Both Quorum Sensing (Qs)-I and Ii Systems Regulate Escherichia coli Flagellin Expression

Yang Yang; Yun Liu; Mingxu Zhou; Guoqiang Zhu

doi:10.17582/journal.pjz/2018.50.5.1807.1813

Research Article · Volume 50, Issue 5, 6 August 2018 · Open Access

Both Quorum Sensing (Qs)-I and Ii Systems Regulate Escherichia coli Flagellin Expression

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Affiliations & Notes ⌄

¹Jiangsu Co-Innovation Center for Important Animal Infectious Diseases and Zoonoses, College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China 2Institute of Epigenetics and Epigenomics and College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China , * Corresponding author: yzgqzhu@yzu.edu.cn
²yzgqzhu@hotmail.com

Article Info ⌄

Journal:: Pakistan Journal of Zoology
DOI:: 10.17582/journal.pjz/2018.50.5.1807.1813
Published:: 6 August 2018

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From the article

Overall, we show here that expressing QS-1 in E. coli inhibits flagella expression, whereas the LuxS QS-II system up-regulates flagella expression.
These systems are coordinately regulated, as QS-I inhibited QS-II and flagellin expression positively regulated LuxS.
These data suggest that E. coli flagella expression is also regulated by AHLs.

Selected from the article's own text.

Abstract

For elucidating effect of quorum sensing (QS) systems I and II (QS-1 and QS-II) on Escherichia coli flagellin expression, E. coli F18ab strain 107/86 was modified to either express acyl-homoserine lactone (AHL) synthase (QS-I) or deleted for autoinducer 2 (AI-2) expression (QS-II). AHL expression and deletion of luxS (AI-2) both inhibited flagellin expression, as measured by motility assays, bacterial gene expression, and host responses to infection. The QS systems and flagellin were coordinately regulated, as deleting fliC caused decreased QS-II activity.

Introduction

Porcine edema disease and porcine post-weaning diarrhea are two important diseases which bring pigs high morbidity and mortality. Shiga toxin-producing E. coli (STEC) is major pathogen of the diseases ; . Flagella participate in bacterial pathogenicity as important virulence factor. Besides providing motility, it also contributes to bacterial initial adhesion or colonization to host cells. In vivo, enteric bacteria could take advantage of flagella motility to compete with intestinal microbiota by exploiting inflammation , 2008; ; .

Quorum sensing (QS) represents one crucial communication system, and was considered as a kind of bacterial-population based language between bacteria ; . QS-I positive bacteria normally express acyl-homoserine lactone (AHL) synthase, whereas the QS-II system is regulated by LuxS and autoinducer 2 (AI-2) . We previously reported that QS-I expression in E. coli suppresses flagella expression . QS-II also regulates bacterial virulence strategies, including regulate motility by flhDC, type III secretion systems ; ; , as well as biofilm formation and bacterial pathogenicity ; ; .

Here we investigated the extent to which QS-II can also regulate flagellin expression in STEC and examined the potential for coordinate regulation between two QS systems.

Materials and methods

Strains used in this study

Strains and plasmids used are listed in Table I. LB broth or LB agar plates were used for bacterial growth. Caco-2 cell line was cultivated in DMEM with 10 % FBS (37 ˚C, 5 % CO2). Human TNF and IL-8 immunoassay Kits (R&D Systems, Inc.) were purchased for relative experiments.

Construction of recombinant strains

The F18ab luxS gene in-frame deletion mutant (F18abΔluxS) was constructed using λRed-based recombination system . The luxS open reading frame (ORF) was amplified by primers LuxS-1/ LuxS-2 (Table II). Plasmid pBR-luxS was constructed and then transformed into F18abΔluxS to obtain the complemented strain F18abΔluxS/pluxS.

To over-express uvrY and csrB in F18ab, the primers uvrY-F/uvrY-R and csrB-F/csrB-R were used to PCR amplify uvrY and csrB, respectively. uvrY and csrB were cloned into pBR322 and transformed into F18ab E. coli.

AI-2 bioassays and motility assays

After grown to an OD600 of 1.3, supernatants of strains were collected. Bioluminescence was measured in luminescence mode by Tecan GPM reader ; . For motility assays, strains were seeded in the middle of motility agar plates. After appropriate growth time, motility halos were measured .

Table I.- Strains and plasmids used in this study.

Strain or plasmid	Description	Source or reference
Strains
E. coli F18ab 107/86	Wild-type: O139:H1:F18ab, Stx2e; O139:H1:F18ab, Stx2e	Duan et al. (2012)
E. coli F18ab/pyenI	107/86 carrying pyenI	Yang et al. (2013)
E. coli F18ab/pBR	107/86 carrying pBR322	Yang et al. (2013)
E. coli F18abΔfliC	fliC deletion mutant	Duan et al. (2012)
E. coli F18abΔfliC/pfliC	F18abΔfliC carrying pBR-fliC	Duan et al. (2012)
E. coli F18abΔluxS	luxS deletion mutant	This study
E. coli F18abΔluxS/pluxS	F18abΔluxS carrying pBR-luxS	This study
E. coli F18ab/pcsrB	107/86 carrying pcsrB	This study
E. coli F18ab/puvrY	107/86 carrying puvrY	This study
E. coli DH5a	AI-2 bioassay negative control	Takara Ltd.
Vibrio harveyi BB170	AI-2 bioassay reporter strain	Bassler et al. (1994); Yang et al. (2013)
Plasmids
pBR322	Expression vector, Ampr	Takara Ltd.
pBR-luxS	pBR322 carrying LuxS ORF	This study
pKD3	Cmr; Cm cassette template	Datsenko and Wanner (2000); Duan et al. (2012)
pKD46	Ampr, λRed recombinase expression	Datsenko and Wanner (2000); Duan et al. (2012)
pCP20	Ampr,Cmr; Flp recombinase expression	Datsenko and Wanner (2000); Duan et al. (2012)

Table II.- Primers used in this study.

Primer	Sequence (5’-3’)	Primer	Sequence (5’-3’)
LuxS-1	ATGCCGTTGTTAGAT AGCTTCAC	csrA-RT-F	AGCCTGGATACG CTGGTAGA
LuxS-2	CTAGATGTGCAGTTC CTGCAACT	csrA-RT-R	CGAGTTGGTGAG ACCCTCAT
ΔLuxS-1	TGCAGTTCGGGTGGCG AAAACAATGA ACACCCCGCATGGCGA CGCAATCATGT GTAGGCTGGAGCTGCTTCG	barA-RT-F	GCTGCGTACACC ACTGAATG
		barA-RT-R	TGCGTAGTGGGA ATGGAATAC
		fliC-RT –F	CAGCAAGCGGTG AAGTGAA
ΔLuxS-2	TCTGATTCTGATCCTGCAC TTTCAGCAC GTCTTCCATTGCCGCTTTC CCATATGAAT ATCCTCCTTAG	fliC-RT-R	AAGCGTAGCCAC AGTAGCA
		flhD-RT-F	ACTGACTCTTCCG CAAATGGT
		flhD-RT-R	TGGCTGTCAAAAC GGAAGTG
uvrY-F	TAAGGATCCATGGAC ATGAGTAT	il8-RT-F	TGCAGCTCTGTGT GAAGGTG
uvrY-R	TTAGTCGACTCACTGA CTTGATAAT	il8-RT-R	ACTTCTCCACAACC CTCTGC
csrB-F	TAAGGATCCGTCGAC AGGGAGT	il10-RT-F	CCACGCTTTCTAGC TGTTGA
csrB-R	CGCGTCGACAATAAAA AAAGGG	il10-RT-R	CTCCGAGACACTG GAAGGTG
gapA-RT-F	CGTTAAAGGCGCTA ACTTCG	tnfa-RT –F	CCCAGGGACCTCT CTCTAATC
gapA-RT-R	ACGGTGGTCATCAG ACCTTC	tnfa-RT-R	TGAGGTACAGGCC CTCTGAT
uvrY-RT-F	TACCAGCGAAAGTC ATGCAG	GAPDH-RT-F	GATGGGCGTGAAC CATGAG
uvrY-RT-R	CGTTCAGACAAACT GGCAAA	GAPDH-RT-R	GAGGCATTGCTGAC GATCTTG

Measurement of mRNA level

Tiangen RNA Extraction Kit (DP419) was employed in this study, through which total RNA from each strain was prepared . Primers for flhD, fliC, csrA, barA, uvrY, pfs, and luxS genes were designed and listed in Table II. Gene gapA was chosen as the endogenous reference. Caco-2 (1×106 cells/well density) was plated in 6-well plates. 107 CFU of relative strains were injected into each well, and infected for 2 h. Then cells were dealt with Tiangen RNA Extraction Kit following the standard protocol. 2-ΔΔCT method was employed for data analysis.

ELISA assay

Monolayer of Caco-2 was prepared for infection of individual E. coli strains. After 2h incubation, supernatants were obtained by centrifugation . With commercial kits, expression levels of IL-8 and TNF were then measured.

Statistics

All experiments were repeated at least 3 times. Data are presented as the mean + standard deviation. To evaluate statistical significance with p < 0.05 considered significant, the Student’s t-test method was employed.

Results and discussion

QS-1 and QS-II have differential impact on bacterial motility and affect E. coli-induced pro-inflammatory responses

F18ab E. coli was transformed with the yenI gene from Y. enterocolitica to induce endogenous AHL production (QS-1) . Flagella involves in bacterial motility, adhesion, invasion. Furthermore, it could induce inflammation response in host cells. With the recombinant strain, function of AHL (QS-1 signals) upon flagella expression could be identified. Subsequently, expressing pyenI inhibited bacterial motility on swim agar plates (Fig. 1A). Reduced flagella expression was observed in AHL positive strain F18ab/pyenI, as well as decreased motility ability.

QS-II manipulates multiple genes expression through AI-2. In many pathogenic bacteria, AI-2 participates in regulating bacterial virulence strategies. To assess a similar role for QS-2 on motility, we deleted the luxS gene. F18abΔluxS was deficient in AI-2 production (Fig. 1B) and was less motile than the WT strain (Fig. 1A). Consistent with their impaired motility, fliC expression was inhibited in both pyenI and in ΔluxS (Fig. 1C).

Bacterial flagellin can induce pro-inflammatory responses through TLR5. TLR5 stimulates pro-inflammatory genes in NF-κB and MAPK pathways ; . Researchers found that as one pathogen-associated molecular pattern (PAMP), flagellin also have TLR5-independent pro-inflammatory ability by Naip5 and Ipaf, members of the NLR family ; .

These F18ab E. coli strains did not activate the pro-inflammatory IL-8 or TNF responses of infected Caco-2 cells to a magnitude equal to that of infection by WT F18ab E. coli, as measured by both RT-PCR (Fig. 2A, B) or by ELISA (Fig. 2C, D). QS-1 expression inhibits F18 E. coli motility, whereas QS-II expression enhances motility by affecting fliC expression.

AI-1 and flagella expression influence AI-2

AI-2 activity was impaired in F18ab/pyenI, indicating that QS-1 influences AI-2 production (Fig. 1B). The phenomenon was consistent with the decreased mRNA level of both luxS and pfs in F18ab/pyenI (Fig. 3), which encode enzymes involved in AI-2 synthesis in E. coli . Pfs, an important functional enzyme in AI-2 signal synthesis, encounter 25 % decrease of mRNA level under QS-1 influence, while flagella motility was reduced heavily in luxS mutant. FliC expression also regulated QS-II, as deleting fliC inhibited pfs and luxS expression (Fig. 3).

Coordinate regulation of flagella and QS expression

Bacteria utilize two-component systems for adaptation to environmental changes , 2003; ; . The BarA/UvrY and the CsrA/CsrB two-component systems regulate flagella expression . UvrY can activate barA expression through an auto-regulatory loop. Influence of CsrA upon csrB is regulated partly by barA, and a BarA-independent, UvrY-dependent mechanism also involves. CsrA indirectly induces csrB transcription. UvrY can directly activate csrB transcription, and also is included in up-regulation of CsrA. Increased transcription of uvrY has been observed when E. coli is sustained in an AHL-positive environment ; .

In this study, expression of barA and uvrY were increased by 2.3- and 2.7-fold, respectively, in F18ab/pyenI (Fig. 4). Up-regulation of uvrY and barA can induce csrB transcription, which binds to CsrA and antagonizes its regulatory effects upon flhDC ; ; . flhD expression did decreased 2.1-fold in pyenI (Fig. 4). Over-expressing uvrY and csrB caused a 1.7- and 2.3-fold reduction in fliC expression, respectively (Fig. 1C).

Conclusions

Overall, we show here that expressing QS-1 in E. coli inhibits flagella expression, whereas the LuxS QS-II system up-regulates flagella expression. These systems are coordinately regulated, as QS-I inhibited QS-II and flagellin expression positively regulated LuxS. We implicate the BarA/UvrY and the CsrA/CsrB two-component systems as possible regulators of this coordinated regulation. In the presence of cattle rumen AHLs, E. coli O157:H7 represses LEE gene expression and activates gad expression to improve acid tolerance ; . Other aspects of E. coli biology are also regulated by AHLs, including cell division and antibiotic resistance . These data suggest that E. coli flagella expression is also regulated by AHLs.

Acknowledgements

This study was supported by grants from the 13th Five-Year National Key Development Program (2016YFD0501000), Natural Science Foundation of Jiangsu Province (BK20150442), the Chinese National Science Foundation Grants (Nos. 31502075, 31072136, 31270171 and 30771603), the Genetically Modified Organisms Technology Major Project of China (2014ZX08006-001B), Program for Chang Jiang Scholars and Innovative Research Team In University “PCSIRT” (IRT0978), 948 programme from Ministry of Agriculture of the People’s Republic of China (grant No. 2011-G24) and the Priority Academic Program Development of Jiangsu Higher Education Institutions.

Statement of conflict of interest

The authors or their institution do not have any relationships that may influence or bias the results and data presented in this manuscript. There is no conflict of interests regarding the publication of the manuscript.

Figures

Fig. 1..
QS-1 and QS-II have differential impact on bacterial motility. A, motility diameters were quantified after 12 h growth on 0.3 % swim agar plates; B, AI-2 production, AI-2 activity was measured using a bioluminescence assay after growing the indicated bacterial strains to an OD600 of 1.3. AI-2 activity is expressed as relative light units measured; C, fliC expression. fliC expression was measured using qRT-PCR with data normalized to the endogenous reference gene gapA. Data are expressed relative to expression in the WT strain.

Fig. 2..
Host IL-8 and TNF expression in response to F18 E. coli infection. A-B, transcription of il8 and tnfa in Caco-2 cells after a 2 h infection with the indicated bacterial strains. Data were normalized to the housekeeping gene gapdh; C-D, ELISA, secretion of IL-8 and TNF into Caco-2 cell supernatants after a 2 h infection with the indicated bacterial strains was quantified using ELISAs.

Fig. 3..
AI-1 and flagella expression influence AI-2 expression. luxS and pfs expression were measured using qRT-PCR with data normalized to the endogenous reference gene gapA. Data are expressed relative to expression in the WT strain.

Fig. 4..
Coordinate regulation of flagella and QS expression. Transcription of the indicated genes was measured using qRT-PCR. Data are shown as expression in pyenI vs. WT.

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[1] Anand, S.K. and Griffiths, M.W., 2003. Quorum sensing and expression of virulence in Escherichia coli O157:H7. Int. J. Fd. Microbiol., 85: 1-9. https://doi.org/10.1016/S0168-1605(02)00482-8[CrossRef]

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