Arginine Deiminase and Biotin Metabolism Signaling Pathways Play an Important Role in Human-Derived Serotype V, ST1 Streptococcus agalactiae Virulent Strain upon Infected Tilapia

Our previous study showed that human-derived Streptococcus agalactiae (serotype V) could infect tilapia, but the mechanism underlying the cross-species infection remains unrecognized. In this study, a multi-omics analysis was performed on human-derived S.agalactiae strain NNA048 (virulent to tilapia...

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Main Authors: Yu Liu, Liping Li, Zhiping Luo, Rui Wang, Ting Huang, Wanwen Liang, Qunhong Gu, Fangzhao Yu, Ming Chen
Format: Article
Language:English
Published: MDPI AG 2020-05-01
Series:Animals
Subjects:
Online Access:https://www.mdpi.com/2076-2615/10/5/849
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author Yu Liu
Liping Li
Zhiping Luo
Rui Wang
Ting Huang
Wanwen Liang
Qunhong Gu
Fangzhao Yu
Ming Chen
author_facet Yu Liu
Liping Li
Zhiping Luo
Rui Wang
Ting Huang
Wanwen Liang
Qunhong Gu
Fangzhao Yu
Ming Chen
author_sort Yu Liu
collection DOAJ
description Our previous study showed that human-derived Streptococcus agalactiae (serotype V) could infect tilapia, but the mechanism underlying the cross-species infection remains unrecognized. In this study, a multi-omics analysis was performed on human-derived S.agalactiae strain NNA048 (virulent to tilapia, serotype V, ST1) and human-derived S.agalactiae strain NNA038 (non-virulent to tilapia, serotype V, ST1). The results showed that 907 genes (504 up/403 down) and 89 proteins (51 up/38 down) were differentially expressed (p < 0.05) between NNA038 and NNA048. Among them, 56 genes (proteins) were altered with similar trends at both mRNA and protein levels. Functional annotation of them showed that the main differences were enriched in the arginine deiminase system signaling pathway and biotin metabolism signaling pathway: gdhA, glnA, ASL, ADI, OTC, arcC, FabF, FabG, FabZ, BioB and BirA genes may have been important factors leading to the pathogenicity differences between NNA038 and NNA048. We aimed to provide a comprehensive analysis of the human-derived serotype V ST1 S.agalactiae strains, which were virulent and non-virulent to tilapia, and provide a more comprehensive understanding of the virulence mechanism.
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spelling doaj.art-be8b1313abe948a4a8be04862b6bd7b32023-11-20T00:28:31ZengMDPI AGAnimals2076-26152020-05-0110584910.3390/ani10050849Arginine Deiminase and Biotin Metabolism Signaling Pathways Play an Important Role in Human-Derived Serotype V, ST1 Streptococcus agalactiae Virulent Strain upon Infected TilapiaYu Liu0Liping Li1Zhiping Luo2Rui Wang3Ting Huang4Wanwen Liang5Qunhong Gu6Fangzhao Yu7Ming Chen8Guangxi Academy of Fishery Sciences, Nanning 530021, ChinaGuangxi Academy of Fishery Sciences, Nanning 530021, ChinaZhuhai modern agriculture development center, Zhuhai 519000, ChinaGuangxi Academy of Fishery Sciences, Nanning 530021, ChinaGuangxi Academy of Fishery Sciences, Nanning 530021, ChinaGuangxi Academy of Fishery Sciences, Nanning 530021, ChinaZhuhai modern agriculture development center, Zhuhai 519000, ChinaZhuhai modern agriculture development center, Zhuhai 519000, ChinaGuangxi Academy of Fishery Sciences, Nanning 530021, ChinaOur previous study showed that human-derived Streptococcus agalactiae (serotype V) could infect tilapia, but the mechanism underlying the cross-species infection remains unrecognized. In this study, a multi-omics analysis was performed on human-derived S.agalactiae strain NNA048 (virulent to tilapia, serotype V, ST1) and human-derived S.agalactiae strain NNA038 (non-virulent to tilapia, serotype V, ST1). The results showed that 907 genes (504 up/403 down) and 89 proteins (51 up/38 down) were differentially expressed (p < 0.05) between NNA038 and NNA048. Among them, 56 genes (proteins) were altered with similar trends at both mRNA and protein levels. Functional annotation of them showed that the main differences were enriched in the arginine deiminase system signaling pathway and biotin metabolism signaling pathway: gdhA, glnA, ASL, ADI, OTC, arcC, FabF, FabG, FabZ, BioB and BirA genes may have been important factors leading to the pathogenicity differences between NNA038 and NNA048. We aimed to provide a comprehensive analysis of the human-derived serotype V ST1 S.agalactiae strains, which were virulent and non-virulent to tilapia, and provide a more comprehensive understanding of the virulence mechanism.https://www.mdpi.com/2076-2615/10/5/849Streptococcus agalactiaeOreochromis niloticuscross-species infectiontranscriptomeproteome
spellingShingle Yu Liu
Liping Li
Zhiping Luo
Rui Wang
Ting Huang
Wanwen Liang
Qunhong Gu
Fangzhao Yu
Ming Chen
Arginine Deiminase and Biotin Metabolism Signaling Pathways Play an Important Role in Human-Derived Serotype V, ST1 Streptococcus agalactiae Virulent Strain upon Infected Tilapia
Animals
Streptococcus agalactiae
Oreochromis niloticus
cross-species infection
transcriptome
proteome
title Arginine Deiminase and Biotin Metabolism Signaling Pathways Play an Important Role in Human-Derived Serotype V, ST1 Streptococcus agalactiae Virulent Strain upon Infected Tilapia
title_full Arginine Deiminase and Biotin Metabolism Signaling Pathways Play an Important Role in Human-Derived Serotype V, ST1 Streptococcus agalactiae Virulent Strain upon Infected Tilapia
title_fullStr Arginine Deiminase and Biotin Metabolism Signaling Pathways Play an Important Role in Human-Derived Serotype V, ST1 Streptococcus agalactiae Virulent Strain upon Infected Tilapia
title_full_unstemmed Arginine Deiminase and Biotin Metabolism Signaling Pathways Play an Important Role in Human-Derived Serotype V, ST1 Streptococcus agalactiae Virulent Strain upon Infected Tilapia
title_short Arginine Deiminase and Biotin Metabolism Signaling Pathways Play an Important Role in Human-Derived Serotype V, ST1 Streptococcus agalactiae Virulent Strain upon Infected Tilapia
title_sort arginine deiminase and biotin metabolism signaling pathways play an important role in human derived serotype v st1 streptococcus agalactiae virulent strain upon infected tilapia
topic Streptococcus agalactiae
Oreochromis niloticus
cross-species infection
transcriptome
proteome
url https://www.mdpi.com/2076-2615/10/5/849
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