Cao Thu Thuy
University of Oxford
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BMC Infectious Diseases | 2009
Ha Vinh; Nguyen Thi Khanh Nhu; Tran Vu Thieu Nga; Pham Thanh Duy; James I. Campbell; Nguyen Van Minh Hoang; Maciej F. Boni; Phan Vu Tra My; Christopher M. Parry; Tran Thi Thu Nga; Pham Van Minh; Cao Thu Thuy; To Song Diep; Le Thi Phuong; Mai Thu Chinh; Ha Thi Loan; Nguyen Thi Hong Tham; Mai Ngoc Lanh; Bui Li Mong; Vo Thi Cuc Anh; Phan Van Be Bay; Nguyen Van Vinh Chau; Jeremy Farrar; Stephen Baker
BackgroundShigellosis remains considerable public health problem in some developing countries. The nature of Shigellae suggests that they are highly adaptable when placed under selective pressure in a human population. This is demonstrated by variation and fluctuations in serotypes and antimicrobial resistance profile of organisms circulating in differing setting in endemic locations. Antimicrobial resistance in the genus Shigella is a constant threat, with reports of organisms in Asia being resistant to multiple antimicrobials and new generation therapies.MethodsHere we compare microbiological, clinical and epidemiological data from patients with shigellosis over three different periods in southern Vietnam spanning14 years.ResultsOur data demonstrates a shift in dominant infecting species (S. flexneri to S. sonnei) and resistance profile of the organisms circulating in southern Vietnam. We find that there was no significant variation in the syndromes associated with either S. sonnei or S. flexneri, yet the clinical features of the disease are more severe in later observations.ConclusionsOur findings show a change in clinical presentation of shigellosis in this setting, as the disease may be now more pronounced, this is concurrent with a change in antimicrobial resistance profile. These data highlight the socio-economic development of southern Vietnam and should guide future vaccine development and deployment strategies.Trial RegistrationCurrent Controlled Trials ISRCTN55945881
Proceedings of the National Academy of Sciences of the United States of America | 2013
Kathryn E. Holt; Tran Vu Thieu Nga; Duy Pham Thanh; Ha Vinh; Dong Wook Kim; My Phan Vu Tra; James I. Campbell; Nguyen Van Minh Hoang; Nguyen Thanh Vinh; Pham Van Minh; Cao Thu Thuy; Tran Thi Thu Nga; Corinne N. Thompson; Tran Thi Ngoc Dung; Nguyen Thi Khanh Nhu; Phat Voong Vinh; Pham Thi Ngoc Tuyet; Hoang Le Phuc; Nguyen Thi Nam Lien; Bui Duc Phu; Nguyen Thi Thuy Ai; Nguyen Manh Tien; Nguyen Dong; Christopher M. Parry; Tran Tinh Hien; Jeremy Farrar; Julian Parkhill; Gordon Dougan; Nicholas R. Thomson; Stephen Baker
Significance Shigella sonnei is a globally emerging agent of bacterial dysentery. Here, we use genomics to examine the microevolution of S. sonnei in Vietnam. We show that S. sonnei was introduced into Vietnam in the early 1980s, where it continued to evolve, spreading geographically to establish localized founder populations. The population in Ho Chi Minh City has undergone several localized clonal replacement events, during which a small number of microevolutionary changes have risen to dominance. These changes, induced by horizontal gene transfer and substitution mutations, confer high-level antimicrobial resistance and the ability to kill other gut bacteria. This work provides a unique, high-resolution insight into the microevolution of a pioneering human pathogen during its establishment in a new host population. Shigella sonnei is a human-adapted pathogen that is emerging globally as the dominant agent of bacterial dysentery. To investigate local establishment, we sequenced the genomes of 263 Vietnamese S. sonnei isolated over 15 y. Our data show that S. sonnei was introduced into Vietnam in the 1980s and has undergone localized clonal expansion, punctuated by genomic fixation events through periodic selective sweeps. We uncover geographical spread, spatially restricted frontier populations, and convergent evolution through local gene pool sampling. This work provides a unique, high-resolution insight into the microevolution of a pioneering human pathogen during its establishment in a new host population.
Journal of Medical Microbiology | 2009
Le Thi Minh Vien; Stephen Baker; Le Thi Phuong Thao; Le Thi Phuong Tu; Cao Thu Thuy; Tran Thi Thu Nga; Nguyen Van Minh Hoang; James I. Campbell; Lam Minh Yen; Nguyen Trong Hieu; Nguyen Van Vinh Chau; Jeremy Farrar; Constance Schultsz
Antimicrobial-resistant pathogenic members of the Enterobacteriaceae are a well-defined global problem. We hypothesized that one of the main reservoirs of dissemination of antimicrobial resistance genes in Vietnam is non-pathogenic intestinal flora, and sought to isolate antimicrobial-resistant organisms from hospitalized patients and non-hospitalized healthy individuals in Ho Chi Minh City. The results identified substantial faecal carriage of gentamicin-, ceftazidime- and nalidixic acid-resistant members of the Enterobacteriaceae in both hospitalized patients and non-hospitalized healthy individuals. A high prevalence of quinolone resistance determinants was identified, particularly the qnrS gene, in both community- and hospital-associated strains. Furthermore, the results demonstrated that a combination of quinolone resistance determinants can confer resistance to nalidixic acid and ciprofloxacin, even in the apparent absence of additional chromosomal resistance mutations in wild-type strains and laboratory strains with transferred plasmids. These data suggest that intestinal commensal organisms are a significant reservoir for the dissemination of plasmid-mediated quinolone resistance in Ho Chi Minh City.
PLOS Neglected Tropical Diseases | 2010
Nguyen Thi Khanh Nhu; Ha Vinh; Tran Vu Thieu Nga; Richard A. Stabler; Pham Thanh Duy; Le Thi Minh Vien; H. Rogier van Doorn; Ana Cerdeño-Tárraga; Nicholas R. Thomson; James I. Campbell; Nguyen Van Minh Hoang; Tran Thi Thu Nga; Pham Van Minh; Cao Thu Thuy; Brendan W. Wren; Jeremy Farrar; Stephen Baker
Background Plasmid mediated antimicrobial resistance in the Enterobacteriaceae is a global problem. The rise of CTX-M class extended spectrum beta lactamases (ESBLs) has been well documented in industrialized countries. Vietnam is representative of a typical transitional middle income country where the spectrum of infectious diseases combined with the spread of drug resistance is shifting and bringing new healthcare challenges. Methodology We collected hospital admission data from the pediatric population attending the hospital for tropical diseases in Ho Chi Minh City with Shigella infections. Organisms were cultured from all enrolled patients and subjected to antimicrobial susceptibility testing. Those that were ESBL positive were subjected to further investigation. These investigations included PCR amplification for common ESBL genes, plasmid investigation, conjugation, microarray hybridization and DNA sequencing of a bla CTX–M encoding plasmid. Principal Findings We show that two different bla CTX-M genes are circulating in this bacterial population in this location. Sequence of one of the ESBL plasmids shows that rather than the gene being integrated into a preexisting MDR plasmid, the bla CTX-M gene is located on relatively simple conjugative plasmid. The sequenced plasmid (pEG356) carried the bla CTX-M-24 gene on an ISEcp1 element and demonstrated considerable sequence homology with other IncFI plasmids. Significance The rapid dissemination, spread of antimicrobial resistance and changing population of Shigella spp. concurrent with economic growth are pertinent to many other countries undergoing similar development. Third generation cephalosporins are commonly used empiric antibiotics in Ho Chi Minh City. We recommend that these agents should not be considered for therapy of dysentery in this setting.
PLOS ONE | 2010
Tran Tinh Hien; Nguyen Thi Dung; Nguyen Thanh Truong; Ninh Thi Thanh Van; Tran Nguyen Bich Chau; Nguyen Van Minh Hoang; Tran Thi Thu Nga; Cao Thu Thuy; Pham Van Minh; Nguyen Thi Cam Binh; Tran Thi Diem Ha; Pham Van Toi; To Song Diep; James I. Campbell; Elaine Stockwell; Constance Schultsz; Cameron P. Simmons; Clare Glover; Winnie Lam; Filipe Marques; James P. May; Anthony Upton; Ronald Budhram; Gordon Dougan; Jeremy Farrar; Nguyen Van Vinh Chau; Christiane Dolecek
Background The emergence of drug resistant typhoid fever is a major public health problem, especially in Asia. An oral single dose typhoid vaccine would have major advantages. M01ZH09 is a live oral single dose candidate typhoid vaccine containing Salmonella enterica serovar Typhi (Ty2 aroC − ssaV −) ZH9 with two independently attenuating deletions. Studies in healthy adults demonstrated immunogenicity and an acceptable safety profile. Objectives We conducted a randomised placebo controlled, single-blind trial to evaluate the safety and immunogenicity of M01ZH09 in healthy Vietnamese children aged 5 to 14 years. Methods Subjects were randomly assigned to receive either a nominal dose of 5×109 CFU of M01ZH09 or placebo and were followed up for 28 days. The primary safety outcome was the proportion of subjects with any adverse event attributed to M01ZH09. The primary immunogenicity endpoint was the proportion of subjects who showed a positive immune response to M01ZH09 in the Salmonella Typhi lipopolysaccharide (LPS) specific serum IgA and IgG ELISA. Principal Findings One hundred and fifty-one children were enrolled, 101 subjects received M01ZH09 and 50 subjects received placebo. An intention to treat analysis was conducted. There were no serious adverse events and no bacteraemias. In the M01ZH09 group, 26 (26%; 95% CI, 18–5%) of 101 subjects experienced adverse events compared to 11 (22%; 95% CI, 12–36%) of 50 subjects in the placebo group (odds ratio (OR) [95%CI] = 1.23 [0.550–2.747]; p = 0.691). Faecal shedding of S. Typhi (Ty2 aroC − ssaV −) ZH9 was detected in 51 (51%; 95% CI, 41–61%) of 100 M01ZH09 subjects. No shedding was detected beyond day 3. A positive immune response, defined as 70% increase (1.7 fold change) in LPS specific serum IgG (day 14 or 28) and/or 50% increase (1.5 fold change) in LPS specific serum IgA (day 7 or 14) from baseline was detected in 98 (97%; 95% CI, 92–99%) of 101 M01ZH09 recipients and 8 (16%; 95% CI, 7–29%) of 50 placebo recipients. Twenty-eight (100%; 95% CI, 88–100%) of 28 vaccine recipients who were evaluated in the LPS specific IgA ELISPOT assay showed a positive response compared to none of the 14 placebo recipients tested. Conclusions This was the first phase II trial of a novel oral candidate typhoid vaccine in children in an endemic country. M01ZH09 had an appropriate safety profile and was immunogenic in children. Trial Registration Controlled-trials.comISRCTN91111837
Journal of Virological Methods | 2013
Tran Thi Ngoc Dung; Voong Vinh Phat; Tran Vu Thieu Nga; Phan Vu Tra My; Pham Thanh Duy; James I. Campbell; Cao Thu Thuy; Nguyen Van Minh Hoang; Pham Van Minh; Hoang Le Phuc; Pham Thi Ngoc Tuyet; Ha Vinh; Duong Thi Hue Kien; Huynh Le Anh Huy; Nguyen Thanh Vinh; Tran Thi Thu Nga; Nguyen Thi Thu Hau; Nguyen Tran Chinh; Tang Chi Thuong; Ha Manh Tuan; Cameron P. Simmons; Jeremy Farrar; Stephen Baker
Highlights ► A multiplex real-time PCR was developed for the detection and quantitation of Rotavirus A and Norovirus genogroup II. ► An internal extraction and amplification control was incorporated. ► Real-time PCR was compared to the current gold standard, enzyme immunoassay. ► Real-time PCR was significantly more sensitive than enzyme immunoassay. ► Quantitation demonstrated that the viral loads of both pathogens were ten times greater in stools children with diarrhea than in children without diarrhea.
American Journal of Tropical Medicine and Hygiene | 2015
Corinne N. Thompson; My V. T. Phan; Nguyen Van Minh Hoang; Pham Van Minh; Nguyen Thanh Vinh; Cao Thu Thuy; Tran Thi Thu Nga; Maia A. Rabaa; Pham Thanh Duy; Tran Thi Ngoc Dung; Voong Vinh Phat; Tran Vu Thieu Nga; Le Thi Phuong Tu; Ha Thanh Tuyen; Keisuke Yoshihara; Claire Jenkins; Vu Thuy Duong; Hoang Le Phuc; Pham Thi Ngoc Tuyet; Nguyen Minh Ngoc; Ha Vinh; Nguyen Tran Chinh; Tang Chi Thuong; Ha Manh Tuan; Tran Tinh Hien; James I. Campbell; Nguyen Van Vinh Chau; Guy Thwaites; Stephen Baker
We performed a prospective multicenter study to address the lack of data on the etiology, clinical and demographic features of hospitalized pediatric diarrhea in Ho Chi Minh City (HCMC), Vietnam. Over 2,000 (1,419 symptomatic and 609 non-diarrheal control) children were enrolled in three hospitals over a 1-year period in 2009–2010. Aiming to detect a panel of pathogens, we identified a known diarrheal pathogen in stool samples from 1,067/1,419 (75.2%) children with diarrhea and from 81/609 (13.3%) children without diarrhea. Rotavirus predominated in the symptomatic children (664/1,419; 46.8%), followed by norovirus (293/1,419; 20.6%). The bacterial pathogens Salmonella, Campylobacter, and Shigella were cumulatively isolated from 204/1,419 (14.4%) diarrheal children and exhibited extensive antimicrobial resistance, most notably to fluoroquinolones and third-generation cephalosporins. We suggest renewed efforts in generation and implementation of policies to control the sale and prescription of antimicrobials to curb bacterial resistance and advise consideration of a subsidized rotavirus vaccination policy to limit the morbidity due to diarrheal disease in Vietnam.
Emerging Infectious Diseases | 2013
Phan Vu Tra My; Corinne N. Thompson; Hoang Le Phuc; Pham Thi Ngoc Tuyet; Ha Vinh; Nguyen Van Minh Hoang; Pham Van Minh; Nguyen Thanh Vinh; Cao Thu Thuy; Tran Thi Thu Nga; Nguyen Thi Thu Hau; James D. Campbell; Nguyen Tran Chinh; Tang Chi Thuong; Ha Manh Tuan; Jeremy Farrar; Stephen Baker
We performed a case–control investigation to identify risk factors for norovirus infections among children in Vietnam. Of samples from 1,419 children who had diarrhea and 609 who were asymptomatic, 20.6% and 2.8%, respectively, were norovirus positive. Risk factors included residential crowding and symptomatic contacts, indicating person-to-person transmission of norovirus.
Journal of Medical Microbiology | 2014
Nguyen Thi Khanh Nhu; Nguyen Phu Huong Lan; James I. Campbell; Christopher M. Parry; Corinne N. Thompson; Ha Thanh Tuyen; Nguyen Van Minh Hoang; Pham Thi Thanh Tam; Vien Minh Le; Tran Vu Thieu Nga; Tran Do Hoang Nhu; Pham Van Minh; Nguyen Thi Thu Nga; Cao Thu Thuy; Le Thi Dung; Nguyen Thi Thu Yen; Nguyen Van Hao; Huynh Thi Loan; Lam Minh Yen; Ho Dang Trung Nghia; Tran Tinh Hien; Louise Thwaites; Guy Thwaites; Nguyen Van Vinh Chau; Stephen Baker
Ventilator-associated pneumonia (VAP) is a serious healthcare-associated infection that affects up to 30 % of intubated and mechanically ventilated patients in intensive care units (ICUs) worldwide. The bacterial aetiology and corresponding antimicrobial susceptibility of VAP is highly variable, and can differ between countries, national provinces and even between different wards in the same hospital. We aimed to understand and document changes in the causative agents of VAP and their antimicrobial susceptibility profiles retrospectively over an 11 year period in a major infectious disease hospital in southern Vietnam. Our analysis outlined a significant shift from Pseudomonas aeruginosa to Acinetobacter spp. as the most prevalent bacteria isolated from quantitative tracheal aspirates in patients with VAP in this setting. Antimicrobial resistance was common across all bacterial species and we found a marked proportional annual increase in carbapenem-resistant Acinetobacter spp. over a 3 year period from 2008 (annual trend; odds ratio 1.656, P = 0.010). We further investigated the possible emergence of a carbapenem-resistant Acinetobacter baumannii clone by multiple-locus variable number tandem repeat analysis, finding a blaOXA-23-positive strain that was associated with an upsurge in the isolation of this pathogen. We additionally identified a single blaNDM-1-positive A. baumannii isolate. This work highlights the emergence of a carbapenem-resistant clone of A. baumannii and a worrying trend of antimicrobial resistance in the ICU of the Hospital for Tropical Diseases in Ho Chi Minh City, Vietnam.
PLOS Neglected Tropical Diseases | 2011
Ha Vinh; Vo Thi Cuc Anh; Nguyen Duc Anh; James I. Campbell; Nguyen Van Minh Hoang; Tran Vu Thieu Nga; Nguyen Thi Khanh Nhu; Pham Van Minh; Cao Thu Thuy; Pham Thanh Duy; Le Thi Phuong; Ha Thi Loan; Mai Thu Chinh; Nguyen Thi Thu Thao; Nguyen Thi Hong Tham; Bui Li Mong; Phan Van Be Bay; Jeremy N. Day; Christiane Dolecek; Nguyen Phu Huong Lan; To Song Diep; Jeremy Farrar; Nguyen Van Vinh Chau; Marcel Wolbers; Stephen Baker
Background The bacterial genus Shigella is the leading cause of dysentery. There have been significant increases in the proportion of Shigella isolated that demonstrate resistance to nalidixic acid. While nalidixic acid is no longer considered as a therapeutic agent for shigellosis, the fluoroquinolone ciprofloxacin is the current recommendation of the World Health Organization. Resistance to nalidixic acid is a marker of reduced susceptibility to older generation fluoroquinolones, such as ciprofloxacin. We aimed to assess the efficacy of gatifloxacin versus ciprofloxacin in the treatment of uncomplicated shigellosis in children. Methodology/Principal Findings We conducted a randomized, open-label, controlled trial with two parallel arms at two hospitals in southern Vietnam. The study was designed as a superiority trial and children with dysentery meeting the inclusion criteria were invited to participate. Participants received either gatifloxacin (10 mg/kg/day) in a single daily dose for 3 days or ciprofloxacin (30 mg/kg/day) in two divided doses for 3 days. The primary outcome measure was treatment failure; secondary outcome measures were time to the cessation of individual symptoms. Four hundred and ninety four patients were randomized to receive either gatifloxacin (n = 249) or ciprofloxacin (n = 245), of which 107 had a positive Shigella stool culture. We could not demonstrate superiority of gatifloxacin and observed similar clinical failure rate in both groups (gatifloxacin; 12.0% and ciprofloxacin; 11.0%, p = 0.72). The median (inter-quartile range) time from illness onset to cessation of all symptoms was 95 (66–126) hours for gatifloxacin recipients and 93 (68–120) hours for the ciprofloxacin recipients (Hazard Ratio [95%CI] = 0.98 [0.82–1.17], p = 0.83). Conclusions We conclude that in Vietnam, where nalidixic acid resistant Shigellae are highly prevalent, ciprofloxacin and gatifloxacin are similarly effective for the treatment of acute shigellosis. Trial Registration Controlled trials number ISRCTN55945881