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Article ; Online: Comparison of Captia

Wong, Ann H / Ho, Yolanda I I / Tang, Kevin P S / Lai, Raymond W M

Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology

2020 Volume 127, Page(s) 104342

Abstract: Background: Correlation of the assay cut-off values for Captia: Objective: The aim of this study was to compare the relative performance of the Captia: Study design: Correlation of the cut-off value of both assays with the immunoprotective level ... ...

Abstract	Background: Correlation of the assay cut-off values for Captia Objective: The aim of this study was to compare the relative performance of the Captia Study design: Correlation of the cut-off value of both assays with the immunoprotective level was determined with the 3rd WHO Measles IgG International Standard. One hundred clinical samples including frozen and fresh were tested with both assays. The positive percentage agreement (PPA) based on the manufacturers' interpretation and the WHO recommended immunoprotective level was compared. Results: Samples tested positive by the Captia Conclusions: Captia
MeSH term(s)	Antibodies, Viral/blood ; Humans ; Immunoassay/methods ; Immunoglobulin G/blood ; Measles/diagnosis ; Measles/immunology ; Measles virus/immunology ; Reagent Kits, Diagnostic ; Sensitivity and Specificity ; World Health Organization
Chemical Substances	Antibodies, Viral ; Immunoglobulin G ; Reagent Kits, Diagnostic
Language	English
Publishing date	2020-04-06
Publishing country	Netherlands
Document type	Comparative Study ; Journal Article
ZDB-ID	1446080-4
ISSN	1873-5967 ; 1386-6532
ISSN (online)	1873-5967
ISSN	1386-6532
DOI	10.1016/j.jcv.2020.104342
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Article ; Online: Comparison of the Cepheid Xpert Xpress Flu/RSV Assay to in-house Flu/RSV triplex real-time RT-PCR for rapid molecular detection of Influenza A, Influenza B and Respiratory Syncytial Virus in respiratory specimens.

Ho, Yolanda I I / Wong, Ann H / Lai, Raymond W M

Journal of medical microbiology

2018 Volume 67, Issue 11, Page(s) 1576–1580

Abstract: This study compared the performance of the commercially available Xpert Xpress Flu/RSV assay to an in-house FluAB/RSV triplex real-time RT-PCR assay for the detection of influenza A/B viruses and respiratory syncitial virus (RSV) from both nasopharyngeal ...

Abstract	This study compared the performance of the commercially available Xpert Xpress Flu/RSV assay to an in-house FluAB/RSV triplex real-time RT-PCR assay for the detection of influenza A/B viruses and respiratory syncitial virus (RSV) from both nasopharyngeal aspirate (NPA) and nasopharyngeal flocked swab (NPS). A total of 20 external quality assurance (EQA) samples and 172 clinical respiratory samples were tested prospectively using both the Xpert Xpress Flu/RSV assay and the in-house FluAB/RSV triplex assay. For the EQA samples, concordance rate was 100 % when tested with both assays. For clinical samples, there was 100 % agreement between the two assays for detection of influenza A and influenza B, 96.7 % agreement for detection of RSV and 99.7 % agreement for negative results. With a shortened turnaround time and good diagnostic performance, application of the Xpert Xpress Flu/RSV assay can facilitate patient triage for prompt implementation of infection control measures and management of high-risk patients during influenza epidemics.
MeSH term(s)	Biological Assay ; DNA Primers/genetics ; Humans ; Influenza A virus/genetics ; Influenza A virus/isolation & purification ; Influenza B virus/genetics ; Influenza B virus/isolation & purification ; Influenza, Human/diagnosis ; Influenza, Human/virology ; Molecular Diagnostic Techniques/instrumentation ; Molecular Diagnostic Techniques/methods ; Multiplex Polymerase Chain Reaction/methods ; Nasopharynx/virology ; Real-Time Polymerase Chain Reaction/instrumentation ; Real-Time Polymerase Chain Reaction/methods ; Respiratory Syncytial Virus Infections/diagnosis ; Respiratory Syncytial Virus Infections/virology ; Respiratory Syncytial Viruses/genetics ; Respiratory Syncytial Viruses/isolation & purification ; Sensitivity and Specificity
Chemical Substances	DNA Primers
Language	English
Publishing date	2018-09-12
Publishing country	England
Document type	Comparative Study ; Journal Article
ZDB-ID	218356-0
ISSN	1473-5644 ; 0022-2615
ISSN (online)	1473-5644
ISSN	0022-2615
DOI	10.1099/jmm.0.000841
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Article ; Online: Performance evaluation of the re-standardized Abbott Architect anti-HBs assay.

Wong, Ann H / Ho, Yolanda I I / Lai, Raymond W M

Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology

2018 Volume 111, Page(s) 1–3

Abstract: Background: As defined by World Health Organization (WHO), an antibody level of ≥ 10mIU/mL to hepatitis B virus confers protection. With the launching of Abbott anti-HBs assay re-standardized to the 2: Objectives: To evaluate the performance of the ... ...

Abstract	Background: As defined by World Health Organization (WHO), an antibody level of ≥ 10mIU/mL to hepatitis B virus confers protection. With the launching of Abbott anti-HBs assay re-standardized to the 2 Objectives: To evaluate the performance of the re-standardized Abbott Architect anti-HBs assay and to determine the impact of the upward shift. Study design: A total of 52 samples, including 12 external quality assurance programme samples and 40 clinical samples were tested with both the Abbott 1 Results: Verification of the re-standardized assay with the 2 Conclusions: Final interpretation of immune status to hepatitis B was not affected by the upward shift following introduction of the new Abbott anti-HBs assay except for previously negative samples with anti-HBs levels between >5.00 to <10.00 mIU/mL.
MeSH term(s)	Hepatitis B/diagnosis ; Hepatitis B Antibodies/blood ; Hepatitis B virus/immunology ; Humans ; Reagent Kits, Diagnostic/standards ; Reference Standards ; Serologic Tests/standards ; World Health Organization
Chemical Substances	Hepatitis B Antibodies ; Reagent Kits, Diagnostic
Language	English
Publishing date	2018-12-15
Publishing country	Netherlands
Document type	Evaluation Study ; Journal Article
ZDB-ID	1446080-4
ISSN	1873-5967 ; 1386-6532
ISSN (online)	1873-5967
ISSN	1386-6532
DOI	10.1016/j.jcv.2018.12.003
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Article ; Online: Comparison of three commercial SARS-CoV-2 assays for pooled testing of deep throat saliva for surveillance of patients attending general outpatient clinics.

Ho, Yolanda I / Wong, Ann H / Tang, Kevin P S / Wong, River C W / Leung, Eddie C M / Lai, Raymond W M

Journal of medical virology

2021 Volume 93, Issue 4, Page(s) 1917–1919

MeSH term(s)	COVID-19/diagnosis ; COVID-19 Nucleic Acid Testing ; Humans ; Nasopharynx/virology ; SARS-CoV-2/isolation & purification ; Saliva/virology ; Specimen Handling
Language	English
Publishing date	2021-01-11
Publishing country	United States
Document type	Comparative Study ; Letter
ZDB-ID	752392-0
ISSN	1096-9071 ; 0146-6615
ISSN (online)	1096-9071
ISSN	0146-6615
DOI	10.1002/jmv.26764
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Article ; Online: Rapid adaptation and continuous performance evaluation of SARS-CoV-2 envelope gene (E-gene) real-time RT-PCR assays to support the hospital surge in test demand.

Ho, Yolanda I I / Wong, Ann H / Leung, Eddie C M / Wong, River C W / Lai, Raymond W M

Journal of medical virology

2020 Volume 93, Issue 3, Page(s) 1824–1827

Abstract: We describe the timely adaption of both published WHO E-gene protocol and commercially available LightMix Modular E-gene assay to the test platform (ABI 7900 Fast real-time analyzer and TaqMan Fast One-step Virus Master Mix) available in an accredited ... ...

Abstract	We describe the timely adaption of both published WHO E-gene protocol and commercially available LightMix Modular E-gene assay to the test platform (ABI 7900 Fast real-time analyzer and TaqMan Fast One-step Virus Master Mix) available in an accredited tertiary hospital laboratory with an on-going evaluation to ensure the provision of quality service within the time constraint. The LightMix Modular E-gene was slightly more sensitive when compared to the WHO E-gene, both analytically and diagnostically. The assay was recommended for screening of SARS-CoV-2 infection. With the availability of technically competent staff through continuous training, the provision of round-the-clock service is feasible despite the test is of high complexity. The thermal cycling duration of the adapted LightMix E-gene and WHO E-gene is shortened by half and one hour respectively and allows the number of runs to double when 24-h round-the-clock service is provided. An increase in testing capacity could support surges in testing demand, which is essential to control the current SARS-CoV-2 pandemic, to prevent potential overwhelming of the healthcare system, and to optimize utilization of the isolation beds.
MeSH term(s)	COVID-19/diagnosis ; COVID-19/virology ; COVID-19 Testing/methods ; Clinical Laboratory Techniques/methods ; Coronavirus Envelope Proteins/genetics ; Genes, env/genetics ; Hospitals ; Humans ; Pandemics/prevention & control ; RNA, Viral/genetics ; Real-Time Polymerase Chain Reaction/methods ; Reverse Transcriptase Polymerase Chain Reaction/methods ; SARS-CoV-2/genetics ; Sensitivity and Specificity
Chemical Substances	Coronavirus Envelope Proteins ; RNA, Viral ; envelope protein, SARS-CoV-2
Keywords	covid19
Language	English
Publishing date	2020-11-22
Publishing country	United States
Document type	Journal Article
ZDB-ID	752392-0
ISSN	1096-9071 ; 0146-6615
ISSN (online)	1096-9071
ISSN	0146-6615
DOI	10.1002/jmv.26660
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Article ; Online: Higher Viral Load of Emerging Norovirus GII.P16-GII.2 than Pandemic GII.4 and Epidemic GII.17, Hong Kong, China.

Cheung, Sarah K C / Kwok, Kirsty / Zhang, Lin-Yao / Mohammad, Kirran N / Lui, Grace C Y / Lee, Nelson / Nelson, E Anthony S / Lai, Raymond W M / Leung, Ting F / Chan, Paul K S / Chan, Martin Chi-Wai

Emerging infectious diseases

2019 Volume 25, Issue 1, Page(s) 119–122

Abstract: We compared viral load of emerging recombinant norovirus GII.P16-GII.2 with those for pandemic GII.Pe-GII.4 and epidemic GII.P17-GII.17 genotypes among inpatients in Hong Kong. Viral load of GII.P16-GII.2 was higher than those for other genotypes in ... ...

Abstract	We compared viral load of emerging recombinant norovirus GII.P16-GII.2 with those for pandemic GII.Pe-GII.4 and epidemic GII.P17-GII.17 genotypes among inpatients in Hong Kong. Viral load of GII.P16-GII.2 was higher than those for other genotypes in different age groups. GII.P16-GII.2 is as replication competent as the pandemic genotype, explaining its high transmissibility and widespread circulation.
MeSH term(s)	Adolescent ; Adult ; Caliciviridae Infections/epidemiology ; Caliciviridae Infections/virology ; Child ; Child, Preschool ; Communicable Diseases, Emerging/epidemiology ; Communicable Diseases, Emerging/virology ; Female ; Gastroenteritis/epidemiology ; Gastroenteritis/virology ; Genotype ; Hong Kong/epidemiology ; Humans ; Infant ; Male ; Middle Aged ; Norovirus/genetics ; Pandemics ; Viral Load ; Young Adult
Language	English
Publishing date	2019-02-21
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	1380686-5
ISSN	1080-6059 ; 1080-6040
ISSN (online)	1080-6059
ISSN	1080-6040
DOI	10.3201/eid2501.180395
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Article ; Online: Bimodal Seasonality and Alternating Predominance of Norovirus GII.4 and Non-GII.4, Hong Kong, China, 2014-2017

Chan, Martin Chi-Wai / Kwok, Kirsty / Zhang, Lin-Yao / Mohammad, Kirran N / Lee, Nelson / Lui, Grace C Y / Nelson, E Anthony S / Lai, Raymond W M / Leung, Ting F / Chan, Paul K S

Emerging infectious diseases

2018 Volume 24, Issue 4

Abstract: We report emerging subtropical bimodal seasonality and alternating predominance of norovirus GII.4 and non-GII.4 genotypes in Hong Kong. GII.4 predominated in summer and autumn months and affected young children, whereas emergent non-GII.4 genotypes ... ...

Abstract	We report emerging subtropical bimodal seasonality and alternating predominance of norovirus GII.4 and non-GII.4 genotypes in Hong Kong. GII.4 predominated in summer and autumn months and affected young children, whereas emergent non-GII.4 genotypes predominated in winter months and affected all age groups. This highly dynamic epidemiology should inform vaccination strategies.
Language	English
Publishing date	2018-04-17
Publishing country	United States
Document type	Journal Article
ZDB-ID	1380686-5
ISSN	1080-6059 ; 1080-6040
ISSN (online)	1080-6059
ISSN	1080-6040
DOI	10.3201/eid2404.171791
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Article ; Online: Surveillance of antibiotic resistance among common Clostridium difficile ribotypes in Hong Kong.

Chow, Viola C Y / Kwong, Thomas N Y / So, Erica W M / Ho, Yolanda I I / Wong, Sunny H / Lai, Raymond W M / Chan, Raphael C Y

Scientific reports

2017 Volume 7, Issue 1, Page(s) 17218

Abstract: Incidence of Clostridium difficile infection (CDI) is rapidly increasing and it poses a major health burden globally. However, data regarding the epidemiology of CDI in Asia are limited. We aimed to characterize the antimicrobial susceptibility patterns ... ...

Abstract	Incidence of Clostridium difficile infection (CDI) is rapidly increasing and it poses a major health burden globally. However, data regarding the epidemiology of CDI in Asia are limited. We aimed to characterize the antimicrobial susceptibility patterns of common ribotypes of toxigenic C. difficile in Hong Kong. Fifty-three PCR ribotypes were identified among 284 toxigenic C. difficile clinical isolates. The five most prevalent ribotypes were 002 (13%), 017 (12%), 014 (10%), 012 (9.2%), and 020 (9.5%). All tested C. difficile strains remained susceptible to metronidazole, vancomycin, meropenem and piperacillin/tazobactam, but highly resistant to cephalosporins. Of the fluoroquinolones, highest resistance to ciprofloxacin was observed (99%), followed by levofloxacin (43%) and moxifloxacin (23%). The two newly emerged PCR ribotypes, 017 and 002, demonstrated high levels of co-resistance towards clindamycin, tetracycline, erythromycin and moxifloxacin. PCR ribotypes 017 and 002 with multi-drug resistance are rapidly emerging and continuous surveillance is important to monitor the epidemiology of C. difficile to prevent outbreaks of CDI.
MeSH term(s)	Anti-Bacterial Agents/pharmacology ; Clostridium difficile/classification ; Clostridium difficile/drug effects ; Clostridium difficile/genetics ; Drug Resistance, Bacterial ; Hong Kong ; Polymerase Chain Reaction ; Ribotyping
Chemical Substances	Anti-Bacterial Agents
Language	English
Publishing date	2017-12-08
Publishing country	England
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2615211-3
ISSN	2045-2322 ; 2045-2322
ISSN (online)	2045-2322
ISSN	2045-2322
DOI	10.1038/s41598-017-17523-7
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Article ; Online: Increased Detection of Emergent Recombinant Norovirus GII.P16-GII.2 Strains in Young Adults, Hong Kong, China, 2016-2017.

Kwok, Kirsty / Niendorf, Sandra / Lee, Nelson / Hung, Tin-Nok / Chan, Lok-Yi / Jacobsen, Sonja / Nelson, E Anthony S / Leung, Ting F / Lai, Raymond W M / Chan, Paul K S / Chan, Martin C W

Emerging infectious diseases

2017 Volume 23, Issue 11, Page(s) 1852–1855

Abstract: A new recombinant norovirus GII.P16-GII.2 outnumbered pandemic GII.4 as the predominant GII genotype in the winter of 2016-2017 in Hong Kong, China. Half of hospitalized case-patients were older children and adults, including 13 young adults. This ... ...

Abstract	A new recombinant norovirus GII.P16-GII.2 outnumbered pandemic GII.4 as the predominant GII genotype in the winter of 2016-2017 in Hong Kong, China. Half of hospitalized case-patients were older children and adults, including 13 young adults. This emergent norovirus targets a wider age population compared with circulating pandemic GII.4 strains.
Language	English
Publishing date	2017
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	1380686-5
ISSN	1080-6059 ; 1080-6040
ISSN (online)	1080-6059
ISSN	1080-6040
DOI	10.3201/eid2311.170561
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Article ; Online: Rapid emergence and predominance of a broadly recognizing and fast-evolving norovirus GII.17 variant in late 2014.

Chan, Martin C W / Lee, Nelson / Hung, Tin-Nok / Kwok, Kirsty / Cheung, Kelton / Tin, Edith K Y / Lai, Raymond W M / Nelson, E Anthony S / Leung, Ting F / Chan, Paul K S

Nature communications

2015 Volume 6, Page(s) 10061

Abstract: Norovirus genogroup II genotype 4 (GII.4) has been the predominant cause of viral gastroenteritis since 1996. Here we show that during the winter of 2014-2015, an emergent variant of a previously rare norovirus GII.17 genotype, Kawasaki 2014, ... ...

Abstract	Norovirus genogroup II genotype 4 (GII.4) has been the predominant cause of viral gastroenteritis since 1996. Here we show that during the winter of 2014-2015, an emergent variant of a previously rare norovirus GII.17 genotype, Kawasaki 2014, predominated in Hong Kong and outcompeted contemporary GII.4 Sydney 2012 in hospitalized cases. GII.17 cases were significantly older than GII.4 cases. Root-to-tip and Bayesian BEAST analyses estimate GII.17 viral protein 1 (VP1) evolves one order of magnitude faster than GII.4 VP1. Residue substitutions and insertion occur in four of five inferred antigenic epitopes, suggesting immune evasion. Sequential GII.4-GII.17 infections are noted, implicating a lack of cross-protection. Virus bound to saliva of secretor histo-blood groups A, B and O, indicating broad susceptibility. This fast-evolving, broadly recognizing and probably immune-escaped emergent GII.17 variant causes severe gastroenteritis and hospitalization across all age groups, including populations who were previously less vulnerable to GII.4 variants; therefore, the global spread of GII.17 Kawasaki 2014 needs to be monitored.
MeSH term(s)	Adolescent ; Adult ; Aged ; Australia/epidemiology ; Caliciviridae Infections/epidemiology ; Caliciviridae Infections/virology ; Child ; Child, Preschool ; Disease Outbreaks ; Evolution, Molecular ; Female ; Gastroenteritis/epidemiology ; Gastroenteritis/virology ; Genotype ; Hong Kong/epidemiology ; Humans ; Male ; Middle Aged ; Molecular Sequence Data ; Norovirus/classification ; Norovirus/genetics ; Norovirus/isolation & purification ; Phylogeny ; Seasons ; Viral Proteins/genetics ; Young Adult
Chemical Substances	Viral Proteins
Language	English
Publishing date	2015-12-02
Publishing country	England
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ISSN	2041-1723
ISSN (online)	2041-1723
DOI	10.1038/ncomms10061
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