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1.
Parasit Vectors ; 16(1): 295, 2023 Aug 24.
Article in English | MEDLINE | ID: mdl-37620979

ABSTRACT

BACKGROUND: The Coronavirus disease 2019 (COVID-19) pandemic was marked by an increase in diagnosis and treatment delays for a range of medical conditions. Yet the impact of the pandemic on the management of tick-borne diseases, which frequently manifest as an acute febrile illness similar to COVID-19, has not been well described. METHODS: In this retrospective cohort study of patients with suspected tick-borne disease attending the University of North Carolina Health facilities, we compared the timeliness of diagnosis and treatment in a "pre-COVID" period (March 2019 to February 2020) and a "post-COVID" period (March 2020 to February 2021). Participants included patients with an ICD-10 diagnosis code of spotted fever group rickettsiosis or ehrlichiosis and a positive Rickettsia rickettsii or Ehrlichia indirect immunofluorescence assay immunoglobulin G antibody test result. Of the 897 patients who had an eligible diagnosis, 240 (26.8%) met the inclusion criteria. The main outcome was time from initial presentation to definitive diagnosis and treatment. RESULTS: During the 2-year study period, 126 (52.5%) patients were grouped in the pre-COVID period and 114 (47.5%) were grouped in the post-COVID period; 120 (50.0%) were female; and 139 (57.9%) were aged > 50 years. Comparing the post-COVID to the pre-COVID period, the adjusted odds ratio (aOR) for delay in treatment > 0 days was 1.81 (95% confidence interval [CI] 1.07-3.07, P = 0.03), and for a treatment delay > 7 days, 1.65 (95% CI 0.94-2.90, P = 0.08). The odds of a delay in diagnosis were similar for patients in the post- and pre-COVID periods, with an aOR of 1.61 (95% CI 0.96-2.72, P = 0.07) for delays > 0 days, and aOR of 1.72 (95% CI 0.99-3.00, P = 0.05) for delays > 7 days. CONCLUSIONS: The odds of a delay in treatment > 0 days were significantly higher in the post-COVID period than in the pre-COVID period. However, the odds of a delay in treatment > 7 days, or a delay in diagnosis, were similar between these two periods. Shifts in care-seeking, alternative care delivery models and prioritization of COVID-19 may contribute to diminished timeliness of treatment for patients with tick-borne diseases.


Subject(s)
COVID-19 , Ehrlichiosis , Tick-Borne Diseases , Humans , Female , Male , Pandemics , Retrospective Studies , COVID-19/diagnosis , COVID-19/epidemiology , Tick-Borne Diseases/diagnosis , Tick-Borne Diseases/drug therapy , Tick-Borne Diseases/epidemiology , COVID-19 Testing
2.
N C Med J ; 83(5): 322-326, 2022.
Article in English | MEDLINE | ID: mdl-37158555

ABSTRACT

Social vulnerabilities affect life expectancy across North Carolina. From 2018 to 2020, we observed that counties with low life expectancy had higher Social Vulnerability Index (SVI) scores. Counties with low SVI scores had higher life expectancy compared to sister counties with higher SVI scores.


Subject(s)
Life Expectancy , Social Vulnerability , Humans , North Carolina/epidemiology
3.
Sci Rep ; 10(1): 4196, 2020 03 06.
Article in English | MEDLINE | ID: mdl-32144374

ABSTRACT

Tail Tubular Protein A (TTPA) was long thought to be strictly a structural protein of environmental bacteriophages. However, our recent work has suggested that some TTPAs have additional functional features and thus are dual-function proteins. This study introduces a new TTPA family member, TTPAgp11, which belongs to Yersinia phage phiYeO3-12. We cloned the gene, expressed it and then purified the phage protein. The protein, including its hydrolytic activity, was characterized. Our enzymatic activity tests showed that TTPAgp11 displayed hydrolytic activity towards Red-starch, suggesting that this enzyme could be classified as part as the α - 1, 4-glucosidase family. Protein folding and aggregation tests indicated that TTPAgp11 is a single-domain protein whose aggregation can be induced by maltose or N-acetylglucosamine. The spatial structure of TTPAgp11 seemed to resemble that of the first reported dual-function TTPA, TTPAgp31, which was isolated from Klebsiella pneumoniae phage 32.


Subject(s)
Viral Proteins/chemistry , Viral Proteins/metabolism , Amino Acid Sequence , Bacteriophages/genetics , Genome, Viral/genetics , Hydrolysis , Molecular Sequence Data , Viral Proteins/genetics
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