Jamie Fraser
Uniformed Services University of the Health Sciences
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American Journal of Tropical Medicine and Hygiene | 2017
David A. Lindholm; Todd Myers; Susana Widjaja; Edward Grant; Kalyani Telu; Tahaniyat Lalani; Jamie Fraser; Mary P. Fairchok; Anuradha Ganesan; Mark D. Johnson; Anjali N. Kunz; David R. Tribble; Heather C. Yun
AbstractTravelers are at risk for arbovirus infection. We prospectively enrolled 267 Department of Defense beneficiaries traveling to chikungunya-outbreak regions in the Americas between December 2013 and May 2015 and assessed travel characteristics and serologic exposure to chikungunya virus (CHIKV) and dengue virus (DENV). Ten ill-returning travelers were also assessed retrospectively. Self-reported mosquito exposure was common (64% of 198 evaluable travelers saw mosquitoes; 53% of 201 reported ≥ 1 bite). Increased exposure was associated with active-duty travelers (odds ratio [OR] = 2.6 [1.3-5.4] for seeing mosquitoes) or travelers visiting friends and relatives (VFR) (OR = 3.5 [1.0-10.0] for high-intensity bite exposure). Arbovirus infection was defined as seroconversion on plaque reduction neutralization testing (PRNT) of pre- and posttravel sera. For ill subjects enrolled posttravel, infection was defined by a positive convalescent PRNT and/or a positive reverse transcription polymerase chain reaction for CHIKV or DENV. We identified seven cases of arbovirus infection: four with CHIKV, five with DENV, and two with both. The composite attack rate for CHIKV and DENV infection was 3.7% of 108 evaluable, immunologically naïve, prospectively assessed travelers; there was serologic and/or polymerase chain reaction evidence of arbovirus infection in three of four evaluable (three of 10 total) ill-returning travelers. We identified both symptomatic and asymptomatic cases. Military purpose of travel and VFR travel accounted for five of seven cases. Pretravel counseling is important and should target higher risk groups. Given a shared vector between CHIKV, DENV, and Zika virus (ZIKV), this study can also help guide counseling for travelers to ZIKV-outbreak regions.
Military Medicine | 2016
Jennifer A. Curry; Jason D. Maguire; Jamie Fraser; David R. Tribble; Robert Deiss; Coleman Bryan; Michele D. Tisdale; Katrina Crawford; Michael W. Ellis; Tahaniyat Lalani
Staphylococcal skin and soft tissue infections (SSTIs), especially those due to methicillin-resistant Staphylococcus aureus (MRSA) are an important public health issue for the military. Limited data exist regarding the prevalence of S. aureus colonization in the shipboard setting. We conducted a cross-sectional, observational study to determine the point prevalence of S. aureus colonization among military personnel onboard a naval vessel. Asymptomatic active duty personnel completed a survey for risk factors associated with colonization and SSTIs. Culture specimens were obtained from the anterior nares, pharynx, groin, and perirectal regions. MRSA isolates underwent testing for antimicrobial resistance, virulence factors, and pulsed-field type. 400 individuals were enrolled, 198 (49.5%) of whom were colonized with S. aureus, with MRSA identified in 14 participants (3.5%). No significant risk factors were associated with MRSA colonization. USA800 was the most common colonizing MRSA strain in the cohort and was detected in 10 participants (71%). Two participants (14%) were colonized with USA300 MRSA. In this first report of S. aureus epidemiology in a shipboard setting, we observed high rates of S. aureus and MRSA colonization. Longitudinal studies are needed to document the incident rates of S. aureus colonization during shipboard deployment and its impact on SSTI risk.
PLOS ONE | 2018
Tahaniyat Lalani; Michele D. Tisdale; Jie Liu; Indrani Mitra; Cliff Philip; Elizabeth Odundo; Faviola Reyes; Mark P. Simons; Jamie Fraser; Emma Hutley; Patrick M. O’Connor; Brett E. Swierczewski; Eric R. Houpt; David R. Tribble; Mark S. Riddle
The use of Polymerase Chain Reaction (PCR) assays for pathogen detection in travelers’ diarrhea (TD) field studies is limited by the on-site processing and storage requirements for fecal specimens. The objectives of this investigation were to i) characterize the pathogen distribution in deployed military personnel with TD using the TaqMan® Array Card PCR (TAC) on frozen stool and diarrheal smears on Whatman FTA Elute cards (FTA cards), and to ii) compare TAC detection of enteropathogen targets using smeared FTA cards and frozen stool, using TAC on frozen stool as the ‘reference standard’. Stool samples, obtained from active duty personnel with acute TD enrolled in a field trial, were smeared onto FTA cards and stored at room temperature. A corresponding aliquot of stool was frozen in a cryovial. FTA cards and frozen stool samples were tested at a central lab, using a customized TAC for detection of TD pathogens. 187 paired frozen stool samples and smeared FTA cards were stored for a median of 712 days (IQR 396–750) before testing. Overall detection rates were 78.6% for frozen stool and 73.2% for FTA cards. Diarrheagenic Escherichia coli were the most common bacteria identified. Using the TAC results on frozen stool as the reference, the overall sensitivity and specificity of TAC on FTA cards was 72.9% and 98.0% respectively. TAC on FTA cards demonstrated a decrease in sensitivity with increasing frozen stool quantification cycle (Cq) (90.0% in FTA cards with a corresponding frozen stool Cq < 30, and 72.9% in samples with a corresponding frozen stool Cq < 35). Our findings support the use and further development of FTA cards in combination with a quantitative PCR assay for enteropathogen detection in TD field studies.
American Journal of Tropical Medicine and Hygiene | 2018
Stuart Wood; Mary P. Fairchok; Heather C. Yun; Anjali Kunz; Mark Johnson; Elizabeth Schnaubelt; Jamie Fraser; Ryan C. Maves; Tahaniyat Lalani; Kalyani Telu; Anuradha Ganesan; Indrani Mitra; David R. Tribble
Travelers to developing regions are at risk for development of influenza-like illness (ILI). Little is known of traveler and trip characteristics associated with the development of ILI. TravMil is a prospective observational study, enrolling subjects presenting to six military travel clinics or predeployment-screening sites. We analyzed pre- and post-travel surveys from travelers visiting regions outside of the continental United States, Western or Northern Europe, Canada, Australia, or New Zealand between January 2010 and March 2016. Influenza-like illness was defined as a self-reported fever associated with either sore throat or cough. Trip and traveler characteristics were analyzed to determine risk factors for the development of ILI. Two thousand nine hundred and thirty-two trips were recorded (55% male, median age 45 years, 69% white, 51% on vacation, median travel duration 17 days). The 2,337 trips included the number of self-reported influenza vaccinations in the preceding 5 years (median 5). Eleven percent of the trips were complicated by an ILI lasting a median of 5 days; 70% and 17% of these reported upper and lower respiratory tract infection, respectively, and 12% reported both. On multivariate analysis, increased risk of ILI was associated with female gender (odds ratio [OR]: 1.60 [confidence interval (CI): 1.25-2.05], P < 0.01), age (years) (OR: 1.01 [CI: 1.01-1.02], P < 0.01); and duration of travel (days) (OR: 1.01 [CI: 1.00-1.01], P < 0.01). Influenza-like illness is common in travelers, regardless of traveler characteristics, purpose of travel, destination, or season of year. Female gender, older age, and longer duration of travel were associated with an increased risk of ILI. Additional tools and strategies are needed to prevent ILI in international travelers.
Journal of Travel Medicine | 2015
Tahaniyat Lalani; Jason Maguire; Edward Grant; Jamie Fraser; Anuradha Ganesan; Mark D. Johnson; Robert Deiss; Mark S. Riddle; Timothy H. Burgess; David R. Tribble
Journal of Travel Medicine | 2016
Tahaniyat Lalani; Heather C. Yun; David R. Tribble; Anuradha Ganesan; Anjali Kunz; Mary P. Fairchok; Elizabeth Schnaubelt; Jamie Fraser; Indrani Mitra; Karl Kronmann; Timothy Burgess; Robert Deiss; Mark S. Riddle; Mark D. Johnson
Military Medicine | 2017
Mark S. Riddle; Gregory J. Martin; Clinton K. Murray; Timothy Burgess; Patrick Connor; James D. Mancuso; Elizabeth R. Schnaubelt; Timothy P. Ballard; Jamie Fraser; David R. Tribble
Clinical Infectious Diseases | 2017
Mark S. Riddle; Patrick Connor; Jamie Fraser; Chad K. Porter; Brett Swierczewski; Emma Hutley; Brook Danboise; Mark P. Simons; Christine Hulseberg; Tahaniyat Lalani; Ramiro L. Gutierrez; David R. Tribble; Matthew Adam; Ernest Akorli; Rachael Armstrong; Lucy Ashford-Brown; Jaime Alvarado; Ricardo Aviles; Charlotte Ayres; Timothy Ballard; Liam Barry; Catherine Berjohn; Robert Bjoraker; Peter Blenkinsop; Jason Blitz; Jeromy Boucher; Timothy Burgess; Daniel Burns; Jenna Burns; Shauna Butler
Open Forum Infectious Diseases | 2016
Stuart Wood; Kalyani Telu; David R. Tribble; Anuradha Ganesan; Anjali N. Kunz; Mary Fairchok; Elizabeth Schnaubelt; Jamie Fraser; Indrani Mitra; Mark D. Johnson; Tahaniyat Lalani; Heather C. Yun
Open Forum Infectious Diseases | 2016
Jack N. Hutter; Tahaniyat Lalani; Heather C. Yun; David R. Tribble; Anjali Kunz; Mary P. Fairchok; Elizabeth Schnaubelt; Jamie Fraser; Indrani Mitra; Timothy Burgess; Mark S. Riddle; Mark Johnson; Anuradha Ganesan