Quang Luong

Dr. Quang Luong

orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 July 2022 in International Journal of Infectious Diseases
Verified
Journal Article
Open access
TNThi Huyen Trang Nguyen
Thi Huyen Trang Nguyen
TNThuong Vu Nguyen
Thuong Vu Nguyen
QLQuang Luong
Quang Luong
THThang Vinh Ho
Thang Vinh Ho
CFChristel Faes
Christel Faes
NHNiel Hens
Niel Hens
Southern Vietnam experienced a large measles outbreak of over 26,000 cases during 2018-2020. We aimed to understand and quantify the measles spread in space-time dependence and the transmissibility during the outbreak. Measles surveillance reported cases between January 2018 and June 2020, vaccination coverage, and population data at provinicial level were used. To illustrate the spatio-temporal pattern of disease spread, we employed the endemic-epidemic multivariate time series model decomposing measles risk additively into autoregressive, spatio-temporal, and endemic components. Likelihood-based estimation procedures were performed to determine the time-varying reproductive number Re of measles. Our analysis showed that the incidence of measles was associated with vaccination coverage heterogeneity and spatial interaction between provincial units. The risk of infections was dominated by between-province transmission (36.1% to 78.8%), followed by local endogenous transmission (4.1% to 61.5%). In contrast, the endemic behavior had a relatively small contribution (2.4% to 33.4%) across provinces. In the exponential phase of the epidemic, Re was above the threshold with a maximum value of 2.34 (95% CI: 2.20-2.46). Local vaccination coverage and human mobility are important factors contributing to the measles dynamics in Southern Vietnam, and the high risk of inter-provincial transmission is of most concern. Strengthening the disease surveillance is recommended, and further research is essential to understand the relative contribution of population immunity and control measures in measles epidemics.

1 December 2010 in Genomics
Verified
Journal Article
Closed access
GBGary A. Bulla
Gary A. Bulla
QLQuang Luong
Quang Luong
SSSushma Shrestha
Sushma Shrestha
SRSarah Reeb
Sarah Reeb
SHSharon Hickman
Sharon Hickman

8 October 2023 in Viruses
Verified
Journal Article
Open access
PDF file
TNThanh Vu Nguyen
Thanh Vu Nguyen
MTMya Myat Ngwe Tun
Mya Myat Ngwe Tun
MCMinh Thang Cao
Minh Thang Cao
HDHuy Manh Dao
Huy Manh Dao
QLQuang Luong
Quang Luong
FHFutoshi Hasebe
Futoshi Hasebe
Chikungunya fever is an acute febrile illness caused by the chikungunya virus (CHIKV), which is transmitted by Aedes mosquitoes. Since 1965, only a few studies with limited scope have been conducted on CHIKV in Vietnam. Thus, this study aimed to determine the seroprevalence and molecular epidemiology of CHIKV infection among febrile patients in Vietnam from 2017 to 2019. A total of 1063 serum samples from 31 provinces were collected and tested for anti-CHIKV IgM and IgG ELISA. The 50% focus reduction neutralization test (FRNT50) was used to confirm CHIKV-neutralizing antibodies. Quantitative real-time RT–PCR (RT–qPCR) was performed to confirm the presence of the CHIKV genome. The results showed that 15.9% (169/1063) of the patients had anti-CHIKV IgM antibodies, 20.1% (214/1063) had anti-CHIKV IgG antibodies, 10.4% (111/1063) had CHIKV-neutralizing antibodies, and 27.7% (130/469) of the samples were positive in RT–qPCR analysis. The E1 CHIKV genome sequences were detected among the positive RT–qPCR samples. Our identified sequences belonged to the East/Central/South/African (ECSA) genotype, which has been prevalent in Vietnam previously, suggesting CHIKV has been maintained and is endemic in Vietnam. This study demonstrates a high prevalence of CHIKV infection in Vietnam and calls for an annual surveillance program to understand its impact.

18 November 2023 in IJID Regions
Verified
Journal Article
Open access
TPThanh Van Phan
Thanh Van Phan
DVDai Thi Trang Vo
Dai Thi Trang Vo
HNHoang Thi Kim Nguyen
Hoang Thi Kim Nguyen
THThuy Nguyen Loc Ho
Thuy Nguyen Loc Ho
QPQuang Duy Pham
Quang Duy Pham
TNTrung Vu Nguyen
Trung Vu Nguyen
Our goal was to describe Invasive Meningococcal Disease (IMD) in Southern Vietnam over the last 10 years. We characterized 109 Neisseria meningitidis strains in Southern Vietnam isolated between 1980s to 2021, that were collected from IMD (n = 44), sexually transmitted infections (n = 2), and healthy carriage (n = 63). IMD were confirmed by bacterial culture and/or real-time polymerase chain reaction at the national reference laboratory in Pasteur Institute of Ho Chi Minh City (PIHCM). Antimicrobial resistance was determined on 31 IMD and two sexually transmitted infection isolates with E-test for chloramphenicol (CHL), penicillin (PEN), ciprofloxacin (CIP), ceftriaxone (CRO), and rifampicin (RIF). Sequencing was performed for analyzing of multilocus-sequence-typing (MLST), porA, fetA, and antibiotic resistance genes, including gyrA, penA, and rpoB. The incidence rate during this period was 0.02 per 100,000 persons/year. Serogroup B accounted for over 90% of cases (50/54). ST-1576 were mainly responsible for IMD, 27/42 MLST profiles, and associated with CHL resistance. Resistance was prevalent among IMD isolates. Thirteen were resistant to CHL (minimum inhibitory concentration [MIC] ≥16 mg/l), 12 were intermediate to PEN (MIC between 0.19 and 0.5 mg/l), and five were CIP-resistant (MIC between 0.19 and 0.5 mg/l). Particularly, one was non-susceptible to CRO (MIC at 0.125 mg/l), belonging to ST-5571 lineage. The resistance was due to carrying resistant alleles of penA and gyrA genes, and catP gene. Notably, seven isolates were resistant/non-susceptible to two or more antibiotics. Our results suggest the persistence of the circulating ST-1576 in Southern Vietnam, with a spread of antimicrobial resistance across the community.

29 April 2019 in Western Pacific Surveillance and Response Journal
Verified
Journal Article
Open access
PDF file
LPLan Trong Phan
Lan Trong Phan
QLQuang Luong
Quang Luong
TDThi Hong Hien Do
Thi Hong Hien Do
CCCindy H Chiu
Cindy H Chiu
TCThang Minh Cao
Thang Minh Cao
MKMasaya Kato
Masaya Kato
Findings and lessons from establishing Zika virus surveillance in southern Viet Nam, 2016

19 December 2020 in medRxiv
Verified
Preprint
Open access
PDF file
QPQuang D. Pham
Quang D. Pham
RSRobyn Margaret Stuart
Robyn Margaret Stuart
TNThuong V. Nguyen
Thuong V. Nguyen
QLQuang Luong
Quang Luong
DTDai Q. Tran
Dai Q. Tran
CKCliff Kerr
Cliff Kerr
Background: Vietnam has emerged as one of the world’s leading success stories in responding to COVID-19. After prolonged zero-low transmission, a summer outbreak of unknown source at Da Nang caused the country’s first COVID-19 deaths, but was quickly suppressed. Vietnam recently reopened its borders to international travelers. Understanding the attendant risks and how to minimize them is crucial as Vietnam moves into this new phase. Methods: We create an agent-based model of COVID-19 in Vietnam, using regional testing data and a detailed linelist of the 1,014 COVID-19 cases, including 35 deaths, identified across Vietnam. We investigate the Da Nang outbreak, and quantify the risk of another outbreak under different assumptions about behavioral/policy responses and ongoing testing. Results: The Da Nang outbreak, although rapidly contained once detected, nevertheless caused significant community transmission before it was detected; higher symptomatic testing could have mitigated this. If testing levels do not increase, the adoption of past policies in response to newly-detected cases may reduce the size of potential outbreaks but will not prevent them. Compared to a baseline symptomatic testing rate of 10%, we estimate half as many infections under a 20% testing rate, and a quarter as many with 40-50% testing rates, over the four months following border reopenings. Conclusions: Vietnam’s success in controlling COVID-19 is largely attributable to its rapid response to detected outbreaks, but the speed of response could be improved even further with higher levels of symptomatic testing.