- Methodology article
- Open Access
An improved multiple-locus variable-number of tandem repeat analysis (MLVA) for the fish pathogen Francisella noatunensis using capillary electrophoresis
© Duodu et al.; licensee BioMed Central Ltd. 2013
- Received: 10 May 2013
- Accepted: 2 December 2013
- Published: 13 December 2013
Francisellosis, caused by the bacterium Francisella noatunensis subsp. noatunensis, remains a serious threat to Atlantic cod (Gadhus morhua) farming in Norway and potentially in other countries. As outbreak strains appear clonal in population structure, access to highly discriminatory typing tools is critical for understanding the epidemiology of francisellosis infections in aquaculture. In this study, a simplified multiple-locus variable-number of tandem repeat analysis (MLVA) targeting five highly polymorphic variable number of tandem repeat (VNTR) loci in a single multiplex PCR was developed to rapidly discriminate between outbreak strains.
The assay resulted in identification of at least 13 different allelic profiles or subpopulations among 91 F. noatunensis isolates from farmed cod in Norway. The VNTR loci appear relatively stable, with isolates originating from individual outbreaks showing identical MLVA profiles following repeated passage. MLVA displayed greater discriminatory power than pulse-field gel electrophoresis (PFGE). Both MLVA and PFGE show good epidemiological concordance by their abilities to separate outbreak strains from epidemiologically unrelated isolates.
The MLVA method presented here is robust, easy to perform and provides a good alternative to other typing systems for F. noatunensis subsp. noatunensis and epidemiological study of francisellosis in cod.
- Capillary electrophoresis
- Francisella noatunensis
Francisella noatunensis is an emergent fish pathogen of major concern. It causes francisellosis, a systemic bacterial disease characterized by the presence of multi-organ granuloma with high morbidity and varying associated mortality levels . The disease affects several important cultured fish species in fresh, brackish and marine water environments. Francisellosis in farmed Atlantic cod Gadhus morhua L. was first reported in 2004/2005, when an outbreak caused by F. noatunensis subsp. noatunensis was discovered in Norway [2, 3]. Since then, many cases of F. noatunensis infection have been diagnosed in cod from numerous grow-out facilities spanning most of the mid-and south-western Norwegian coastline. Outbreaks caused by different strains of F. noatunensis have also been linked to other important cultured fish species around the globe . As no vaccine is yet available and antibiotic treatment largely ineffective, understanding the infection dynamics and spread of the disease may be important in regard to management of francisellosis in aquaculture.
Genetically, F. noatunensis subsp. noatunensis is a monomorphic pathogen, showing very little intra-species variation [4, 5]. As a result, few genetic tools with the necessary resolution to track and link individual disease outbreaks are available. An increasingly applied molecular typing tool for discrimination of bacterial species with stable clonal population structures is multiple locus variable-number tandem repeat analysis (MLVA). The method is based upon PCR amplification of variable tandem repeats (VNTRs), which are short polymorphic DNA sequences located at several loci in many microbial genomes . Isolates belonging to single bacterial species generally maintain the same sequence elements but show variation in the number of repeat units through the activity of a strand-slippage mechanism introduced by DNA polymerase during replication [7–9]. The different variants are most commonly resolved by standard agarose gel electrophoresis or capillary electrophoresis on a DNA sequencer .
To date, there is limited information on MLVA application relating to pathogenic fish Francisella species. In a recently published study, DNA sequencing was used to determine variations in the number of repeats at seven VNTR loci . Although the study highlighted the value of using MLVA as a typing system for F. noatunensis subsp. noatunensis, DNA sequencing is costly and labour intensive. Typing of a single isolate may require seven different PCRs and 14 sequencing reactions. The primary aim of the present study was, therefore, to improve the efficiency of MLVA as a typing scheme for discrimination of F. noatunensis isolates, through development of a single tube multiplex PCR amplification followed by automated fragment analysis using capillary electrophoresis. The epidemiological utility of the developed assay was compared with Pulsed-field gel electrophoresis (PFGE), which has been the gold standard method for epidemiological investigation of disease outbreaks in many pathogenic bacteria.
In vitro stability of the VNTR loci was evaluated after multiple subcultures of four F. noatunensis subsp. noatunensis isolates displaying genetically distinct MLVA profiles. The isolates were passaged at 5 day intervals for nearly 30 weeks on CHAB incubated at 22°C. Screening of single colonies picked from passage 10, 20, 30 and 40 revealed the same MLVA profile as the original isolates (data not shown).
Characteristics of VNTR loci used in MLVA for F. noatunensis subsp. noatunensis isolates
GeneBank accession no.
Number of repeats
Fragment size range (bp)
No. of alleles
TPR repeat protein
ThiJ/PfpI family protein
DNA-directed DNA polymerase
In this study we validated a novel MLVA assay for the fish pathogen F. noatunensis subsp. noatunensis using capillary electrophoresis. The presented assay relies on multiplex PCR amplification of five VNTR loci visualised in a single electrophoretic run, allowing typing of many or few isolates simultaneously. The MLVA protocol is robust, easy to perform and generates unambiguous numerical profiles for individual strain identification.
Not surprisingly, independent searches within highly similar genomes performed during the same time periods identified several common informative VNTR loci. Brevik et al.  published an MLVA assay for F. noatunensis, in which sequencing was used to identify polymorphisms in seven VNTR loci. Four of these loci were also identified and included in the present study. The fnVNTR-1 marker was, however, unique to the present study. The high degree of polymorphism identified in each VNTR loci suggests that the optimal markers were selected by both MLVA schemes. For all loci, with the exception of fnVNTR-1, accurate size estimation of PCR products was achieved by capillary electrophoresis. Sizing by capillary, although reproducible for this locus, failed to correspond to the actual fragment size identified by sequencing. This discrepancy could be due to the nature of the gel matrix, or to slightly biased flanking sequences or differences in mobility patterns of specific repeat units as previously mentioned by other investigators [12, 13]. Nonetheless, this did not interfere with the overall results, as alleles were correctly assigned with or without adjustment of the number of repeats deduced by capillary electrophoresis.
The specificity of the present assay was demonstrated by the amplification of all 5 VNTRs in all Norwegian isolates. As the primers were designed to exclusively detect F. noatunensis subsp. noatunensis isolates from cod, the lack of amplification from some loci in other bacterial subspecies/species may be due to either sequence variability in the primer regions or the absence of the locus altogether.
Generally, informative VNTR loci require a good balance between variability and stability. Although the studied loci appeared relatively stable over several generations in vitro, a single repeat change was previously reported for fnVNTR-4 in F. noatunensis subsp. noatunensis GM2212 following successive culturing at 20°C . Nevertheless, the fact that isolates from different outbreaks in the same locality (exemplified by MVT 10), displayed identical MLVA patterns over a period of 3 years, indicates that the loci are of sufficient stability to be used as VNTR markers for typing of F. noatunensis subsp. noatunensis.
Our MLVA assay provided high resolution typing and clustered the Norwegian F. noatunensis subsp. noatunensis isolates into three major clonal groups, consistent with previous MLVA findings . However, in the previous study, they indicated low diversity among 17 F. noatunensis subsp. noatunensis isolates collected from outbreaks in cultured cod populations. A total of four different allelic profiles were identified compared with 13 MLVA profiles detected from the 91 outbreak isolates included in the present study. Although polymorphisms in fnVNTR-1 may have contributed to the greater discriminatory ability of the present assay, it is more likely related to the greater number of isolates included in the present analysis. It was also reported that isolates from wild cod are more diverse than those from farmed cod . That the least polymorphic locus identified in the present study (fnVNTR-2) was among the most diverse loci identified in isolates from wild cod , suggests that the discriminatory power of the present assay for F. noatunensis subsp. noatunensis may be underestimated.
At the time of sampling, the epidemiological situation was complex with movement of juvenile fish common over long distances along the Norwegian coast. Thus, the information generated during the present study is difficult to interpret in terms of ‘natural’ or anthropological spread of infection. Our data shows, however, that several clones were present within the Norwegian cod-farming industry over a short period of time. Interpretation of these results in relation to microevolution will require knowledge of the mutation rates and understanding of how VNTRs in F. noatunensis subsp. noatunensis change with time. The situation could also be explained by the existence of many clones of which we have only identified a few. MVT1 may represent a highly successful spreading clone, as this genotype was detected at high frequency each sampling year. As with other theories relating to bacterial clonal expansion, the widespread dissemination of MVT1 could have been caused by human activities [11, 14]. While any significance of the demonstrated diversity within noatunensis to pathogenesis remains unclear, the current study helps define and differentiate epizootic F. noatunensis clones causing francisellosis in Norwegian cod populations.
Our data indicated better resolution for MLVA compared to PFGE. The two methods, however, assess different genetic events in different parts of the chromosome. While mutation, recombination or replication error may affect the number and frequency of tandem repeats, variations in PFGE profiles are caused by mutations in restriction enzyme sites. Generally, isolates belonging to the same cluster or PFGE type were identified with the same MLVA type. It should be noted, however, that isolates used for PFGE analysis were chosen based on differences in MLVA profile, which might have introduced selection bias. We observed two isolates, including the type strain NCIMB14265T that were inseparable by MLVA, but were resolved by PFGE. The PFGE profiles of these isolates differed by only one band, consistent with a single genetic event such as a point mutation, insertion or deletion . NCIMB14265T has been cultured repeatedly over time, which could explain the minor genetic changes.
We found the described MLVA scheme to meet all the performance criteria proposed for a good typing method . It shows good stability, provided 100% typeability of the isolates, is reproducible and has a high discriminatory power. These performance qualities do not differ significantly from the previous F. noatunensis MLVA assay , however, the main advantage of our MLVA is the high throughput that is facilitated by using a single multiplex PCR and capillary electrophoresis. The epidemiological concordance was demonstrated by the ability of MLVA typing to correctly cluster isolates within an outbreak and separate these from epidemiologically unrelated isolates. Thus, the assay has a great potential as a high-resolution molecular typing tool for the study of outbreaks of cod francisellosis. By using allele string codes based on repeat copy numbers for strain identification, the assay can easily be standardised to facilitate exchange of data among laboratories. Compared to PFGE, it lacks subjectivity, is less time-consuming and more discriminatory. However, as MLVA and PFGE target different parts of the chromosome, combined analyses of these two methods may result in a more discriminatory approach to understanding the processes of transmission of this fish pathogen in aquaculture.
Bacterial strains and culture conditions
Ninety-one isolates of F. noatunensis subsp. noatunensis, including the type strain NCIMB14265T, from disease outbreaks in Norwegian cod farms during the period 2005 to 2011, were studied. For comparative purposes, single isolates derived originally from Atlantic salmon Salmo salar L. (F. noatunensis subsp. noatunensis PQ 1106) in Chile, three line-grunt Parapristipoma trilineatum Thunberg (F. noatunensis subsp. orientalis Ehime-1) in Japan, and from a captive wild Atlantic cod (F. noatunensis subsp. noatunensis) in Ireland were included in the analysis. The collection also included three reference strains of F. philomiragia (CCUG 12603, CCUG 13404 and CCUG 19701). Details of source of isolation and country of origin of the strains can be found in supplementary material Additional file 1: Figure S1. Stock cultures of bacterial strains were stored in cryo-broth with 20% (v/v) glycerol at -80°C. Individual colonies of each strain were revived by streaking on Cysteine Heart Agar with Blood (CHAB) and incubated at 22°C for 7 days. F. philomiragia was incubated under the same conditions for 3 days. The Irish isolate was kindly provided by Dr Neil Ruane, Marine Institute, Oranmore, Ireland. The Chilean PQ 1106 isolate and the two F. noatunensis subsp. orientalis strains were kindly provided by PHARMAQ AS, Norway.
Identification and selection of VNTR loci
Tandem repeats (TRs) were identified in the published complete genome sequence of F. philomiragia subsp. philomiragia (ATCC 25017) and three draft genome sequences of F. noatunensis subsp. noatunensis (NCIMB14265T, GM 2212T, PQ 1106) , using Tandem Repeats Finder (http://tandem.bu.edu/trf/trf.html) . Initially, variability of 25 potential VNTR loci were tested in temporally and geographically discrete F. noatunensis subsp. noatunensis isolates using conventional PCR and gel-based analysis. Primers targeting flanking regions of each locus were designed using Primer3 software . DNA was prepared by boiling bacterial cells in TZ lysis buffer  and used directly in PCR after brief centrifugation at 10,000 × g for 3 minutes. Alternatively, genomic DNA was purified using the QIAamp DNA mini kit (Qiagen) following the manufacturer’s instructions. PCR amplification reactions were carried out with a PTC- 100 Programmable Thermal Controller (MJ Research Inc. Watertown, Massachusetts, USA). Each 25-μl reaction mixture contained 1 × PCR buffer, 0.4 μM of each primer (Invitrogen), 0.2 mM dNTP mix, 1.5 mM MgCl2, 2U Taq DNA polymerase (GE Healthcare) and 2 μl of DNA as template. The thermal cycling conditions were as follows: Initial denaturation cycle at 95°C for 5 min, followed by 35 cycles of amplification at 95°C for 30 s, 53°C for 30 s and 72°C for 1 min and a final extension at 72°C for 4 min. A portion of the amplified PCR products (10 μl) were size-fractionated by electrophoresis on 3% agarose gel in 1 × TBE buffer at constant voltage of 70 V (3–4 V/cm) for 4 h and visualized after staining with ethidium bromide. As control, DNA from NCIMB14265T was included in each experiment. Loci resulting in polymorphic banding patterns were considered suitable for further analysis.
Primers used for MLVA in this study
Verification by DNA sequencing
To verify the accuracy of sizing determined by capillary electrophoresis, PCR fragments representing all variants of each tandem repeat were sequenced. For fnVNTR-4 and fnVNTR-5 new sequencing primers were designed (Table 2), while for the other loci the primers used to amplify the VNTRs were also used for sequencing. PCR products were purified using Nucleospin® Extract II (Macherey-Nagel, Germany) following the manufacturer’s instructions. Two μL of purified PCR product was added to 4 μL DYEnamic™ Dye Terminator Cycle Sequencing Kit (Amersham Biosciences), 1 μL sequencing primer (5 μM) and 3 μl sterile dH2O. Sequencing products were purified using the DYE Terminator Removal Kit (ABgene®) and sequenced on MegaBACE 1000 sequencing instrument (Amersham Biosciences). Consensus sequences were determined using Vector NTI (Invitrogen).
Stability of VNTR loci after in-vitropassage
The stability of each VNTR locus was determined in-vitro after a number of laboratory passages (40 passages at 5 days intervals) using four F. noatunensis subsp. noatunensis isolates showing distinct MLVA profiles. For each passage, single colonies were streaked on CHAB agar plates. Bacterial growth conditions, preparation of DNA, VNTR PCR amplification and MLVA were carried out on single colonies from passage 10, 20, 30 and 40 as described above.
Prior to PFGE analysis, in silico searches for rare-cutting restriction enzymes were made from the available in-house Francisella genomes . In all, five candidate endonucleases (PasI, SacII, ApaI, NaeI) were evaluated. Of these enzymes, PasI (Fermentas) was the most discriminatory on the preliminary panel of five F. noatunensis isolates tested (data not shown). PFGE using PasI was then performed on a subset of 54 isolates including members from each representative MLVA group, using the PulseNet protocol for subtyping of Francisella tularensis (CDC, Atlanta, GA, USA).
Bacterial cells were embedded in 1.2% agarose plugs (SeaKem Gold agarose; FMC Bioproduct, Rockland, ME), lysed, washed, and genomic DNA digested with 30 U PasI enzyme for at least 3 h at 37°C. Salmonella enterica serotype Braenderup (H9812) was used as a reference standard, and restricted with 50 U XbaI (Roche Diagnostics, Indianapolis, IN, USA) for 3 hours at 37°C. The digests were resolved by electrophoresis on the CHEF-DRIII apparatus (Bio-Rad Laboratories, Hercules, CA) with 1% agarose gel in 0.5× Tris-borate –EDTA (TBE) buffer and running conditions set at voltage, 6 V/cm; initial switch time, 5.0 s; final switch time 30 s; runtime 18 h at 14°C. Gels were stained with ethidium bromide (1 mg/mL) and images of individual DNA fingerprints were captured using the Bio-Rad Gel Doc system (Bio-Rad Laboratories).
Cluster analysis of MLVA and PFGE profiles was performed in BioNumerics 6.1 (Applied Maths, Saint-Martens-Latem, Belgium). Dendrograms were created using the categorical similarity coefficient or the Dice correlation coefficient coupled with WARD algorithm. A minimum spanning tree (MST) was created to illustrate the distribution and inter-relationships of the MLVA genotypes within the F. noatunensis subsp. noatunensis population (Figure 2). The discriminatory capacity of the MLVA assay was evaluated using the Simpson’s index of diversity , which was calculated for both individual and combined VNTR markers on a data subset containing single representatives of each genotype identified in individual diagnostic cases. The degree of linkage disequilibrium, as an indicator of the statistical independence of each of the five loci was tested using the LIAN Linkage analysis 3.5 Software as described by Haubold & Hudson  on a data subset representing single representatives of each genotype.
This work was supported financially by the Norwegian Research Council (Grant no. 185362), the Swedish Civil Contingencies Agency (Grant no. 08-H189) and the Swedish Ministry of Defence (Project A4042) to whom we express our gratitude. We thank Hilde Welde for technical assistance.
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