-12 mRNA were dramatically reduced relative to earlier time points, but increased to a steady state with age. Exposure effects were observed for monocyte numbers, as well as CCR3, FoxP3, and IL-12 mRNA levels in peripheral blood. Significant differences in cell surface marker and cytokine expression were detected following in vitro HDM or PMA/ionomycin stimulation of PBMC isolated from animals exposed to either HDM or ozone. Lavage revealed a mixed immune phenotype of FoxP3, IFNγ and eosinophilia in association with combined HDM plus ozone exposure, which was not observed in blood. Collectively, our findings show that airborne challenges during postnatal development elicit measureable cell and cytokine changes in peripheral blood over time, but exposure-induced immune profiles are not mirrored in the lung.
    MeSH term(s) Aerosols ; Aging/immunology ; Air Pollutants/toxicity ; Allergens/toxicity ; Animals ; Antigens, Dermatophagoides ; Blood/immunology ; Bronchoalveolar Lavage Fluid/chemistry ; Bronchoalveolar Lavage Fluid/cytology ; Gene Expression Regulation/drug effects ; Inhalation Exposure ; Interferon-gamma/analysis ; Macaca mulatta ; Male ; Monocytes/metabolism
    Chemical Substances Aerosols ; Air Pollutants ; Allergens ; Antigens, Dermatophagoides ; Interferon-gamma (82115-62-6)
    Language English
    Publishing date 2017--01
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 204477-8
    ISSN 1096-0333 ; 0041-008X
    ISSN (online) 1096-0333
    ISSN 0041-008X
    DOI 10.1016/j.taap.2017.05.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Occurrence and correlations between coliphages and anthropogenic viruses in the Massachusetts Bay using enrichment and ICC-nPCR.

    Ballester, Nicola A / Fontaine, Justin H / Margolin, Aaron B

    Journal of water and health

    2005  Volume 3, Issue 1, Page(s) 59–68

    Abstract: We evaluated a two-step enrichment procedure to detect coliphages and an integrated cell culture-nested polymerase chain reaction (ICC-nPCR) to detect human astrovirus, enteroviruses, rotavirus and adenovirus type 40 and 41 in marine water samples ... ...

    Abstract We evaluated a two-step enrichment procedure to detect coliphages and an integrated cell culture-nested polymerase chain reaction (ICC-nPCR) to detect human astrovirus, enteroviruses, rotavirus and adenovirus type 40 and 41 in marine water samples collected by the Massachusetts Water Resource Authority (MWRA). MWRA has been monitoring its receiving waters for coliphages, anthropogenic viruses and indicator bacteria in order to evaluate the impact of Boston's Deer Island Sewage Treatment Plant discharge. Coliphages and enteric viruses were originally assayed using single agar overlay and most probable number cell culture (MPN) methods, respectively. Reanalysis of these samples for enteric viruses by ICC-nPCR demonstrated that 46% were positive for at least one virus compared with 23% with the MPN method. Use of the enrichment method showed a 47% increase in the detection of male specific and somatic coliphages compared with the single agar overlay method. Correlations between the presence of coliphages, enteric viruses and indicator bacteria were based on proximity to the treatment plant discharge, seasonal variations and site levels. The presence of enteric viruses was significantly correlated to coliphages but not to indicator bacteria. Preliminary comparative results demonstrate that effective and efficient monitoring of anthropogenic contamination can be achieved using these more sensitive and specific techniques.
    MeSH term(s) Base Sequence ; Coliphages/isolation & purification ; Colony Count, Microbial ; DNA Primers ; Massachusetts ; Polymerase Chain Reaction/methods ; Prevalence ; Viruses/classification ; Viruses/genetics ; Viruses/isolation & purification ; Water Microbiology
    Chemical Substances DNA Primers
    Language English
    Publishing date 2005-03
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2123845-5
    ISSN 1996-7829 ; 1477-8920
    ISSN (online) 1996-7829
    ISSN 1477-8920
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Innate immune response to LPS in airway epithelium is dependent on chronological age and antecedent exposures.

    Maniar-Hew, Kinjal / Clay, Candice C / Postlethwait, Edward M / Evans, Michael J / Fontaine, Justin H / Miller, Lisa A

    American journal of respiratory cell and molecular biology

    2013  Volume 49, Issue 5, Page(s) 710–720

    Abstract: The immune mechanisms for neonatal susceptibility to respiratory pathogens are poorly understood. Given that mucosal surfaces serve as a first line of host defense, we hypothesized that the innate immune response to infectious agents may be ... ...

    Abstract The immune mechanisms for neonatal susceptibility to respiratory pathogens are poorly understood. Given that mucosal surfaces serve as a first line of host defense, we hypothesized that the innate immune response to infectious agents may be developmentally regulated in airway epithelium. To test this hypothesis, we determined whether the expression of IL-8 and IL-6 in airway epithelium after LPS exposure is dependent on chronological age. Tracheas from infant, juvenile, and adult rhesus monkeys were first exposed to LPS ex vivo, and then processed for air-liquid interface primary airway epithelial cell cultures and secondary LPS treatment in vitro. Compared with adult cultures, infant and juvenile cultures expressed significantly reduced concentrations of IL-8 after LPS treatment. IL-8 protein in cultures increased with animal age, whereas LPS-induced IL-6 protein was predominantly associated with juvenile cultures. Toll-like receptor (TLR) pathway RT-PCR arrays showed differential expressions of multiple mRNAs in infant cultures relative to adult cultures, including IL-1α, TLR10, and the peptidoglycan recognition protein PGLYRP2. To determine whether the age-dependent cytokine response to LPS is reflective of antecedent exposures, we assessed primary airway epithelial cell cultures established from juvenile monkeys housed in filtered air since birth. Filtered air-housed animal cultures exhibited LPS-induced IL-8 and IL-6 expression that was discordant with age-matched ambient air-housed animals. A single LPS aerosol in vivo also affected this cytokine profile. Cumulatively, our findings demonstrate that the innate immune response to LPS in airway epithelium is variable with age, and may be modulated by previous environmental exposures.
    MeSH term(s) Aerosols ; Age Factors ; Aging/immunology ; Animals ; Animals, Newborn ; Carrier Proteins/genetics ; Carrier Proteins/metabolism ; Cells, Cultured ; Dose-Response Relationship, Drug ; Environmental Exposure ; Epithelial Cells/drug effects ; Epithelial Cells/immunology ; Gene Expression Regulation ; Immunity, Innate/drug effects ; Inflammation Mediators/metabolism ; Interleukin-1alpha/genetics ; Interleukin-1alpha/metabolism ; Interleukin-6/metabolism ; Interleukin-8/metabolism ; Lipopolysaccharides/pharmacology ; Macaca mulatta ; Male ; RNA, Messenger/metabolism ; Respiratory Mucosa/drug effects ; Respiratory Mucosa/immunology ; Tissue Culture Techniques ; Toll-Like Receptors/drug effects ; Toll-Like Receptors/genetics ; Toll-Like Receptors/metabolism
    Chemical Substances Aerosols ; Carrier Proteins ; Inflammation Mediators ; Interleukin-1alpha ; Interleukin-6 ; Interleukin-8 ; Lipopolysaccharides ; RNA, Messenger ; Toll-Like Receptors ; lipopolysaccharide, E. coli O26-B6 ; peptidoglycan recognition protein
    Language English
    Publishing date 2013-04-22
    Publishing country United States
    Document type Comparative Study ; Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 1025960-0
    ISSN 1535-4989 ; 1044-1549
    ISSN (online) 1535-4989
    ISSN 1044-1549
    DOI 10.1165/rcmb.2012-0321OC
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Airway epithelial wounds in rhesus monkey generate ionic currents that guide cell migration to promote healing.

    Sun, Yao-Hui / Reid, Brian / Fontaine, Justin H / Miller, Lisa A / Hyde, Dallas M / Mogilner, Alex / Zhao, Min

    Journal of applied physiology (Bethesda, Md. : 1985)

    2011  Volume 111, Issue 4, Page(s) 1031–1041

    Abstract: Damage to the respiratory epithelium is one of the most critical steps to many life-threatening diseases, such as acute respiratory distress syndrome and chronic obstructive pulmonary disease. The mechanisms underlying repair of the damaged epithelium ... ...

    Abstract Damage to the respiratory epithelium is one of the most critical steps to many life-threatening diseases, such as acute respiratory distress syndrome and chronic obstructive pulmonary disease. The mechanisms underlying repair of the damaged epithelium have not yet been fully elucidated. Here we provide experimental evidence suggesting a novel mechanism for wound repair: endogenous electric currents. It is known that the airway epithelium maintains a voltage difference referred to as the transepithelial potential. Using a noninvasive vibrating probe, we demonstrate that wounds in the epithelium of trachea from rhesus monkeys generate significant outward electric currents. A small slit wound produced an outward current (1.59 μA/cm(2)), which could be enhanced (nearly doubled) by the ion transport stimulator aminophylline. In addition, inhibiting cystic fibrosis transmembrane conductance regulator (CFTR) with CFTR(Inh)-172 significantly reduced wound currents (0.17 μA/cm(2)), implicating an important role of ion transporters in wound induced electric potentials. Time-lapse video microscopy showed that applied electric fields (EFs) induced robust directional migration of primary tracheobronchial epithelial cells from rhesus monkeys, towards the cathode, with a threshold of <23 mV/mm. Reversal of the field polarity induced cell migration towards the new cathode. We further demonstrate that application of an EF promoted wound healing in a monolayer wound healing assay. Our results suggest that endogenous electric currents at sites of tracheal epithelial injury may direct cell migration, which could benefit restitution of damaged airway mucosa. Manipulation of ion transport may lead to novel therapeutic approaches to repair damaged respiratory epithelium.
    MeSH term(s) Animals ; Cell Movement/physiology ; Cells, Cultured ; Cystic Fibrosis Transmembrane Conductance Regulator/metabolism ; Electrodes ; Epithelial Cells/metabolism ; Epithelial Cells/physiology ; Ion Transport ; Macaca mulatta ; Membrane Potentials/physiology ; Respiratory Mucosa/metabolism ; Respiratory Mucosa/physiology ; Trachea/metabolism ; Trachea/physiology ; Wound Healing/physiology
    Chemical Substances Cystic Fibrosis Transmembrane Conductance Regulator (126880-72-6)
    Language English
    Publishing date 2011-06-30
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 219139-8
    ISSN 1522-1601 ; 0021-8987 ; 0161-7567 ; 8750-7587
    ISSN (online) 1522-1601
    ISSN 0021-8987 ; 0161-7567 ; 8750-7587
    DOI 10.1152/japplphysiol.00915.2010
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Early life ozone exposure results in dysregulated innate immune function and altered microRNA expression in airway epithelium.

    Clay, Candice C / Maniar-Hew, Kinjal / Gerriets, Joan E / Wang, Theodore T / Postlethwait, Edward M / Evans, Michael J / Fontaine, Justin H / Miller, Lisa A

    PloS one

    2014  Volume 9, Issue 3, Page(s) e90401

    Abstract: Exposure to ozone has been associated with increased incidence of respiratory morbidity in humans; however the mechanism(s) behind the enhancement of susceptibility are unclear. We have previously reported that exposure to episodic ozone during postnatal ...

    Abstract Exposure to ozone has been associated with increased incidence of respiratory morbidity in humans; however the mechanism(s) behind the enhancement of susceptibility are unclear. We have previously reported that exposure to episodic ozone during postnatal development results in an attenuated peripheral blood cytokine response to lipopolysaccharide (LPS) that persists with maturity. As the lung is closely interfaced with the external environment, we hypothesized that the conducting airway epithelium of neonates may also be a target of immunomodulation by ozone. To test this hypothesis, we evaluated primary airway epithelial cell cultures derived from juvenile rhesus macaque monkeys with a prior history of episodic postnatal ozone exposure. Innate immune function was measured by expression of the proinflammatory cytokines IL-6 and IL-8 in primary cultures established following in vivo LPS challenge or, in response to in vitro LPS treatment. Postnatal ozone exposure resulted in significantly attenuated IL-6 mRNA and protein expression in primary cultures from juvenile animals; IL-8 mRNA was also significantly reduced. The effect of antecedent ozone exposure was modulated by in vivo LPS challenge, as primary cultures exhibited enhanced cytokine expression upon secondary in vitro LPS treatment. Assessment of potential IL-6-targeting microRNAs miR-149, miR-202, and miR-410 showed differential expression in primary cultures based upon animal exposure history. Functional assays revealed that miR-149 is capable of binding to the IL-6 3' UTR and decreasing IL-6 protein synthesis in airway epithelial cell lines. Cumulatively, our findings suggest that episodic ozone during early life contributes to the molecular programming of airway epithelium, such that memory from prior exposures is retained in the form of a dysregulated IL-6 and IL-8 response to LPS; differentially expressed microRNAs such as miR-149 may play a role in the persistent modulation of the epithelial innate immune response towards microbes in the mature lung.
    MeSH term(s) 3' Untranslated Regions/genetics ; Animals ; Animals, Newborn ; Cells, Cultured ; Epithelial Cells/drug effects ; Epithelial Cells/metabolism ; Epithelium/drug effects ; Epithelium/immunology ; Fluorescent Antibody Technique ; Gene Expression Profiling ; Gene Expression Regulation/drug effects ; Humans ; Immunity, Innate/drug effects ; Immunity, Innate/genetics ; Interleukin-6/genetics ; Interleukin-6/metabolism ; Interleukin-8/genetics ; Interleukin-8/metabolism ; Lipopolysaccharides/pharmacology ; Lung/immunology ; Macaca mulatta/genetics ; Macaca mulatta/immunology ; Male ; MicroRNAs/genetics ; MicroRNAs/metabolism ; Ozone/pharmacology ; Protein Binding/drug effects
    Chemical Substances 3' Untranslated Regions ; Interleukin-6 ; Interleukin-8 ; Lipopolysaccharides ; MicroRNAs ; Ozone (66H7ZZK23N)
    Language English
    Publishing date 2014-03-04
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0090401
    Database MEDical Literature Analysis and Retrieval System OnLINE

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