Phan Ngoc Quang

Dr. Phan Ngoc Quang

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Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

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

Representative Publications

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3 June 2022 in Ethics, Medicine and Public Health
Verified
Journal Article
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QTQuang Duc Tran
Quang Duc Tran
TVThi Quynh Chi Vu
Thi Quynh Chi Vu
Phan Ngoc QuangPhan Ngoc Quang
Phan Ngoc Quang

15 September 2015 in Journal of Bacteriology
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Journal Article
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Phan Ngoc QuangPhan Ngoc Quang
Phan Ngoc Quang
TUTakashi Uebanso
Takashi Uebanso
TSTakaaki Shimohata
Takaaki Shimohata
MNMutsumi Nakahashi
Mutsumi Nakahashi
KMKazuaki Mawatari
Kazuaki Mawatari
ATAkira Takahashi
Akira Takahashi
HU is one of the most abundant nucleoid-associated proteins in bacterial cells and regulates the expression of many genes involved in growth, motility, metabolism, and virulence. It is known that Vibrio parahaemolyticus pathogenicity is related to its characteristic rapid growth and that type III secretion system 1 (T3SS1) contributes to its cytotoxicity. However, it is not known if HU plays a role in the pathogenicity of V. parahaemolyticus . In the present study, we investigated the effect of HU proteins HU-2 (HUα) ( V. parahaemolyticus 2911 [vp2911]) and HUβ (vp0920) on the pathogenicity of V. parahaemolyticus . We found that a deletion of both HU subunits (yielding the ΔHUs [Δ vp0920 Δ vp2911 ] strain), but not single deletions, led to a reduction of the growth rate. In addition, expression levels of T3SS1-related genes, including exsA (positive regulator), exsD (negative regulator), vp1680 (cytotoxic effector), and vp1671 (T3SS1 apparatus), were reduced in the ΔHUs strain compared to the wild type (WT). As a result, cytotoxicity to HeLa cells was decreased in the ΔHUs strain. The additional deletion of exsD in the ΔHUs strain restored T3SS1-related gene expression levels and cytotoxicity but not the growth rate. These results suggest that the HU protein regulates the levels of T3SS1 gene expression and cytotoxicity in a growth rate-independent manner. IMPORTANCE Nucleoid-binding protein HU regulates cellular behaviors, including nucleoid structuring, general recombination, transposition, growth, replication, motility, metabolism, and virulence. It is thought that both the number of bacteria and the number of virulence factors may affect the pathogenicity of bacteria. In the present study, we investigated which factor(s) has a dominant role during infection in one of the most rapidly growing bacterial species, Vibrio parahaemolyticus . We found that V. parahaemolyticus cytotoxicity is regulated, in a growth rate-independent manner, by the HU proteins through regulation of a number of virulence factors, including T3SS1 gene expression.


2 February 2024 in Current Problems in Cancer
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Journal Article
Closed access
DTDuc Quang Tran
Duc Quang Tran
TTThanh Luong Thi
Thanh Luong Thi
KDKhanh Nguyen Di
Khanh Nguyen Di
CQChi Vu Thi Quynh
Chi Vu Thi Quynh
HHHuyen Nguyen Thi Hoa
Huyen Nguyen Thi Hoa
Phan Ngoc QuangPhan Ngoc Quang
Phan Ngoc Quang

1 October 2019 in Infection and Drug Resistance
Verified
Journal Article
Open access
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RKRyuji Kawahara
Ryuji Kawahara
DKDiep Thi Khong
Diep Thi Khong
HLHa Viet Le
Ha Viet Le
Phan Ngoc QuangPhan Ngoc Quang
Phan Ngoc Quang
TNThang Nam Nguyen
Thang Nam Nguyen
YYYoshimasa Yamamoto
Yoshimasa Yamamoto
Purpose: The dissemination of colistin-resistant bacteria harboring the colistin-resistance gene mcr-1 in developing countries has recently entered the spotlight as an emerging public health threat, which is attributed to the abuse of colistin use in these countries. However, the prevalence of these bacteria in developing countries has not been extensively investigated. Therefore, in the present study, we examined the prevalence of cefotaxime-resistant commensal Escherichia coli harboring mcr-1 among residents of a representative Vietnamese village and assessed the characteristics of these isolates. Materials and methods: The stool samples, one stool sample per resident, of 612 residents were cultured on MacConkey agar with cefotaxime. Resulting E. coli-like colonies were isolated and examined further for the presence of colistin-resistant extended-spectrum β-lactamase (ESBL)-producing E. coli with mcr-1. Antibiotic susceptibility tests were performed, and clonal relationship among colistin-resistant isolates was assessed. Results: Thirty-one of the 451 cefotaxime-resistant E. coli isolates were resistant to colistin and the majority possessed mcr-1, blaCTX-M, and/or blaTEM, except for two isolates that produced the AmpC β-lactamase. All mcr-1 ESBL-producing E. coli isolates were multidrug-resistant (5–11 antibiotics). The isolates contained various plasmid replicon types, including the most prevalent types IncHI2 (54.8%), IncFIB (48.4%), and IncN (41.9%). In addition, 83.9% of the mcr-1 ESBL-E. coli isolates possessed a transposon ISApl1-mcr-1 segment. Furthermore, 77.4% of the mcr-1 ESBL-E. coli isolates belonged to phylogenetic group A. Pulsed-field gel electrophoresis analysis indicated limited clonal expansion of a specific strain. Conclusion: These results demonstrate the wide dissemination of colistin-resistant ESBL-E. coli harboring mcr-1 among commensal bacteria of rural residents in Vietnam, suggesting possible mobilization of the mcr-1 gene among ESBL-producing microbiota, which is a great public health concern.