BioMed Research International

Volume 2013 (2013), Article ID 295050, 10 pages

http://dx.doi.org/10.1155/2013/295050

Research Article

A New Protocol to Detect Multiple Foodborne Pathogens with PCR Dipstick DNA Chromatography after a Six-Hour Enrichment Culture in a Broad-Range Food Pathogen Enrichment Broth

Masahiro Hayashi,1,2 Tatsuya Natori,² Sayoko Kubota-Hayashi,² Machiko Miyata,² Kiyofumi Ohkusu,² Keiko Kawamoto,³ Hisao Kurazono,³ Souichi Makino,⁴ and Takayuki Ezaki²

¹Division of Anaerobe Research, Life Science Research Center, Gifu University, 1-1 Yanagido, Gifu 501-1194, Japan

²Department of Microbiology, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu 501-1194, Japan

³Division of Food Hygiene, Department of Animal and Food Hygiene, Obihiro University of Agriculture & Veterinary Medicine Inada-cho, Obihiro, Hokkaido 080-8555, Japan

⁴Department of Domestic Science, Kyoto Seibo College, Kyoto 612-0878, Japan

Received 27 September 2013; Revised 5 November 2013; Accepted 5 November 2013

Academic Editor: Hiroshi Asakura

Copyright © 2013 Masahiro Hayashi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

A quick foodborne pathogen screening method after six-hour enrichment culture with a broad-range food pathogen enrichment broth is described. Pathogenic factors of Salmonella enterica, Shigella spp., enteroinvasive Escherichia coli, and enterohemorrhagic E. coli are amplified with a cocktail primer and rapid polymerase chain reaction (PCR), which finishes amplification in 30 min. The PCR amplicon was differentiated with a dipstick DNA chromatography assay in 5–10 min. Starting from a four- to six-hour enrichment culture, this assay was finished within 45 min. Detection sensitivity of this protocol was less than 2.5 CFU/25 g for S. enterica and 3.3 CFU/25 g for enterohemorrhagic E. coli in spiked ground meat experiments.

1. Introduction

Infectious gastroenteritis is a leading cause of morbidity and mortality worldwide, particularly in developing countries [1]. Risk factors for infectious gastroenteritis include exposure to various contaminated food products [2]. Several methods to detect pathogens directly in food samples have been reported [3, 4]; however, most food analysis requires a 25 g food sample. Ideally, pathogen detection in food should be at the single-cell level [5].

Several methods based on polymerase chain reaction (PCR) have been developed to detect a single-cell pathogen from enrichment culture [6–8]. Cocktail PCR, carried out in a single PCR tube for simultaneous detection of more than one bacterial target, has been investigated as a more cost-effective and time-saving method [9, 10]. However, it is difficult for small food laboratories to use ethidium bromide-based agarose gel. On the other hand, real-time PCR assays employing various types of fluorescence systems allow multiple detection during PCR [11–13]. This is an excellent method, but it requires an expensive real-time thermal cycler and reagents. Thus, small laboratories cannot afford this real-time method.

Another aspect of food analysis is the analysis time. Fresh food products must arrive to the market quickly, but current culture-based protocols require several days to confirm that the products are pathogen-free. Confirmation that fresh food is safe before shipping is, therefore, desired, but difficult in practice.

To solve these problems, we developed a quick cocktail PCR and dipstick DNA chromatography to differentiate PCR amplicons for Salmonella enterica, Shigella spp., enteroinvasive Escherichia coli (EIEC), and enterohemorrhagic E. coli (EHEC) from a single enrichment culture broth. In our previous report, we described a food pathogen enrichment (FPE) broth that supports the growth of Campylobacter without adding lysed blood and carbon dioxide [14]. The method detected a few Campylobacter cells in 25 g of chicken within 24 hours and was better than the conventional Bolton-based enrichment culture.

In this report, we describe a new protocol to detect S. enterica, Shigella spp., EIEC, and EHEC from the FPE broth. DNA preparation from the FPE broth was simplified and the cocktail PCR was designed to finish within 30 min. The PCR amplicon was visually differentiated using dipstick DNA chromatography within 5–10 min.

2. Materials and Methods

2.1. Bacterial Strains

The bacterial strains of S. enterica, Shigella spp., EIEC, and EHEC and other strains are listed in Table 1. All strains were supplied from the Gifu Type Culture Collection of the Microbial Genetic Resource Stock Center, Gifu University Graduate School of Medicine (Gifu, Japan), supported by the Ministry of Education, Culture, Sports, Science, and Technology of Japan. All strains were cultured on heart infusion agars (BD, Tokyo, Japan) at 37°C under an aerobic atmosphere overnight. A fresh culture was used for each experiment.

Table 1: List of bacterial strains used in this study.

Bacteria
Serotype
Toxin
Strains
Number of strain

EHEC

(Enterohemorrhagic E. coli)
O26: H-
Shiga toxin 1
GTC14538, GTC14548, GTC14605, GTC14606
4

O26: H11
Shiga toxin 1
GTC14516, GTC14540, GTC14549, GTC14557, GTC14558
5

Shiga toxin 1 and 2
GTC14515, GTC14539, GTC14567
3

O111: H-
Shiga toxin 1
GTC14517, GTC14528, GTC14541
3

Shiga toxin 1 and 2
GTC14508, GTC14582
2

O115: H10
Shiga toxin 1
GTC14518
1

O119: H2
Shiga toxin 1
GTC14529
1

O121: H19
Shiga toxin 2
GTC14530, GTC14577, GTC14601, GTC14602
4

O128: H-
Shiga toxin 1 and 2
GTC14603
1

O157: H7
Shiga toxin 2
GTC14513, GTC14514,GTC14524, GTC14525, GTC14537 GTC14546, GTC14547, GTC14550, GTC14553, GTC14560
10

Shiga toxin 1 and 2
GTC14510, GTC14511, GTC14512, GTC14521, GTC14535 GTC14536, GTC14544, GTC14545, GTC14551, GTC14552,
10

O157: H-
Shiga toxin 1 and 2
GTC14507, GTC14520, GTC14530, GTC14543, GTC14555 GTC14556, GTC14566, GTC14571, GTC14587, GTC14588
10

EIEC

(Enteroinvasive E. coli)
O28: H-

GTC14240, GTC14243, GTC14251, GTC14259, GTC14260
5

O124: H-

GTC14241, GTC14242, GTC14245, GTC14262
4

O136: H-

GTC13248, GTC14254
2

O144: H-

GTC14249, GTC14252, GTC14256
3

O164:H-

GTC14244, GTC14246, GTC14247,
3

Salmonella enterica

    subsp.enterica    
serovar Typhimurium

GTC02557, GTC02561, GTC02562, GTC02563, GTC02564
10

GTC02571, GTC02572, GTC-2573, GTC02574, GTC02575

    subsp.enterica
serovar Enteritidis

GTC03838, GTC00131, GTC02377, GTC02382, GTC02387
7

GTC02389, GTC02390

    subsp.enterica
serovar Dublin

GTC13214, GTC13215, GTC13216, GTC13217,GTC13218
10

GTC13219, GTC13220, GTC13221. GTC02558, GTC02560

    subsp.enterica
serovar Typhi

GTC3P001, GTC3P074,GTC3P076, GTC3P081, GTC3P085
10

GTC3P087, GTC3P091, GTC3P095, GTC3P100, GTC3P106

    subsp.enterica
serovar ParaTyphi A

GTC3P002, GTC3P082, GTC3P083
3

Salmonella bongori

GTC03793T
1

Shigella boydii

GTC00779T, GTC01912, GTC01913, GTC01914, GTC01915
8

GTC01915, GTC01916, GTC01917,

Shigella dysenteriae

GTC01057T, GTC00786, GTC01929, GTC01930, GTC14808
17

GTC14809, GTC14810, GTC14811, GTC14812, GTC14813,

GTC14814, GTC14815, GTC14816, GTC14817, GTC14818,

GTC14819, GTC14820,

Shigella flexneri

GTC 0780T, GTC01918, GTC01920, GTC02007, GTC02008
13

GTC02009, GTC02010, GTC02011, GTC02012, GTC02013,

GTC02015, GTC02016, GTC02014,

Shigella sonnei

GTC00781T, GTC01909, GTC01910, GTC01911, GTC01931
7

GTC01932, GTC01933,

Escherichia coli

GTC00503 T
1

Escherichia albertii

GTC 16441T
1

Escherichia fergusonii

GTC 01720T
1

Escherichia vulneris

GTC 10613T
1

Escherichia hermannii

GTC 10612T
1

Escherichia blattae

GTC 01342T
1

Citrobacter freundii

GTC 14890T
1

Citrobacter diversus

GTC 00114T
1

Citrobacter rodentium

GTC 14911T
1

Citrobacter youngae

GTC 14914T
1

Klebsiella pneumoniae

GTC 14868T
1

Enterobacter cloacae

GTC 00109T
1

Enterobacter aerogenes

GTC 14962T
1

Cronobacter sakazakii

GTC 14952T
1

Serratia marcescens

GTC 14672
1

Yersinia enterocolitica

GTC 00127T
1

Pseudomonas aeruginosa

GTC 00002T
1

Vibrio parahaemolyiticus

GTC 02055
1

Staphylococcus aureus

GTC 00286T
1

GTC is the Gifu Type Culture Collection supported by the National Bioresource Project (NBRP: http://www.nbrp.jp/) of the Ministry of Education, Culture, Sports, Science,and Technology.

“T” after the strain number means type strain.

2.2. Determination of Optimal Enrichment Culture with FPE Broth

FPE broth is designed to support the growth of Campylobacter species without blood and carbon dioxide [14]. This broth was used in the present study to simplify the total food analysis protocol because the FPE broth supported most food borne pathogens in our preliminary experiment. The growth of the foodborne pathogen in the FPE broth was compared with that in conventional selective enrichment broth (Figure 1). In the spiked ground meat experiment, diluted fresh bacterial solution and 25 g of beef were mixed in 225 mL of FPE broth and incubated at 37°C.

(a)

(b)

(c)

(d)

(e)

(f)

Figure 1: Growth of reference strains in FPE broth and established reference media. The initial number of bacteria was defined as one and the multiplication number is indicated on the -axis. The -axis represents incubation time.

2.3. DNA Extraction

DNA was extracted from 1 mL of culture broth using a physical disruption method (MORA-EXTRACT, AMR, Gifu, Japan) according to the manufacturer’s instructions, with a final DNA elution volume of 200–400 μL.

DNA extraction from FPE broth was performed using a simplified protocol. One milliliter of 2 to 18 hours enrichment culture was collected in a 2 mL Eppendorf tube and centrifuged at 12,000 g. The supernatant was completely removed and 1 mL of T10E1 buffer was added and centrifuged under the same conditions. After the complete removal of the supernatant, 200 μL of T10E1 buffer was added to the tube and mixed. The solution was transferred to a tube containing beads and physically disrupted for 1 min with a Disrupter Genie (Scientific Industry Inc., Bohemia, NY, USA). The tube was boiled at 100°C for 3 min. Five microliters of the solution were used for the cocktail PCR assay.

2.4. Cocktail PCR

The cocktail PCR conditions used in the present study are described below. The primers used are described in Table 2. PCR amplification was performed in 10 μL of reaction mixture containing 5 μL of 2× premix Ex Taq (Takara Bio, Shiga, Japan), 2.5 μL of primer mixture, 0.5 μL of distilled water, and 2 μL of DNA template. PCR was carried out using the QuickBath thermal cycler (ThermoGen Ltd., Nagano, Japan) under the following conditions: 95°C for 3 min, 40 cycles of 95°C for 10 s, and 65°C for 10 s. The PCR cycles finished within 30 min.

Table 2: Cocktail primer list.

Pathogen
Targeted gene
Primer name
Sequence (5′-3′)

EHEC
stx1
Forward stx1
Biotin-ACAGGATTTGTTAACAGGAC

Reverse stx1
Tag1-TCTGTATTTGCCGAAAACGT

stx2
Forward stx2
Biotin-GATACAGAGAGAATTTCGTC

Reverse stx2
Tag1-GCCAGTTATCTGACATTCTG

Shigella spp. and EIEC
ipaH
Forward ipaHF
Biotin-CTCGCAGAGAAACTTCAGCTCT

Reverse ipaHR
Tag2-TTCTCTTCACGGCTTCTGACCAT

Salmonella spp.
invA
Forward invA
Biotin-TGACAGAATCCTCAGTTTTTCA

Reverse invA
Tag3-AGATAAGACGGCTGGTACTGAT

Internal control

Forward IPC
Biotin-ACTCTTCCTAGCAGGATCCCTCTAAG

Reverse IPC
Tag4-GCAATTCTAATACGACTCACTATAGG

2.5. Dipstick DNA Chromatography

The 5 terminus of the cocktail PCR amplicon was labeled with biotin, and the 3 terminus was labeled with four different tags. Streptavidin-coated blue latex, kindly provided from Fujikura (Saitama, Japan), bound the biotinylated 5 terminal amplicon and the tagged 3 terminus was bound on the antitag lines printed on the DNA strip (Figure 2).

(a)

(b)

Figure 2: DNA strip for chromatography (a) and reaction results (b) for three pathogens and a negative control. (a) Line 1 (Tag1): EHEC, Line 2 (Tag2): Shigella spp. and EIEC, Line 3 (Tag3): Salmonella spp., Line 4 (Tag4): internal control, Line 5: flow control. (b) Strains: no. 1 Eschesrichia coli O157 (shiga toxin 1 and 2) GTC14510; no. 2 Shigella dysenteriae O1 (shiga toxin 1 and IpaH) GTC01057; no. 3 Salmonella enterica serovar Enteritidis GTC03838; and no. 4 internal positive control. All of amplicons are reacted with each tag.

After PCR, 30 μL of streptavidin-coated blue latex solution was added to the PCR tube, and then the DNA strip was inserted into the PCR tube. The hybridized PCR amplicon was visualized in 5 to 10 min as a blue line, which represented the bound streptavidin-coated blue latex and biotin-labeled 5 terminus of the PCR amplicon.

2.6. A Protocol to Detect Multiple Foodborne Pathogens after 6 Hours Enrichment Culture of Ground Meat

For detection of foodborne pathogens with our protocol, 25 g of beef and 225 mL of FPE broth were homogenized in Stomacher bags (Eiken Chemical Co., Tokyo, Japan). The entire homogenate was transferred to a culture bottle and incubated with shaking at 37°C. After incubation, 1 mL of the supernatant was collected, and DNA was extracted using the physical disruption method described above. Subsequently, 5 μL of the extracted DNA was analyzed by cocktail PCR primers (Table 2) using premix Ex Taq (Takara Bio, Shiga, Japan) and the QuickBath thermal cycler. After 30 min, the PCR amplicon was analyzed by dipstick DNA chromatography. Thirty microliters of streptavidin-coated blue latex solution were added to each tube. Subsequently, the DNA strip was inserted into each tube. After 5–10 min at room temperature, the amplicon bound on the appropriate line on the dipstick surface (Figure 2) was visualized by the blue latex of the biotin-labeled 5 terminus of the PCR amplicon.

2.7. Sensitivity and Specificity of the Cocktail PCR Dipstick DNA Chromatography (CPDC) Assay

To measure the sensitivity of the CPDC assay, purified chromosomal DNA of E. coli O157 GTC14510 and S. enterica serovar Enteritidis GTC03838 were prepared at six different concentrations (2 ng, 200 pg, 20 pg, 2 pg, 200 fg, and 20 fg) and assayed (Table 3). Another sensitivity assay starting from quantitatively diluted culture supernatants was also performed (Table 4). The specificity of the CPDC assay was determined using the 176 strains listed in Table 5.

Table 3: Detection sensitivity of CPDC assay.

DNA concentration
EHEC serovar O111, GTC14517 (stx1)
EHEC serovar O157, GTC14513 (stx2)
Shigella dysenteriae serovar 2, GTC01929 (ipaH)
Salmonella enterica serovar Enteritidis GTC03838 (invA)

2 ng/assay
+
+
+
+

200 pg/assay
+
+
+
+

20 pg/assay
+
+
+
+

2 pg/assay
+
+
+
+

200 fg/assay
+
+
+
+

20 fg/assay
−
−
−
−

Serially diluted purified DNA of each strain was used to count detection sensitivity.

Table 4: Detection sensitivity of CPDC assay and immunochromatography.

Bacterial concentration (CFU/mL)
EHEC O157 GTC14510
Bacterial concentration (CFU/mL)
Salmonella enterica serovar

Enteritidis GTC03838

Immunochromat.
CPDC assay
Immunochromat.
CPDC assay

+
+

+
+

+
+

+
+

+
+

+
+

+
+

+
+

+
+

+
+

−
+

−
+

−
+

−
+

−
−

−
−

−
−

−
−

3.3
−
−
2.5
−
−

Table 5: Specificity of CPDC assay.

Bacteria
Serotype (Virulence factor)
Reacted Dipstick line
CPDC assay (positive/strains)

EHEC
O26: H- (stx1)
Line 1
4/4

O26: H11(stx1)
Line 1
5/5

O26: H11(stx1/2)
Line 1
3/3

O111: H- (stx1)
Line 1
3/3

O111: H- (stx1/2)
Line 1
2/2

O115: H10(stx1)
Line 1
1/1

O119: H2(stx1)
Line 1
1/1

O121: H19(stx2)
Line 1
4/4

O128: H- (stx1/2)
Line 1
1/1

O157: H7(stx2)
Line 1
10/10

O157: H7(stx1/2)
Line 1
10/10

O157: H-(stx1/2)
Line 1
10/10

EIEC
O28: H- (IpaH)
Line 2
5/5

O124: H- (IpaH)
Line 2
4/4

O136: H- (IpaH)
Line 2
10/10

O144: H- (IpaH)
Line 2
3/3

O164:H- (IpaH)
Line 2
3/3

Shigella boydii
(IpaH)
Line 2
8/8

Shigella dysenteriae
(IpaH)
Line 2
16/16

Shigella flexneri
(IpaH)
Line 2
13/13

Shigella sonnei
(IpaH)
Line 2
7/7

Salmonella enterica

    subsp.enterica
serovar Typhimurium (InvA)
Line 3
10/10

    subsp.enterica
serovar Typhi (InvA)
Line 3
10/10

    subsp.enterica
serovar Enteritidis (InvA)
Line 3
7/7

    subsp.enterica
serovar Dublin (InvA)
Line 3
10/10

    subsp.enterica
serovar paratyphi A (InvA)
Line 3
3/3

Salmonella bongoriGTC 03793 T
(InvA)
Line 3
1/1

Escherichia coli GTC00503 T

N*
0/1

Escherichia albertiiGTC 16441 T

N
0/1

Escherichia fergusoniiGTC 01720 T

N
0/1

Escherichia vulneris GTC 10613 T

N
0/1

Escherichia hermanniiGTC 10612 T

N
0/1

Escherichia blattaeGTC 01342 T

N
0/1

Citrobacter freundiiGTC 14890 T

N
0/1

Citrobacter diversusGTC 00114 T

N
0/1

Citrobacter rodentium GTC 14911 T

N
0/1

Citrobacter youngaeGTC 14914

N
0/1

Klebsiella pneumonia GTC 14868 T

N
0/1

Enterobacter cloacaeGTC 00109 T

N
0/1

Enterobacter aerogenesGTC 14962 T

N
0/1

Cronobacter sakazakiiGTC 14952 T

N
0/1

Serratia marcescensGTC 14672

N
0/1

Yersinia enterocoliticaGTC 00127 T

N
0/1

Vibrio parahaemolyticus GTC02055

N
0/1

Pseudomonas aeruginosaGTC 00002 T

N
0/1

Staphylococcus aureusGTC 00286 T

N
0/1

N*: no positive line.

Reacted line no. 1 is stx1 and 2 for EHEC, line 2 is ipaH for Shigella spp. and EIEC, and line 3 is for invA for Salmonella.

2.8. Evaluation of CPDC Assay with Spiked Ground Meat

The CPDC assay after enrichment culture in FPE broth was compared with a commercial immunochromatography system (Wako Pure Chem. Industries, Ltd., Osaka, Japan). Ground beef collected from local supermarkets was immediately transported to our laboratory in an insulated cooler box at 4°C. However, the isolation frequency of the target Shigella spp., Salmonella enterica, and E. coli O157 : H7 was less than 0.1% by culture-based conventional methods in our preliminary experiments. We decided, therefore, to evaluate the CPDC assay with spiked ground meat experiments. Ground meat was collected from a supermarket and confirmed target to be pathogen free by conventional methods. One milliliter of a mixed culture containing Shigella dysenteriae, S. enterica subspecies enterica serovar Enteritidis, and E. coli O157:H7 at three different concentrations were mixed with 25 g of ground meat, and 225 mL of FPE broth was then added. The total volume was incubated at 37°C. Immediately, and 4 hours, 6 hours, 8 hours, and 18 hours, 1 mL of the enrichment was used for extraction and then used in the CPDC assay. Another aliquot was used for the commercial immunochromatography kit for S. enterica serovar Enteritidis and E. coli O157.

3. Results and Discussion

Conventional culture has been the “gold standard” method for the detection of enteric bacterial pathogens. The advantages of this method include identification, facilitation of outbreak management, and generation of an antimicrobial susceptibility profile [15]. However, this conventional method has many disadvantages. Many different enrichment broths and solid media are used to screen for all possible foodborne pathogens, and time-consuming protocols are prepared to generate a result. FPE broth is designed to support Campylobacter without adding lysed blood and carbon dioxide. Campylobacter, however, is a slow-growing organism and needs 24 hours to reach 10⁴ CFU/mL. Therefore, addition of selective antibiotics to the FPE broth was essential to suppress contaminating other bacteria for 24 hours enrichment culture. FPE broth could also support the growth of Listeria without adding blood, but the growth of Listeria is also slow, needing 24 hours to reach 10⁴ CFU/mL (unpublished data).

The growth of pathogens in conventional enrichment culture and FPE broths were measured (Figure 1). Approximately 1–10 bacteria were spiked in 225 mL of enrichment broth. S. enterica and E. coli reached 10⁴ CFU/mL after 6-hours incubation in FPE broth, buffered peptone water broth, and mEC broth, as shown in Figure 1. V. parahaemolyticus reached 10⁴ CFU/mL after 4-hours incubation in both FPE and alkaline peptone broths. Based on these data, we selected 6 hours incubation for the CPDC assay.

In the present study, cocktail PCR was capable of simultaneously determining the presence of Salmonella spp., Shigella spp., EIEC, and EHEC by targeting invA, ipaH, stx1, and stx2 genes (Figure 2).

To evaluate the detection limit of the CPDC assay for each pathogen, 2 ng to 20 fg of DNA per reaction was prepared. The sensitivity and specificity of this assay are shown in Tables 3–5. The detection limit was 200 fg for each pathogen per CPDC assay (Table 3). The presence of the products with expected sizes was also confirmed by agarose gel electrophoresis, and nonspecific products were not observed (data not shown). The specificity of this CPDC assay was evaluated using 157 target strains (45 strains of Shigella spp., 54 strains of EHEC, 17 strains of EIEC, and 41 strains of Salmonella spp.) and 19 nontarget strains shown in Table 5. The detection limit of Salmonella and Escherichia from FPE culture supernatant (Table 4) was 10³ CFU/mL, while the commercial immunochromatography kit required 10⁵ CFU/mL. No false positive lines appeared on the dipstick DNA chromatography for any of the nontarget strains.

Immunochromatography is a simple technology to detect antigen in culture supernatant. However, immunochromatography targeting EHEC serotypes is not useful for testing food, because many kinds of E. coli serotypes produce shiga toxins. Thus, it is practically difficult to cover all of the EHEC serotypes by immunochromatography. Our method targeted both shiga toxin 1 and shiga toxin 2 toxins and detected non-O157 shiga toxin-producing serotypes (O26, O111, and O121). Three serotype (O45, O103, and O145) strains were not used because they are not available from our collection.

Shiga toxin 1 and shiga toxin 2 PCR products were designed to be bound on line 1 of the dipstick (Figure 2). The two genes were not equally amplified. The signal of the shiga toxin 2 amplicon was always bigger than the signal of the shiga toxin 1 amplicon.

The invasion plasmid antigen H (ipaH) gene is often used to diagnosis dysentery [16], because ipaH is carried by all four Shigella species as well as EIEC. In our cocktail primer, therefore, we selected the ipaH-specific primer to detect both Shigella and EIEC. The ipaH amplicon was designed to react on the second line of the dipstick chromatography strip, as shown in Figure 2. The CPDC assay was found to be effective at detecting Shigella species and EIEC from 4 to 6 hours FPE broth.

The CPDC assay required 4 to 6 hours FPE broth for the detection of S. enterica serovar Enteritidis. The detection limit of chromatography for Salmonella was, however, 10⁵ CFU/mL in culture supernatant. To reach this cell number in FPE broth, incubation for more than 6 hours was necessary (Table 6). There is another disadvantage to using immunochromatography. The commercially available immunochromatography kits for Salmonella serovars are limited. The products only detect serovar Enteritidis. Thus, it is difficult to screen many different Salmonella serotypes simultaneously, such as serovar Typhimurium, serovar Choleraesuis, serovar Dublin, serovar Typhi, and others.

Table 6: Result of CPDC assay in spiked ground meat samples.

Inoculated level

(CFU/25 g)
CPDC assay
Immunochromatography

Enrichment time (h)
Enrichment time (h)

0
4
6
8
18
0
4
6
8
18

Enterohemorrhagic E. coli O157 GTC14510

13.3
−
−
+
+
+
−
−
−
−
+

6.7
−
−
+
+
+
−
−
−
−
+

3.3
−
−
+
+
+
−
−
−
−
+

Control
−
−
−
−
−
−
−
−
−
−

Salmonella enterica serovar Enteritidis GTC03838

10.0
−
+
+
+
+
−
−
−
−
+

5.0
−
+
+
+
+
−
−
−
−
+

2.5
−
+
+
+
+
−
−
−
−
+

Control
−
−
−
−
−
−
−
−
−
−

The CPDC assay for Salmonella was evaluated by spiked ground meat experiments with three different inoculation levels from 2.5 to 10 CFU/25 g (Table 6). The CPDC assay detected target pathogens on the third line of a dipstick DNA strip from 4 to 6 hours culture with FPE broth. On the other hand, the commercial immunochromatography kit only detected antigens from 18 hours enrichment culture because the method requires 10⁵ CFU/mL of organism (Tables 4 and 6).

Multiplex PCR to detect many Salmonella serovars has been reported [17, 18]; however, we selected the invA gene for our assay because all Salmonella serovars carry this gene [19].

Internal amplification control (IAC) is designed to bind to line 4 of the dipstick chromatography strip to check for the presence of PCR inhibitor and false negatives [20]. A general guideline proposed for PCR testing of foodborne pathogens also requires the presence of IAC in the reaction mixture [21].

Systematic review of clinical implications, public health considerations, and the cost effectiveness of rapid diagnostic tests for detection and identification of bacterial pathogens in feces and food suggests that adoption of rapid test methods, especially for PCR, in combination with a routine culture is unlikely to be cost-effective [7, 22]. However, as the cost of rapid technologies decreases, total replacement with rapid technologies may be feasible.

The clinical impact of the decreased turnaround time means that bacterial diarrhea is more promptly ruled out using the CPDC assay compared to using conventional culture in small laboratories. This reduces the expenditure of infection control resources and, in particular, in cases of sporadic diarrhea, helps to reduce the requirement for scarce isolation rooms. In addition, the earlier availability of results is helpful in community-based management of outbreaks.

For detection of Salmonella spp., Shigella spp., EIEC, and EHEC, the overall time to confirm a positive result by conventional culture plus immunochromatography is at least two working days. Generating a negative report requires 48 hours. In contrast, a report can be generated for the CPDC assay within one working day. One advantage of an early laboratory report is early judgment of contamination, which can prevent food poisoning and additional outbreaks. The method also contributes to the quick shipment of fresh food products to the markets.

4. Conclusion

Cocktail PCR targeting multiple foodborne pathogens and simple dipstick DNA chromatography to differentiate the PCR product was designed. The method was applied to detect pathogens in ground meat after 6 hours enrichment broth, which supports the growth of broad range foodborne pathogens. This single tube PCR and enrichment method help to simplify food analysis protocol. As a result, the method offers rapid report to food suppliers and helps the quick shipment of safety-confirmed food products to markets.

Acknowledgments

This work was partially funded by the Regional Innovation Strategy Support Program of the Ministry of Education, Culture, Sports, Science, and Technology of Japan, and Grant for Health and Labour Sciences Research, Research on Global Health Issues supported by the United States-Japan Cooperative Medical Science Program.

References

R. A. Britton and J. Versalovic, “Probiotics and gastrointestinal infections,” Interdisciplinary Perspectives on Infectious Diseases, vol. 2008, Article ID 290769, 10 pages, 2008.

S. P. Oliver, B. M. Jayarao, and R. A. Almeida, “Foodborne pathogens in milk and the dairy farm environment: food safety and public health implications,” Foodborne Pathogens and Disease, vol. 2, no. 2, pp. 115–129, 2005.

P. Amavisit, G. F. Browning, D. Lightfoot et al., “Rapid PCR detection of Salmonella in horse faecal samples,” Veterinary Microbiology, vol. 79, no. 1, pp. 63–74, 2001.

G. D. Inglis and L. D. Kalischuk, “Direct quantification of Campylobacter jejuni and Campylobacter lanienae in feces of cattle by real-time quantitative PCR,” Applied and Environmental Microbiology, vol. 70, no. 4, pp. 2296–2306, 2004.

A. N. Sharpe, “Preparing samples for rapid detection of microbes,” in Rapid Methods and Automation in Microbiology and Immunology, Intercept Ltd., Andover, UK, 1994.

B. Melero, L. Cocolin, K. Rantsiou, I. Jaime, and J. Rovira, “Comparison between conventional and qPCR methods for enumerating Campylobacter jejuni in a poultry processing plant,” Food Microbiology, vol. 28, no. 7, pp. 1353–1358, 2011.

K. Rantsiou, C. Lamberti, and L. Cocolin, “Survey of Campylobacter jejuni in retail chicken meat products by application of a quantitative PCR protocol,” International Journal of Food Microbiology, vol. 141, pp. S75–S79, 2010.

B. Swaminathan and P. Feng, “Rapid detection of food-borne pathogenic bacteria,” Annual Review of Microbiology, vol. 48, pp. 401–426, 1994.

M. Wagner, T. Potocnik, A. Lehner, J. Dengg, P. Pless, and E. Brandl, “A two step multiplex-seminested Polymerase Chain Reaction assay (m-sn PCR) for the simultaneous identification of four major foodborne pathogens,” Milchwissenschaft, vol. 55, no. 9, pp. 500–503, 2000.

Y. S. Park, S. R. Lee, and Y. G. Kim, “Detection of Escherichia coli O157:H7, Salmonella spp., Staphylococcus aureus and Listeria monocytogenes in Kimchi by multiplex polymerase chain reaction (mPCR),” Journal of Microbiology, vol. 44, no. 1, pp. 92–97, 2006.

R. D. Oberst, M. P. Hays, L. K. Bohra et al., “PCR-based DNA amplification and presumptive detection of Escherichia coli O157:H7 with an internal fluorogenic probe and the 5' nuclease (TaqMan) assay,” Applied and Environmental Microbiology, vol. 64, no. 9, pp. 3389–3396, 1998.

B. Kimura, S. Kawasaki, T. Fujii, J. Kusunoki, T. Itoh, and S. J. A. Flood, “Evaluation of TaqMan PCR assay for detecting Salmonella in raw meat and shrimp,” Journal of Food Protection, vol. 62, no. 4, pp. 329–335, 1999.

Y. Yuan, W. Xu, Z. Zhai et al., “Universal primer-multiplex pcr approach for simultaneous detection of Escherichia coli, Listeria monocytogenes, and Salmonella spp. in food samples,” Journal of Food Science, vol. 74, no. 8, pp. M446–M452, 2009.

M. Hayashi, S. Kubota-Hayashi, T. Natori et al., “Use of blood-free enrichment broth in the development of a rapid protocol to detect Campylobacter in twenty-five grams of chicken meat,” International Journal of Food Microbiology, vol. 163, no. 1, pp. 41–46, 2013.

J. O'Leary, D. Corcoran, and B. Lucey, “Comparison of the EntericBio multiplex PCR system with routine culture for detection of bacterial enteric pathogens,” Journal of Clinical Microbiology, vol. 47, no. 11, pp. 3449–3453, 2009.

O. Sethabutr, M. Venkatesan, G. S. Murphy, B. Eampokalap, C. W. Hoge, and P. Echeverria, “Detection of shigellae and enteroinvasive Escherichia coli by amplification of the invasion plasmid antigen H DNA sequence in patients with dysentery,” Journal of Infectious Diseases, vol. 167, no. 2, pp. 458–461, 1993.

E. O'Regan, E. McCabe, C. Burgess et al., “Development of a real-time multiplex PCR assay for the detection of multiple Salmonella serotypes in chicken samples,” BMC Microbiology, vol. 8, article 156, 2008.

S. H. Lee, B. Y. Jung, N. Rayamahji et al., “A multiplex real-time PCR for differential detection and quantification of Salmonella spp., Salmonella enterica serovar Typhimurium and Enteritidis in meats,” Journal of Veterinary Science, vol. 10, no. 1, pp. 43–51, 2009.

J. E. Galan, C. Ginocchio, and P. Costeas, “Molecular and functional characterization of the Salmonella invasion gene invA: homology of InvA to members of a new protein family,” Journal of Bacteriology, vol. 174, no. 13, pp. 4338–4349, 1992.

J. Hoorfar, P. Ahrens, and P. Radstrom, “Automated 5' nuclease PCR assay for identification of Salmonella enterica,” Journal of Clinical Microbiology, vol. 38, no. 9, pp. 3429–3435, 2000.

“Microbiology of food and animal feeding stuffs. Polymerase chain reaction (PCR) for the detection of foodborne pathogens. General method specific requirements,” Draft International Standard EN ISO 22174, International Organization for Standardization, Geneva, Switzerland, 2002.

I. Abubakar, L. Irvine, C. F. Aldus et al., “A systematic review of the clinical, public health and cost-effectiveness of rapid diagnostic tests for the detection and identification of bacterial intestinal pathogens in faeces and food,” Health Technology Assessment, vol. 11, no. 36, pp. 1–216, 2007.