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Epidemiology of Human Seasonal Coronaviruses Among People With Mild and Severe Acute Respiratory Illness in Blantyre, Malawi, 2011-2017

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Epidemiology of Human Seasonal Coronaviruses Among People With Mild and Severe Acute Respiratory Illness in Blantyre, Malawi, 2011-2017. / Kovacs, Dory; Mambule, Ivan; Read, Jonathan M et al.
In: The Journal of infectious diseases, 14.02.2024.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Kovacs, D, Mambule, I, Read, JM, Kiran, A, Chilombe, M, Bvumbwe, T, Aston, S, Menyere, M, Masina, M, Kamzati, M, Ganiza, TN, Iuliano, D, McMorrow, M, Bar-Zeev, N, Everett, D, French, N & Ho, A 2024, 'Epidemiology of Human Seasonal Coronaviruses Among People With Mild and Severe Acute Respiratory Illness in Blantyre, Malawi, 2011-2017', The Journal of infectious diseases. https://doi.org/10.1093/infdis/jiad587

APA

Kovacs, D., Mambule, I., Read, J. M., Kiran, A., Chilombe, M., Bvumbwe, T., Aston, S., Menyere, M., Masina, M., Kamzati, M., Ganiza, T. N., Iuliano, D., McMorrow, M., Bar-Zeev, N., Everett, D., French, N., & Ho, A. (2024). Epidemiology of Human Seasonal Coronaviruses Among People With Mild and Severe Acute Respiratory Illness in Blantyre, Malawi, 2011-2017. The Journal of infectious diseases. Advance online publication. https://doi.org/10.1093/infdis/jiad587

Vancouver

Kovacs D, Mambule I, Read JM, Kiran A, Chilombe M, Bvumbwe T et al. Epidemiology of Human Seasonal Coronaviruses Among People With Mild and Severe Acute Respiratory Illness in Blantyre, Malawi, 2011-2017. The Journal of infectious diseases. 2024 Feb 14. Epub 2024 Feb 14. doi: 10.1093/infdis/jiad587

Author

Bibtex

@article{6a4b4d07bdec43288eb2941a6b07a0c4,
title = "Epidemiology of Human Seasonal Coronaviruses Among People With Mild and Severe Acute Respiratory Illness in Blantyre, Malawi, 2011-2017",
abstract = "The aim of this study was to characterize the epidemiology of human seasonal coronaviruses (HCoVs) in southern Malawi. We tested for HCoVs 229E, OC43, NL63, and HKU1 using real-time polymerase chain reaction (PCR) on upper respiratory specimens from asymptomatic controls and individuals of all ages recruited through severe acute respiratory illness (SARI) surveillance at Queen Elizabeth Central Hospital, Blantyre, and a prospective influenza-like illness (ILI) observational study between 2011 and 2017. We modeled the probability of having a positive PCR for each HCoV using negative binomial models, and calculated pathogen-attributable fractions (PAFs). Overall, 8.8% (539/6107) of specimens were positive for ≥1 HCoV. OC43 was the most frequently detected HCoV (3.1% [191/6107]). NL63 was more frequently detected in ILI patients (adjusted incidence rate ratio [aIRR], 9.60 [95% confidence interval {CI}, 3.25-28.30]), while 229E (aIRR, 8.99 [95% CI, 1.81-44.70]) was more frequent in SARI patients than asymptomatic controls. In adults, 229E and OC43 were associated with SARI (PAF, 86.5% and 89.4%, respectively), while NL63 was associated with ILI (PAF, 85.1%). The prevalence of HCoVs was similar between children with SARI and controls. All HCoVs had bimodal peaks but distinct seasonality. OC43 was the most prevalent HCoV in acute respiratory illness of all ages. Individual HCoVs had distinct seasonality that differed from temperate settings. ",
keywords = "severe acute respiratory illness, human, seasonal coronavirus, Malawi, pathogen-attributable fraction",
author = "Dory Kovacs and Ivan Mambule and Read, {Jonathan M} and Anmol Kiran and Moses Chilombe and Thandiwe Bvumbwe and Stephen Aston and Mavis Menyere and Mazuba Masina and Moses Kamzati and Ganiza, {Thokozani Namale} and Danielle Iuliano and Meredith McMorrow and Naor Bar-Zeev and Dean Everett and Neil French and Antonia Ho",
year = "2024",
month = feb,
day = "14",
doi = "10.1093/infdis/jiad587",
language = "English",
journal = "The Journal of infectious diseases",
issn = "0022-1899",
publisher = "Oxford University Press",

}

RIS

TY - JOUR

T1 - Epidemiology of Human Seasonal Coronaviruses Among People With Mild and Severe Acute Respiratory Illness in Blantyre, Malawi, 2011-2017

AU - Kovacs, Dory

AU - Mambule, Ivan

AU - Read, Jonathan M

AU - Kiran, Anmol

AU - Chilombe, Moses

AU - Bvumbwe, Thandiwe

AU - Aston, Stephen

AU - Menyere, Mavis

AU - Masina, Mazuba

AU - Kamzati, Moses

AU - Ganiza, Thokozani Namale

AU - Iuliano, Danielle

AU - McMorrow, Meredith

AU - Bar-Zeev, Naor

AU - Everett, Dean

AU - French, Neil

AU - Ho, Antonia

PY - 2024/2/14

Y1 - 2024/2/14

N2 - The aim of this study was to characterize the epidemiology of human seasonal coronaviruses (HCoVs) in southern Malawi. We tested for HCoVs 229E, OC43, NL63, and HKU1 using real-time polymerase chain reaction (PCR) on upper respiratory specimens from asymptomatic controls and individuals of all ages recruited through severe acute respiratory illness (SARI) surveillance at Queen Elizabeth Central Hospital, Blantyre, and a prospective influenza-like illness (ILI) observational study between 2011 and 2017. We modeled the probability of having a positive PCR for each HCoV using negative binomial models, and calculated pathogen-attributable fractions (PAFs). Overall, 8.8% (539/6107) of specimens were positive for ≥1 HCoV. OC43 was the most frequently detected HCoV (3.1% [191/6107]). NL63 was more frequently detected in ILI patients (adjusted incidence rate ratio [aIRR], 9.60 [95% confidence interval {CI}, 3.25-28.30]), while 229E (aIRR, 8.99 [95% CI, 1.81-44.70]) was more frequent in SARI patients than asymptomatic controls. In adults, 229E and OC43 were associated with SARI (PAF, 86.5% and 89.4%, respectively), while NL63 was associated with ILI (PAF, 85.1%). The prevalence of HCoVs was similar between children with SARI and controls. All HCoVs had bimodal peaks but distinct seasonality. OC43 was the most prevalent HCoV in acute respiratory illness of all ages. Individual HCoVs had distinct seasonality that differed from temperate settings.

AB - The aim of this study was to characterize the epidemiology of human seasonal coronaviruses (HCoVs) in southern Malawi. We tested for HCoVs 229E, OC43, NL63, and HKU1 using real-time polymerase chain reaction (PCR) on upper respiratory specimens from asymptomatic controls and individuals of all ages recruited through severe acute respiratory illness (SARI) surveillance at Queen Elizabeth Central Hospital, Blantyre, and a prospective influenza-like illness (ILI) observational study between 2011 and 2017. We modeled the probability of having a positive PCR for each HCoV using negative binomial models, and calculated pathogen-attributable fractions (PAFs). Overall, 8.8% (539/6107) of specimens were positive for ≥1 HCoV. OC43 was the most frequently detected HCoV (3.1% [191/6107]). NL63 was more frequently detected in ILI patients (adjusted incidence rate ratio [aIRR], 9.60 [95% confidence interval {CI}, 3.25-28.30]), while 229E (aIRR, 8.99 [95% CI, 1.81-44.70]) was more frequent in SARI patients than asymptomatic controls. In adults, 229E and OC43 were associated with SARI (PAF, 86.5% and 89.4%, respectively), while NL63 was associated with ILI (PAF, 85.1%). The prevalence of HCoVs was similar between children with SARI and controls. All HCoVs had bimodal peaks but distinct seasonality. OC43 was the most prevalent HCoV in acute respiratory illness of all ages. Individual HCoVs had distinct seasonality that differed from temperate settings.

KW - severe acute respiratory illness

KW - human

KW - seasonal coronavirus

KW - Malawi

KW - pathogen-attributable fraction

U2 - 10.1093/infdis/jiad587

DO - 10.1093/infdis/jiad587

M3 - Journal article

C2 - 38365443

JO - The Journal of infectious diseases

JF - The Journal of infectious diseases

SN - 0022-1899

ER -