Antony Vinh
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Associate Professor
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About
Antony Vinh is an Associate Professor at La Trobe University in Australia. His research primarily focuses on the interplay between gut microbiome, cardiovascular health, and metabolic disorders, as evidenced by his recent publications on neurotransmitter regulation, aortic function, and the implications of diet on health outcomes. Professor Vinh also explores cellular mechanisms in disease progression and the therapeutic potential of cellular therapies for hypertension-related complications.
Recent Grants
Grant: Open
Targeting interleukin 18-mediated inflammation to treat advanced kidney disease
Open Date: 2023-01-01
Close Date: 2028-12-01
Grant: Close
INFLAMMASOMES AND INTERLEUKIN-18 SIGNALLING: NOVEL BIOMARKERS AND THERAPEUTIC TARGETS FOR KIDNEY DISEASE
Open Date: 2018-01-01
Close Date: 2021-12-31
Grant: Close
B cells and autoantibodies in the pathogenesis of hypertension
Open Date: 2018-01-01
Close Date: 2021-12-31
Grant: Close
Dissecting the contribution of T cells and the adaptive immune system to hypertension
Open Date: 2015-01-01
Close Date: 2015-12-01
Grant: Close
Identifying the Function of Tissue-Infiltrating T cells in Hypertension
Open Date: 2013-01-01
Close Date: 2014-01-01
Articles (12)
Year:
2025
Year:
2025
Introduction Animal models are regularly used to test the role of the gut microbiome in hypertension. Small-scale pre-clinical studies have investigated changes to the gut microbiome in the angiotensin II hypertensive model. However, the gut microbiome is influenced by internal and external experimental factors which are not regularly considered in the study design. Once these factors are accounted for, it is unclear if microbiome signatures are reproduceable. We aimed to determine the influence of angiotensin II treatment on the gut microbiome using a large and diverse cohort of mice and to quantify the magnitude by which other factors contribute to microbiome variations. Methods and Results We conducted a retrospective study to establish a diverse mouse cohort resembling large human studies. We sequenced the V4 region of the 16S rRNA gene from 538 samples across the gastrointestinal tract of 303 male and female C57BL/6J mice randomised into sham or angiotensin II treatment from different genotypes, diets, animal facilities, and age groups. Analysing over 17 million sequencing reads, we observed that angiotensin II treatment influenced α-diversity (P = 0.0137) and β-diversity (i.e., composition of the microbiome, P < 0.001). Bacterial abundance analysis revealed patterns consistent with a reduction in short-chain fatty acid-producers, microbial metabolites that lower blood pressure. Furthermore, animal facility, genotype, diet, age, sex, intestinal sampling site, and sequencing batch had significant effects on both α- and β-diversity (all P < 0.001). Sampling site (6.8%) and diet (6%) had the largest impact on the microbiome, while angiotensin II and sex had the smallest effect (each 0.4%). Conclusions Our large-scale data confirmed findings from small-scale studies that angiotensin II impacted the gut microbiome. However, this effect was modest relative to most of the other factors studied. Accounting for these factors in future pre-clinical hypertensive studies will increase the likelihood that microbiome findings are replicable and translatable.
Year:
2024
Year:
2024
Year:
2024
Year:
2024
Year:
2023
Year:
2023
Year:
2023
Year:
2023
Year:
2022
Year:
2022
Collaborators (7)
Grant Drummond
Professor of Physiology
La Trobe University
Katerina Sarapis
Lecturer
La Trobe University
Christopher Sobey
La Trobe University
Alexander Pinto
Baker Heart and Diabetes Institute
Francine Z Marques
MONASH UNIVERSITY
Jessica R. Biesiekierski
-
Rikeish R. Muralitharan
Graduate Teaching Associate
MONASH UNIVERSITY
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