Department of Health and Human Services
Centers for Disease Control and Prevention

Emerging Infectious Diseases

ISSN: 1080-6059

Email this page

Printer-friendly version

Download this article as PDF

Article Contents

Volume 13, Number 6–June 2007

Dispatch

Loop-Mediated Isothermal Amplification for Influenza A (H5N1) Virus

Shanthi Jayawardena,* Chung Y. Cheung,* Ian Barr,† Kwok H. Chan,* Honglin Chen,* Yi Guan,* J.S. Malik Peiris,* and Leo L.M. Poon*
*The University of Hong Kong, Hong Kong Special Administrative Region, People's Republic of China; and †World Health Organization Collaborating Centre for Influenza, Melbourne, Victoria, Australia

The Study

We aimed to develop a reverse transcription (RT) LAMP assay that could detect a variety of highly pathogenic influenza (H5N1) viruses. For primer design, we used highly pathogenic influenza (H5N1) sequences publicly available from the Influenza Sequence Database (www.flu.lanl.gov/index.html) in August 2006. We used hemagglutinin (HA) from an influenza (H5N1) prototype vaccine strain (A/Vietnam/1203/2004, GenBank accession no. AY651334) as the reference for this study. The sequences included highly pathogenic influenza (H5N1) viruses identified in the past 2 years. In addition, sequences from all the other HA subtypes (e.g., 1,127 for H1 and 1,472 for H3) in the above database were used for the analysis. Because highly pathogenic influenza (H5N1) gene sequences are genetically diverse, all studied H5 sequences (n = 711) were aligned, and a highly conserved region at the 5´ end of HA2 encoding sequence (corresponding to nt 1,065–1,298 of the reference sequence) was selected as the target (Appendix Figure 2A [ 33 KB, 2 pages] and Appendix Figure 3 [ 22 KB, 1 page] ). Of all the downloaded highly pathogenic influenza (H5N1) sequences, 115 did not contain the target site and were excluded from analysis. The GenBank accession numbers for the highly pathogenic influenza (H5N1) sequences used for the primer design are listed in the Appendix Table.

Previous demonstration that degenerate primers could be used in LAMP assays (6) led us to use the same approach for designing a set of degenerate primers for the targeted region (Appendix Figure 2A [ 33 KB, 2 pages] ). Our HA sequence analysis also showed that HA sequences from influenza (H5N2) viruses of North American lineage and other viruses with other HA subtypes contain extensive mismatches to the primers used in the LAMP assay (Appendix Figure 2A,B [ 33 KB, 2 pages] ). In the initial phase of the study, we used the reference strain (A/Vietnam/1203/2004) to determine the sensitivity of the assay. Purified RNA from a viral supernatant with a known titer was serially diluted and subjected to the LAMP assay. As shown in the Figure, panel A, the detection limit of the assay was found to be 2×10–3 plaque-forming units (pfu) per reaction. The sensitivity of this assay was also compared with that of an optimized RT-PCR assay recommended by the World Health Organization (7). As shown in the Figure, panel A, the detection limit of the RT-PCR assay was identical to that from the LAMP assay. We also spiked various amounts of influenza (H5) viruses into non-H5 nasopharyngeal aspirate samples and tested the purified RNA from these clinical specimens by the LAMP and RT-PCR assays. The results from these assays were identical (data not shown). These findings are in accordance with previous findings that the sensitivity of LAMP assays is comparable to that of conventional PCR methods (5,6,8). In addition, all positive reactions were visually examined for the presence of white precipitate at the end of the reaction incubation. As expected, all results correlated exactly with those deduced by the real-time turbidity meter (data not shown).

We also tested the feasibility of using this assay to detect influenza (H5) viruses in clinical specimens from a patient with influenza (H5). RNA from 2 different postmortem lung tissue samples from a patient infected with influenza A/HK/212/03 was subjected to the LAMP assay. As shown in the Figure, panel B, both RNA samples had positive results for the influenza (H5) viruses.

To evaluate the specificity of the LAMP assay for influenza (H5) viruses, a comparative study including all 16 HA subtypes and a variety of H5N1 strains was performed (Table). All 14 H5N1 strains isolated from different geographic regions during the past 10 years were positive, whereas none of the non-H5 samples were positive (Table). All the reactions were visually examined, and the results corresponded with those generated from the real-time turbidity meter. Influenza A/chicken/Wajo/BBVM/2005, A/duck/Vietnam/568/2005, and A/bar-headed goose/Qinghai/5/2005 are clade 2 influenza (H5N1) viruses that have recently emerged from different geographic regions (9), and these 3 viruses are phylogenetically distinct (10,11). Our results demonstrate that this assay is applicable to a wide variety of highly pathogenic influenza (H5N1) viruses. In addition, other virus reassortants with the HA of this lineage are expected to be positive in the assay.

We previously demonstrated that heat-treated blood samples could be directly tested by a LAMP assay specific for DNA of a bloodborne pathogen (5). These modifications could avoid the need for nucleic acid purification, thereby reducing the cost and turnaround time for molecular diagnosis. We tested the feasibility of detecting the H5 sequence from viral cultures without RNA extraction. In a Biosafety Level 3 facility, 50 μL of viral culture of the prototype virus was heat inactivated (99°C for 10 min), the heat-treated sample was serially diluted with standard viral culture medium, and 2 μL of serially diluted samples was added to the LAMP assay. As shown in the Figure, panel C, and in online Appendix Figure 1, H5N1 subtype could still be detected by the assay. However, the detection limit (9.6 pfu/reaction) was ≈1,000× less sensitive than the limit with purified RNA as an input.

Conclusions

The RT-LAMP assay is highly specific, and its sensitivity is comparable to that of an optimized RT-PCR assay for influenza (H5N1) viruses. The detection limit is equivalent to that of a similar LAMP assay (12), but our assay was extensively tested by using a wide variety of influenza (H5) viruses, including recent clade 2 influenza (H5) viruses (9). LAMP does not require thermocyclers and gel electrophoresis. Reactions can simply be incubated in a water bath or heating block, and the results can be confirmed by direct visual inspection. Because early identification of influenza (H5) is crucial for the containment of the disease, this novel assay can provide an efficient option for the preliminary molecular detection of highly pathogenic influenza (H5) viruses in basic laboratory or clinical settings. Combined with the use of a turbidity meter, which costs much less than a real-time RT-PCR system, RT-LAMP can provide quantitative data for viral load studies. In conclusion, the LAMP assay is a promising tool for the detection of influenza (H5) viruses.

Acknowledgments

We thank Bonnie W.Y. Wong for her technical assistance.

We acknowledge research funding from Public Health Research Grant A195357 from the US National Institutes of Health, the Research Grant Council of Hong Kong (HKU 7530/06M), and the Seed Funding Programme for Basic Research from HKU.

Ms Jayawardena is a PhD student in the Department of Microbiology of The University of Hong Kong. Her research interests mainly relate to the molecular biology of influenza viruses.

References

Perez DR, Sorrell EM, Donis RO. Avian influenza: an omnipresent pandemic threat. Pediatr Infect Dis J. 2005;24:S208–16.
Brown IH. Advances in molecular diagnostics for avian influenza. Dev Biol (Basel). 2006;124:93–7.
Notomi T, Okayama H, Masubuchi H, Yonekawa T, Watanabe K, Amino N, et al. Loop-mediated isothermal amplification of DNA. Nucleic Acids Res. 2000;28:e63.
Mori Y, Nagamine K, Tomita N, Notomi T. Detection of loop-mediated isothermal amplification reaction by turbidity derived from magnesium pyrophosphate formation. Biochem Biophys Res Commun. 2001;289:150–4.
Poon LLM, Wong BWY, Ma EHT, Chan KH, Chow LMC, Abeyewickreme W, et al. Sensitive and inexpensive molecular test for falciparum malaria: detecting Plasmodium falciparum DNA directly from heat-treated blood by loop-mediated isothermal amplification. Clin Chem. 2006;52:303–6.
Poon LLM, Leung CSW, Chan KH, Lee JHC, Yuen KY, Guan Y, et al. Detection of human influenza A viruses by loop-mediated isothermal amplification. J Clin Microbiol. 2005;43:427–30.
World Health Organization. Recommended laboratory tests to identify avian influenza A virus in specimens from humans. 2005 [cited 2006 September 24]. Available from http://www.who.int/csr/disease/avian_influenza/guidelines/avian_labtests2.pdf
Parida M, Posadas G, Inoue S, Hasebe F, Morita K. Real-time reverse transcription loop-mediated isothermal amplification for rapid detection of West Nile virus. J Clin Microbiol. 2004;42:257–63.
Webster RG, Govorkova EA. H5N1 influenza–continuing evolution and spread. N Engl J Med. 2006;355:2174–7.
Chen H, Smith GJD, Li KS, Wang J, Fan XH, Rayner JM, et al. Establishment of multiple sublineages of H5N1 influenza virus in Asia: implications for pandemic control. Proc Natl Acad Sci U S A. 2006;103:2845–50.
Smith GJ, Naipospos TS, Nguyen TD, de Jong MD, Vijaykrishna D, Usman TB, et al. Evolution and adaptation of H5N1 influenza virus in avian and human hosts in Indonesia and Vietnam. Virology. 2006;350:258–68.
Imai M, Ninomiya A, Minekawa H, Notomi T, Ishizaki T, Tashiro M, et al. Development of H5-RT-LAMP (loop-mediated isothermal amplification) system for rapid diagnosis of H5 avian influenza virus infection. Vaccine. 2006;24:6679–82.

Figures

Figure. Detection of influenza (H5) virus by loop-mediated isothermal amplification (LAMP). A) Serially diluted RNA from A/Vietnam/1203/2004 was tested...
Appendix Figure 1. Visual inspection of the positivity of LAMPreactions. Heated, treated viral culture was serially diluted and tested by the LAMP assay...
Appendix Figure 2. Target sites for the loop-mediated isothermal amplification (LAMP) assay. A) Alignment of H1–16 sequences...
Appendix Figure 3. Target site for the loop-mediated isothermal amplification (LAMP) assay. A) Alignment of H1 to H16 sequence...

Tables

Table. RT-LAMP assay results for highly pathogenic influenza A (H5N1)
Appendix Table. Influenza A virus (H5N1) sequences used in the primer design