- Research article
- Open Access
A simple and rapid identification method for newly emerged porcine Deltacoronavirus with loop-mediated isothermal amplification
- Fanfan Zhang†1,
- Yu Ye†1,
- Deping Song1,
- Nannan Guo1,
- Qi Peng1,
- Anqi Li1,
- Xingrong Zhou1,
- Yanjun Chen1,
- Min Zhang1,
- Dongyan Huang1 and
- Yuxin Tang1Email author
© The Author(s) 2017
- Received: 26 October 2016
- Accepted: 8 August 2017
- Published: 21 September 2017
Porcine Deltacoronavirus (PDCoV) is a newly emerged enteropathogenic coronavirus that causes diarrhea and mortality in neonatal piglets. PDCoV has spread to many countries around the world, leading to significant economic losses in the pork industry. Therefore, a rapid and sensitive method for detection of PDCoV in clinical samples is urgently needed.
In this study, we developed a single-tube one-step reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay specific for nucleocapsid gene to diagnose and monitor PDCoV infections. The detection limit of RT-LAMP assay was 1 × 101 copies of PDCoV, which was approximately 100-fold more sensitive than gel-based one-step reverse transcription polymerase chain reaction (RT-PCR). This assay could specifically amplify PDCoV and had no cross amplification with porcine epidemic diarrhea virus (PEDV), transmissible gastroenteritis virus (TGEV), porcine kobuvirus (PKoV), porcine astrovirus (PAstV), porcine reproductive and respiratory syndrome virus (PRRSV), classic swine fever virus (CSFV), and porcine circovirus type 2 (PCV2). By screening a panel of clinical specimens (N = 192), this method presented a similar sensitivity with nested RT-PCR and was 1–2 log more sensitive than conventional RT-PCR in detection of PDCoV.
The RT-LAMP assay established in this study is a potentially valuable tool, especially in low-resource laboratories and filed settings, for a rapid diagnosis, surveillance, and molecular epidemiology investigation of PDCoV infections. To the best of our knowledge, this is the first work for detection of newly emerged PDCoV with LAMP technology.
- Porcine Deltacoronavirus (PDCoV)
- Rapid diagnosis
Porcine Deltacoronavirus (PDCoV) is a member of the genus Deltacoronavirus in the family Coronaviridae [1, 2]. PDCoV was first identified in Hong Kong in 2012, and then isolated in the United States [2, 3]. Afterwards, PDCoV was reported in Korea, China, and Thailand [4–6]. PDCoV causes an acute, highly contagious, and devastating enteric disease that is characterized by severe diarrhea, vomiting, dehydration, and a high number of deaths in nursing piglets [3–7]. Clinical symptoms of infected swine are indistinguishable from those caused by porcine epidemic diarrhea virus (PEDV) and transmissible gastroenteritis virus (TGEV) [3, 8, 9]. Experimental studies on gnotobiotic and conventional piglets showed that isolated PDCoVs caused similar clinical signs to the disease of field infections, from mild to severe diarrhea and intestinal lesions . Molecular surveillance on diarrheal samples of swine from USA indicated a 30% infection rate of PDCoV, and a similar frequency of PDCoV (31.33%) in China was also detected in fecal and intestinal samples of diarrheic pigs . Therefore, a simple, rapid, and highly sensitive diagnostic method for detection of PDCoV is urgently needed for the prevention and control of the virus infections and spread.
Currently, available methods for detection of PDCoVs include conventional reverse transcription—polymerase chain reaction (RT-PCR), nested RT-PCR, real-time RT-PCR, and ELISA [6, 10–13]. However, these techniques have some shortcomings, such as higher requirements for equipment, high cost, extended detection period, and/or low sensitivity . Reverse transcription loop-mediated isothermal amplification (RT-LAMP) provides a potential effective tool for rapid and accurate identification of viral pathogens, which amplifies nucleic acids under isothermal conditions with high sensitivity and specificity. This novel gene detection technique is cost-effective and time-saving, and only requires a constant temperature water bath. RT-LAMP has been widely used in clinical diagnosis for detection of the presence of several important viral pathogens, including PEDV, TGEV, classic swine fever virus (CSFV), and H10N8 subtype of influenza A virus [14–17]. The improved LAMP assays, such as visual detection of amplified products by adding SYBR Green I or hydroxynaphthol blue (HNB), have made it easier to apply in primary clinical settings or for field use. In the present work, we developed and evaluated a specific and sensitive RT-LAMP assay for visual detection of PDCoV, which might be a good tool for the diagnosis of PDCoV in field samples.
Optimization of RT-LAMP assay for detection of PDCoV
Sensitivity of RT-LAMP with conventional RT-PCR and nested RT-PCR
Specificity of RT-LAMP
Clinical sample detection
Detection results of PDCoV in clinical samples by conventional RT-PCR, nested RT-PCR and RT-LAMP
Total number of samples
Positive rate of PDCoV
PDCoV was first described as a newly emerged coronavirus in swine from rectal swabs in 2012 by Woo . Since then, PDCoV infections have been reported in America, Europe, and Asia, and caused substantial economic losses [4–7, 18, 19]. As a result, it is urgently needed to develop an easy, rapid and highly sensitive diagnostic method for detection of PDCoV. The current methods for the diagnosis of PDCoV include conventional RT-PCR, nested RT-PCR, real-time RT-PCR, and ELISA. However, these methods are inappropriate for detection of PDCoV in the field settings and resource-poor laboratories, due to lack of sophisticated instruments.
In this study, a RT-LAMP assay was developed and evaluated for PDCoV detection. A set of primers was designed against the conserved coding regions of the N gene of PDCoV and the reaction conditions were optimized. The RT-LAMP assay was able to detect PDCoV with a detection limit of 10 copies, which was 100-fold more sensitive than conventional RT-PCR. Furthermore, the RT-LAMP assay only needs a water bath for 70 min incubation to accomplish efficient amplification, which was much fast and simple when compared with conventional RT-PCR and nested RT-PCR.
It is obvious that the RT-LAMP has some advantages over the conventional PCR-based tests and serological tests. The selected set of four primes specific to the N gene of PDCoV dramatically enhanced the specificity of RT-LAMP assay in contrast of the traditional diagnostic methods [4–7, 18, 19]. The fact that the RT-LAMP assay could not detect several reference swine viruses (PEDV, TGEV, PKoV, PAsTV, PRRSV, CSFV, and PCV2) demonstrated that this method established was highly specific. In addition, the results of sensitivity/detection limit comparisons indicated that the assay was the most sensitive among the tests employed for the evaluation of the assay in this study. Moreover, the RT-LAMP was a one-step assay in which the reverse transcription and LAMP reaction were combined, which further simplified the procedure and shortened the time of the reaction of the assay. The RT-LAMP was simple and user-friendly, and only required a water bath with a constant temperature feature or a traditional heat block to perform. To evaluate the practicability of RT-LAMP in the field, 192 clinical diarrhea samples of piglets were examined. The results showed that the RT-LAMP had a similar sensitivity with nested RT-PCR and was much sensitive than conventional RT-PCR in detection of PDCoV. These data further suggested that PDCoV was a leaved out pathogen related to swine diarrhea in China, and might cause the high mortality in diarrheal piglets.
This one step RT-LAMP established in this study will provide an effective technique tool for the rapid diagnosis, surveillance, and the investigation of molecular epidemiology of PDCoV.
All samples, including feces and intestinal contents, were collected from suckling piglets of 1–2 weeks old on 35 pig farms with acute diarrhea outbreaks in Jiangxi, China during 2014–2015, and were tested for PDCoV, PEDV, TGEV, CSFV, porcine kobuvirus (PKoV), porcine astrovirus (PAstV), porcine reproductive and respiratory syndrome virus (PRRSV), and porcine circovirus type 2 (PCV2) by RT-PCR or PCR. Corresponding positive controls of the viruses used in the study are preserved in our labs.
The total RNAs of the samples were extracted by using the RNAiso Plus (Takara, Japan) and the genomic DNAs of PCV2 were extracted with the DNAiso reagent (Takara, Japan) according to the manufacturer’s instructions. The extracted RNAs/DNAs were dissolved in 30 μL of nuclease-free water. RNA samples were stored at −80 °C and DNA samples were stored at −20 °C until use.
Targeted region selection and LAMP primers design
The primers for detection of PDCoV used in this study
The construction of standards
In order to construct the standards of PDCoV N gene, the targeted RNA of PDCoV was reversely transcribed into single-stranded cDNA by a random primer and then amplified by PCR using forward primer PDCoV-NWF and reverse primer PDCoV-NWR (Table 2). The reaction conditions were as follows: denaturation at 95 °C for 5 min, 38 cycles of 94 °C for 30 s, 53 °C for 30 s, 72 °C for 2 min, and a final extension at 72 °C for 7 min. The amplified products were purified by E.Z.N.A™ Gel Extraction Kit (Omega, USA) and subsequently cloned into E. coli JM109 using the pGEM-T easy vector (Promega, USA). The recombinant plasmid was extracted using TIANprep Mini Plasmid Kit (TIANGEN, China) following the protocol of the manufacturer. The concentration and quality of the plasmid DNA was determined by NanoDrop 2000 spectrophotometer (Thermo scientific, USA), which was then used as the standards for the quantitative analysis.
The RT-LAMP reaction was carried out in a final volume of 25 μL. To optimize the reaction parameters, reactions containing different concentrations of MgSO4 (at 2, 4, 6, 8 mM, and 10 m, Sigma, USA), dNTPs mix (at 1.0, 1.2, 1.4, and 1.6 mM, Promega, USA), each of inner primer FIP and BIP (at 0.6, 0.8, 1.0, 1.2, 1.4, and 1.6 µM), each of outer primer F3 and B3 (0.2 µM), Bst DNA polymerase (8 U, New England Biolabs, USA), AMV reverse transcriptase (2 U, Takara, Japan), betaine (0.8 M, Sigma, USA), 2 μL of RNA template per reaction were tested. Furthermore, the temperature of the RT-LAMP reaction was determined by incubating the reaction systems at 60, 61, 62, 63, and 64 °C for 70 min in a water bath, respectively, and then the reactions were terminated by heating up at 80 °C for 10 min. The RT-LAMP products were electrophoresed on 2.0% agarose gel in 1× TAE buffer, or directly visualized by adding 1× SYBR green I in the reaction system for diction by a color change. In addition, the RT-LAMP products were identified by the digestion of SmlI (New England Biolabs, USA).
Conventional RT-PCR and nested RT-PCR
To identify PDCoV in diarrheal samples of piglets, a N-gene-based conventional RT-PCR assay previously established in our lab was employed . The first-strand cDNA was synthesized with reverse primers PDCoV-NR, followed by PCR with primer pairs of PDCoV-NF and PDCoV-NR under the following conditions: denaturation at 94 °C for 5 min, 38 cycles of 94 °C 30 s, 54 °C 30 s, 72 °C 40 s, and consequently with a final extension at 72 °C for 10 min. Expected PCR products of 329 bp in size were purified, cloned and sequenced. The nested RT-PCR method for detection of PDCoV was performed as reported previously . Finally, the amplicons were subjected to electrophoresis on 2% agarose gel, and the target bands were visualized under UV light by staining with ethidium bromide.
Determination of the sensitivity and specificity of the RT-LAMP assay
To determine the sensitivity of the RT-LAMP assay, the constructed recombinant standards with known concentration were made tenfold serial dilutions (from 1 × 108 to 1 × 100 copies), and served as the templates for conventional RT-PCR, nested RT-PCR and the RT-LAMP assay. To evaluate the specificity of the RT-LAMP assay, RNAs/DNAs of several important pathogenic viral agents of pigs, including PEDV, TGEV, PKoV, PAsTV, PRRSV, CSFV, and PCV2, were used in the RT-LAMP assay under optimized reaction conditions. The standards of PDCoV and blank template were served as the positive and negative controls, respectively. All reactions were carried out in triplicates.
Detection of PDCoV in clinical samples by conventional RT-PCR, nested RT-PCR, and RT-LAMP
A total of 192 fecal/intestinal clinical samples of piglets with severe watery diarrhea were collected from 35 pig farms in Jiangxi, China during 2014 and 2015. All samples were then selected to detect the presence of PDCoV by conventional RT-PCR, nested RT-PCR, and RT-LAMP. The samples were resuspended in saline, subsequently vortexed and then centrifuged at 8000×g for 5 min at 4 °C. The supernatants were harvested and stored at −80 °C until use. Viral RNA was extracted and used as a template for conventional RT-PCR, nested RT-PCR, and RT-LAMP according to aforementioned methods.
FZ carried out data analysis, experiment design and manuscript writing. YY carried out data analysis and manuscript writing. DS, NG, QP, AL, XZ, YC, MZ, and DH participated in manuscript preparation. YT conceived the studies, and prepared the manuscript. All authors read and approved the final manuscript.
This work is funded by the National Natural Science Foundation of China (31260611 and 31372457), the Natural Science Foundation of Jiangxi Province (2013BAB204017), the Landing Program Fund of Jiangxi Province (KJLD13029), and Science and Technology Project of Education Department of Jiangxi Province (GJJ150388). We would like to thank the advisory group members for their guidance and input into the overall project.
The authors declare that they have no competing interests.
Availability of data and materials
Consent for publication
The Experimental Animal Ethics Committee in Jiangxi Agricultural University (JXND 2012-0025) approved this study. All procedures involving animals were conducted according to the guidelines for the care and use of experimental animals established by the Ministry of Agriculture of China. The intestinal samples used in this study were obtained from the dead diarrheal piglets and the fecal samples were non-invasively collected immediately after excretion from diarrheal pigs in Jiangxi, China.
The research was supported by the National Natural Science Foundation of China (31260611 and 31372457), the Natural Science Foundation of Jiangxi Province (2013BAB204017), the Landing Program Fund of Jiangxi Province (KJLD13029), and Science and Technology Project of Education Department of Jiangxi Province (GJJ150388). The external funding body had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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