Salmonella Typhimurium fepB negatively regulates C. elegans behavioral plasticity

秀丽隐杆线虫 生物 突变体 沙门氏菌 微生物学 拉伤 运动性 免疫系统 生物膜 细菌 基因 细胞生物学 遗传学 解剖
作者
Swarupa Mallick,Neha Mishra,Bedanta Kumar Barik,Vidya Devi Negi
出处
期刊:Journal of Infection [Elsevier BV]
卷期号:84 (4): 518-530 被引量:4
标识
DOI:10.1016/j.jinf.2021.12.043
摘要

Dauer is an alternative developmental stage of Caenorhabditis elegans (C. elegans) that gives survival benefits under unfavorable environmental conditions. Our study aims to decipher C. elegans dauer larvae development upon Salmonella Typhimurium infection and how the bacterial gene regulating the worm's behavioural plasticity for better survival.Age-synchronized L4 C. elegans worms were infected with Salmonella Typhimurium 14028s (WT-STM) strain and mutant strains to check the dauer larvae development using 1% SDS. Besides, bacterial load in animals' gut, pharyngeal pumping rate and viability were checked. Worm's immune genes (e.g., ilys-3, lys-7, pmk-1, abf-2, clec-60) and dauer regulatory genes (e.g., daf-7, daf-11, daf-12, daf-16, daf-3) were checked by performing qRT-PCR under infection conditions.We found that deletion of the fepB gene in S. Typhimurium strain became less pathogenic with reduced flagellar motility and biofilm-forming ability. Besides, there was decreased bacterial burden in the worm's gut with no damage to their pharynx. The fepB mutant strain was also able to enhance the immune responses for better survival of worms. Infection with mutant strain could activate dauer signaling via the TGF-β pathway leading to a significant increase in dauer formation than WT-STM infection.Our study indicated that the bacteria act as a food source for the growth of C. elegans and development and can act as a signal that might be playing an essential role in regulating the host physiology for their survival. Such a study can help us in understanding the complex host-pathogen interaction benefiting pathogen in host dissemination.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Lucas应助科研通管家采纳,获得10
1秒前
英姑应助科研通管家采纳,获得10
1秒前
上官若男应助科研通管家采纳,获得10
1秒前
李健应助科研通管家采纳,获得10
1秒前
冰魂应助科研通管家采纳,获得10
1秒前
科研通AI5应助科研通管家采纳,获得50
1秒前
Hello应助科研通管家采纳,获得10
1秒前
小蘑菇应助科研通管家采纳,获得10
1秒前
1秒前
1秒前
1秒前
纸芯完成签到 ,获得积分10
1秒前
djdh完成签到 ,获得积分10
4秒前
魏白晴发布了新的文献求助10
5秒前
无语的凡梦完成签到 ,获得积分10
5秒前
dnbe完成签到 ,获得积分10
5秒前
科研通AI5应助HYLJ采纳,获得10
6秒前
8秒前
jagger完成签到,获得积分10
10秒前
杨炀发布了新的文献求助10
12秒前
Orange应助Gakay采纳,获得10
15秒前
Gino完成签到,获得积分0
15秒前
16秒前
gstsgd完成签到 ,获得积分10
17秒前
17秒前
18秒前
空白完成签到,获得积分10
19秒前
20秒前
青山落日秋月春风完成签到,获得积分10
21秒前
小白发布了新的文献求助10
21秒前
科研通AI5应助杨炀采纳,获得10
23秒前
Wjh123456完成签到,获得积分10
23秒前
笑点低静竹关注了科研通微信公众号
24秒前
沉默的小耳朵完成签到 ,获得积分10
24秒前
nwds完成签到,获得积分10
24秒前
木香发布了新的文献求助10
24秒前
刘七七努力搞科研完成签到 ,获得积分10
25秒前
25秒前
25秒前
眼睛大的电脑完成签到 ,获得积分10
25秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024) 3000
Continuum Thermodynamics and Material Modelling 2000
Encyclopedia of Geology (2nd Edition) 2000
105th Edition CRC Handbook of Chemistry and Physics 1600
Maneuvering of a Damaged Navy Combatant 650
Fashion Brand Visual Design Strategy Based on Value Co-creation 350
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3777767
求助须知:如何正确求助?哪些是违规求助? 3323293
关于积分的说明 10213450
捐赠科研通 3038542
什么是DOI,文献DOI怎么找? 1667545
邀请新用户注册赠送积分活动 798152
科研通“疑难数据库(出版商)”最低求助积分说明 758275