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1.
Nat Commun ; 13(1): 3215, 2022 06 09.
Article in English | MEDLINE | ID: mdl-35680857

ABSTRACT

The effectiveness of the inactivated BBIBP-CorV vaccine against severe COVID-19 outcomes (hospitalization, critical care admission and death due to COVID-19) and its long-term effectiveness have not been well characterized among the general population. We conducted a retrospective cohort study using electronic health records of 3,147,869 adults, of which 1,099,886 vaccinated individuals were matched, in a 1:1 ratio to 1,099,886 unvaccinated persons. A Cox-proportional hazard model with time varying coefficients was used to assess the vaccine effectiveness adjusting for age, sex, comorbidity, ethnicity, and the calendar month of entry into the study. Our analysis showed that the effectiveness was 79.6% (95% CI, 77.7 to 81.3) against hospitalization, 86% (95% CI, 82.2 to 89.0) against critical care admission, and 84.1% (95% CI, 70.8 to 91.3) against death due to COVID-19. The effectiveness against these severe outcomes declined over time indicating the need for booster doses to increase protection against severe COVID-19 outcomes.


Subject(s)
COVID-19 , Adult , COVID-19/epidemiology , COVID-19/prevention & control , Humans , Retrospective Studies , United Arab Emirates/epidemiology
2.
Sci Rep ; 12(1): 490, 2022 01 11.
Article in English | MEDLINE | ID: mdl-35017530

ABSTRACT

Based on the findings from the Phase III clinical trials of inactivated SARS COV-2 Vaccine, (BBIBP-CORV) emergency use authorization (EUA) was granted for the vaccine to frontline workers in the UAE. A prospective cohort study was conducted among frontline workers to estimate the incidence rate and risk of symptomatic COVID-19 infection 14 days after the second dose of inoculation with BBIBP-CORV inactivated vaccine. Those who received two doses of the BBIBP-CORV vaccine in the period from 14th of September 2020 (first dose) to 21st of December 2020 (second dose) were followed up for COVID-19 infections. 11,322 individuals who received the two-dose BBIBP-CORV vaccine were included and were followed up post the second dose plus fourteen days. The incidence rate of symptomatic infection was 0.08 per 1000-person days (95% CI 0.07, 0.10). The estimated absolute risk of developing symptomatic infection was 0.97% (95% CI 0.77%, 1.17%). The confirmed seroconversion rate was 92.8%. There were no serious adverse events reported and no individuals suffered from severe disease. Our findings show that vaccinated individuals are likely to remain protected against symptomatic infection or becoming PCR positive for SARS COV 2 following the second dose of the vaccination.


Subject(s)
COVID-19 Vaccines/administration & dosage , COVID-19/diagnosis , Vaccines, Inactivated/administration & dosage , Adult , COVID-19/epidemiology , COVID-19/virology , COVID-19 Vaccines/adverse effects , Clinical Trials, Phase III as Topic , Female , Follow-Up Studies , Headache/etiology , Health Personnel , Humans , Incidence , Male , Middle Aged , Prospective Studies , SARS-CoV-2/genetics , SARS-CoV-2/isolation & purification , United Arab Emirates/epidemiology , Vaccines, Inactivated/adverse effects
4.
Sci Rep ; 11(1): 13971, 2021 07 07.
Article in English | MEDLINE | ID: mdl-34234167

ABSTRACT

To unravel the source of SARS-CoV-2 introduction and the pattern of its spreading and evolution in the United Arab Emirates, we conducted meta-transcriptome sequencing of 1067 nasopharyngeal swab samples collected between May 9th and Jun 29th, 2020 during the first peak of the local COVID-19 epidemic. We identified global clade distribution and eleven novel genetic variants that were almost absent in the rest of the world and that defined five subclades specific to the UAE viral population. Cross-settlement human-to-human transmission was related to the local business activity. Perhaps surprisingly, at least 5% of the population were co-infected by SARS-CoV-2 of multiple clades within the same host. We also discovered an enrichment of cytosine-to-uracil mutation among the viral population collected from the nasopharynx, that is different from the adenosine-to-inosine change previously reported in the bronchoalveolar lavage fluid samples and a previously unidentified upregulation of APOBEC4 expression in nasopharynx among infected patients, indicating the innate immune host response mediated by ADAR and APOBEC gene families could be tissue-specific. The genomic epidemiological and molecular biological knowledge reported here provides new insights for the SARS-CoV-2 evolution and transmission and points out future direction on host-pathogen interaction investigation.


Subject(s)
COVID-19/epidemiology , COVID-19/immunology , Coinfection/epidemiology , Genomics , Immunity, Innate , Mutation , SARS-CoV-2/genetics , Adult , COVID-19/transmission , Cytidine Deaminase/genetics , Female , Gene Expression Profiling , Genome, Viral/genetics , Humans , Male , Middle Aged , Nasopharynx/virology , Organ Specificity , SARS-CoV-2/immunology
5.
Clin Infect Dis ; 68(3): 409-418, 2019 01 18.
Article in English | MEDLINE | ID: mdl-29905769

ABSTRACT

Background: Although there is evidence of person-to-person transmission of Middle East respiratory syndrome coronavirus (MERS-CoV) in household and healthcare settings, more data are needed to describe and better understand the risk factors and transmission routes in both settings, as well as the extent to which disease severity affects transmission. Methods: A seroepidemiological investigation was conducted among MERS-CoV case patients (cases) and their household contacts to investigate transmission risk in Abu Dhabi, United Arab Emirates. Cases diagnosed between 1 January 2013 and 9 May 2014 and their household contacts were approached for enrollment. Demographic, clinical, and exposure history data were collected. Sera were screened by MERS-CoV nucleocapsid protein enzyme-linked immunosorbent assay and indirect immunofluorescence, with results confirmed by microneutralization assay. Results: Thirty-one of 34 (91%) case patients were asymptomatic or mildly symptomatic and did not require oxygen during hospitalization. MERS-CoV antibodies were detected in 13 of 24 (54%) case patients with available sera, including 1 severely symptomatic, 9 mildly symptomatic, and 3 asymptomatic case patients. No serologic evidence of MERS-CoV transmission was found among 105 household contacts with available sera. Conclusions: Transmission of MERS-CoV was not documented in this investigation of mostly asymptomatic and mildly symptomatic cases and their household contacts. These results have implications for clinical management of cases and formulation of isolation policies to reduce the risk of transmission.


Subject(s)
Antibodies, Viral/blood , Coronavirus Infections/epidemiology , Coronavirus Infections/transmission , Disease Transmission, Infectious , Middle East Respiratory Syndrome Coronavirus/immunology , Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Coronavirus Infections/immunology , Enzyme-Linked Immunosorbent Assay , Family Health , Female , Fluorescent Antibody Technique, Indirect , Humans , Infant , Infant, Newborn , Male , Middle Aged , Risk Factors , Seroepidemiologic Studies , United Arab Emirates/epidemiology , Young Adult
6.
Emerg Microbes Infect ; 6(11): e101, 2017 Nov 08.
Article in English | MEDLINE | ID: mdl-29116217

ABSTRACT

Middle East respiratory syndrome coronavirus (MERS-CoV) was identified on the Arabian Peninsula in 2012 and is still causing cases and outbreaks in the Middle East. When MERS-CoV was first identified, the closest related virus was in bats; however, it has since been recognized that dromedary camels serve as a virus reservoir and potential source for human infections. A total of 376 camels were screened for MERS-Cov at a live animal market in the Eastern Region of the Emirate of Abu Dhabi, UAE. In all, 109 MERS-CoV-positive camels were detected in week 1, and a subset of positive camels were sampled again weeks 3 through 6. A total of 126 full and 3 nearly full genomes were obtained from 139 samples. Spike gene sequences were obtained from 5 of the 10 remaining samples. The camel MERS-CoV genomes from this study represent 3 known and 2 potentially new lineages within clade B. Within lineages, diversity of camel and human MERS-CoV sequences are intermixed. We identified sequences from market camels nearly identical to the previously reported 2015 German case who visited the market during his incubation period. We described 10 recombination events in the camel samples. The most frequent recombination breakpoint was the junctions between ORF1b and S. Evidence suggests MERS-CoV infection in humans results from continued introductions of distinct MERS-CoV lineages from camels. This hypothesis is supported by the camel MERS-CoV genomes sequenced in this study. Our study expands the known repertoire of camel MERS-CoVs circulating on the Arabian Peninsula.


Subject(s)
Camelus/virology , Genetic Variation , Middle East Respiratory Syndrome Coronavirus/classification , Middle East Respiratory Syndrome Coronavirus/genetics , Animals , Cluster Analysis , Female , Genome, Viral , Genotype , Male , Middle East Respiratory Syndrome Coronavirus/isolation & purification , Phylogeny , Recombination, Genetic , Sequence Analysis, DNA , Spike Glycoprotein, Coronavirus/genetics , United Arab Emirates
7.
Emerg Infect Dis ; 22(7): 1162-8, 2016 07.
Article in English | MEDLINE | ID: mdl-27314227

ABSTRACT

In January 2013, several months after Middle East respiratory syndrome coronavirus (MERS-CoV) was first identified in Saudi Arabia, Abu Dhabi, United Arab Emirates, began surveillance for MERS-CoV. We analyzed medical chart and laboratory data collected by the Health Authority-Abu Dhabi during January 2013-May 2014. Using real-time reverse transcription PCR, we tested respiratory tract samples for MERS-CoV and identified 65 case-patients. Of these patients, 23 (35%) were asymptomatic at the time of testing, and 4 (6%) showed positive test results for >3 weeks (1 had severe symptoms and 3 had mild symptoms). We also identified 6 clusters of MERS-CoV cases. This report highlights the potential for virus shedding by mildly ill and asymptomatic case-patients. These findings will be useful for MERS-CoV management and infection prevention strategies.


Subject(s)
Coronavirus Infections/epidemiology , Coronavirus Infections/virology , Middle East Respiratory Syndrome Coronavirus , Adult , Communicable Diseases, Emerging , Female , Humans , Male , Middle Aged , Retrospective Studies , United Arab Emirates/epidemiology , Young Adult
8.
Emerg Infect Dis ; 22(4): 647-56, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26981708

ABSTRACT

Middle East respiratory syndrome coronavirus (MERS-CoV) infections sharply increased in the Arabian Peninsula during spring 2014. In Abu Dhabi, United Arab Emirates, these infections occurred primarily among healthcare workers and patients. To identify and describe epidemiologic and clinical characteristics of persons with healthcare-associated infection, we reviewed laboratory-confirmed MERS-CoV cases reported to the Health Authority of Abu Dhabi during January 1, 2013-May 9, 2014. Of 65 case-patients identified with MERS-CoV infection, 27 (42%) had healthcare-associated cases. Epidemiologic and genetic sequencing findings suggest that 3 healthcare clusters of MERS-CoV infection occurred, including 1 that resulted in 20 infected persons in 1 hospital. MERS-CoV in healthcare settings spread predominantly before MERS-CoV infection was diagnosed, underscoring the importance of increasing awareness and infection control measures at first points of entry to healthcare facilities.


Subject(s)
Coronavirus Infections/transmission , Cross Infection/transmission , Hospitals , Middle East Respiratory Syndrome Coronavirus/genetics , Adult , Aged , Aged, 80 and over , Animals , Camelus/virology , Communicable Disease Control , Coronavirus Infections/epidemiology , Coronavirus Infections/virology , Cross Infection/epidemiology , Cross Infection/virology , Female , Health Personnel , Humans , Incidence , Male , Middle Aged , Middle East Respiratory Syndrome Coronavirus/classification , Middle East Respiratory Syndrome Coronavirus/isolation & purification , United Arab Emirates/epidemiology
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