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Brazilian Journal of Poultry Science

Print version ISSN 1516-635X

Rev. Bras. Cienc. Avic. vol.14 no.3 Campinas July/Sept. 2012

https://doi.org/10.1590/S1516-635X2012000300003 

Potential use of molecular-typing methods for the identification and characterization of salmonella enterica serotypes isolated in the poultry production chain

 

 

Baratto CM; Gelinski JMLN ; Bernardi AZ ; Marafon A; Braun F

Correponding author

 

 


ABSTRACT

Salmonella is widespread in nature and can be found in all links of the poultry production chain. Due to its high impact on meat processing, techniques for the rapid detection and reproducible characterization of Salmonella serotypes in foods are needed. The present study investigated the potential of molecular profiling to identify and differentiate 15 Salmonella serotypes isolated from the poultry production chain, based on 5 primers by random amplified polymorphic DNA (RAPD), enterobacterial repetitive intergenic consensus (ERIC-PCR), amplification of rDNA internal spacer analysis (RISA), and amplified ribosomal DNA restriction analysis (ARDRA) of 16S-23S rRNA internal spacer region (ISR) cleaved with Alu I and Hha I restriction enzymes. Three isolates of each serotype were analyzed for the identification of similar and different profiles. Dendrograms were constructed from molecular profiles using the UPGMA method (unweighted pair-group method for the arithmetic averages) and the software program WinBoot. The present study indicates the usefulness of RISA and ARDRA of the 16S-23S rRNA intergenic spacer region (ISR) for systematic, epidemiological, and diagnostic purposes. Since these techniques can be used for the differentiation of serotypes, they are highly promising for the characterization of Salmonella serotypes and intra-serotypes. Data indicate that these techniques may be used to produce more consistent, reliable, and reproducible results in the identification and epidemiological study (traceability) of Salmonella in the poultry industry.

Keywords: Molecular analysis, Salmonella, serotypes, typing.


 

 

INTRODUCTION

Salmonellosis is one of the most common infectious diseases in the world and affects both animals and humans. Salmonella infections may cause gastroenteritis, involving an abrupt onset of nausea, fever, vomiting, and diarrhea, with several virulence factors involved (Baumler et al., 1998; Schaechter et al., 2001). Some outbreaks affecting the population are caused by specific Salmonella serovars (serotypes), and the difficulty in detecting carriers makes these a potential source of contamination, particularly due to detection limitations of culture techniques, which are also time-consuming (Robinson et al., 1995; Aspinall et al., 1992).

Moreover, about 2,600 Salmonella serovars are known and new serovars, which may potentially be foodborne pathogens, have been discovered (Guibourdenche et al., 2010). This high number and wide diversity of serovars causes the nomenclature of the Salmonella genus, species and serovars to be very complex (Smith et al., 2011).

There is a high incidence of S. Enteritidis in broiler breeder (57.5%) and broiler flocks (84.0%), and it is the serovar most frequently responsible for foodborne outbreaks and sporadic cases of salmonellosis in humans (Kanashiro et al., 2005).

When dealing with the epidemiology of Salmonella infections, determining how humans acquire the infection is essential (Dhillon et al., 2001). Therefore, when monitoring the health quality of poultry meat used for human consumption, it is important to identify which Salmonella serotypes are present in the production chain. Aiming at developing a more robust assessment of intraspecific diversity within Salmonella species using genetic markers, some techniques based on PCR were devised (Tindall et al., 2005; Wang et al., 2009).

Among the methods used to identify Salmonella isolates are random amplified polymorphic DNA (RAPD) analysis (Betancor et al., 2004; Smith et al., 2011), which is based on the amplification of repetitive elements present in several copies in the chromosome; enterobacterial repetitive intergenic consensus (ERIC-PCR) (Rasschaert et al., 2005; Anderson et al., 2010); repetitive extragenic palindrome (REP-PCR) sequences (Merino et al., 2003; Woo & Lee, 2006); Salmonella enteritidis repetitive extragenic (SERE) sequences (Rajashekara et al., 1998); and BOX elements (Woo & Lee, 2006; Suh & Song, 2006). Previous studies have shown PCR fingerprinting techniques to be strain specific and highly useful in Salmonella strain typing (Woo & Lee, 2006; Suh & Song, 2006; Merino et al., 2003; Smith et al., 2011; Kumao et al., 2002).

Another PCR-based method that enables the study of the biodiversity of Salmonella isolates is amplification followed by product separation of the spacer between the 16S and 23S rRNA genes (intergenic spacer region - ISR) (Baudart et al., 2000; Luz et al., 1998; Lagatolla et al., 1996). This method, identified by the acronym RISA (rDNA internal spacer analysis),   provides products with a highly variable size because of its hypervariable nature (García-Martínez et al., 1999).

In addition, the amplification of this region followed by restriction digestion and analyses of its products is another potential use of ISR. This technique, called ARDRA (amplified ribosomal DNA restriction analysis), is easy, fast and accurate to identify and characterize Lactobacillus sp. and Bradyrhizobium sp. isolates (Moreira et al., 2005; Han et al., 2005; Mohania et al., 2008; Vinuesa et al., 1998). However, despite its great potential, ISR-ARDRA has not yet been used for the identification or characterization of Salmonella serotypes.

The purpose of the present study was to evaluate the usefulness and the potential application of different techniques based on PCR analysis (RAPD, ERIC, RISA and ARDRA) for the differentiation of 15 Salmonellaenterica subsp. enterica serotypes isolated from the poultry meat production chain.

 

MATERIAL AND METHODS

Salmonella strains

The Salmonella isolates used in this study were obtained from  poultry production chain environments, including hatcheries, broiler breeder farms, broiler farms and slaughterhouses located in the states of Santa Catarina and Rio Grande do Sul, between 2006 and 2010 (data not shown). Salmonella sp. were isolated and identified following the recommendations of Oliveira et al. (2006). The colonies suspected of Salmonella were collected for presumptive identification by biochemistry tests and the positive isolates were submitted to serologic tests using polyvalent serum against Salmonella O antigens. The positive isolates were submitted to reference official laboratories (Oswaldo Cruz Institute Foundation; FIOCRUZ, Rio de Janeiro, Brazil) for complete identification and serotyping. A total of 15 different serotypes of Salmonella enterica subsp. enterica were chosen for the study and isolated during that period, including S. Infantis, S. Tennessee, S. Bredeney, S. Schwarzengrund, S. Ohio, S. Montevideo, S. Newport, S. Sandiego, S. Panama, S. Hadar, S. Rissen, S. Anatum, S. Muenchen, S. Typhimurium and S. Saintpaul. Three isolates of each serotype were randomly selected and analyzed for the determination of common profiles.

DNA extraction and characterization by RAPD

For the molecular characterization of Salmonella serotypes, DNA extractions were performed using the extraction kit Whatman FTA® Classic Card (Whatman, USA), as specified by the manufacturer.

The RAPD profiles of Salmonella isolates were generated from five different primers: P1254 (5'-CCGCAGCCAA-3'), 784 (5'-GCGGAAATAG-3'), 23L (5'-CCGAAGCTGC-3'), OPA-4 (5'-AATCGGGCTG-3') and OPB-15 (5'-CCAGGGTGTT-3') (Woo & Lee, 2006; Malorny et al., 2001). The PCR mixture contained 2 mM MgCl2, 0.25 mM dNTP, 2.5 U of Taq polymerase (Invitrogen), PCR buffer (Invitrogen), 50 ρmol of primer and DNA template. Amplification was performed as previously described with minor modifications (Betancor et al., 2004), using the following program: 4 cycles of 94°C for 4 min, 37ºC for 4 min and 72ºC for 4 min; then 35 cycles of 94ºC for 30 s, 37ºC for 1 min, and 72ºC for 2 min, followed by final 10 min at 72ºC with PCR thermal cycler HBSP02110 (Thermo Electron Corp.). The PCR products (15 ml of each sample) were loaded on 1.5% agarose gel with 0.5 μ/ml of ethidium bromide in the electrophoresis tank, using 0.5 X TBE buffer, at 3 Vcm-1 for 2 hours. A DNA molecular weight marker, 100-bp DNA ladder (Ludwig Biotec, Brazil), was used as standard. Gels were observed under UV light and a digital image was captured (Photo Capt Software version 12.5 for Windows - Vilber Lourmat) for analysis. In order too confirm the reproducibility of the method, each experiment was repeated three times.

ERIC-PCR analysis

For the amplification of ERIC motifs, the PCR mixture and reaction programs were utilized according to similar conditions reported on previous studies (Suh & Song, 2006), using 1R (5'-ATGTAAGCTCCTGGGGATTCAC-3') and 2R (5'-AAGTAAGTGACTGGGGTGAGCG-3') primers. The gel and digital image were produced as previously described.

Molecular analysis by RISA and ARDRA methods

The amplification of the 16S-23S rRNA intergenic spacer region (ISR) was performed using a 50 µL mix (10X PCR buffer with MgCl2 1.5mM, 0.25mM dNTP, 2.5U of Taq polymerase (Invitrogen), 50 ρmol of each primer and DNA template) and the following universal primers: P1 (5'-TTGTACACACCGCCCGTCA-5') and P2 (5'-GGTACTTAGATGTTTCAGTTC-3') (Lagatolla et al., 1996). Samples were submitted to the following program: 35 cycles of 94ºC for 1 min, 53ºC for 1 min and 72ºC for 1 min and 30 sec, and the reaction products were analyzed by electrophoresis as described. For the ARDRA method, 14 microliters of the amplification product of each Salmonella isolate were digested with restriction endonucleases. Ten units of enzymes - Alu I and Hha I (Invitrogen) - were added to each reaction and the mixture was incubated at 37ºC for 2 hours. The restriction fragments were separated by electrophoresis on 3% agarose gel at 2 Vcm-1 for 4 hours.

Phylogenetic data analysis

Dendrograms were constructed by UPGMA (unweighted pair-group method for the arithmetic average) based on Jaccard's similarity coefficient from a matrix based on the binary code of molecular profile data for bootstrapping. Each phenogram was reconstructed 2000 times by repeated sampling with replacement using computer program WinBoot (Yap & Nelson, 1996).

 

RESULTS AND DISCUSSION

A total of 15 different serotypes of Salmonellaenterica subsp. enterica isolated from the poultry production chain were typed using different molecular methods for the purpose of obtaining a common molecular profile. Three isolates of each serotype were used.

Salmonellosis is a worldwide problem in the poultry industry, affecting both animal and public health. Studies in several regions of Brazil have shown that S. Enteritidis, S. Typhimurium, S. Panama, S. Newport, S. Infantis, S. Senftenberg, S. Heidelberg, S. Saintpaul, S. Indiana, S. Agona, and S. London are  the most common Salmonella serovars found in poultry commercial breeders and broiler flocks (Ribeiro et al., 2006; Oliveira et al., 2006; Kanashiro et al., 2005). As expected, these serovars were found in the present study and were submitted to molecular analyses. However, the most prevalent Salmonella serotypes causing human toxic infections are S. Enteritidis and S. Typhimurium (Robeson et al., 2008; Oliveira et al., 2006).

Because of the need of detecting and identifying  infections to prevent disease and their dissemination, methods are required for the epidemiological study of salmonellosis (Dhillon et al., 2001). The genetic characteristics of Salmonella serotypes must be accurately and objectively analyzed using an efficient, reliable, and discriminatory genetic analysis method (Christensen et al., 1998). Thus far, several genetic analysis methods for the genotyping of Salmonella serotypes have become available (Lagatolla et al., 1996; Baudart et al., 2000).

Because of it is easy to use and it has discriminatory power, RAPD-PCR has become an important tool to fingerprint bacteria involved in disease outbreaks and to determine the sources, vectors and vehicles of transmission (Betancor et al., 2004). For RAPD analysis, five known primers used for Salmonella characterization were selected, as well as the best simplification conditions to differentiate each serotype based on their DNA amplification profiles. The use of RAPD enabled the differentiation of most genotypes (Betancor et al., 2000). Primers P1254, 784, 23L, OPA-4 and OPB-15 were effective for the differentiation of most Salmonella serotypes isolated from the broiler production chain (Figure 1).

DNA fragments  ranging from approximately 2.5 to 0.3 kbp were generated, providing the molecular profile from which a dendrogram was constructed using UPGMA by profile numerical analysis to group isolates by similarity. This approach allowed molecular analyses because, due to the high number of molecular markers developed over the last decades, it has been difficult to associate genetic diversity or molecular profiles with classification and phylogeny, especially of closely-related Salmonella isolates (Yap & Nelson, 1996; Baudart et al., 2000).

Similarly to the RAPD results,  ERIC-PCR results (Figure 2A) provided evidences of clear molecular diversity among the Salmonella serotypes isolated in this study. As suggested earlier, the molecular profile obtained by ERIC, associated with the dendrogram (Figure 2B), proved to be a convenient method for fingerprinting and therefore, a good typing tool.

According to Rasschaert et al. (2005), it is possible to use the ERIC1R–ERIC2 primer set to differentiate Salmonella serotypes and to improve the reproducibility and resolving power of the method by using appropriate annealing temperatures in order to obtain a correlation between the molecular pattern (footprinting) and the specific serotype.

The results obtained by RISA (rDNA internal spacer analysis) demonstrated that 16S-23S rRNA intergenic spacer regions (ISR) are highly polymorphic in Salmonella isolates, and therefore, it is possible to use this method to detect variability . Amplification generated DNA fragments of approximately 500 to 1000 pb, and it was possible to differentiate most of the isolates analyzed (Figure 3A-RISA). The high polymorphism of the DNA spacer in the regions between 16S and 23S is due to the fact that  sp., as well as , has seven ribosomal operons, and they are usually not identical (intercistronic heterogeneity) (García-Martínez et al., 1999; Jensen et al., 1993; Thomson et al., 2998). In consequence, spacer region polymorphisms have been useful in the identification of Listeria, Staphylococcus, and Salmonella, as well as the identification of Salmonella serotypes (Jensen et al., 1993), and the intraserovar or subtyping discrimination of Salmonella (Baudart et al., 2000; Lagatolla et al., 2006 ). From the results obtained, most of the examined serotypes could be differentiated by their profile. The length and sequence polymorphisms present in the PCR product can therefore be used for the recognition of genotypic diversity.

The most direct and rapid method to visualize the polymorphic character of 16-23S rRNA ISR is PCR amplification of the spacer regions with the use of primers from highly-conserved flanking sequences (García-Martínez et al., 1999).

A second approach is to use the PCR product digested with a restriction enzyme (amplified ribosomal DNA restriction analysis - ARDRA), and have the resulting fragments resolved electrophoretically (Moreira et al., 2005). If the PCR product contains the restriction endonuclease recognition sequence at unique or different locations, then the resultant fragment size pattern can indicate a particular profile.

In this study, the results of 16S-23S rRNA ISR – ARDRA using Alu I and Hha I restriction enzymes for the 15 serotypes analyzed showed very complex molecular profile patterns (Figure 3A-ARDRA), and no common patterns among the three isolates tested of most serotypes (data not shown). Profiles were differentiated according to band number and position, as suggested by Betancor et al. (2000). The number of bands per profile varied, and most fragments were below 500 pb. Additional information may be inherent in the polymorphic character of the amplified and digested products. This indicates the great potential of the technique for footprinting.

However, as those fragments were very small, possibly having small differences in length (few pb), they were not perceptible when the products were separated by agarose gel electrophoresis. In these cases the molecular profile may be obtained by other means, such as thermal gradient gel electrophoresis (TGGE) analysis (Yasuda & Shiaris, 2005), denaturing gradient gel electrophoresis (DGGE) (Anderson et al., 2010), or on 4-8 % polyacrylamide gel (Jensen et al., 1993; Baudart et al., 2000), although these methods are more expensive and time-consuming.

A dendogram was constructed by UPGMA from the molecular profiles obtained using RISA and ARDRA (Figure 3B). The clusters generated were different from those obtained by RAPD (Figure 1) and ERIC (Figure 2B), but the highest numbers on a branch, from the high bootstrap values, indicated the percentage that reflected on the concordant structure with which the nodes were supported, meaning that data were more robust than in the other dendograms.

The 16S-23S rRNA ISR (intergenic sequence region) is a hypervariable region, which is useful for the fine discrimination of operational taxonomic units, but limited work has been found focusing on Salmonella or other enteric pathogens. However, despite the advantages of the ISR-ARDRA method and its usefulness in the characterization of others organisms (Jensen et al., 1993; Luz et al., 1998), it had not been used for the identification of  serotypes or the analysis of isolates, possibly due to the difficulty in visualizing the results, whereas rDNA internal spacer analysis (RISA), RAPD, repetitive extragenic palindromic-PCR (REP-PCR) and ERIC are more common (Rasschaert et al., 2005; Woo & Lee, 2006).

In conclusion, the main Salmonella serotypes found in poultry products to be sources of infection may be identified by molecular techniques such as RAPD and ERIC. Depending on the conditions of the reactions, these methods may also be used for footprinting analyses. On the other hand, RISA and ARDRA techniques, especially  the 16S-23S rRNA intergenic spacer regions, are primarily intended for intra-serotype characterization, that is, the differentiation of Salmonella strains at the intra-serovar level. Moreover, the use of a complementary method is essential for obtaining more reliable and accurate results both in serotype determination and isolate characterization. Methods should be combined as needed. Therefore, the new approach to the ISR-ARDRA technique will possibily have important practical implications for the epidemiological analysis of Salmonella. The method has proven to be an important tool for Salmonella fingerprinting and was highly discriminatory among Salmonella isolates; therefore, it may potentially detect wider variability among fingerprint profiles.

 

ACKNOWLEDGEMENTS

This study was funded by CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico) and FAPESC (Fundação de Amparo à Pesquisa e Inovação do Estado de Santa Catarina) grants.

 

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Correponding author
César Milton Baratto.
Universidade do Oeste de Santa Catarina –
Molecular Biology Laboratory - building K.
198, Paese Street. CEP.89560-000 Videira-SC-Brazil.
E-mail: cesar.baratto@unoesc.edu.br
Phone number: +55 49 35334479 Fax: +55 49 35334422

Submitted: December/2011
Approved: September/2012

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