Charting the trajectories of music piracy in Ho Chi Minh City, Vietnam

This study focuses on how the expanding market for pirated music in Vietnam has led to transnational flows of texts and genres, and to changes in how the state, music companies, pirates, and consumers deal with one another. Using theories put forth by Roger Wallis and Krister Malm (1984) and Shujen Wang and Jonathan Zhu (2003), the goal of my research is to identify major technological, economic, and organizational shifts taking place within the distribution and consumption of compact discs (CDs) in Ho Chi Minh City. This work suggests that Vietnam operates outside of our traditional understanding of the music industry or cultural flows. Unauthorized music products are helping to create a demand for all types of music in Vietnam and this begs us to question whether piracy is as negative for this country as previously thought. This thesis argues that the piracy in HCMC is a rare case of defiance and triumph over major global corporations. This study explores the magnitude of international copyright conventions, intellectual property rights enforcement, the structure of the domestic industry and the high profitability and affordability of piracy. Using a qualitative case studies approach, this examination looks at the different political, legal and regulatory frameworks that control the trajectories of music piracy in Ho Chi Minh City

Fonction de CFTR dans les processus de réparation de l’épithélium des voies aériennes et développement de nouvelles stratégies thérapeutiques en fibrose kystique

La pathologie de la fibrose kystique (FK) est causée par des mutations dans le gène codant pour le canal CFTR. La mutation la plus commune est la délétion du résidu Phe508 (∆F508), qui entraîne un mauvais repliement et la dégradation de la protéine mutée. Ainsi, l’absence du CFTR cause un dysfonctionnement du transport ionique et liquidien qui altère le phénomène de clairance mucociliaire. Il en résulte une accumulation de mucus visqueux obstruant les voies aériennes favorisant une colonisation bactérienne, spécialement par P. aeruginosa, et une inflammation chronique. Ces phénomènes entraînent des lésions épithéliales et un remodelage des voies aériennes. Selon nos analyses ultrastructurales de poumons issus de patients FK au moment de la transplantation, certaines zones de l’épithélium FK montrait des signes de d’initiation des processus de réparation. Malgré cela, un dommage épithélial progressif est observé chez les patients FK et il apparaît évident que les processus de réparation sont insuffisants pour permettre le rétablissement de l’intégrité épithéliale. Le principal objectif de mon étude était d’étudier le rôle du CFTR dans les mécanismes de réparation de l’épithélium FK et de déterminer l’impact de la correction du CFTR sur la réparation épithéliale et ce, en condition aseptique et en présence d’infection. Mes travaux montrent que l’épithélium des voies aériennes FK présente un défaut de réparation, associé, du moins en partie, à l’absence d’un CFTR fonctionnel. De plus, nous avons démontré pour la première fois que l’application du correcteur du CFTR VRT-325 permettait, non seulement, la maturation du CFTR, mais également une amélioration de la capacité des monocouches de cellules des voies aériennes FK à se réparer. D’autre part, nous avons montré que la présence du filtrat bactérien de P. aeruginosa (PsaDM) altérait non seulement l’expression et la fonction du CFTR, mais également les processus de réparation épithéliale. Enfin, nos résultats montrent que l’infection affecte la maturation du CFTR induite par le VRT-325 et diminue les effets bénéfiques du VRT-325 sur la réparation épithéliale. Mes travaux permettent de mieux comprendre le rôle du CFTR dans les processus de réparation de l’épithélium FK et de proposer une nouvelle approche thérapeutique visant à promouvoir la régénération épithéliale chez les patients FK afin de tenter de stabiliser leur état, malgré l’effet délétère de la composante infectieuse.The Cystic fibrosis (CF) pathology is caused by mutations of the gene coding for the CFTR channel. The most common mutation is the deletion of Phe508 (∆F508) causing protein misfolding and degradation. Thus, the absence of CFTR channel causes the dysfunction of ion and fluid transport that impairs mucociliary clearance resulting in mucus thickening and plugging in the airways. These conditions then favor P. aeruginosa bacterial colonisation and inflammation in the airways, which contribute to airway damage and remodeling. Ultrstructural analysis of bronchial sections of lungs collected from CF patients at the time of transplantation showed some area with signs of ongoing epithelial repair. However, a progressive epithelial damage is still observed in CF patients and it appears that the repair process is insufficient to restore epithelial integrity. The main objective of my work was to study the role of CFTR in the CF repair processes and to explore the impact of CFTR correction on epithelial repair under pathogen-free condition as well as in the presence of infectious products. Our study showed that CF airway epithelium exhibits a repair defect, associated, at least in part, to the absence of a functional CFTR channel. Furthermore, we demonstrated for the first time that CFTR rescue with the CFTR corrector VRT-325 significantly improved the wound-healing capacity of CF epithelial cell monolayers. Then, we showed that the presence of bacterial filtrate, more precisely P. aeruginosa diffusible material (PsaDM), not only alter CFTR function and expression, but also impaired epithelial repair processes. Finally, our results suggested that infection has a deleterious impact on CFTR rescue, and affected the beneficial effect on epithelial repair processes induced by VRT-325. My work allows to better understand the role of CFTR in the CF epithelial repair mechanisms and to propose new therapeutic strategies to promote epithelial regeneration in CF patients in attempt to stabilize their condition, despite the deleterious impact of infection

Implication des canaux K+ dans les processus de réparation de l’épithélium respiratoire sain et fibrose kystique

La pathologie de la fibrose kystique (FK) est causée par des mutations du gène codant pour le canal Cl- CFTR. Au niveau respiratoire, cette dysfonction du transport transépithélial de Cl- occasionne une altération de la composition et du volume du liquide de surface des voies aériennes. Une accumulation de mucus déshydraté favorise alors la colonisation bactérienne et une réponse inflammatoire chronique, entraînant des lésions épithéliales sévères au niveau des voies aériennes et des alvéoles pouvant culminer en défaillance respiratoire. Le principal objectif de mon projet de maîtrise était d’étudier les processus de réparation de l’épithélium alvéolaire sain, l’épithélium bronchique sain et FK à l’aide d’un modèle in vitro de plaies mécaniques. Nos résultats démontrent la présence d’une boucle autocrine EGF/EGFR contrôlant les processus de migration cellulaire et de réparation des lésions mécaniques. D’autre part, nos expériences montrent que l’EGF stimule l’activité et l’expression des canaux K+ KATP, KvLQT1 et KCa3.1 des cellules épithéliales respiratoires. L’activation de ces canaux est cruciale pour les processus de réparation puisque la majeure partie de la réparation stimulée à l’EGF est abolie en présence d’inhibiteurs de ces canaux. Nous avons également observé que les cellules FK présentent un délai de réparation, probablement causé par un défaut de la réponse EGF/EGFR et une activité/expression réduite des canaux K+. Nos résultats permettent de mieux comprendre les mécanismes de régulation des processus de réparation de l’épithélium sain et FK. De plus, ils ouvrent de nouvelles options thérapeutiques visant à promouvoir, à l’aide d’activateurs de canaux K+ et de facteurs de croissance, la régénération de l’épithélium respiratoire chez les patients atteints de FK.The cystic fibrosis pathology (CF) is caused by mutations of the gene coding for the Cl- channel, CFTR. In the lungs, the dysfunction of transepithelial ion transport leads to an alteration of airway surface liquid volume and composition. Dehydrated mucus accumulation then favors chronic bacterial colonisation and inflammatory response, inducing severe epithelial injuries in the airways and the alveoli and then, respiratory failure. The main objective of my master degree project was to study normal alveolar, normal and CF bronchial epithelia repair processes using an in vitro model of mechanical wound-healing. Our results reveal the presence of an EGF/EGFR autocrine loop that controls cell migration and wound-healing. Our results show also that EGF signaling stimulate KATP, KvLQT1 and KCa3.1 K+ channel activity and expression in epithelial cells. K+ channel activation is crucial for repair processes since K+ channel inhibitors prevent most of EGF-stimulated wound-healing. We also observed that CF cells present delayed repair processes, probably caused by an EGF signaling defect and reduced K+ channel activity and expression. Our results allow us to better understand the regulatory mechanisms of normal and CF epithelial repair processes. Futhermore, our results open to new therapeutic options that promote, with K+ channel activators and growth factors, respiratory epithelium regeneration in CF patients

Social capital, trust, and bank tail risk: The value of ESG rating and the effects of crisis shocks

Using a global sample of 244 banks in 52 stock markets, we investigate the effect of corporate social responsibility (CSR) on bank tail risk in normal and turbulent times. Our analysis shows no significant evidence that CSR intensity protects banks from tail risks ex ante or during the global financial crisis of 2007–2009. However, investors appear to become more tolerant and more lenient towards banks with stronger CSR post ante economic recession by reducing the likelihood of extreme devaluation of banking stocks. Socially responsible banks with higher social capital and trust (associated with superior CSR performance) experience lower idiosyncratic and systematic tail risks even in the context of the COVID-19 pandemic in 2020. Our empirical evidence implies that the trust between banks and investors started to build through banks’ investments in social capital through committed CSR performance since the credit crunch erupted

Novel Human Parechovirus, Sri Lanka

Of 362 fecal samples collected from children with acute gastroenteritis in Sri Lanka during 2005–2006, 30 (8.3%) were positive for human parechovirus (HPeV) by reverse transcription–PCR. A novel HPeV, designated as HPeV10, was identified in 2 samples by sequence analysis of the viral protein 1 gene of the detected HPeVs

The responsibility of C-terminal domain in the thermolabile haemolysin activity of Vibrio parahaemolyticus and inhibition treatments by Phellinus sp. extracts

The thermolabile haemolysin (tlh) of Vibrio parahaemolyticus (Vptlh) from V. parahaemolyticus is a multiple-function enzyme, initially describes as a haemolytic factor activated by lecithin and phospholipase A2 enzymatic activity (Shinoda, 1991; Vazquez-Morado, 2021; Yanagase et al., 1970). Until now, the tlh structure has hypothesized including N-terminal and C-terminal domain, but what domain of the Vptlh structure does the haemolytic activity has not been refined yet. In this study, a 450-bp VpTLH nucleotide sequence of the entire Vptlh gene encoded the C-terminal domain cloned firstly to examine its responsibility in the activity of the Vptlh. The C-terminal domain fused with a 6-His-tag named the His-tag-VpC-terminal domain was expressed successfully in soluble form in the BL21 (DE3) PlysS cell. Remarkably, both expression and purification results confirmed a high agreement in the molecular weight of the His-tag-VpC-terminal domain was 47 kDa. This work showed the His-tag-VpC-terminal domain lysed the erythrocyte membranes in the blood agar and the phosphate buffered saline (0.9%) media without adding the lecithin substrate of the phospholipase enzyme. Haemolysis occurred at all tested diluted concentrations of His-tag-VpC-terminal domain (p < 0.05), providing evidence for the independent haemolytic activity of the His-tag-VpC-terminal domain. The content of 100 μg of the His-tag-VpC-terminal domain brought the highest haemolytic activity of 80% compared to that in the three remaining contents. Significantly, the His-tag-VpC-terminal domain demonstrated not to involve the phospholipase activity in Luria-Bertani agar supplemented with 1% (vol/vol) egg yolk emulsion. All results proved the vital responsibility of the His-tag-VpC-terminal domain in causing the haemolytic activity without the required activation by the phospholipase enzyme. Raw extracts of Phellinus igniarus and Phellinus pipi at 10-1 mg/mL inhibited the haemolytic activity of the His-tag-VpC-terminal domain from 67.7% to 87.42%, respectively. Hence applying the His-tag-VpC-terminal domain as a simple biological material to evaluate quickly potential derivatives against the Vptlh in vivo conditions will accessible and more advantageous than using the whole of the Vptlh

Research on chemical constituents, anti-bacterial and anti-cancer effects of components isolated from Zingiber officinale Roscoe from Vietnam

Ginger, a commonly used spice and medicinal herb, is an abundant source of bioactive compounds. However, the utilization of ginger in the pharmaceutical industry is still moderate and not commensurate with the potential of the Vietnamese horticulture industry, mainly due to a lack of information about the quality of input materials. In this study, we compared the volatile compounds of gingers collected from 13 provinces of Vietnam using GC/MS and GC-FID analysis to provide a basis for selecting and standardizing input materials. Furthermore, ginger essential oil from Ben Tre province of Vietnam exhibited significant antibacterial activity particularly in inhibiting Gram-positive bacteria, including S. aureus and S. epidermidis, with inhibition zones of 30.00 ± 1.41 and 24.67 ± 3.30 mm, respectively. However, no significant inhibition was observed against Gram-negative bacteria P. aeruginosa and E. coli. We also isolated 5 non-volatile compounds from ginger extract, namely 6-shogaol (1), quercetin (2), rutin (3), beta-sitosterol (4) and beta-sitosterol-3-O-beta-D-glucopyranoside (5). Among them, compounds 1–3 displayed cytotoxicity against Hep3B, SK-LU-1, MCF-7, SK-LU-1, SW480 and HepG2 tumour cell lines, with an IC50 values ranging between 62.7 ± 2.1 and 97.6 ± 1.1 µM, using Ellipticine as a positive control. Compounds 4 and 5 showed cytotoxicity against Hep3B and HepG2 tumor cells, with the IC50 values ranging between 21.5 ± 5.1 and 46.9 ± 3.7 µM but did not exhibit any significant cytotoxicity against SW480 and SK-LU-1 cells. Compound 4 also demonstrated middling cytotoxicity against the MCF7 cell line, with an IC50 value of 43.6 ± 5.1 µM. These findings suggest further applications of Vietnamese ginger for the treatment of infectious and cancer-related diseases

Assessment of physical land suitability by GIS-based fuzzy AHP for rubber plantation at the Nam Dong district, Thua Thien Hue province

This research was conducted to determine the main influences and physical factors of land suitability for rubber plantation in the Nam Dong district, Thua Thien Hue province. Six factors such as soil type, soil texture, soil thickness, slope, soil pH and soil organic matter content were considered. Results indicate that soil thickness is has the highest role on the land suitability analysis while soil pH has the lowest. The physical land suitability of rubber plantation was divided into 4 levels: very suitable (10.1%), suitable (15.5%), slightly suitable (3.6%), and currently not suitable (70,8%). This research provides important information for rubber cultivation in projected agricultural land use planning of the Nam Dong district.Nghiên cứu này được thực hiện nhằm xác định sự ảnh hưởng của các yếu tố tự nhiên đến sự thích nghi đất đai của loại hình sử dụng đất trồng cây cao su trên địa bàn huyện Nam Đông, tỉnh Thừa Thiên Huế. Có 6 yếu tố được xem xét trong nghiên cứu này bao gồm: loại đất, thành phần cơ giới, tầng dày canh tác, độ dốc, độ chua và hàm lượng mùn trong đất. Kết quả nghiên cứu chỉ ra rằng tầng dày canh tác là yếu tố có ảnh hưởng lớn nhất đến việc sử dụng đất trồng cây cao su, trong khi đó độ chua là yếu tố có ảnh hưởng ít nhất. Sự thích nghi tự nhiên của loại hình sử dụng đất trồng cây cao su được chia thành 4 mức độ bao gồm rất thích nghi (10,1%), thích nghi (15,5%), tương đối thích nghi (3,6%) và hiện taị không thích nghi (70,8%). Nghiên cứu này cung cấp những thông tin cần thiết và hữu ích cho việc quy hoạch sử dụng đất trồng cây cao su trên địa bàn huyện Nam Đông

When Intervention Becomes Imperative: A Case Report of Spontaneous Vulvar Edema During Pregnancy

Spontaneous idiopathic vulvar edema during the second trimester is a rare condition. The approach to managing this condition involves relieving symptoms, identifying underlying causes, and implementing appropriate treatment. Managing such cases during pregnancy is challenging because of concerns for potential adverse fetal outcomes. Conservative management expects the condition to be relieved spontaneously postpartum, whereas invasive treatment offers a more rapid resolution. Treatment choices are controversial because each method has its pros and cons and influences the delivery process to a certain extent. Surgical drainage becomes a viable option when patients are not responsive to medications. We report a case of spontaneous massive vulvar edema in a 22-year-old primigravida in her 23rd week of pregnancy. After ruling out other notable causes of vulvar edema, we decided to intervene using an invasive procedure because she complained of progressive symptoms and discomfort. Subsequently, the edema subsided postprocedure, and the patient experienced successful labor with no complications. This report aims to alert clinicians that drainage attempts should be considered in pregnant patients with worsening symptoms

Clinical outcomes and response to treatment of patients receiving topical treatments for pyoderma gangrenosum: a prospective cohort study

Background: pyoderma gangrenosum (PG) is an uncommon dermatosis with a limited evidence base for treatment. Objective: to estimate the effectiveness of topical therapies in the treatment of PG. Methods: prospective cohort study of UK secondary care patients with a clinical diagnosis of PG suitable for topical treatment (recruited July 2009 to June 2012). Participants received topical therapy following normal clinical practice (mainly Class I-III topical corticosteroids, tacrolimus 0.03% or 0.1%). Primary outcome: speed of healing at 6 weeks. Secondary outcomes: proportion healed by 6 months; time to healing; global assessment; inflammation; pain; quality-of-life; treatment failure and recurrence. Results: Sixty-six patients (22 to 85 years) were enrolled. Clobetasol propionate 0.05% was the most commonly prescribed therapy. Overall, 28/66 (43.8%) of ulcers healed by 6 months. Median time-to-healing was 145 days (95% CI: 96 days, ∞). Initial ulcer size was a significant predictor of time-to-healing (hazard ratio 0.94 (0.88;80 1.00); p = 0.043). Four patients (15%) had a recurrence. Limitations: No randomised comparator Conclusion: Topical therapy is potentially an effective first-line treatment for PG that avoids possible side effects associated with systemic therapy. It remains unclear whether more severe disease will respond adequately to topical therapy alone