LncRNA BACE1-AS delays the propagation of Cryptosporidium parvum through regulating cell apoptosis by targeting the miR-6805-5p/IRF3 axis

ABSTRACT Cryptosporidium spp. are important zoonotic pathogens causing diarrhea in humans and various animals. To date, there are still no effective drugs and vaccines for the prevention and treatment of cryptosporidiosis, mainly due to the absence of knowledge on the interaction mechanisms between...

Full description

Saved in:
Bibliographic Details
Main Authors: Shuang Huang, Xin Yang, Ting-Li Liu, Gui-Rong Hu, Qian Yao, Jun-Ke Song, Ying-Ying Fan, Guang-Hui Zhao
Format: Article
Language:English
Published: American Society for Microbiology 2025-07-01
Series:Microbiology Spectrum
Subjects:
Online Access:https://journals.asm.org/doi/10.1128/spectrum.02022-24
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849429410076164096
author Shuang Huang
Xin Yang
Ting-Li Liu
Gui-Rong Hu
Qian Yao
Jun-Ke Song
Ying-Ying Fan
Guang-Hui Zhao
author_facet Shuang Huang
Xin Yang
Ting-Li Liu
Gui-Rong Hu
Qian Yao
Jun-Ke Song
Ying-Ying Fan
Guang-Hui Zhao
author_sort Shuang Huang
collection DOAJ
description ABSTRACT Cryptosporidium spp. are important zoonotic pathogens causing diarrhea in humans and various animals. To date, there are still no effective drugs and vaccines for the prevention and treatment of cryptosporidiosis, mainly due to the absence of knowledge on the interaction mechanisms between hosts and Cryptosporidium. Increasing evidence has indicated that long non-coding RNAs (lncRNAs) play significant roles in various physiological and pathological processes. Our previous study showed that Cryptosporidium parvum infection induced significant differential changes in lncRNA expression profiles in HCT-8 cells. BACE1-AS was a significantly downregulated lncRNA in HCT-8 cells during C. parvum infection, but its roles were still unknown. Results of the present study indicated that C. parvum infection significantly downregulated the expression of BACE1-AS probably through regulating the nuclear factor kappa-B (NF-κB) signaling pathway, and the expression of BACE1-AS was negatively related to the propagation of C. parvum in HCT-8 cells. BACE1-AS was mainly localized outside of the nucleus of HCT-8 cells and promoted the expression of IRF3 by sponging miR-6805-5p during C. parvum infection. Further studies indicated that the BACE1-AS/miR-6805-5p/IRF3 axis delayed in vitro propagation of C. parvum through regulating BCL2-mediated apoptosis of HCT-8 cells. The present study enriches our knowledge on the function of host lncRNAs during Cryptosporidium infection and contributes to our understanding of the interaction between hosts and Cryptosporidium.IMPORTANCERecent studies indicate that Cryptosporidium can regulate cell apoptosis to promote its development in host cells, but the mechanism is still unclear. This study identified a significantly downregulated host lncRNA BACE1-AS during C. parvum infection, which could regulate cell apoptosis to affect the propagation of C. parvum in vitro by targeting the miR-6805-5p/IRF3 axis. The present study contributes to our understanding of the pathogenesis of Cryptosporidium and provides potential targets for the development of drugs and vaccines against cryptosporidiosis.
format Article
id doaj-art-8b5d7274d5a0458aaace8bb2f7ade29a
institution Kabale University
issn 2165-0497
language English
publishDate 2025-07-01
publisher American Society for Microbiology
record_format Article
series Microbiology Spectrum
spelling doaj-art-8b5d7274d5a0458aaace8bb2f7ade29a2025-08-20T03:28:22ZengAmerican Society for MicrobiologyMicrobiology Spectrum2165-04972025-07-0113710.1128/spectrum.02022-24LncRNA BACE1-AS delays the propagation of Cryptosporidium parvum through regulating cell apoptosis by targeting the miR-6805-5p/IRF3 axisShuang Huang0Xin Yang1Ting-Li Liu2Gui-Rong Hu3Qian Yao4Jun-Ke Song5Ying-Ying Fan6Guang-Hui Zhao7College of Veterinary Medicine, Northwest A&F University, Yangling, ChinaCollege of Veterinary Medicine, Northwest A&F University, Yangling, ChinaCollege of Veterinary Medicine, Northwest A&F University, Yangling, ChinaCollege of Veterinary Medicine, Northwest A&F University, Yangling, ChinaCollege of Veterinary Medicine, Northwest A&F University, Yangling, ChinaCollege of Veterinary Medicine, Northwest A&F University, Yangling, ChinaCollege of Veterinary Medicine, Northwest A&F University, Yangling, ChinaCollege of Veterinary Medicine, Northwest A&F University, Yangling, ChinaABSTRACT Cryptosporidium spp. are important zoonotic pathogens causing diarrhea in humans and various animals. To date, there are still no effective drugs and vaccines for the prevention and treatment of cryptosporidiosis, mainly due to the absence of knowledge on the interaction mechanisms between hosts and Cryptosporidium. Increasing evidence has indicated that long non-coding RNAs (lncRNAs) play significant roles in various physiological and pathological processes. Our previous study showed that Cryptosporidium parvum infection induced significant differential changes in lncRNA expression profiles in HCT-8 cells. BACE1-AS was a significantly downregulated lncRNA in HCT-8 cells during C. parvum infection, but its roles were still unknown. Results of the present study indicated that C. parvum infection significantly downregulated the expression of BACE1-AS probably through regulating the nuclear factor kappa-B (NF-κB) signaling pathway, and the expression of BACE1-AS was negatively related to the propagation of C. parvum in HCT-8 cells. BACE1-AS was mainly localized outside of the nucleus of HCT-8 cells and promoted the expression of IRF3 by sponging miR-6805-5p during C. parvum infection. Further studies indicated that the BACE1-AS/miR-6805-5p/IRF3 axis delayed in vitro propagation of C. parvum through regulating BCL2-mediated apoptosis of HCT-8 cells. The present study enriches our knowledge on the function of host lncRNAs during Cryptosporidium infection and contributes to our understanding of the interaction between hosts and Cryptosporidium.IMPORTANCERecent studies indicate that Cryptosporidium can regulate cell apoptosis to promote its development in host cells, but the mechanism is still unclear. This study identified a significantly downregulated host lncRNA BACE1-AS during C. parvum infection, which could regulate cell apoptosis to affect the propagation of C. parvum in vitro by targeting the miR-6805-5p/IRF3 axis. The present study contributes to our understanding of the pathogenesis of Cryptosporidium and provides potential targets for the development of drugs and vaccines against cryptosporidiosis.https://journals.asm.org/doi/10.1128/spectrum.02022-24Cryptosporidium parvumBACE1-ASmiR-6805-5pIRF3apoptosispropagation
spellingShingle Shuang Huang
Xin Yang
Ting-Li Liu
Gui-Rong Hu
Qian Yao
Jun-Ke Song
Ying-Ying Fan
Guang-Hui Zhao
LncRNA BACE1-AS delays the propagation of Cryptosporidium parvum through regulating cell apoptosis by targeting the miR-6805-5p/IRF3 axis
Microbiology Spectrum
Cryptosporidium parvum
BACE1-AS
miR-6805-5p
IRF3
apoptosis
propagation
title LncRNA BACE1-AS delays the propagation of Cryptosporidium parvum through regulating cell apoptosis by targeting the miR-6805-5p/IRF3 axis
title_full LncRNA BACE1-AS delays the propagation of Cryptosporidium parvum through regulating cell apoptosis by targeting the miR-6805-5p/IRF3 axis
title_fullStr LncRNA BACE1-AS delays the propagation of Cryptosporidium parvum through regulating cell apoptosis by targeting the miR-6805-5p/IRF3 axis
title_full_unstemmed LncRNA BACE1-AS delays the propagation of Cryptosporidium parvum through regulating cell apoptosis by targeting the miR-6805-5p/IRF3 axis
title_short LncRNA BACE1-AS delays the propagation of Cryptosporidium parvum through regulating cell apoptosis by targeting the miR-6805-5p/IRF3 axis
title_sort lncrna bace1 as delays the propagation of cryptosporidium parvum through regulating cell apoptosis by targeting the mir 6805 5p irf3 axis
topic Cryptosporidium parvum
BACE1-AS
miR-6805-5p
IRF3
apoptosis
propagation
url https://journals.asm.org/doi/10.1128/spectrum.02022-24
work_keys_str_mv AT shuanghuang lncrnabace1asdelaysthepropagationofcryptosporidiumparvumthroughregulatingcellapoptosisbytargetingthemir68055pirf3axis
AT xinyang lncrnabace1asdelaysthepropagationofcryptosporidiumparvumthroughregulatingcellapoptosisbytargetingthemir68055pirf3axis
AT tingliliu lncrnabace1asdelaysthepropagationofcryptosporidiumparvumthroughregulatingcellapoptosisbytargetingthemir68055pirf3axis
AT guironghu lncrnabace1asdelaysthepropagationofcryptosporidiumparvumthroughregulatingcellapoptosisbytargetingthemir68055pirf3axis
AT qianyao lncrnabace1asdelaysthepropagationofcryptosporidiumparvumthroughregulatingcellapoptosisbytargetingthemir68055pirf3axis
AT junkesong lncrnabace1asdelaysthepropagationofcryptosporidiumparvumthroughregulatingcellapoptosisbytargetingthemir68055pirf3axis
AT yingyingfan lncrnabace1asdelaysthepropagationofcryptosporidiumparvumthroughregulatingcellapoptosisbytargetingthemir68055pirf3axis
AT guanghuizhao lncrnabace1asdelaysthepropagationofcryptosporidiumparvumthroughregulatingcellapoptosisbytargetingthemir68055pirf3axis