Last data update: Mar 21, 2025. (Total: 48935 publications since 2009)
Records 1-4 (of 4 Records) |
Query Trace: Marinova-Petkova A[original query] |
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Melioidosis in a resident of Texas with no recent travel history, United States
Cossaboom CM , Marinova-Petkova A , Strysko J , Rodriguez G , Maness T , Ocampo J , Gee JE , Elrod MG , Gulvik CA , Liu L , Bower WA , Hoffmaster AR , Blaney DD , Salzer JS , Yoder JS , Mattioli MC , Sidwa TJ , Ringsdorf L , Morrow G , Ledezma E , Kieffer A . Emerg Infect Dis 2020 26 (6) 1295-1299 To our knowledge, environmental isolation of Burkholderia pseudomallei, the causative agent of melioidosis, from the continental United States has not been reported. We report a case of melioidosis in a Texas resident. Genomic analysis indicated that the isolate groups with B. pseudomallei isolates from patients in the same region, suggesting possible endemicity to this region. |
First reported human cases of leptospirosis in the United States Virgin Islands in the aftermath of Hurricanes Irma and Maria, September-November 2017
Marinova-Petkova A , Guendel I , Strysko JP , Ekpo LL , Galloway R , Yoder J , Kahler A , Artus A , Hoffmaster AR , Bower WA , Walke H , Ellis BR , Hunte-Ceasar T , Ellis EM , Schafer IJ . Open Forum Infect Dis 2019 6 (7) ofz261 Objective: Following Hurricanes Irma and Maria, the first case of human leptospirosis ever identified in the US Virgin Islands (USVI) was reported to the Virgin Islands Department of Health. Leptospirosis is a potentially fatal bacterial disease caused by Leptospira species found in animal urine and urine-contaminated water and soil. Outbreaks can occur following extreme weather events. Method: Additional cases of leptospirosis were identified in the 2.5 months post-hurricanes by reviewing emergency department (ED) records from territorial hospitals for patients demonstrating leptospirosis-consistent symptoms, testing symptomatic patients previously enrolled in the USVI arbovirus surveillance system (VIASS), and adding leptospirosis testing prospectively to VIASS. Available patient sera underwent local rapid diagnostic testing for anti-Leptospira IgM followed by confirmatory microscopic agglutination testing at the US Centers for Disease Control and Prevention. Water was collected from cisterns with epidemiologic links to confirmed cases and tested by real-time PCR (qPCR) for pathogenic Leptospira spp. Results: Sixteen retrospectively identified symptomatic patients were enrolled in VIASS; 15 with available samples tested negative. Based on review of 5226 ED charts, 6 patients were further investigated; of these, 5 were tested of which 1 was positive. Prospective leptospirosis surveillance tested 57 additional patients; of these, 1 was positive. Water from 1 of 5 tested cisterns was found positive by qPCR. Conclusions: This investigation documents the first 3 cases of leptospirosis reported in the USVI and demonstrates how VIASS successfully was adapted to establish leptospirosis surveillance. Contaminated cistern water was identified as a potential source for Leptospira spp. transmission, highlighting the need for additional post-hurricane remediation and disinfection guidance. |
Comparison of nucleic acid extraction methods for next-generation sequencing of avian influenza A virus from ferret respiratory samples.
Di H , Thor S , Trujillo AA , Stark T , Marinova-Petkova A , Jones J , Wentworth DE , Barnes J , Davis CT . J Virol Methods 2019 270 95-105 ![]() ![]() Influenza A virus is a negative-sense RNA virus with a segmented genome consisting of eight RNA segments. Avian influenza A virus (AIV) primarily infects avian hosts and sporadically infects mammals, which can lead to adaptation to new species. Next-generation sequencing (NGS) of emerging AIV genomes extracted from respiratory samples collected on sequential days from animal models and clinical patients enables analysis of the emergence of evolutionary variants within the virus population over time. However, obtaining codon complete AIV genome at a sufficient coverage depth for nucleotide variant calling remains a challenge, especially from post-inoculation respiratory samples collected at late time points that have low viral titers. In this study, nasal wash samples from ferrets inoculated with different subtypes of AIV were collected on various days post-inoculation. Each nasal wash sample was aliquoted and extracted using five commercially available nucleic acid extraction methods. Extracted influenza virus RNA was amplified and NGS conducted using Illumina Mi-Seq. For each nasal wash sample, completeness of AIV genome segments and coverage depth were compared among five extraction methods. Nucleic acids extracted by MagNA pure compact RNA isolation consistently yielded codon complete sequences for all eight genome segments at the required coverage depth at each time point sampled. The study revealed that DNase treatment was critical to the amplification of influenza genome segments and the downstream success of codon complete NGS from nasal wash samples. The findings from this study can be applied to improve NGS of influenza and other RNA viruses that infect the respiratory tract and are collected from respiratory samples. |
Avian influenza A(H7N2) virus in human exposed to sick cats, New York, USA, 2016
Marinova-Petkova A , Laplante J , Jang Y , Lynch B , Zanders N , Rodriguez M , Jones J , Thor S , Hodges E , De La Cruz JA , Belser J , Yang H , Carney P , Shu B , Berman L , Stark T , Barnes J , Havers F , Yang P , Trock SC , Fry A , Gubareva L , Bresee JS , Stevens J , Daskalakis D , Liu D , Lee CT , Torchetti MK , Newbury S , Cigel F , Toohey-Kurth K , St George K , Wentworth DE , Lindstrom S , Davis CT . Emerg Infect Dis 2017 23 (12) 2046-9 An outbreak of influenza A(H7N2) virus in cats in a shelter in New York, NY, USA, resulted in zoonotic transmission. Virus isolated from the infected human was closely related to virus isolated from a cat; both were related to low pathogenicity avian influenza A(H7N2) viruses detected in the United States during the early 2000s. |
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