Influence of pCP1NetB ancillary genes on the virulence of Clostridium perfringens poultry necrotic enteritis strain CP1
© Crown copyright; licensee BioMed Central Ltd. 2017
Received: 1 October 2016
Accepted: 15 December 2016
Published: 21 January 2017
Necrotic enteritis (NE) is an economically important disease of poultry caused by certain Clostridium perfringens type A strains. The NetB toxin plays a critical role in the pathogenesis of NE. We previously demonstrated that netB is located within a 42 kb plasmid-encoded pathogenicity locus (NELoc-1), which also encodes 36 additional genes. Although NetB clearly plays a role in pathogenesis, the involvement of the other NELoc-1 genes has not yet been established. The current study was to provide experimental evidence to confirm the involvement of these genes in NE pathogenesis.
The present study has characterized a virulent C. perfringens strain (CP1) that has spontaneously lost the NELoc-1-encoding plasmid, pCP1netB. When assessed for cytotoxicity on Leghorn Male Hepatoma (LMH) cells, the culture supernatant of the pCP1netB-deficient CP1 variant (CP1ΔpCP1netB) demonstrated significantly reduced cytotoxicity compared to the wild-type. In addition, CP1ΔpCP1netB was unable to cause intestinal lesions in chickens in a NE disease model. When netB alone was introduced into CP1ΔpCP1netB, in vitro cytotoxicity was restored to the wild-type level; however, it did not completely restore virulence when used to challenge broiler chickens [mean lesion score of 0.71 compared to 3.23 in the wild type control group (n = 14)].
The results of this study suggest that other genes present in NELoc-1, in addition to netB, are required for full virulence in the chicken challenge model.
Avian necrotic enteritis (NE) is caused by certain strains of type A Clostridium perfringens, an anaerobic Gram-positive bacterium. It is of significant economic importance to the poultry industry, estimated to cost approximately US$6 billion worldwide in 2015 . The necrotic enteritis beta toxin-like (NetB) toxin was recently identified and shown to be a critical virulence factor in NE pathogenesis . In these studies, a netB knockout mutant was unable to induce disease in an NE challenge chicken model system, while complementation with netB restored the virulence of the mutant . Furthermore, several studies have examined netB prevalence in a wide variety of C. perfringens strains and found a strong correlation between the presence of netB and host disease status [3–6]. Recently, we took the approach of comparative genomics and identified a genetic “signature” of NE disease in chickens . We found that netB resides on a 42 kb pathogenicity locus, NELoc-1, located on a plasmid (pNetB) and associated specifically with virulent strains. This locus contains 36 genes in addition to netB, several of which are predicted to play a role in virulence. Two other loci (NELoc-2 and -3) associated with NE-producing strains were also identified: NELoc-2 consists of 11 genes and is chromosomally-encoded, whereas NELoc-3 consists of five genes and is located on a plasmid (pCpb2) distinct from that harboring NELoc-1. The complete sequences of pNetB and pCpb2 from virulent strains originating in Canada and Australia have been reported and contain sequences with >99% identity to NELoc-1 and NELoc-3, respectively [8, 9]. The strict conservation of these loci suggests that they may encode genes important in the pathogenesis of NE. However, functional confirmation of these putative additional virulence factors has yet to be provided. The extrachromosomal location of most of the NE-associated genes (i.e. NELoc-1 and NELoc-3) presents an opportunity to remove these genes en masse, through plasmid loss, and thereby assess their collective role in virulence in a common genetic background. Furthermore, putative virulence genes may be reintroduced into the strains cured of their virulence plasmids, either individually or in combination, to assess each gene for phenotypic effects and possible interactions.
To extend our previous findings from the comparative genomic analyses, we have characterized a virulent C. perfringens strain (CP1) that has spontaneously lost its netB-carrying plasmid (pCP1netB). The virulence of the mutant, a netB-complemented derivative, and the wild-type strain has also been assessed both in vitro and in vivo. The results are reported herein.
Bacterial strains, media and growth conditions
Clostridium perfringens strain CP1 used in this study was a field isolate from an NE case in Ontario . C. perfringens strains were routinely grown anaerobically at 37 °C in Brain Heart Infusion (BHI), Tryptone Proteose peptone Glucose (TPG), or Fluid Thioglycollate (FTG) broth (Difco). C. perfringens media were supplemented with 34 µg/ml chloramphenicol (Sigma-Aldrich, St. Louis, MO, USA) as required to retain the plasmid pJIR750::netB that carries a chloramphenicol resistance gene. E. coli Top 10 was used for cloning and grown at 37 °C in Luria–Bertani (LB) broth or agar (Difco), supplemented with 34 µg/ml chloramphenicol as required.
Pulsed field gel electrophoresis (PFGE)
Pulsed field gel electrophoresis was performed on chromosomal and plasmid DNA as previously described . DNA plugs for PFGE were prepared from overnight cultures of C. perfringens grown in BHI and the bacterial pellets incorporated into a final agarose concentration of 1% in PFGE-certified agarose (Bio-Rad, Hercules, CA, USA). Plugs were incubated overnight with gentle shaking at 37 °C in lysis buffer (0.5 M EDTA pH 8.0, 2.5% of 20% sarkosyl), 0.25% lysozyme (Sigma-Aldrich) and subsequently incubated in 2% proteinase K (Roche, Laval, QC, Canada) buffer for 2 days at 55 °C. Then plugs were equilibrated in 200 µl restriction buffer at room temperature for 20 min and digested with 10 U of NotI (New England Biolabs, Ipswich, MA) at 37 °C overnight. Electrophoresis was performed in a 1% PFGE-certified gel and separated with the CHEF-III PFGE system (Bio-Rad) in 0.5X Tris–borate-EDTA buffer at 14 °C at 6 V for 19 h with a ramped pulse time of 1–12 s. Gels were stained in ethidium bromide and visualized by UV light. Mid-Range II PFG markers (New England Biolabs) were used as a molecular DNA ladder.
Genome sequencing and phylogenetic analysis
Total genomic DNA was isolated from strains CP1 and CP1ΔpCP1netB using the Gentra Puregene kit (Qiagen). Sequencing libraries were prepared with the Nextera XT DNA sample preparation kit (Illumina, San Diego, CA) according to the manufacturer’s instructions, using 1 ng of total gDNA as input. The library concentration was determined by quantitative PCR, and diluted to a final concentration of 8 ρM in 10 mM Tris–HCl, pH 8. Sequencing was performed on a MiSeq instrument (Illumina) using the 600v3 kit, to generate 300 bp paired-end reads. The quality of the resulting Fastq files was assessed with FastQC (http://www.bioinformatics.bbsrc.ac.uk/projects/fastqc), and reads were quality filtered and assembled with SPAdes v3.0 . Phylogenetic trees based on whole genome sequence data were built using REALPHY , which uses Bowtie 2  for mapping reads to a reference genome and RAxML  for tree-building. The ATCC13124 genome (gi_110798562) was used as a reference and C. perfringens strains ATCC3626 (gi_151558394), JGS1721 (gi_177911222), F262 (gi_422872590), NCTC8239 (gi_151558627), WAL-14572 (gi_373228597), JGS1987 (gi_151558496), JGS1495 (gi_151558295), Str.13 (gi_18308982), F4969 (gi_151558571), 1207_CPER (gi_875303967), JJC (gi_558869255), and CP4 (gi_942714078) were also included in the comparison.
Construction of plasmid pJIR750::netB and complementation of CP1ΔpCP1netB
The netB complementation plasmid pJIR750::netB was constructed using primers CTC_netBF (CGGGATCCGTACCATTTAAATTAAGCAC) and CTC_netBR (TCGAGCTCCCCTCTATATACTATTGATTG), which contain BamHI and SacI restriction sites (underlined), respectively. They were used to amplify a 1551 bp fragment encompassing the wildtype netB gene and 300 bp of upstream sequence. Following digestion with BamHI and SacI, the fragment was purified with the Qiagen PCR purification kit (Qiagen, Mississauga, Ontario, Canada), and ligated into the BamHI/SacI sites of the E. coli-C. perfringens shuttle vector pJIR750 (a gift from Dr. Julian I. Rood, Monash University, Australia), which confers chloramphenicol resistance, and the resulting pJIR750::netB plasmid was confirmed by sequencing. pJIR750::netB was then introduced into CP1ΔpCP1netB by electroporation to generate CP1ΔpCP1netB(netB +). The transformation mixture was plated onto BHI agar supplemented with 34 μg/ml chloramphenicol and incubated overnight at 37 °C under anaerobic conditions. The CP1ΔpCP1netB(netB +) transformants were confirmed by PCR amplification of a 302 bp fragment using primers QnetBF (AGTGTAATTAGTACAAGCC) and QnetBR (GGCCATTTCATTTTTCCGTAA) and the following cycling conditions: initial denaturation at 94 °C for 5 min; 30 cycles at 94 °C for 30 s, 47 °C for 30 s and 68 °C for 25 s; final extension at 68 °C for 10 min.
LMH cytotoxicity assay
Lactate dehydrogenase (LDH) cytotoxicity assays were performed essentially as described [15, 16]. Briefly, chicken Leghorn male hepatoma (LMH) cells (ATCC CRL-2117) were maintained in Earl’s minimum essential medium (EMEM) (Invitrogen) supplemented with l-glutamine, MEM Non-Essential Amino Acids Solution, 100 U/ml penicillin, 100 µg/ml streptomycin and 10% fetal bovine serum. Flasks and 96-well plates were pre-coated with 0.1% gelatine (Millipore, Billerica, MA, USA) for adherence to surfaces. Cells were incubated in a humidified environment of 5% CO2 at 37 °C.
For the cell cytotoxicity assays, 96-well cell culture plates (BD Biosciences) were seeded with ~4 × 104 LMH cells/well and incubated for 2–3 days until just 100% confluent. C. perfringens strains were grown in TPG broth to an OD600nm of 0.6–0.8, and broth culture supernatants were obtained by centrifugation at 18,000×g for 15 min. The supernatants were filter-sterilized and added to the LMH cell medium (all samples were performed in triplicate), then incubated for 4 h at 37 °C with 5% CO2. Lactate dehydrogenase (LDH) release into the supernatant was measured as an indicator of cytolysis using the Cyto-Tox Non-Radioactive (Promega) kit. Triton-X 100 (1%) was used as positive control, which gave 100% cell death; the experiment was repeated three times.
Total RNA was isolated from overnight cultures of C. perfringens strains using RiboPure™-Bacteria Kit (Applied Biosystems) and DNase treated with the Ambion Turbo DNase kit (BioRad). All first-strand cDNAs were prepared from same amount of approximately 2.5 µg of total RNA in a 20 µl reaction containing 0.5 mM dNTPs, 1 µg random hexamers (Invitrogen), 1× First strand buffer, 10 mM dithiothreitol, 40 U RNasin (Promega) and 200 U Superscript II (Invitrogen). The reaction was incubated at 25 °C for 10 min, 42 °C for 50 min and 70 °C for 15 min. PCR amplification of transcribed netB was carried out using 2 µl of cDNA as template and primers QnetBF and QnetBR as described above.
Infection of chickens
Fifty-four commercial 1-day-old male white Plymouth Rock broiler chickens (Bonnie’s Chick Hatchery, Elmira, ON, Canada) were randomly divided into 4 experimental groups (n = 13–14 per group). The chickens were fed an antibiotic-free chicken starter containing 20% protein for 11 days followed by turkey starter containing 28% protein (Arkell Research Station, University of Guelph). For the experimental infection (challenge) of birds, wild type CP1, CP1ΔpCP1netB and CP1ΔpCP1netB(netB +) were grown in cooked meat medium (Difco) (CMM) for 24 h at 37 °C under anaerobic conditions. FTG medium (Difco) was then inoculated 3% (v/v) with an overnight CMM culture and incubated aerobically at 37 °C for 15 h. The growth at 15 h was approximately log10 8.45 ± 0.14 C. perfringens colony-forming units (CFUs) per ml. The FTG-grown culture was then mixed with feed at a ratio of 2:1 (v/w). The chickens were starved for 24 h before the C. perfringens contaminated feed was administered on day 13. Inoculated feed was prepared fresh twice daily and fed to chickens for 5 days.
Chickens were euthanized with carbon dioxide on the day following a 5-day challenge, and at necropsy the small intestine was examined for grossly visible lesions. Necrotic enteritis lesions were scored blindly using the system described by Keyburn et al. .
To determine if there were differences in the number of birds with lesions between two challenge groups, a two-tailed Fisher’s exact test was used to assess the null hypothesis that the proportion of birds with lesions among the two groups was the same. The null hypothesis was rejected at p ≤ 0.05.
Identification of a CP1 isolate deficient in pCP1netB
Complementation of mutant CP1ΔpCP1netB with netB alone
Cytotoxic effects towards LMH cells
Virulence of CP1ΔpCP1netB and CP1ΔpCP1netB(netB+) in vivo
In this study, we have characterized a C. perfringens mutant from a chicken NE strain (CP1) that spontaneously lost the plasmid carrying the NE-specific locus NELoc-1, including investigating its cytotoxicity towards the chicken male Leghorn hepatoma cell-line and capacity to produce NE lesions in broilers. The validity of this CP1 mutant (CP1ΔpCP1netB) as lacking only the pNetB plasmid and having no other gene changes was confirmed by PFGE of plasmid and chromosomal DNA and genome sequencing (Figs. 1, 2).
Previously, our group reported on three highly conserved NE-associated loci that were designated NELoc-1 (42 kb), NELoc-2 (11.2 kb) and NELoc-3 (5.6 kb). The largest locus, NELoc-1, consists of netB and 36 additional genes . In the present study, we tested the virulence conferred by netB alone, in the absence of the other NELoc-1 genes. The expression of netB was sufficient to restore the in vitro cytotoxicity of CP1ΔpCP1netB to wildtype levels, as observed when supernatant from the complemented CP1ΔpCP1netB(netB +) was tested in the LMH cytotoxicity assay (Fig. 4). Cytotoxicity of C. perfringens culture supernatants towards the LMH cell-line has been demonstrated to be specifically attributable to NetB , and has been used extensively to assay the activity of NetB [2, 15, 18]. Our study importantly suggests that genes on the pNetB pathogenicity island (other than netB) are not involved directly in regulating expression of NetB.
When assessed in vivo, the complemented group failed to fully restore the ability of CP1ΔpCP1netB to cause NE (Fig. 5). While it has been reported that there is not always a direct correlation between in vitro cytotoxicity and the development of NE , the inability of netB complementation alone to restore full virulence to CP1ΔpCP1netB also suggests that other genes present on pCP1netB are required during NE pathogenesis in a role not related to NetB expression. NELoc-1 encodes a number of genes with putative virulence-related functions, including adhesins, glycosidases, and a cyclic-di-GMP signaling system , which plausibly influence the survival and colonization of C. perfringens in the intestinal mucosa during NE pathogenesis, as well as other possible functions. The fact that neither netB transcription determined through semi-quantitative RT-PCR, nor in vitro LMH cytotoxicity appeared to be reduced by CP1ΔpCP1netB(netB +), indicates that this isolate has the capacity similar to the wild-type strain in the production of NetB toxin. In addition, the uneven distribution of NE disease (approximately one-third of the birds showed NE disease but two-thirds had no NE lesion) and less severe NE lesions in the complemented group make it difficult to attribute the results to the loss of the vector, given that all the birds received the same delivery of the isolate through a diet during the challenge. Thus, our results support the hypothesis that although NetB is the essential factor which initiates NE disease, its delivery to target cells clearly involves a complex delivery system likely including mucus and mucosal adhesion .
It should be noted that the disease model system employed in this study, and by others, may be insufficient for assessing the contribution to pathogenesis of all accessory virulence factors, which could each play a role at any point during the infection cycle of the pathogen [20, 21]. For example, genes involved in environmental survival, transmission, competition with the indigenous intestinal microbiota, or other activities that may normally be essential for pathogenesis, may no longer be required due to the severe challenge used in this model system. Hence, more sensitive in vivo assays directly suited to evaluate these functions need to be explored.
The current study found that netB, in the absence of other NELoc-1 genes, was able to completely restore in vitro cytotoxicity, but only partially restore virulence in vivo. These results importantly support the hypothesis that other genes present on NELoc-1 are involved in NE pathogenesis and have functions other than controlling the expression of NetB.
HZ, DL, and JG designed the study and wrote the manuscript. HZ and DL performed laboratory experiments and data analyses. JP and YL designed and conducted the chicken trial with support from other authors. ML identified CP1 strain as a transformable recipient of plasmids. XY and RM contributed to data analyses and discussion. JG supervised the research. All authors read and approved the final manuscript.
Plasmid pJIR750 was a gift from Dr. Julian I. Rood, Monash University, Australia. HZ was a visiting Ph.D. student to Guelph Research and Development Centre supported by the China Scholarship Council through the MOE-AAFC Ph.D. Student Research Program. ML was a NSERC Visiting Fellow to Canadian Federal Government Laboratories.
The authors declare that they have no competing interests.
Availability of data and materials
The data supporting the findings of this study are contained within the manuscript.
Ethics approval and consent to participate
The experiment with chickens and conditions for their use was approved by the University of Guelph Animal Care Committee (Reference# AUP 1936) in accordance with the Canadian Council on Animal Care’s Guidelines.
This work was supported by Agriculture and Agri-Food Canada and Canadian Poultry Research Council through the Poultry Cluster program. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Open AccessThis is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited
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