23 results on '"Olson, Alex"'
Search Results
2. Mycobacterium tuberculosis disease associates with higher HIV-1-specific antibody responses
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Adeoye, Bukola, Nakiyingi, Lydia, Moreau, Yvetane, Nankya, Ethel, Olson, Alex J., Zhang, Mo, Jacobson, Karen R., Gupta, Amita, Manabe, Yukari C., Hosseinipour, Mina C., Kumwenda, Johnstone, and Sagar, Manish
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- 2023
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3. Microphysics and Optical Attenuation in Fog: Observations from Two Coastal Sites
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Wang, Qing, Yamaguchi, Ryan T., Kalogiros, John A., Daniels, Zachary, Alappattu, Denny P., Jonsson, Haflidi, Alvarenga, Oswaldo, Olson, Alex, Wauer, Benjamin J., Ortiz-Suslow, David G., and Fernando, Harindra Joseph
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- 2021
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4. Vδ1 Effector and Vδ2 γδ T-Cell Subsets Shift in Frequency and Are Linked to Plasma Inflammatory Markers During Antiretroviral Therapy-Suppressed HIV Infection.
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Pihl, Riley M F, Smith-Mahoney, Erika L, Olson, Alex, Yuen, Rachel R, Asundi, Archana, Lin, Nina, Belkina, Anna C, and Snyder-Cappione, Jennifer E
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HIV infections ,T cells ,IMMUNE reconstitution inflammatory syndrome ,HIV ,OLDER people ,ANTIRETROVIRAL agents - Abstract
Background Chronic inflammation is prevalent with antiretroviral therapy (ART)-suppressed human immunodeficiency virus (HIV) infection and one immune cell subset putatively driving this phenomenon is TIGIT
+ γδ T cells. Methods To elucidate γδ T-cell phenotypic diversity, spectral flow cytometry was performed on blood lymphocytes from individuals of a HIV and aging cohort and data were analyzed using bioinformatic platforms. Plasma inflammatory markers were measured and correlated with γδ T-cell subset frequencies. Results Thirty-nine distinct γδ T-cell subsets were identified (22 Vδ1+ , 14 Vδ2+ , and 3 Vδ1− Vδ2− Vγ9+ ) and TIGIT was nearly exclusively found on the Vδ1+ CD45RA+ CD27− effector populations. People with ART-suppressed HIV infection (PWH) exhibited high frequencies of distinct clusters of Vδ1+ effectors distinguished via CD8, CD16, and CD38 expression. Among Vδ2+ cells, most Vγ9+ (innate-like) clusters were lower in PWH; however, CD27+ subsets were similar in frequency between participants with and without HIV. Comparisons by age revealed lower 'naive' Vδ1+ CD45RA+ CD27+ cells in older individuals, regardless of HIV status. Plasma inflammatory markers were selectively linked to subsets of Vδ1+ and Vδ2+ cells. Conclusions These results further elucidate γδ T-cell subset complexity and reveal distinct alterations and connections with inflammatory pathways of Vδ1+ effector and Vδ2+ innate-like subsets during ART-suppressed HIV infection. [ABSTRACT FROM AUTHOR]- Published
- 2024
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5. Targeting HIV-1 proviral transcription
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Olson, Alex, Basukala, Binita, Wong, Wilson W, and Henderson, Andrew J
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- 2019
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6. Vaccine elicitation of HIV broadly neutralizing antibodies from engineered B cells
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Huang, Deli, Tran, Jenny Tuyet, Olson, Alex, Vollbrecht, Thomas, Tenuta, Mary, Guryleva, Mariia V., Fuller, Roberta P., Schiffner, Torben, Abadejos, Justin R., Couvrette, Lauren, Blane, Tanya R., Saye, Karen, Li, Wenjuan, Landais, Elise, Gonzalez-Martin, Alicia, Schief, William, Murrell, Ben, Burton, Dennis R., Nemazee, David, and Voss, James E.
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- 2020
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7. HIV-1 replicates and persists in vaginal epithelial dendritic cells
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Pena-Cruz, Victor, Agosto, Luis M., Akiyama, Hisashi, Olson, Alex, Moreau, Yvetane, Larrieux, Jean-Robert, Henderson, Andrew, Gummuluru, Suryaram, and Sagar, Manish
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HIV infections -- Health aspects ,HIV -- Care and treatment -- Prevention ,Dendritic cells -- Health aspects ,Women -- Health aspects ,Health care industry - Abstract
HIV-1 acquisition occurs most commonly after sexual contact. To establish infection, HIV-1 must infect cells that support high-level replication, namely [CD4.sup.+] T cells, which are absent from the outermost genital epithelium. Dendritic cells (DCs), present in mucosal epithelia, potentially facilitate HIV-1 acquisition. We show that vaginal epithelial DCs, termed [CD1a.sup.+] VEDCs, are unlike other blood- and tissue-derived DCs because they express langerin but not DC-SIGN, and unlike skin-based [langerin.sup.+] DC subset Langerhans cells (LCs), they do not harbor Birbeck granules. Individuals primarily acquire HIV-1 that utilizes the CCR5 receptor (termed either R5 or R5X4) during heterosexual transmission, and the mechanism for the block against variants that only use the CXCR4 receptor (classified as X4) remains unclear. We show that X4 as compared with R5 HIV-1 shows limited to no replication in [CD1a.sup.+] VEDCs. This differential replication occurs after fusion, suggesting that receptor usage influences postentry steps in the virus life cycle. Furthermore, [CD1a.sup.+] VEDCs isolated from HIV-1-infected virologically suppressed women harbor HIV-1 DNA. Thus, [CD1a.sup.+] VEDCs are potentially infected early during heterosexual transmission and also retain virus during treatment. Understanding the interplay between HIV-1 and [CD1a.sup.+] VEDCs is important for future prevention and cure strategies., Introduction The majority of new HIV-1 infections occur in women after heterosexual contact. To establish a systemic infection in a naive woman, HIV-1 must cross the genital epithelium and infect [...]
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- 2018
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8. Brief Report: Pulmonary Tuberculosis Is Associated With Persistent Systemic Inflammation and Decreased HIV-1 Reservoir Markers in Coinfected Ugandans
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Olson, Alex, Ragan, Elizabeth J., Nakiyingi, Lydia, Lin, Nina, Jacobson, Karen R., Ellner, Jerrold J., Manabe, Yukari C., and Sagar, Manish
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- 2018
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9. Intercropping perennial cereal grain crops in alternate or same row seeding method for improved forage yield and quality.
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Ugwu, Cosmas, Omokanye, Akim, Ramirez Hernandez, Guillermo, Thilakrathna, Malinda S., Hostetller, Chelsey, Arora, Naveen, Puurveene, Dick, Singh, Kabal, Olson, Alex, and Ahmed, Khalil
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Intercropping perennial cereal crops with legume species can offer multiple ecosystem functions and agronomic benefits. This study evaluated the forage dry matter yield (FDMY) and the nutritive value of two perennial cereal grain crop species [ACE 1-rye and Kenza, intermediate wheatgrass (IWG)] intercropped with three perennial legume species (alfalfa, white clover, and sainfoin) using alternate- and same-row seeding methods at five different sites in Alberta. The experimental sites were established in June 2022 using a factorial experimental model with eight treatment factors, including perennial monocultures or intercrop with a legume species. One year after establishment in 2023, the forage dry matter yield (FDMY) varied significantly (P < 0.05) across experimental sites, ranging from 228 kgּ·ha-1ּ·yr-1 for the IWG/sainfoin intercrop to 6,833 kgּ·ha-1ּ·yr-1 for the IWG and alfalfa intercrop treatment. Seeding methods (Same or Alternate row) and site location had a significant effect on the FDMY (P = 0.00126), indicating consistent performance in the two cropping systems across diverse environments and site locations. The study assessed eight treatments (cereal-legume combinations) for forage quality performance, of which seven treatments, including RyeClover, Rye-Sainfoin, Wheat-Alfalfa, Wheat-Clover, Wheat-Sainfoin, Wheat mono, and Rye mono, showed significant effects on forage quality factors of crude protein (CP), NDF, NDFD-48, and the Relative Feed Value (RFV). The nutritive value of forage varied across different treatments, with CP content ranging from 6.28% to 18.94% and acid detergent fiber (ADF) content ranging from 10.28% to 40.27%. This variation suggests that the protein and digestibility requirements for livestock consumption are met at different stages. Additionally, the study suggests that intercropping perennial cereal grain crops with legume species using either alternate or the same row seeding methods can lead to consistent forage productivity across different sites. The forages from these intercropping systems exhibit adequate concentrations of CP and total digestible nutrient (TDN), with an average TDN concentration across all sites of approximately 59.3%. This makes them suitable for fulfilling the dietary requirements of beef or dairy cows at various developmental stages. Further research is ongoing to investigate ecosystem functions such as biological nitrogen fixation and water-use efficiency to optimize management practices for sustainable forage production. [ABSTRACT FROM AUTHOR]
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- 2024
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10. Integrase Inhibitor Use Associated with Weight Gain in Women and Incident Diabetes Mellitus.
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Asundi, Archana, Olson, Alex, Jiang, Wenqing, Varshney, Swati P., White, Laura F., Sagar, Manish, and Lin, Nina H.
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Excessive weight gain associated with integrase strand transfer inhibitor (InSTI) antiretrovirals is an emerging issue; however, the metabolic consequences of this effect have not been established. Our objective was to evaluate for InSTI-emergent weight gain and potential associated type 2 diabetes mellitus (T2DM) among a diverse HIV patient cohort. For this retrospective cohort study, we obtained clinical warehouse data for HIV+ patients between fiscal years 2007–17. We compared patients initiated on an InSTI with those started on an alternate regimen. Our primary outcome was percentage weight change from baseline to 24 months postinitiation using the linear mixed-effects model fit by restricted maximum likelihood. Our secondary outcome was incident T2DM as defined by a new prescription for antihyperglycemic medication within 18 months after antiretroviral therapy (ART) start. Diabetes-free survival was estimated using the Kaplan–Meier method, log-rank test, and Cox proportional-hazards model. The cohort included 1,235 individuals initiating ART, 136 (11.0%) with an InSTI. InSTI use in women was significantly associated with greater weight gain compared with non-InSTIs (11.0%, 95% confidence interval, CI: 5.22 to 16.8, p < .01), after adjusting for potential confounding variables. In a univariate analysis, InSTI use was associated with more incident T2DM diagnoses compared with non-InSTI regimens (unadjusted hazard ratio = 3.27, p = .01), although incident T2DM was not associated with weight gain. InSTIs were significantly associated with weight gain among females. We also observed an increased risk of incident diabetes mellitus among both sexes, however, unrelated to weight changes. Further prospective studies will be necessary to confirm this finding and investigate its mechanism. [ABSTRACT FROM AUTHOR]
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- 2022
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11. Intragenic proviral elements support transcription of defective HIV-1 proviruses.
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Kuniholm, Jeffrey, Armstrong, Elise, Bernabe, Brandy, Coote, Carolyn, Berenson, Anna, Patalano, Samantha D., Olson, Alex, He, Xianbao, Lin, Nina H., Fuxman Bass, Juan I., and Henderson, Andrew J.
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HIV ,T cells ,HIV-positive persons ,ANTIRETROVIRAL agents - Abstract
HIV-1 establishes a persistent proviral reservoir by integrating into the genome of infected host cells. Current antiretroviral treatments do not target this persistent population of proviruses which include latently infected cells that upon treatment interruption can be reactivated to contribute to HIV-1 rebound. Deep sequencing of persistent HIV proviruses has revealed that greater than 90% of integrated HIV genomes are defective and unable to produce infectious virions. We hypothesized that intragenic elements in the HIV genome support transcription of aberrant HIV-1 RNAs from defective proviruses that lack long terminal repeats (LTRs). Using an intact provirus detection assay, we observed that resting CD4+ T cells and monocyte-derived macrophages (MDMs) are biased towards generating defective HIV-1 proviruses. Multiplex reverse transcription droplet digital PCR identified env and nef transcripts which lacked 5' untranslated regions (UTR) in acutely infected CD4+ T cells and MDMs indicating transcripts are generated that do not utilize the promoter within the LTR. 5'UTR-deficient env transcripts were also identified in a cohort of people living with HIV (PLWH) on ART, suggesting that these aberrant RNAs are produced in vivo. Using 5' rapid amplification of cDNA ends (RACE), we mapped the start site of these transcripts within the Env gene. This region bound several cellular transcription factors and functioned as a transcriptional regulatory element that could support transcription and translation of downstream HIV-1 RNAs. These studies provide mechanistic insights into how defective HIV-1 proviruses are persistently expressed to potentially drive inflammation in PLWH. Author summary: People living with HIV establish a persistent reservoir which includes latently infected cells that fuel viral rebound upon treatment interruption. However, the majority of HIV-1 genomes in these persistently infected cells are defective. Whether these defective HIV genomes are expressed and whether they contribute to HIV associated diseases including accelerated aging, neurodegenerative symptoms, and cardiovascular diseases are still outstanding questions. In this paper, we demonstrate that acute infection of macrophages and resting T cells is biased towards generating defective viruses which are expressed by DNA regulatory elements in the HIV genome. These studies describe an alternative mechanism for chronic expression of HIV genomes. [ABSTRACT FROM AUTHOR]
- Published
- 2021
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12. HIV-1 Transcription but Not Intact Provirus Levels are Associated With Systemic Inflammation.
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Olson, Alex, Coote, Carolyn, Snyder-Cappione, Jennifer E, Lin, Nina, and Sagar, Manish
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MONONUCLEAR leukocytes , *HIV , *HIV infections , *VIRAL physiology , *VIRUSES , *INFLAMMATION , *RNA , *FIBRIN fibrinogen degradation products - Abstract
Individuals infected with human immunodeficiency virus (HIV) 1 have increased inflammation, which has been associated with age-associated diseases. Plasma markers, cell-associated virus levels, and ability to stimulate RNA transcription in latently infected cell lines was examined in younger and older HIV-1-infected individuals with suppressed virus. Cell-associated RNA, but not intact provirus level, had positive correlation with plasma D-dimer levels. Compared with the younger group, the older group had higher D-dimer levels and a trend toward more cell-associated RNA but similar levels of intact proviruses. Even though all measured inflammatory markers were relatively higher in the older group, this greater inflammation did not induce more HIV-1 transcription in latently infected cell lines. Inflammation and HIV-1 RNA expression increase with age despite similar levels of intact infectious HIV DNA. While plasma inflammation is correlated with HIV-1 RNA expression in peripheral blood mononuclear cells, it does not induce HIV-1 transcription in latently infected cell lines. [ABSTRACT FROM AUTHOR]
- Published
- 2021
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13. Novel ELISA Protocol Links Pre-Existing SARS-CoV-2 Reactive Antibodies With Endemic Coronavirus Immunity and Age and Reveals Improved Serologic Identification of Acute COVID-19 via Multi-Parameter Detection.
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Yuen, Rachel R., Steiner, Dylan, Pihl, Riley M.F., Chavez, Elizabeth, Olson, Alex, Smith, Erika L., Baird, Lillia A., Korkmaz, Filiz, Urick, Patricia, Sagar, Manish, Berrigan, Jacob L., Gummuluru, Suryaram, Corley, Ronald B., Quillen, Karen, Belkina, Anna C., Mostoslavsky, Gustavo, Rifkin, Ian R., Kataria, Yachana, Cappione III, Amedeo J., and Gao, Wenda
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SARS-CoV-2 ,COVID-19 ,COVID-19 pandemic ,VIRAL proteins ,IMMUNOGLOBULINS ,SYSTEMIC lupus erythematosus - Abstract
The COVID-19 pandemic has drastically impacted work, economy, and way of life. Sensitive measurement of SARS-CoV-2 specific antibodies would provide new insight into pre-existing immunity, virus transmission dynamics, and the nuances of SARS-CoV-2 pathogenesis. To date, existing SARS-CoV-2 serology tests have limited utility due to insufficient reliable detection of antibody levels lower than what is typically present after several days of symptoms. To measure lower quantities of SARS-CoV-2 IgM, IgG, and IgA with higher resolution than existing assays, we developed a new ELISA protocol with a distinct plate washing procedure and timed plate development via use of a standard curve. Very low optical densities from samples added to buffer coated wells at as low as a 1:5 dilution are reported using this 'BU ELISA' method. Use of this method revealed circulating SARS-CoV-2 receptor binding domain (RBD) and nucleocapsid protein (N) reactive antibodies (IgG, IgM, and/or IgA) in 44 and 100 percent of pre-pandemic subjects, respectively, and the magnitude of these antibodies tracked with antibody levels of analogous viral proteins from endemic coronavirus (eCoV) strains. The disease status (HIV, SLE) of unexposed subjects was not linked with SARS-CoV-2 reactive antibody levels; however, quantities were significantly lower in subjects over 70 years of age compared with younger counterparts. Also, we measured SARS-CoV-2 RBD- and N- specific IgM, IgG, and IgA antibodies from 29 SARS-CoV-2 infected individuals at varying disease states, including 10 acute COVID-19 hospitalized subjects with negative serology results by the EUA approved Abbott IgG chemiluminescent microparticle immunoassay. Measurements of SARS-CoV-2 RBD- and N- specific IgM, IgG, IgA levels measured by the BU ELISA revealed higher signal from 9 of the 10 Abbott test negative COVID-19 subjects than all pre-pandemic samples for at least one antibody specificity/isotype, implicating improved serologic identification of SARS-CoV-2 infection via multi-parameter, high sensitive antibody detection. We propose that this improved ELISA protocol, which is straightforward to perform, low cost, and uses readily available commercial reagents, is a useful tool to elucidate new information about SARS-CoV-2 infection and immunity and has promising implications for improved detection of all analytes measurable by this platform. [ABSTRACT FROM AUTHOR]
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- 2021
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14. SNAPflex: a paper-and-plastic device for instrument-free RNA and DNA extraction from whole blood.
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Kolluri, Nikunja, Albarran, Nikolas, Fan, Andy, Olson, Alex, Sagar, Manish, Young, Anna, Gomez-Marquez, José, and Klapperich, Catherine M.
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NUCLEIC acid isolation methods ,NUCLEIC acid amplification techniques ,DNA ,RNA ,BLOODBORNE infections - Abstract
Nucleic acid amplification tests (NAATs), which amplify and detect pathogen nucleic acids, are vital methods to diagnose diseases, particularly in cases where patients exhibit low levels of infection. For many blood-borne pathogens such as HIV or Plasmodium falciparum, it is necessary to first extract pathogen RNA or DNA from patient blood prior to NAAT analysis. Traditional nucleic acid extraction methods are expensive, resource-intensive and are often difficult to deploy to resource-limited areas where many blood-borne infections are widespread. Here, we describe a portable, paper-and-plastic device, called SNAPflex, for instrument-free nucleic acid extraction from whole blood, which builds upon our previous work for RNA extraction using a pressure-driven extraction system. SNAPflex shows improved HIV RNA extraction from simulated patient samples compared to traditional extraction methods as well as long-term stability of extracted RNA without the need for cold storage. We further demonstrated successful extraction and recovery of P. falciparum DNA from cultured parasites in whole blood. SNAPflex was designed to be easily manufacturable and deployable to resource-limited settings. [ABSTRACT FROM AUTHOR]
- Published
- 2020
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15. Jonesville and the Legacy of Slavery at Western Kentucky University
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Doss, Selena Sanderfer, Farmer, Susan, and Olson, Alexander
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- 2021
16. Using morphological, behavioral, and molecular biomarkers in Zebrafish to assess the toxicity of lead-contaminated sediments from a retired trapshooting range within an urban wetland.
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Olson, Alex J, Cyphers, Trevor, Gerrish, Gretchen, Belby, Colin, and King-Heiden, Tisha C
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LEAD toxicology , *LEAD & the environment , *TRAPSHOOTING - Abstract
The widespread use of lead (Pb) shot in shooting activities, including at former shooting ranges, continues to pose environmental risks. The La Crosse River Marsh (located in Wisconsin, USA) is a biologically diverse urban riparian wetland with a legacy of Pb-contaminated sediment resulting from its use as a trap shooting range from 1929-1963. Within the shot fall zone, shot densities exceed 43,000 pellets/m2 and surface sediments exceed 25,000 mg/kg in some areas. This study used the Zebrafish as a model to determine the acute toxicity of these contaminated sediments. Zebrafish were exposed to sediments containing approximately 13 to 13,450 mg/kg Pb for 5 days (8-120 hr post-fertilization). The toxic responses to sediments were non-monotonic. Only exposure to sediments containing “mid-range” concentrations of Pb (4580 mg/kg) induced mild skeletal malformations and a sluggish C-start response indicating that Pb was marginally bioavailable. Expression of δ-aminolevulinic acid dehydratase (ALA-D) also indicated the potential for uptake of Pb from sediments. Our findings suggest that Pb within the La Crosse River Marsh sediments is not readily bioavailable to Zebrafish, and while this metal poses a minimal acute toxicological risk, toxicity due to chronic exposure of low concentrations of Pb is possible. Further, our data demonstrated that induction of ALA-D gene expression in Zebrafish embryos shows promise as an alternative to ALA-D enzyme activity as a biomarker for acute Pb exposure under lab conditions. [ABSTRACT FROM AUTHOR]
- Published
- 2018
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17. MYCOBACTERIUM TUBERCULOSIS ASSOCIATES WITH HIGHER HIV-1- SPECIFIC ANTIBODY RESPONSES.
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Adeoye, Bukola, Nakiyingi, Lydia, Moreau Moreau, Yvetane, Nankya, Ethel, Olson, Alex, Mo Zhang, Jacobson, Karen, Gupta, Amita, Manabe, Yukari C., Hosseinipour, Mina, Kumwenda, Johnstone, and Sagar, Manish
- Published
- 2023
18. The Bitter Waters of Medicine Creek: A Tragic Clash Between White and Native America by <string-name>Richard Kluger</string-name> (review)
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Olson, Alexander I.
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- 2022
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19. Utilizing Machine Learning Algorithms to Evaluate Sex-based Differences in Preoperative Hemoglobin Thresholds in Open Vascular Surgery.
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Raju, Sneha, Roche-Nagle, Graham, Olson, Alex, Eisenberg, Naomi, and Chan, Timothy
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- 2022
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20. Ad Hoc American Studies: Michigan and the Hidden History of a Movement
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Olson, Alexander I. and Kelderman, Frank
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- 2016
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21. Targeted Chromatinization and Repression of HIV-1 Provirus Transcription with Repurposed CRISPR/Cas9.
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Olson, Alex, Basukala, Binita, Lee, Seunghee, Gagne, Matthew, Wong, Wilson W., and Henderson, Andrew J.
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CRISPRS , *HISTONES , *CD4 antigen , *HISTONE acetylation , *TRANSGENIC organisms , *ANTIRETROVIRAL agents , *HIV - Abstract
The major barrier to HIV-1 cure is the persistence of latent provirus, which is not eradicated by antiretroviral therapy. The "shock and kill" approach entails stimulating viral production with latency-reversing agents followed by the killing of cells actively producing the virus by immune clearance. However, this approach does not induce all intact proviruses, leaving a residual reservoir. CRISPR/Cas9 has been utilized to excise integrated Human Immunodeficiency Virus (HIV) DNA from infected cells in an RNA-guided, sequence-specific manner. Here, we seek to epigenetically silence the proviral DNA by introducing nuclease-deficient disabled Cas9 (dCas9) coupled with a transcriptional repressor domain derived from Kruppel-associated box (KRAB). We show that specific guide RNAs (gRNAs) and dCas9-KRAB repress HIV-1 transcription and reactivation of latent HIV-1 provirus. This repression is correlated with chromatin changes, including decreased H3 histone acetylation and increased histone H3 lysine 9 trimethylation, histone marks that are associated with transcriptional repression. dCas9-KRAB-mediated inhibition of HIV-1 transcription suggests that CRISPR can be engineered as a tool for block-and-lock strategies. [ABSTRACT FROM AUTHOR]
- Published
- 2020
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22. ON THE COVER.
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Olson, Alex
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PAINTING ,SENSORY perception - Abstract
A painting of artist Laura Bartlett is presented.
- Published
- 2013
23. A new cell line for assessing HIV-1 antibody dependent cellular cytotoxicity against a broad range of variants.
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Thomas, Allison S., Ghulam-Smith, Melissa, Olson, Alex, Coote, Carolyn, Gonzales, Oscar, and Sagar, Manish
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CELL lines , *ANTIBODY-dependent cell cytotoxicity , *KILLER cells , *HIV , *MONOCLONAL antibodies - Abstract
Human immunodeficiency virus type 1 (HIV-1) studies suggest that antibody-dependent cellular cytotoxicity (ADCC) influences both virus acquisition and subsequent disease outcome. Technical issues with currently available assays, however, have limited the ability to comprehensively assess the impact of ADCC on transmission and disease progression. Commonly used ADCC assays use a target cell line, CEM.NKr-CCR5-Luc, that often does not support replication of relevant HIV-1 variants. Thus, the extent of ADCC responses against a large panel of HIV-1 strains often cannot be assessed using the currently available methods. We developed two new reporter cell-lines (MT4-CCR5-Luc and PM1-CCR5-Luc) to overcome these issues. MT4-CCR5-Luc cells are resistant, whereas PM1-CCR5-Luc cells are susceptible, to killing by a natural killer cell line, CD16+KHYG-1, in the absence of antibody. Polyclonal HIVIG gave similar ADCC estimates against HIV-1 isolate, NL4-3, regardless of which of the three cell lines were used as the targets. In contrast to CEM.NKr-CCR5-Luc and PM1-CCR5-Luc, however, MT4-CCR5-Luc target cells produce significantly higher luciferase after exposure to various HIV-1 strains, including transmitted founder variants and viruses incorporating specific envelopes of interest. This higher luciferase expression does not yield spurious results because ADCC estimates are similar when killing is assessed by both reporter protein expression and flow cytometry. Furthermore, ADCC estimates derived from MT4-CCR5-Luc cells are not skewed by non-antibody contents present in human plasma. In aggregate, the MT4-CCR5-Luc cell line can be used to estimate monoclonal antibody or plasma-induced ADCC responses against a diverse range of HIV-1 envelopes relevant for transmission and disease progression studies. Unlabelled Image • New cell line, MT4-CCR5-Luc, is naturally resistant to CD16+KHYG-1 killing in the absence of antibody. • MT4-CCR5-Luc induce high luciferase expression after exposure to a broad range of HIV-1 variants. • ADCC is similar when estimated from either luciferase reduction or decrease in live infected cells as assessed by flow cytometry. • MT4-CCR5-Luc cells allow for estimation of ADCC against viruses with primary envelopes of interest with luciferase readout. [ABSTRACT FROM AUTHOR]
- Published
- 2020
- Full Text
- View/download PDF
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