Correction
7 Mar 2016: Poly F, Serichantalergs O, Kuroiwa J, Pootong P, Mason C, et al. (2016) Correction: Updated Campylobacter jejuni Capsule PCR Multiplex Typing System and Its Application to Clinical Isolates from South and Southeast Asia. PLOS ONE 11(3): e0151410. https://doi.org/10.1371/journal.pone.0151410 View correction
Figures
Abstract
Campylobacter jejuni produces a polysaccharide capsule that is the major determinant of the Penner serotyping scheme. This passive slide agglutination typing system was developed in the early 1980’s and was recognized for over two decades as the gold standard for C. jejuni typing. A preliminary multiplex PCR technique covering 17 serotypes was previously developed in order to replace this classic serotyping scheme. Here we report the completion of the multiplex PCR technology that is able to identify all the 47 Penner serotypes types known for C. jejuni. The number of capsule types represented within the 47 serotypes is 35. We have applied this method to a collection of 996 clinical isolates from Thailand, Cambodia and Nepal and were able to successfully determine capsule types of 98% of these.
Citation: Poly F, Serichantalergs O, Kuroiwa J, Pootong P, Mason C, Guerry P, et al. (2015) Updated Campylobacter jejuni Capsule PCR Multiplex Typing System and Its Application to Clinical Isolates from South and Southeast Asia. PLoS ONE 10(12): e0144349. https://doi.org/10.1371/journal.pone.0144349
Editor: Mikael Skurnik, University of Helsinki, FINLAND
Received: September 14, 2015; Accepted: November 17, 2015; Published: December 2, 2015
This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication
Data Availability: All relevant data are within the paper.
Funding: This work was supported by U.S. Naval Medical Research and Development Command Work Unit 6000.RAD1.DA3.A0308 (FP JK PP PG). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. US department of agriculture-Agricultural Research Service, CRIS 5325-42000-047 (CTP). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Military Infectious Diseases Research Program, Walter Reed Army Institute of Research, Washington, DC (OS PP CM). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Campylobacter jejuni is among the leading causes of bacterial diarrheal disease worldwide. In the U.S., Campylobacter is currently the second cause of foodborne bacterial disease behind Salmonella with an estimated incidence of 14.22 cases per 100,000 million annually, affecting all age classes [1]. In developing countries, the incidence is higher and predominantly affects children less than two years old [2, 3]. It is estimated that 5.5 to 18% of children under the age of 5 years develop diarrhea caused by this pathogen [4]. In addition, C. jejuni is associated with several sequelae, including irritable bowel syndrome (IBS) [5, 6], reactive arthritis [7], and Guillain-Barré syndrome [8]. Moreover, recent studies suggest the association of repeated C. jejuni infections with malnutrition and stunting [9].
A decade of research utilizing whole genome sequencing and Comparative Genomic Hybridization (CGH) using whole genome microarray analyses has revealed extensive genetic variability among C. jejuni strains [10–19]. The most variable genetic loci are those involved in the synthesis and modification of bacterial surface carbohydrate structures including the genes involved in flagellar O-linked glycosylation, genes involved in biosynthesis of lipooligosachharide (LOS), and the polysaccharide capsule (CPS) [10], all of which contribute to virulence in a variety of ways. Non-encapsulated mutants are defective in colonization of chickens and mice [20, 21], and show reduced virulence in infant ferret [22]. Moreover, the CPS is required for resistance to complement-mediated killing [21–24]. CPS is also the primary determinant of the Penner or heat-stable serotyping scheme, of which there are 47 C. jejuni serotypes [25, 26], some of which fall into complexes of related serotypes (Fig 1) [25, 27, 28]. C. jejuni CPSs are exported via a highly conserved ABC-transporter mechanism similar to class 2 and class 3 capsules of E. coli [29]. The variable genes that encode the enzymes responsible for synthesis of the serotype-specific CPS are located between two blocks of ABC transporter genes (kpsMTEDF at one end of the locus, and kpsCS at the other end. To date the sequence of 18 of these variable CPS loci have been published [10, 15, 19, 30–32], and the remainder are in preparation (C. T Parker, unpublished; F. Poly, unpublished). We are currently evaluating a polysaccharide CPS conjugate approach against C. jejuni -mediated disease [29, 33, 34]. A final vaccine formulation, like most other polysaccharide conjugate vaccines would be multivalent [35]. The criteria for inclusion of specific CPS types into a multivalent formulation would be based on both incidence of specific CPS types and any association of specific CPS types with severity of illness. However, a recent systematic review of published studies on Penner serotyping of strains isolated from 1978–2002 demonstrated a paucity of data from developing countries, where a vaccine is the most needed [27]. Additional information on CPS types present in endemic areas is clearly needed to facilitate development of a multivalent conjugate vaccine approach. Unfortunately, the complexity and costs of Penner serotyping have limited its use in recent years. To circumvent this problem, a partial multiplex PCR methodology was successfully introduced in order to gain more information on C. jejuni CPS distribution worldwide [32]. The initial methodology was able to distinguished 17 of the more frequently isolated CPS types. In this report we present an updated version of the multiplex PCR that is now able to identify all known CPS C. jejuni types. These data indicate that the 47 serotypes can be collapsed into 35 CPS types (Fig 1). Here, we also describe application of this method to a collection of 996 C. jejuni clinical isolates collected from South and Southeast Asia from 1998 to 2010.
Materials and Methods
DNA purification
Frozen stocks of C. jejuni were subcultured on Brucella agar plates with 5% sheep blood (BAP) and incubated at 37°C under microaerobic conditions (5% O2, 10% CO2, 85% N2). Genomic DNA extractions of C. jejuni isolates were performed using DNeasy tissue extraction kits (Qiagen, USA) following the manufacturer’s instructions. Genomic DNAs were routinely stored at -20°C.
Whole genome sequencing and CPS loci annotation
CPS loci sequences were extracted from the USDA-ARS CRIS 5325-42000-047 project aimed at the whole genome sequencing of 45 C. jejuni Penner type strains. Strains are shown in Table 1. Whole-genome sequencing of the 45 C. jejuni Penner type strains to a depth of ~20x was performed using shotgun and paired-end (8 to 12 kb) libraries and was generated on a Roche 454 FLX+ sequencing system with Titanium chemistry. The Roche Newbler assembler (version 2.3) was used to assemble reads into contigs. Genome closing utilized a combination of steps. The contigs were aligned to other C. jejuni genomes. Scaffold gaps were filled by a combination of referenced assemblies of approximately one million Illumina MiSeq reads/strain to the Newbler contigs using Geneious software (Biomatters, New Zealand) and the identification of repeated contigs using the Perlscript contig_extender2. Certain gaps were validated using PCR amplification and Sanger sequencing. All base calls were validated using the Illumina MiSeq reads, which provided an additional 100× coverage. Shotgun library preparations and sequence procedures were performed according to established procedures and manufacturer’s instructions. Annotation of the variable region of CPS biosynthesis, between kpsC and kpsF (Fig 2), was made using Artemis software (Sanger institute).
Putative gene functions were assigned via homology to a protein database by BLAST analyses.
PCR primer design
Selection of CPS regions for primer design was performed as previously described [31, 32]. Briefly, specific CPS sequences (variable capsule region between kpsC and kpsF) for a particular serotype were isolated by performing a local stand alone BLAST using a database encompassing the nucleotides sequences of all 47 available C. jejuni capsule loci (C. T. Parker, unpublished). The selected nucleotide regions were used for multiplex primer design. The sites where the primers were designed are displayed in Fig 2. Multiplex primers were designed via the online software Primer3 [41] using the following parameters: length between 18 and 30 residues, 20 to 50% GC, Tm ranging from 57 to 63°C. Primer sets to be included in the original or new multiplex mixes were designed in order to amplify a PCR of least 20 base pairs smaller/larger than the other amplicons of the same mix. Following design, primers were compared to C. jejuni genomes via NCBI BLAST software to exclude potential amplification outside the CPS locus.
Multiplex PCR parameters
PCRs were performed using 0.4 μM of each primers of their respective mixes in 25-μl reactions containing 1–10 ng DNA template, 1× PCR Gold Buffer, 2.0 mM MgCl2, 0.3 mM each dNTP and 1.25 U of AmpliTaq Gold DNA Polymerase (Life Technologies, USA) using Dyad thermal cycler (Bio-Rad, USA). DNA amplification was performed using an initial denaturation step at 94°C for 5 min; followed by 30 cycles of amplification (denaturation at 94°C for 1 min, annealing at 52°C for 1 min, and extension at 72°C for 1 min and ending with a final extension at 72°C for 10 min. At the end of the reaction, the PCR amplicons were analyzed by gel electrophoresis on 10-cm-long 2% agarose gels in 0.5× TBE (Tris-borate-EDTA) buffer at 175 V for 75 min. The serotypes were determined by the size of the PCR amplicons by comparison with a 100-bp molecular size standard (New England BioLabs, USA).
Validation of PCR primers and multiplex mixes
Primer sets were validated individually on their respective DNA type, and, if an amplicon of the predicted size was observed, the primer set was included in its multiplex mix. The newly generated multiplex mix was then used in a PCR reaction on a collection of 47 C. jejuni DNA (Table 1). The newly designed primer pair was selected and incorporated in multiplex mixes only if it yielded the right size amplicon during PCR performed on its target or related DNA CPS type (i.e. a strain that was part of the same complex) and if no false amplification was observed on the remaining CPS types tested. The newly formulated multiplex mix was finally tested against the DNA of 47 CPS types individually and deemed worthy only if the expected right size amplicons were obtained and no false positives were observed. There are four exceptions to this rule, as discussed below.
Clinical C. jejuni isolates
A total of 996 archived C. jejuni isolates were included in this study. These isolates were from twelve studies on etiology of diarrhea among travelers, military personnel and indigenous population from Southeast Asia during 1998–2010 as shown in Table 2. All stool samples were routinely cultured for enteric bacteria pathogens at the Armed Forces Research Institute of Medical Sciences (AFRIMS). The Cobra Gold exercises in 1998–2003 were approved by ethical review committees from Walter Reed Army Institute of Research (WRAIR) IRB. The travelers’ diarrhea and diarrhea surveillance studies in Thailand, Cambodia and Nepal were approved by ethical review committees from WRAIR IRB as well as host nation IRB (Thailand, Cambodia and Nepal). The studies involve using de-identify archived frozen C. jejuni isolated from stool samples with appropriate consent for samples donation in the future use and currently stored at the Department of Enteric Diseases, AFRIMS without any identifiable information. The studies were closed. Specimens are labeled by subject numbers and date of collection without any personal identifiers. A link to subject name, number, and personal identifier was destroyed. Data to be included in the analysis portion of this study will be demographic (age and gender), clinical (associated symptoms), and laboratory (results) data and will not include any confidential or sensitive data.
Cary Blair medium were used as transportation medium in these study sites. For C. jejuni culture and isolation, fresh stool or stool in Carry Blair medium was processed by a modified filtration method [42]. After filtration, the millipore membranes were incubated on BAP at 37°C under microaerobic conditions. The suspected colonies of C. jejuni were identified by catalase test, nitrate tests and hippurate hydrolysis. Confirmed C. jejuni isolates were kept frozen at -70°C in 15% glycerol medium.
Results and Discussion
Description of primers and multiplex mixes
The previous C. jejuni CPS multiplex version was composed of two mixes, alpha and beta, that contained eight and six primer sets, respectively [32]. A total of 23 new primer sets were added for a total of four mixes, alpha, beta, gamma and delta. The alpha mix of the second version contains three additional primers sets (HS19, HS33 and HS63) compared to the initial published version, for a total of 11 primers sets. The beta mix was revised by moving the HS44 primer set to mix gamma and adding five new primer sets (HS5, HS12, HS21, HS27 and HS57). A positive control primer set for C. jejuni sp. was included in mix gamma following observations that other non-jejuni Campylobacter spp. were cross reacting with the multiplex PCR scheme (data not shown). This C. jejuni-specific primer set amplifies a 331bp region of the lpxA gene (involved in lipid A biosynthesis) [44]. Thus, results should be interpreted only if a positive amplification of a 331 bp amplicon is observed in mix gamma. Finally, mix delta contains an additional eight primer mixes. Primers and their respective PCR product sizes are listed in Table 3 and illustrated in Fig 3. All primer sets were tested as described in Materials and Methods.
Lane 1, 100-bp NEB DNA standard; lane 2, mixture of PCR products obtained with all the templates from the alpha mix; lane 3, 100-bp NEB DNA standard; lane 4, mixture of PCR products obtained with all the templates from the beta mix; lane 5, 100-bp NEB DNA standard; lane 6, mixture of PCR products with all the templates from the gamma mix; lane 7, 100-bp NEB DNA standard; lane 8, mixture of PCR products with all the templates from the gamma mix.
Interpretation of results
As shown in Table 4, some primer sets can show extraneous bands, but the system has been designed to facilitate discrimination. For example, the HS5 template should yield an 857 bp product in mix beta, but it also yields a 129 bp product with the HS45 primer set found in mix gamma. Therefore, if an unknown template yields only a 129 bp product in mix gamma, the CPS type is HS45, but if it yields both a 129 bp product in mix gamma and an 857 bp product in mix beta, the strain is an HS5. Similarly, as described previously [32], HS31 DNA templates should produce a 857 bp product in mix beta, but they also produce a 325 bp product with the HS15 primer set found in mix alpha. The designed HS45 and HS15 primers do not match any sequences of HS5 and HS31 genomes respectively when compared by BLAST algorithm. The reason for these amplifications is still unclear. Nevertheless these additional bands do not interfere with the attribution of HS5 and HS31 CPS types.
During validation, it was also observed that Mu_HS15 primers (325 bp), which were in the alpha mix in the original multiplex, also recognized the HS58 type strain DNA template found in mix delta (89 bp). This observation would suggest that the first generation multiplex was falsely recognizing HS58 strains as HS15. Nucleotide sequence comparisons confirmed a region of homology within the CPS loci of both HS15 and HS58. However, in the current multiplex, amplification of this product does not interfere with attribution of both HS15 or HS58 CPS types, and the Mu_HS15 original primer set was retained in the current multiplex PCR.
Similarly, the Mu_HS8 primers used in the original mix were found to amplify a sugar biosynthesis gene found in the HS32 Penner type strain (Table 4). Thus, the Mu_HS8 primers generate a 342 bp amplicon from mix beta on both strains, but discrimination of HS32 is made by the presence of a 420 bp product (Mu_HS32) in mix delta. In addition, it was observed that HS32 type strain is also recognized by Mu_HS45 primers in mix gamma yielding a 129 bp amplicon. Again because these extraneous amplifications do not interfere with either CPS attribution, the original Mu_HS8 primers were retained in mix beta and Mu_HS32 primers were added to mix delta.
The CPS locus of the type strain of HS45 appeared to be a mosaic of multiple serotypes, an observation that complicated primer design (C. T Parker, unpublished). Primers were designed based on the HS45 sequence with the knowledge that they would also amplify HS5, HS32, and HS60 (Table 4).
Primers for CPS types in related complexes
Many CPS types fall into related complexes, e. g. HS23 and HS36 (Fig 1). DNA sequencing of the CPS loci had previously revealed that the type strains of HS23 and HS36 share 97.6% DNA sequence identity and >87.9% protein identity [31]. Both strains express the same repeating capsular trisaccharide, but the HS23 type strain was shown to lack the MeOPN modification and one of the four variable heptoses found in HS36 [31]. The primer Mu_HS23 developed in the first multiplex version was retained and does not distinguish HS23 and HS36 capsule types.
The HS4 complex is the largest complex and is composed of eight separate serotypes (HS4, HS13, HS16, HS43, HS50, HS62, HS64 and HS65) (Fig 1) [25]. Only the capsule structure of a clinical isolate from Thailand, CG8486, that typed as HS4/13/64 has been published [30]. The primer set named HS4 (alpha mix, 370bp) and CG8486 (beta Mix, 652bp) in the first publication [32] were re-named HS4A and HS4B, respectively. These primer sets were designed based on the MeOPN transferases present in each strain [14, 32]. Due to the high recombination rate of C. jejuni strains, isolates that would react with both HS4A and HS4B primers were anticipated and observed (see below). The CPS biosynthesis loci of all 8 type strains in the complex and of CG8486 are highly conserved (C. T Parker, unpublished). Primers HS4A react positively with all eight individual serotypes associated with the HS4 complex, but not with CG8486, as demonstrated in a previous study [32]. Primers HS4B positively recognize CG8486, HS16 and HS64 and this is consistent with the presence of the CG8486 MeOPN transferase-like gene in these three strains (C. T Parker, unpublished). These data suggest that differences among strains within the HS4 complex include differences in the position of MeOPN attachment, an observation that has been confirmed by determination of CPS structure (Monteiro et al, in preparation).
HS5 and HS31 belong to the same complex [25] and are indistinguishable based on their CPS loci gene content (C. T Parker, unpublished). Thus, both HS5 and HS31 are detected by the presence of an 857 bp amplicon in mix beta generated by the Mu_HS5 primers (Table 4).
The CPS loci of the type strains from three additional Penner complexes, HS6/7, HS8/17, and HS33/35, also showed high conservation. The HS8/17 complex was discussed previously [32]. The Mu_HS6 was designed in the previous CPS multiplex PCR version. The HS6 capsule type remains obscure, due to the fact that CPS has been shown not to be the serodeterminant of the HS6 serotype and might explain the high number of false positive identified with Mu_HS6 designed previously [31, 32]. Nevertheless, sequencing of the HS7 Penner type strain showed that the entire HS7 biosynthesis locus was over 99% identical to that of the HS6 type strain (C. T Parker, unpublished). This result corroborates the frequent association of HS6 and HS7 in the Penner typing literature [27]. Finally, it appears that the CPS biosynthesis loci of the type strains of HS33 and HS35 are over 99% identical at the nucleotide level (C. T Parker, unpublished). The Mu_HS33 primer designed in this new version recognizes both serotypes.
The HS1 complex, which includes HS1 and HS44, can also be detected by the same primer set, producing a 610 bp amplicon in mix beta. Additional information on the HS1 complex will be presented separately (F. Poly, unpublished).
Collectively, the sequencing data suggests that strains within these complexes express similar/related CPS structures despite belonging to different serotypes.
Application of the multiplex to clinical isolates from Thailand
Nine hundred and ninety isolates were positive for the C. jejuni species-specific gene (lpxA) by gamma mix multiplex PCR and six isolates were negative. This result confirms the high level of correlation between the lpxA PCR and classic phenotypical methods for the characterization of C. jejuni sp. [44]. The CPS multiplex PCR assay identified 98% of all 990 C. jejuni isolates in this study. There were a total of 20 untypeable strains, 17 from Nepal (12 from indigenous population, 5 from travelers), and three from Cambodia, representing 12.8 and 12.5% of the isolates in each respective country (Table 5). This higher of level of non-typeable isolates in those countries does not appear to be random or attributable to method failure. This may indicate presence of localized undefined/unreported capsule types that are not included in the current capsule typing method that was developed largely on strains from North America and Europe [45]. Validation of this hypothesis will require further analysis.
In bold are the five most prevalent CPS types in their respective group. Number in parentheses represent the number of strain in the category.
Overall, as shown in Table 5, the five most common CPS types observed from all sites were the HS4 complex (16.1%), HS2 (14.7%), HS5/31 complex (10.6%), HS8/17 complex (9.8%) and HS3 complex (7.8%). In 2013, Pike and colleagues published a longitudinal study of the most common Penner serotypes worldwide. One of the observations of the study is that HS4 complex, HS2 and HS1/44 complex were the most common serotypes in both developing and developed countries. Surprisingly, our survey demonstrates that HS1/44 type is less frequent in this population, but is still significantly represented with 5.4% of cases in the south and Southeast Asian regions (Table 5).
Comparison of capsule distribution of total foreign versus indigenous population, shows some noticeable differences (Fig 4). Isolates from CPS types belonging to HS2 (8.7% vs 18.3%, p<0.01), HS5/31 complex (7.5% vs 12.4%, p = 0.019) HS6/7 complex (1.1% vs 2.7%, p = 0.098), HS8/17 complex (5.3 vs 12.4%, p<0.01), HS9 (1.1% vs 2.5%, p = 0.098), are underrepresented in foreign population, while HS15 (4.7% Vs 0.5%, p<0.01), HS23/36 complex (13.3% Vs 2.2%, p<0.01), HS42 (4.7% Vs 0.5%, p<0.01) and HS53 (12.2% Vs 2.4%, p<0.01) are over represented in isolates collected from foreign visitors. A closer look at the foreign population visiting Thailand, travelers and military population, highlight a dichotomy in those two groups (Table 5): The five most common CPS types in non-military travelers to Thailand are the HS5/31 complex (15.7%), HS3 complex (13.7%), HS15 (11.8%) and the HS23/36 (7.8%) and HS53 (7.8%), whereas the five most common CPS types in military personnel deployed to Thailand were the HS4 complex (22.8%), the HS23/36 complex (16.7%), HS53 (14.8%), HS2 (8%), and HS42 (6.1%). The difference of CPS distribution between those two groups is not easy to explain. However, it is likely that isolates from these military exercises had higher clonal relationships than the other isolates studied. The annual military exercises in Thailand take place for one month or less at different locations, and off-duty military personnel may consume the same contaminated foods from local vendors. In addition while there is no differences of the top five most common CPS types between travelers and indigenous population in Nepal, there are noticeable differences between the travelers and indigenous population in Thailand (Table 5). Capsule types HS2, HS4 and HS8/17 complexes are under-represented and HS15, HS53 and HS23/36 complex are over-represented in travelers to Thailand compared to the Thai population (Table 5). While some of those differences can be explained by clonality/outbreaks, the differences are most likely multifactorial and include regional isolation for foreign visitors, differences in food consumed, and/or seasonal changes. Nonetheless, this is important information to take in account for the development of a capsule based vaccine against C. jejuni.
(*) statistically significant (p<0.01). (**) statistically significant (p<0.05).
Finally, no major temporal difference of capsule types distribution was observed in these pediatric populations during 2004–2006 (n = 302) and 2008–2010 (n = 213) time period. C. jejuni HS2, HS4 complex, HS8/17 complex, HS3, and HS5/31 complex were found as the five most common capsule types, accounting for nearly 70% of isolates in each of these two time periods (data not show).
Conclusions
The burden of disease caused by C. jejuni is undeniable. It represents a major health risk for pediatric population living in developing countries as well as travelers visiting those regions. The most promising vaccine approach to alleviate campylobacteriosis in those populations is a capsule conjugate vaccine. A monovalent vaccine targeting HS23/36 CPS type has shown 100% protection in a non-human primate model [33]. To be efficacious a final vaccine should be multivalent and include the most prevalent and most pathogenic C. jejuni CPS types. In order to gain more information on CPS distribution worldwide we developed a multiplex PCR based approach. In this study we demonstrated the possibility of specifically determining CPS/Penner type through design of specific PCR primer pairs. Typing methods for C. jejuni remains are limited despite the availability of numerous whole genomes sequences in the last decade. The Penner serotyping method is time and labor intensive, and it is now only performed in a handful of laboratories worldwide. One the major drawbacks in addition to the cost and complexity of the typing sera, is the phase variability of CPS expression [22]. In contrast, the multiplex does not require capsule expression for attribution of capsule type.
A recent systematic review of clinical isolates C. jejuni Penner typing since the 80’s demonstrate that over 85% of the typed strains were from developed countries. This result demonstrated the lack of information on pediatric population from the developing countries and the necessity to gain more information on CPS type distribution in those region where a CPS conjugate vaccine is the most needed [27]. This method provides a mechanism to address this deficit.
Analysis on almost 1000 clinical isolates collected from 1998 to 2010 in South East Asian peninsula showed that 98% of the C. jejuni strains were typeable. Knowing the C. jejuni CPS loci plasticity, the C. jejuni non-typeable isolates may represent unknown capsules that were not described in the Penner serotype system. Although there are marked differences between the major capsule types reported in the developed world [27] and those reported here from Asia, a limited number of capsule types account for most of the disease. Thus, the 8 most common CPS types account for 76.7% CPS in that region. Thus, these results suggest that the valency required for an effective C. jejuni conjugate vaccine is similar to that seen in the first pneumococcal conjugate vaccines.
Taken together, these observations validate the development of a multiplex PCR technique. The application of capsule multiplex PCR assay demonstrates simplicity and sensitivity of the technique. All equipment required is standard in most molecular microbiology laboratories. The PCR multiplexing reduces the number of reactions to be performed per samples, and this method is not affected by phase variation of capsule expression. Our study demonstrates the usefulness of the assay in geographical epidemiology for C. jejuni diarrhea and in describing CPS serotype among clonally related C. jejuni isolates from spatial distribution and possible outbreak situations.
Acknowledgments
The views expressed in this article are those of the authors and do not necessarily reflect the official policy or position of the Department of the Navy, Department of the Army, Department of Defense, or the US Government. Authors are military service members (C.M.) and employees of the US government (P.G., O.S., C.T.P.). This work was prepared as part of official duties. Title 17 USC. §105 provides that “Copyright protection under this title is not available for any work of the United States Government.” Title 17 USC §101 defines a US government work as a work prepared by a military service member or employee of the US government as part of that person's official duties.
Author Contributions
Conceived and designed the experiments: FP PG CM CTP. Performed the experiments: OS JK PP. Analyzed the data: FP OS JK PP. Contributed reagents/materials/analysis tools: FP OS JK PP CM PG CTP. Wrote the paper: FP OS PG CTP.
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