key: cord-298076-rujylmib
authors: Chen, Zhiyong; Liao, Yuxue; Ke, Xuemei; Zhou, Jie; Chen, Yixiong; Gao, LuLu; Chen, Qing; Yu, Shouyi
title: Comparison of reverse transcription loop-mediated isothermal amplification, conventional PCR and real-time PCR assays for Japanese encephalitis virus
date: 2010-11-30
journal: Mol Biol Rep
DOI: 10.1007/s11033-010-0525-0
sha: 
doc_id: 298076
cord_uid: rujylmib

We developed and evaluated a reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay for detecting Japanese encephalitis virus (JEV). The sensitivity of the JEV RT-LAMP assay was in concordance with that of real-time RT-PCR and 10-fold more sensitive than that of conventional RT-PCR, which the detection limit was 24 copies/μl. The JEV RT-LAMP was highly specific, which no cross-reactivity was found with dengue-2 virus, rabies virus, norovirus, astrovirus and human enterovirus 71. The JEV RT-LAMP assay was more simple and less time-consuming compared to the conventional RT-PCR and real-time RT-PCR, which the amplification could be completed in a single tube within 1 h under isothermal conditions at temperature of 63°C. The results suggest that the RT-LAMP assay can be applied as a practical molecular diagnostic tool for JEV infection and surveillance.

Japanese encephalitis virus (JEV) is a member of the genus flavivirus of the family flaviviridae. JEV exists in a zoonotic cycle among mosquitoes, pigs and some birds, and human being as incidental and dead-end hosts. In humans, JEV infection can cause Japanese encephalitis (JE) with severe central nervous system disorders. JE is the leading cause of viral encephalitis in China, India, Japan, Southeast Asia and Western Pacific regions, where 30,000-50,000 cases are reported annually, among these cases, about 30% are fatal. 30% of those who survive will remain irreversible neurologic damage [1] . JE can be controlled by vaccination. The implementation of control program is dependent on accurate surveillance data, which include laboratory confirmation of JEV infection.

Diagnosis of JEV infection is mainly based on serological, viral culture and molecular approaches. Serological methods are simple and feasible. However, antibody test results may be confusing due to considerable cross-reactivity with other flaviviruses [2] . Virus isolation is a definitive diagnosis for JEV infection, however, this assay is usually unavailable owing to less sensitive and more time consuming. RT-PCR assays for detection of specific genomic sequence of JEV have been showed high sensitivity and specificity [3] [4] [5] . However, these assays compared with serologic tests are more time-consuming and require expensive and sophisticated equipments. Most of cases of JE occur in rural areas, where routine RT-PCR diagnostic facilities are limited. Therefore, it is necessary to develop a rapid, simple, sensitive, and specific diagnostic method for JEV infection and surveillance.

Loop-mediated isothermal amplification (LAMP) is a novel PCR method developed by Notomi et al. [6] . The most important advantage of the LAMP is amplification of nucleic acids under isothermal conditions at a temperature range of 60-65°C for 1 h or less. Another advantage of the method is that the amplification from stem-loop structures leads to the accumulation of large amounts of products of various lengths, making detection of amplified nucleic acids much easier [7] . Recently, LAMP technology has been successfully applied for rapid detection of various pathogens, such as West Nile virus (WNV), SARS-CoV, Mycobacterium tuberculosis, Paracoccidioides brasiliensis, Plasmodium [8] [9] [10] [11] [12] . A reverse transcription LAMP (RT-LAMP) assay for detecting JEV was firstly reported by Toriniwa and Komiya and the sensitivity similarly to conventional RT-PCR [13] . Later, Parida et al. [14] reported the application of RT-LAMP assay to detect JEV in the cerebrospinal fluid samples from patients with clinical diagnosis of acute encephalitis, which the sensitivity of JEV detection was comparable to conventional RT-PCR. Yet they have not compared the sensitivity and specificity of RT-LAMP with real-time RT-PCR assay. Today, realtime PCR assays have a trend to replace conventional PCR or viral culture method in clinical diagnosis for a lot of viral infections because of their high sensitivity and specificity [15] . Here, we report a comparative study of sensitivity and specificity of RT-LAMP, conventional RT-PCR and real-time RT-PCR assays for detection of JEV.

Nakayama strain of JEV was used as positive standard in the present study. The live-attenuated Japanese encephalitis vaccine (derived from SA14-14-2 viral strain, Chengdu Institute of Biological Products, China) also used as positive control. Negative control included five species of viruses, dengue-2 virus (New Guinea C strain), rabies virus (Flury strain, low egg passage), norovirus, astrovirus and human enterovirus 71. Working stocks of Nakayama strain of JEV and the rabies virus were propagated by inoculation of suckling mouse brains, the dengue virus was propagated by in C6/36 cells. The stool specimens containing norovirus, astrovius or enterovirus 71 were obtained from laboratory confirmed patients. A 10% (wt/vol) suspension of stool was made then kept at -80°C until used.

Two JEV-positive and ten JEV-negative specimens of bat brain tissues that had been confirmed by real-time PCR (data not shown).

Five clinical samples of cerebrospinal fluid (CSF) and two serum samples were collected from patients with non-JE at Nanfang Hospital, Guangzhou city. Simulated JEVpositive samples were prepared as follows. Nakayama strain of JEV propagated in BHK-21 cells. After cultivation and harvest, 10 ll of cultivated viral suspensions were added into sterile tubes containing 300 ll of CSF or serum samples.

The oligonucleotide primers used for the RT-LAMP of JEV were designed from the envelope (E) gene region of the published sequence of strain JaOArS982 (GenBank accession no. M18370). We designed a set of six primers comprising two outer primers (F3 and B3), two inner primers (FIP and BIP) and two loop primers (Loop F and Loop B) that recognizing eight distinct regions on the target sequence by the LAMP primer designing software PrimerExplorer V3 (http://primerexplorer.jp/elamp3.0.0/ index.html). Based on the criteria described by Notomi et al. [6] , the primers were selected. The details of the selected primers with regard to their positions in the genomic sequences are shown in Table 1 .

Extraction of RNA from viral working stocks, suspension of stools, bat brain tissues and clinical samples was performed using QIAamp viral RNA mini kit (Qiagen, Germany), according to the manufacturer's protocols. The viral RNA was eluted from the QIAamp spin columns in a volume of 60 ll of elution buffer and stored at -80°C until used.

In order to evaluate the detection limit of the assays, the amount of JEV RNA was determined by spectrophotometric reading and converted to molecular copies by using the following formula [16] .

Then, 10-fold serial dilutions of the JEV RNA from 10 -1 -10 -8 were used for detection of sensitivity of the assays.

The RT-LAMP reaction was carried out in a total 25 ll reaction volume containing 2. After reaction, the amplified products of RT-LAMP were observed by electrophoresis on a 1.5% agarose gel electrophoresis (Biowest Agarose, Spain) following ethidium bromide staining under ultraviolet light. Besides, the products also were observed directly with the naked eye by adding SYBR Green I. 2 ll of original SYBR Green I (Invitrogen) was added to the reaction mixture tube. The solution turned green in the presence of LAMP amplification products, while it retained orange in the absence of the amplicon.

First-strand cDNA was generated using Superscript III first-strand synthesis system (Invitrogen). The mixture was consisted of 50 ng of random hexamers (50 ng/ll), 1.0 ll of dNTP mix (10 mM) and 8.0 ll of total RNA and incubated at 65°C for 5 min, then on ice for at least 1 min. Afterwards, following reagents were added to each of reactions: 2.0 ll of 10 9 RT buffer, 4.0 ll of 25 mM MgCl 2 , 2.0 ll of 0.1 MDTT, 40U of RNase OUT (40 U/ll, Invitrogen) and 200 U of Superscript III reverse transcriptase (200 U/ll). The reaction mixture was sequentially incubated at 25°C for 10 min, 50°C for 50 min and 85°C for 5 min. The synthesized cDNA was stored at -20°C.

RT-PCR was performed with the JEV specific primers targeting E gene of viral genome (GenBank accession no. L48961), JE1 (5 0 -ACCGTGGGGTCAAAGTCA-3 0 ) (position no. 1590-1607) and JE2 (5 0 -TGCATTTTAGGTG GCCTGAT-3 0 ) (position no. 1820-1839). The reaction was carried out in a total 50 ll mixture volume using Ex Taq The amplification was carried out in a 25 ll total reaction volume using SYBR Ò Premix Ex Taq TM (Perfect Real Time) kit (Takara, Japan). The reaction mixture contained 12.5 ll of 2 9 SYBR Ò Premix Ex Taq TM , 0.5 ll of 50 9 ROX Reference Dye II, 0.5 ll of each of forward and reverse primers (10lL), 2.0 ll of cDNA template and 9.0 ll of nuclease free water. The thermal profile for Real-time PCR was 95°C for 30 s, followed by 40 cycles (95°C for 5 s, 60°C for 10 s, 72°C for 10 s). After amplification, a melting curve analysis was performed to verify the authenticity of the amplified product by its specific melting temperature (Tm).

The reaction mixture containing JEV genome was incubated at 63°C for 1 h, positive amplification could be detected by the presence of a ladder-like pattern on a 1.5% agarose gel electrophoresis under ultraviolet light. No positive reactions were found in dengue-2 virus, rabies virus, norovirus, astrovirus and human enterovirus 71 (Fig. 1) .

The transcript copy number of the initial concentration was deduced from the RNA concentration that was 1.49 lg/ml by using a SmartSpec 3000 spectrophotometer (Bio-Rad, USA). Depending on the formula by Krieg [16] , the JEV RNA initial concentration was converted to 2.4 9 10 8 copies/ll. As observed on 1.5% agarose gel electrophoresis, the detection limit of the RT-LAMP assay was estimated to be 24 copies (Fig. 2) . And the sensitivity of naked-eye inspection with the addition of 2 ll of SYBR GreenI dye was 240 copies (Fig. 3) .

Comparison of the RT-LAMP, RT-PCR and real-time RT-PCR Serial 10-fold dilutions of JEV RNA were parallelly tested by RT-PCR and real-time RT-PCR. The detection limits of conventional RT-PCR and real-time RT-PCR were 240 copies and 24 copies, respectively (Figs. 4, 5). Figure 6 shows JEV special standard curve constructed using the known concentrations of 10-fold serial dilutions of JEV RNA. Melting curve analysis showed that specific amplification melting temperature was 84.7°C (Fig. 7) . According to the amplification and dissociation plots, the amplified product could be assigned as specific genomic sequence.

The JEV RT-LAMP on agarose gel electrophoresis analysis demonstrated an equivalent sensitivity with the real-time RT-PCR, 10-fold more sensitive than conventional RT-PCR. While the sensitivity of RT-LAMP by visual inspection using SYBR GreenI stain was found to be similar to the RT-PCR, which was inferior to the electrophoresis analysis. The details are summarized in Table 2 .

The RT-LAMP amplification was completed within 1 h which was less than that of conventional RT-PCR (3.5 h) and real-time RT-PCR (2.5 h).

Two known JEV positive samples of bat train tissues, seven simulated clinical samples of JEV infection and the SA14-14-2 vaccine were detected for JEV by RT-LAMP assay. All 10 samples were positive by the assay (Fig. 8) . By contrast, no positive amplification was observed in clinical samples from non-JE patients and 10 bat brain tissues that known JEV-negative.

In the past decades, several nucleic acid-based amplification methods for detection of JEV infection have been established, which including conventional RT-PCR, nested RT-PCR, probe real-time RT-PCR, dye real-time RT-PCR and LAMP RT-PCR [3, 4, [18] [19] [20] Compared to conventional RT-PCR and nested RT-PCR, real-time RT-PCR has engendered wider acceptance due to its improved rapidity, sensitivity and the reduced risk of laboratory contamination. However, real-time RT-PCR assays have several disadvantages, such as requiring expensive instruments, high cost of consumables and reagents. Hence, real time RT-PCR assays are often unavailable to routine clinical diagnosis, especially in remote rural areas where are usually at high risk of JEV infection.

The LAMP method does not rely on expensive and sophisticated facilities such as thermal cyclers. The amplified products of the reaction are shown as a ladderlike pattern by agarose gel electrophoresis staining with ethidium bromide under UV light. The products are also observed through naked eye inspection under UV lamp or normal light by adding fluorescent dye such as SYBR Green I. A by-product of the LAMP reaction, magnesium pyrophosphate, can be detected by real-time turbidimeter, or directly can be inspected by naked eye when the Fig. 2 Sensitivity of the RT-LAMP assay for E gene of JEV, the products were electrophoresed on a 1.5% agarose gels. This figure shows that the detection limit of JEV RT-LAMP is 24 copies/ll. The concentrations of JEV RNA are from 2.4 9 10 7 to 2.4 copies/ll in 10-fold serial dilutions (Lanes 1-8). Lane M is DL2000 DNA Marker accumulation of magnesium pyrophosphate forming visual white turbidity [6, 7, 21] .

To date, two reports have described the LAMP assay for detection of JEV. The report by Toriniwa and Komiya have showed that the sensitivity of detection of JEV RNA was 1PFU and 10PFU, with or without loop primers, respectively. The detection limit with loop primer was the same as that of one step RT-PCR [13] . Parida et al. reported a RT-LAMP assay with the added loop primers to detection of JEV in CSF specimens from acute phase patients clinically diagnosed as encephalitis. They compared the RT-LAMP with conventional RT-PCR. Concordance was 85%, sensitivity was 100%, specificity was 86%, none of the samples positive by RT-PCR were missed by RT-LAMP [14] .

Here, we described the establishment of one step, single tube RT-LAMP assay for rapid detection of the envelope gene of JEV genome and compared sensitivity and specificity with conventional RT-PCR and real-time RT-PCR. The JEV RT-LAMP assay showed good specificity due to none of positive results found in negative control samples, including dengue-2 virus, rabies virus, norovirus, astrovirus and human enterovirus 71 under the same experimental conditions. Notwithstanding, it was regret that only two strains of flaviviruses were involved for evaluation of specificity of JEV RT-LAMP in this study. The results showed that the detection limit of the JEV RT-LAMP assay was equivalent to that of SYBR Green real-time RT-PCR when LAMP amplified products by electrophoretic analysis, 10-fold more sensitive than conventional RT-PCR. The detection limit was 24 copies/ll. However, the sensitivity of detection by the naked-eye inspection based on color change was slightly lower than that by electrophoresis. The detection limit of was 240 copies/ll, which was equivalent to conventional RT-PCR assay. Nevertheless, considering the time-consuming of the RT-LAMP obviously less than that of conventional RT-PCR (2.5 h vs. 1 h), the RT-LAMP by the naked-eye inspection is superior to conventional RT-PCR.

In conclusion, this study presented a simple, sensitive and specific RT-LAMP assay for detection of specific nucleic acid sequence of JEV E gene. Considering the advantages of high sensitivity, rapid amplification, simple equipment and operation, the RT-LAMP assay can be applied as a practical molecular diagnostic tool for JEV infection and surveillance. 

Past, present, and future of Japanese encephalitis

Use of recombinant E protein domain III-based enzyme-linked immunosorbent assays for differentiation of tick-borne encephalitis serocomplex flaviviruses from mosquito-borne flaviviruses

Sensitive and specific detection of strains of Japanese encephalitis virus using a one-step TaqMan RT-PCR technique

TaqMan reverse transcription polymerase chain reaction for the detection of Japanese encephalitis virus

Usefulness of RT-PCR for the diagnosis of Japanese encephalitis in clinical samples

Loop-mediated isothermal amplification of DNA

Accelerated reaction by loop-mediated isothermal amplification using loop primers

Detection of gp43 of Paracoccidioides brasiliensis by the loop-mediated isothermal amplification (LAMP) method

Loop-mediated isothermal amplification for direct detection of Mycobacterium tuberculosis complex, M. avium, and M. intracellulare in sputum samples

Rapid detection of the severe acute respiratory syndrome (SARS) coronavirus by a loop-mediated isothermal amplification assay

Rapid identification of Plasmodium-carrying mosquitoes using loop-mediated isothermal amplification

Realtime reverse transcription loop-mediated isothermal amplification for rapid detection of West Nile virus

Rapid detection and quantification of Japanese encephalitis virus by real-time reverse transcription loop-mediated isothermal amplification

Development and evaluation of reverse transcription-loop-mediated isothermal amplification assay for rapid and real-time detection of Japanese encephalitis virus

Real-time PCR in virology

Improved synthesis of full-length RNA probe at reduced incubation temperatures

Development and evaluation of SYBR Green I-based one-step real-time RT-PCR assay for detection and quantitation of Japanese encephalitis virus

Detection of Japanese encephalitis virus in samples of JE patients by RT-PCR

Detection of Japanese encephalitis virus by reverse transcription polymerase chain reaction

Evaluation of reversetranscriptase PCR as a diagnostic tool to confirm Japanese encephalitis virus infection

Detection of loop-mediated isothermal amplification reaction by turbidity derived from magnesium pyrophosphate formation

Acknowledgments This study was funded by National Natural Science Foundation of China (Grant no. 30972525) and Guangdong Province ''211 Project'' (Grant no. GW201004).