Assignment of serotype to Salmonella enterica isolates obtained from poultry and their environment in southern Brazil

 

Brazil currently ranks as the major exporter of chicken meat in the world with markets in more than 150 countries. Salmonella enterica (Salm. enterica) is one of the most important bacterial pathogens that can cause foodborne illness (Schroeder et al. 2006). It is often transmitted to people by eggs and other poultry products (Hogue et al. 1997). The Brazilian poultry industry is committed to the control of Salmonella and its impact on the health of birds and the safety of poultry products. The industry follows the guidelines listed in the National Poultry Health Plan that includes monitoring of Salm. enterica on farms and in poultry products. (www.agricultura.gov.br/ arq_editor/file/Aniamal/Manual). Efforts to control Salm. enterica in poultry are complicated by differences in the predominant serotype, strain heterogeneity, prevalence, biosecurity practices, extent of regulatory control and the nature, size and logistic complexity of this industry (Mead et al. 2010). The increasingly strong demand  for safe poultry products requires application of diagnostic tools that enable rapid and reliable identification of pathogenic micro-organisms.

 

An obstacle to maintaining the safety of poultry products is the difficulty in accessing reliable diagnostic tools to characterize Salm. enterica as part of a continuously operational monitoring programme. Serotyping is an important epidemiological tool in the characterization of Salm. enterica, because it helps determine the prevalence and emergence of pathogenic serotypes in different regions. The Kauffmann–White–Le Minor (KWL) scheme is the historical method for determining serotype (Grimont and Weil 2007; Hendriksen et al. 2009). It is antibody- based and uses a combination of agglutination reactions to determine serotype. More than 2600 serotypes have been described on the basis of the antigenic structure of the cell surface lipopolysaccharide (O antigen) and flagellar proteins (H antigen; Grimont and Weil 2007). The KWL scheme is prone to subjective interpretations arising from combinatorial complexity, mixtures of serotypes in culture, and the absence of cell surface epitopes that are targeted by antisera (Guard et al. 2012). A lack of information about which serotypes are circulating on-farm impedes measures for effective treatment and control because different serotypes have different niches (Dorneles et al. 2010). Molecular methods for subtyping strains have potential for assigning serotype in reference to the historical database developed from the KWL scheme, because serotype is a class of strain variation and thus results from variation in the genome of Salm. Entérica (Murase et al. 1995; McQuiston et al. 2008; Wattiau et al. 2011; Achtman et al. 2012; Fabre et al. 2012). Pulsed-field gel electrophoresis (PFGE) is considered a pivotal DNA-based method that complements the KWL scheme in regard to detecting strain variation occurring within serotype, and it has been used successfully to identify origins of outbreaks. Other DNA-based methods can be used to subtype and may also provide serotype information, and each one has its advantages and disadvantages (Wattiau et al. 2011). Common disadvantages of most DNA-based methods are the need to purchase proprietary equipment, reagents and software for analysis (Tankouo- Sandjong et al. 2008; Wise et al. 2009; McQuiston et al. 2011). Overall, most molecular techniques are restricted to centralized public health laboratories with infrastructure that supports objectives to conduct research and epidemiological studies.

 

Intergenic sequence ribotyping (ISR) is a rapid strain typing method that lowers barriers to implementation because costs for equipment and software are modest (Guard et al. 2012). It is sequence-based and has been shown to distinguish between serotypes at the level of the single nucleotide polymorphism. Cultures with more tan one serotype can be detected when forward and reverse sequences do not align. The attributes of low cost, simplicity of application and the ability to access reference sequences suggested that ISR was suitable for application to widespread use for environmental studies. The objective of the present study was to determine if sequence-based ISR analysis of 155 isolates of Salm. enterica isolated from poultry and their environment from southern Brazil would yield additional information in comparison with those obtained using KWL serotyping. Results suggest that the ecology of Salm. enterica has aspects that have not yet been considered in determining risks to the safety of the food supply.

 

Intergenic sequence ribotyping performed with specific primers assigned a Salm. enterica serotype to 151 of 155 samples collected from poultry in southern Brazil (Tables 1 and 2). The KWL serotype initially reported was confirmed for 85_2% (132/155) of the samples. A total of 15 serotypes were identified, which included S. Enteritidis, S. Heidelberg, S. Hadar, S. Typhimurium, S. Gallinarum, S. Agona, S. Senftenberg, S. Livingstone, S. Cerro, S. Infantis, S. Mbdanka, S. Montevideo, S. Isangi and three different unique sequences (UN0041, UN0042 and UN0043). Of the 155 samples, 23 (14_8%) had an ISR that did not agree with initial KWL serotyping (Table 2). Of the samples reported as S. Heidelberg, two were identified by ISR as S. Enteritidis and two as unique sequence UN0042. S. Hadar had one observed difference, which was S. Heidelberg. In the four samples reported as S. Agona, two sequences were assigned S. Isangi and UN0043. For 8 S. Typhimurium identified by KWL, two were assigned S. Heidelberg by ISR (Table 2).

 

Table 1. Primers used for nested PCR intergenic sequence ribotyping (ISR).

^aSize of amplicon may vary as much as 250 bp between serotypes.

 

Three avian-associated serovar group D Salmonella serovars, namely Enteritidis, Gallinarum and Pullorum, had several disagreements between the KWL serotype and ISR (Table 2). Of the 67 samples, 14 (20_9%) disagreed with KWL serotyping. Of the other 88 isolates that were not group D, nine had disagreement between KWL serotype and ISR (10_2%) (Table 2). S. Pullorum and S. Gallinarum are avian pathogens with a fastidious growth habit that can require longer incubation times. Of the 13 samples in this collection, eight (61_5%) were putatively mixed as detected by an ISR indicating the presence of a different serotype (Table 2). These results suggest that the group D Salmonellae may be prone to overgrowth by minority serotypes present within culture during storage. Alternatively, the group D Salmonellae may have a propensity to associate with other serotypes, and thus, overgrowth is a related outcome. Further research using competition experiments would be required to understand why so many isolates of the group D Salmonellae yielded a secondary serotype. In three cases, S. Enteritidis was isolated after either S. Gallinarum or S. Pullorum had been isolated (B138, B143 and B145). For B137, S. Heidelberg was identified by ISR, but S. Gallinarum was found by KWL serotype. This result supports that mixtures of serotypes in culture were common.

 

Table 2. Variation between reported serotype and serotype as detected by ISR analysis.

ISR, intergenic sequence ribotyping.

 

Salmonella Agona was isolated four times from comercial layer organic farms in 2010, and these results were confirmed by PFGE (Tables 2 and 3). In this study, DNA samples identified as B133 and B134 were again classified as S. Agona by ISR (498 bp), whereas B154 and B155 were not. It is possible that PFGE analysis was not sensitive enough to detect differences between the two S. Agona strains and the other two isolates. However, sequence alignment indicated that disagreement of both B154 and B155 ISRs with the one from S. Agona was substantial, and no alignment was possible at 90% similarity. These results suggest that two isolates of S. Agona were overgrown with serotype S. Isangi in one case and UN0043 in the other.

 

Four sources of isolates included over ten samples, and these were poultry carcass (73), drag swab (27), cloacal swab (11) and 1-day-old chick (13) (Table 3). The 1-dayold chick samples yielded only S. Enteritidis, and there were no mixtures. Cloacal swabs had only S. Heidelberg by KWL serotyping, but one sample (B94) may have been mixed with UN0042. Serotypes from drag swabs were 81_5% S. Enteritidis by KWL serotyping with one sample putatively mixed with S. Mbandaka (B15). The remaining samples were S. Heidelberg with one sample putatively mixed with S. Typhimurium (B146). Poultry carcasses had the most complicated Salmonella flora. According to the KWL scheme, 43 of 73 samples (58_9%) were S. Heidelberg, 16 (21_9%) were S. Enteritidis and 14 (19_2%) were S. Hadar. Of the three serotypes initially recovered from poultry carcasses, 5 of 16 (31_3%) S. Enteritidis cultures may have been mixed. In contrast, 7_1 and 4_7% of samples initially found to have S. Hadar and S. Heidelberg were putatively mixed. These results suggest that S. Enteritidis was frequently overgrown by other Salmonella serotypes when stored. An alternative explanation is that S. Enteritidis had a propensity to associate with other serotypes.

 

Table 3. Salmonella enterica serotypes from southern Brazil as assigned by ISR in reference to the Kauffmann White–Le Minor scheme.

*Strains also identified by pulsed-field gel electrophoresis (PFGE) (Perdoncini, 2011). www.lume.ufrgs.br/bitstream/handle/10183/36857/ 000819160.pdf.

 

Intergenic sequence ribotyping analysis revealed substantially new information about the collection of 155 isolates from southern Brazil that could impact the assessment of risk for emergent foodborne illness in humans or disease in poultry on-farm. The most frequent contributor to disagreement between KLW serotyping and ISR in this study, as it was previously, was the presence of mixed serotypes in culture (Guard et al. 2012). For example, detection of multiple serotypes present when single colonies are passaged strongly suggests that the human pathogen S. Enteritidis circulates with the avian pathogens S. Gallinarum and S. Pullorum on-farm. This finding contradicts the concept that closely related Salm. Entérica serotypes are mutually exclusive (Baumler et al. 2000). It is conceivable that a flock could be infected with two serotypes at one time, and co-infection could affect the percentage of contaminated eggs that enter the market or the health of a flock. Further research is needed to address the impact of co-infection of chickens with serovar group D avian-associated Salmonella, especially as it impacts internal egg contamination, public health and disease in chickens.

 

DNA microarray was used for samples that had unique ISRs because references were not yet available in sequence databases (Guard et al. 2012). Serovars S. Mbandaka, S. Montevideo, S. Livingstone, S. Infantis and S. Cerro were thus assigned to ISRs that are now part of a reference database maintained at the United States Department of Agriculture. Serotypes, S. Mbandaka and S. Infantis, are considered emergent Salmonella serotypes in Brazil with low frequencies of isolation from poultry products (4_8 and 7_6%, respectively) (http://www.anvisa. gov.br/alimentos/relatorios/relatorioprebaf.pdf). The other three serotypes have not yet been reported as prevalent serotypes in Brazil. These results indicate that ISR can be used to find serotypes that may not necessarily have a whole genome reference, but that are represented within DNA microarray hybridization databases.

 

Serotypes may differ in how they are impacted by storage and by how likely they associate with other serotypes. For example, storage of S. Enteritidis at _80°C caused a shift in phenotypes as assayed by composition of the outer membrane, but storage of S. Typhimurium did not (Parker et al. 2001). Another complication of evaluating stored cultures is that a change could occur in the relative prevalence of mixtures of serotypes over time (Borsoi et al., 2009, Oliveira et al., 2002). Access to a less expensive, efficient and highly discriminatory technique for serotyping that can find mixtures should enable appropriate decisions to be made to improve the safety and security of the food supply.

 

A total of 155 isolates of Salm. enterica subsp. Entérica obtained from different poultry sources were evaluated in this study (Table 2). Strains were provided by the Avian Diagnostic and Research Center at the Federal University of Rio Grande do Sul (CDPA – UFRGS for acronym in Portuguese; Table 2). Bacteria were isolated from poultry facilities located in the state of Rio Grande do Sul in southern Brazil between 1995 and 2010. Serotyping, using the KWL scheme, was done by the National Reference Institute Oswaldo Cruz/FIOCRUZ. Strains were conserved at _80°C in 20% glycerol until analysis by ISR.

 

Salmonella strains were revived from freezer stocks in 5 ml of brain–heart infusion (BHI) broth by transferring one 10-ll loop of frozen cells in the media and statically incubating the suspension for 24 h at 37°C. Cultures were streaked on XLD and XLT4agar and incubated for 24 h at 37°C to obtain separated colonies. One colony was transferred to BHI broth and incubated overnight at 37°C. Cell culture was diluted to match a McFarland Turbidity Standard 0_5, and 150 ll of the cell suspension was applied to one circle on Whatman FTA _ classic cards (GE Healthcare Bio-Sciences Corp., Piscataway, NJ, USA). FTA cards were subsequently shipped with an APHIS permit for importation and transportation of controlled materials for analysis at the United States Department of Agriculture, Agricultural Research Service, Egg Safety and Quality Research Unit; (USDA-ARS-ESQRU) in Athens, GA, USA (Pulido-Landinez et al. 2012).

 

Whatman FTA_ cards were processed following manufacturer instructions with some refinements (Pulido- Landinez et al. 2012). Briefly, discs were excised from the cards using a 3_00 mm Harris Uni-Core device and transferred in to sterile 1_5-ml-Eppendorf tubes before adding 200 ll of FTA purification reagent. To avoid crosscontamination between samples, the collecting device was cleaned by cutting two discs from a noninoculated FTA card. Tubes were vortexed for 5 s and incubated at 25°C for 5 min at 450 rpm using an Eppendorf Thermomixer (Eppendorf, Hamburg, Germany). The purification reagent was discarded and replaced with fresh reagent to repeat this step one more time. Discs were then washed twice with 200 ll of TE buffer under the similar conditions indicated for the purification reagent and discarding the buffer in between washes. TE buffer was completely removed before continuing with PCR analysis. Safety testing was conducted on each DNA sample adsorbed in the FTA cards in order to determine if embedded reagents killed bacteria. One disc was placed in BHI broth and incubated with shaking for 24 h at 37°C. If turbidity was observed, culture was streaked on brilliant green (BG) agar (Acumedia, Neogen Corporation, Lansing, MI, USA) to test for the presence of Salmonella.

 

Nested polymerase chain reaction (N-PCR) method was used to obtain PCR products for analysis of sequence. N-PCR and sequencing primers were designed using the Primer-Blast designing tool from the National Center for Biotechnology Information (NCBI; Tables 1 and 2). Purified DNA in FTA discs was amplified using primers ISRF1 and ISR-R1 in the first PCR and primers nISR-F14 and nISR-R14 in the second PCR. Briefly, FTA discs were transferred to 0_2-ml-PCR tubes containing 29 Gene Amp Fast PCR Master Mix (Applied Biosystems, Foster City, CA, USA) and 200 nmol of primers ISR-F1 and ISR-R1 in a volume of 30 ll. One microlitre of the PCR product from this reaction was transferred in to 29 ll of Master Mix solution containing primers nISR-F14 and nISR-R14 in the same aforementioned primer concentrations. Amplification was performed on a Veriti 96-well Fast Thermal cycler (Applied Biosystems) under the following cycling conditions: initial denaturation at 95°C for 10 s followed by 35 cycles of 94°C for 0 s, 64°C for 40 s and 72°C for 10 s with a final extension at 72°C for 10 s. DNA products from the second PCR were resolved in 2% ethidium bromide agarose gels (Invitrogen, Carlsbad, CA, USA). Then, the amplified DNA in those samples containing the expected nucleotide size was purified using a PureLink_ PCR purification kit (Invitrogen). DNA concentrations, ranging from 15 to 50 ng/uL, were measured in a NanoDrop ND-1000, Spectrophotometer (Nano- Drop, Wilmington, DE, USA), and purified PCR products were submitted to Retrogen, Inc. (San Diego, CA, USA) for DNA sequencing in an ABI Prism 3730 DNA analyzer (Life Technologies, Grand Island, NY, USA) using primers ISRs1_F8 and ISRs2_R42 (Table 1).

 

The ISR sequence starts from the nucleotide located immediately after the 23S rRNA gene and the nucleotide located immediately before the tRNA-aspU gene in the Salmonella genome region linked to the dkgB gene (Morales et al. 2006). Finding no ambiguous nucleotides within at least 300 base pairs (bp) of remaining sequence after ends were trimmed assessed the quality of sequence data. In addition, substantial overlap of forward and reverse sequences consisting of at least one flanking intergenic sequence and some of the 5S rRNA gene should be observed. Forward and reverse sequencing data corresponding to each individual sample were aligned using SeqMan Pro Lasergene v8.0 (DNASTAR, Madison, WI, USA), and ISR sequences were assigned serotype. ISR sequences were assigned serotype using SeqMan Pro after a 100% similarity match with the ISR sequence database for Salmonella serotyping maintained at the USDA-ARSESQRU was observed (Guard et al. 2012).

 

The DNA hybridization microarray (DNAhyb) Salmonella serotyping method is AOAC RI certified and marketed as Check&Trace (Checkpoints, Wageningen, the Netherlands) was used to resolve Salmonella serotype identity of the unique ISR sequences detected in this study (Guard et al. 2012). DNAhyb was modified to analyse DNA extracted from FTA discs (Pulido-Landinez et al. 2012), because international restrictions on shipment of live pathogens encourages shipment of DNA only. Salmonella DNA was prepared as suggested by E. Mundt (personal communication). Briefly, three FTA discs were placed into a 1_5-ml-Eppendorf tube containing 0_5% SDS and 0_5 mg ml _1 Proteinase K in 180 ll distiled water. Tubes were briefly vortexed and incubated at 55°C for 60 min at 450 rpm in an Eppendorf Thermomixer. DNA was extracted from the liquid fraction using a PureLinkTM Genomic DNA kit from Invitrogen and following the protocol for Gram-negative bacteria cell lysates after proteinase K digestion. DNA concentrations were measured in a NanoDrop ND-1000 Spectrophotometer (NanoDrop) and 10 ll of extracted DNA were added into the PCR reaction tubes provided within the kit. DNAhyb was otherwise followed as indicated by the manufacturer.

 

This research was supported by the Colombian Veterinary Poultry Association (AMEVEA), the National Council for Scientific and Technological Development (CNPq) from Brazil and the United States Department of Agriculture, Agricultural Research Service (USDA, ARS). Special thanks are made to Tod Stewart (USDA) for technical assistance and professor Nhora Martinez (National University of Colombia) for the assistance in statistical analyses. Authors have no conflict of interest to declare, financial or otherwise.

 

 

 

 

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