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Global metabolomic analysis of blood from mice infected with Brucella abortus

To better understanding Brucella abortus infection, serum metabolites of B. abortus-infected and -uninfected mice were analyzed and twenty-one metabolites were tentatively identified at 3 and 14 days post-infection (d.p.i.). Level of most lysophosphatidylcholines (LPCs) was found to increase in infe...

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Autores principales: VU, Son Hai, KIM, Bomin, REYES, Alisha Wehdnesday Bernardo, HUY, Tran Xuan Ngoc, LEE, John Hwa, KIM, Suk, KIM, Hyun-Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025415/
https://www.ncbi.nlm.nih.gov/pubmed/33473061
http://dx.doi.org/10.1292/jvms.20-0630
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author VU, Son Hai
KIM, Bomin
REYES, Alisha Wehdnesday Bernardo
HUY, Tran Xuan Ngoc
LEE, John Hwa
KIM, Suk
KIM, Hyun-Jin
author_facet VU, Son Hai
KIM, Bomin
REYES, Alisha Wehdnesday Bernardo
HUY, Tran Xuan Ngoc
LEE, John Hwa
KIM, Suk
KIM, Hyun-Jin
author_sort VU, Son Hai
collection PubMed
description To better understanding Brucella abortus infection, serum metabolites of B. abortus-infected and -uninfected mice were analyzed and twenty-one metabolites were tentatively identified at 3 and 14 days post-infection (d.p.i.). Level of most lysophosphatidylcholines (LPCs) was found to increase in infected mice at 3 d.p.i., while it was decreased at 14 d.p.i. as compared to uninfected mice. In contrast, acylcarnitines were initially reduced at 3 d.p.i then elevated after two-weeks of infection, while hydroxysanthine was increased at 14 d.p.i. in infected mice. Our findings suggest that the significant changes in LPCs and other identified metabolites may serve as potential biomarkers in acute phase of B. abortus infection.
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spelling pubmed-80254152021-04-13 Global metabolomic analysis of blood from mice infected with Brucella abortus VU, Son Hai KIM, Bomin REYES, Alisha Wehdnesday Bernardo HUY, Tran Xuan Ngoc LEE, John Hwa KIM, Suk KIM, Hyun-Jin J Vet Med Sci Public Health To better understanding Brucella abortus infection, serum metabolites of B. abortus-infected and -uninfected mice were analyzed and twenty-one metabolites were tentatively identified at 3 and 14 days post-infection (d.p.i.). Level of most lysophosphatidylcholines (LPCs) was found to increase in infected mice at 3 d.p.i., while it was decreased at 14 d.p.i. as compared to uninfected mice. In contrast, acylcarnitines were initially reduced at 3 d.p.i then elevated after two-weeks of infection, while hydroxysanthine was increased at 14 d.p.i. in infected mice. Our findings suggest that the significant changes in LPCs and other identified metabolites may serve as potential biomarkers in acute phase of B. abortus infection. The Japanese Society of Veterinary Science 2021-01-19 2021-03 /pmc/articles/PMC8025415/ /pubmed/33473061 http://dx.doi.org/10.1292/jvms.20-0630 Text en ©2021 The Japanese Society of Veterinary Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Public Health
VU, Son Hai
KIM, Bomin
REYES, Alisha Wehdnesday Bernardo
HUY, Tran Xuan Ngoc
LEE, John Hwa
KIM, Suk
KIM, Hyun-Jin
Global metabolomic analysis of blood from mice infected with Brucella abortus
title Global metabolomic analysis of blood from mice infected with Brucella abortus
title_full Global metabolomic analysis of blood from mice infected with Brucella abortus
title_fullStr Global metabolomic analysis of blood from mice infected with Brucella abortus
title_full_unstemmed Global metabolomic analysis of blood from mice infected with Brucella abortus
title_short Global metabolomic analysis of blood from mice infected with Brucella abortus
title_sort global metabolomic analysis of blood from mice infected with brucella abortus
topic Public Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025415/
https://www.ncbi.nlm.nih.gov/pubmed/33473061
http://dx.doi.org/10.1292/jvms.20-0630
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