Identification of MicroRNAs Regulating <i>Clostridium perfringens</i> Type C Infection in the Spleen of Diarrheic Piglets

<i>Clostridium perfringens</i> (<i>C. perfringens</i>) type C is one of the common bacteria in piglet diarrhea, which seriously affects the swine industry’s development. The spleen plays crucial roles in the resistance and elimination of pathogenic microorganisms, and miRNAs...

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Main Authors: Pengfei Wang, Qiaoli Yang, Zunqiang Yan, Xiaoyu Huang, Xiaoli Gao, Shuangbao Gun
Format: Article
Language:English
Published: MDPI AG 2023-04-01
Series:Current Issues in Molecular Biology
Subjects:
Online Access:https://www.mdpi.com/1467-3045/45/4/208
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author Pengfei Wang
Qiaoli Yang
Zunqiang Yan
Xiaoyu Huang
Xiaoli Gao
Shuangbao Gun
author_facet Pengfei Wang
Qiaoli Yang
Zunqiang Yan
Xiaoyu Huang
Xiaoli Gao
Shuangbao Gun
author_sort Pengfei Wang
collection DOAJ
description <i>Clostridium perfringens</i> (<i>C. perfringens</i>) type C is one of the common bacteria in piglet diarrhea, which seriously affects the swine industry’s development. The spleen plays crucial roles in the resistance and elimination of pathogenic microorganisms, and miRNAs play important roles in regulating piglet diarrhea caused by pathogens. However, the mechanism by which miRNAs in the spleen are involved in regulating <i>C. perfringens</i> type C causing diarrhea in piglets remains unclear. The expression profiles of the spleen miRNAs of 7-day-old piglets challenged by <i>C. perfringens</i> type C were studied using small RNA-sequencing in control (SC), susceptible (SS), and resistant (SR) groups. Eight-eight differentially expressed miRNAs were screened. The KEGG pathway analysis of target genes revealed that the miRNAs were involved in the MAPK, p53, and ECM–receptor interaction signaling pathways. <i>NFATC4</i> was determined to be a direct target of miR-532-3p and miR-133b using a dual-luciferase reporter assay. Thus, miR-133b and miR-532-3p targeted to <i>NFATC4</i> were likely involved to piglet resistance to <i>C. perfringens</i> type C. This paper provides the valuable resources to deeply understand the genetic basis of <i>C. perfringens</i> type C resistance in piglets and a solid foundation to identify novel markers of <i>C. perfringens</i> type C resistance.
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spelling doaj.art-722fb57fe2ed49debf3660531925199d2023-11-17T18:47:48ZengMDPI AGCurrent Issues in Molecular Biology1467-30371467-30452023-04-014543193320710.3390/cimb45040208Identification of MicroRNAs Regulating <i>Clostridium perfringens</i> Type C Infection in the Spleen of Diarrheic PigletsPengfei Wang0Qiaoli Yang1Zunqiang Yan2Xiaoyu Huang3Xiaoli Gao4Shuangbao Gun5College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, ChinaCollege of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, ChinaCollege of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, ChinaCollege of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, ChinaCollege of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, ChinaCollege of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China<i>Clostridium perfringens</i> (<i>C. perfringens</i>) type C is one of the common bacteria in piglet diarrhea, which seriously affects the swine industry’s development. The spleen plays crucial roles in the resistance and elimination of pathogenic microorganisms, and miRNAs play important roles in regulating piglet diarrhea caused by pathogens. However, the mechanism by which miRNAs in the spleen are involved in regulating <i>C. perfringens</i> type C causing diarrhea in piglets remains unclear. The expression profiles of the spleen miRNAs of 7-day-old piglets challenged by <i>C. perfringens</i> type C were studied using small RNA-sequencing in control (SC), susceptible (SS), and resistant (SR) groups. Eight-eight differentially expressed miRNAs were screened. The KEGG pathway analysis of target genes revealed that the miRNAs were involved in the MAPK, p53, and ECM–receptor interaction signaling pathways. <i>NFATC4</i> was determined to be a direct target of miR-532-3p and miR-133b using a dual-luciferase reporter assay. Thus, miR-133b and miR-532-3p targeted to <i>NFATC4</i> were likely involved to piglet resistance to <i>C. perfringens</i> type C. This paper provides the valuable resources to deeply understand the genetic basis of <i>C. perfringens</i> type C resistance in piglets and a solid foundation to identify novel markers of <i>C. perfringens</i> type C resistance.https://www.mdpi.com/1467-3045/45/4/208pigletdiarrheaspleenmiRNA<i>C. perfringens</i> type Cresistance
spellingShingle Pengfei Wang
Qiaoli Yang
Zunqiang Yan
Xiaoyu Huang
Xiaoli Gao
Shuangbao Gun
Identification of MicroRNAs Regulating <i>Clostridium perfringens</i> Type C Infection in the Spleen of Diarrheic Piglets
Current Issues in Molecular Biology
piglet
diarrhea
spleen
miRNA
<i>C. perfringens</i> type C
resistance
title Identification of MicroRNAs Regulating <i>Clostridium perfringens</i> Type C Infection in the Spleen of Diarrheic Piglets
title_full Identification of MicroRNAs Regulating <i>Clostridium perfringens</i> Type C Infection in the Spleen of Diarrheic Piglets
title_fullStr Identification of MicroRNAs Regulating <i>Clostridium perfringens</i> Type C Infection in the Spleen of Diarrheic Piglets
title_full_unstemmed Identification of MicroRNAs Regulating <i>Clostridium perfringens</i> Type C Infection in the Spleen of Diarrheic Piglets
title_short Identification of MicroRNAs Regulating <i>Clostridium perfringens</i> Type C Infection in the Spleen of Diarrheic Piglets
title_sort identification of micrornas regulating i clostridium perfringens i type c infection in the spleen of diarrheic piglets
topic piglet
diarrhea
spleen
miRNA
<i>C. perfringens</i> type C
resistance
url https://www.mdpi.com/1467-3045/45/4/208
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