Please wait a minute...
Journal of Integrative Agriculture  2016, Vol. 15 Issue (06): 1293-1303    DOI: 10.1016/S2095-3119(15)61250-3
Plant Protection Advanced Online Publication | Current Issue | Archive | Adv Search |
An improved method for RNA extraction from urediniospores of and wheat leaves infected by an obligate fungal pathogen, Puccinia striiformis f. sp. tritici
MA Li-Jie1, 3, QIAO Jia-xing1, KONG Xin-yu1, WANG Jun-juan1, XU Xiang-ming1, 2, HU Xiao-ping1
1 State Key Laboratory of Crop Stress Biology for Arid Areas, College of Plant Protection, Northwest A&F University, Yangling 712100, P.R.China
2 Genetics and Crop Improvement, East Malling Research, East Malling ME19 6BJ, UK
3 Erdos Ecological Environment of Career Academy, Ordos 017010, P.R.China
Download:  PDF in ScienceDirect  
Export:  BibTeX | EndNote (RIS)      
Abstract     Stripe rust, caused by Puccinia striiformis f. sp. tritici, is an important wheat disease in China, seriously threatening wheat production. Understanding the winter survival of the fungus is a key for predicting the spring epidemics of the disease, which determines the crop loss. Estimation of P. striiformis f. sp. tritici winter survival requires processing a large number of samples for sensitive detection of the pathogen in wheat leaf tissue using real-time quantitative reverse transcription PCR (qRT-PCR). A bottleneck for the analysis is the acquisition of a good yield of high quality RNA suitable for qRT-PCR to distinguish dead and alive fungal hyphae inside leaves. Although several methods have been described in the literatures and commercial kits are available for RNA extraction, these methods are mostly too complicated, expensive and inefficient. Thus, we modified three previously reported RNA extraction methods with common and low-cost reagents (LiCl, SDS and NaCl) to solve the problems and selected the best to obtain high quality and quantity RNA for use in qRT-PCR. In the three improved methods, the NaCl method was proven to be the best for extracting RNA from urediniospores of and wheat leaves infected by P. striiformis f. sp. tritici, although the modified LiCl and SDS methods also increased yield of RNA compared to the previous methods. The improved NaCl method has the following advantages: 1) Complete transfer of urediniospores of P. striiformis f. sp. tritici from the mortar and pestle can ensure the initial amount of RNA for the qRT-PCR analysis; 2) the use of low-cost NaCl to replace more expensive Trizol can reduce the cost; 3) the yield and quality of RNA can be increased; 4) the improved method is more suitable for a large number and high quantity of samples from fields. Using the improved NaCl method, the amount of RNA was increased three times from urediniospores of P. striiformis f. sp. tritici compared from the extraction kit. Approximately, 10.11 μg total RNA of high quality was obtained from 100 mg of infected leaves, which was 8.8, 6.5, 3.4 and 2.1 folds of the amounts obtained from the previous LiCl, SDS, NaCl and traditional Trizol methods, respectively. The method could be used to study the overwintering rates of P. striiformis f. sp. tritici over a large region of wheat production for predicting epidemic levels by determining pathogen survival levels after winter. The method can also be used in any studies which need a large number of high quality RNA samples.
Keywords:  Puccinia striiformis f. sp. tritici        RNA extraction        RT-PCR        urediniospore, mycelium  
Received: 07 September 2015   Accepted:
Fund: 

This work was supported by the National Key Basic Research Program of China (2013CB127700) and the National Natural Science Foundation of China (31071640 and 31271985), and partially supported by the 111 Project from Education Ministry of China (B07049).

Corresponding Authors:  HU Xiao-ping, Tel/Fax: +86-29-87091095, E-mail: xphu@nwsuaf.edu.cn    
About author:  MA Li-jie, E-mail: malijie1016@163.com

Cite this article: 

MA Li-Jie, QIAO Jia-xing, KONG Xin-yu, WANG Jun-juan, XU Xiang-ming, HU Xiao-ping. 2016. An improved method for RNA extraction from urediniospores of and wheat leaves infected by an obligate fungal pathogen, Puccinia striiformis f. sp. tritici. Journal of Integrative Agriculture, 15(06): 1293-1303.

Asie M H, Dhawan P, Nath P. 2000. A simple procedure for the isolation of high quality RNA from ripening banana fruit. Plant Molecular Biolology, 18, 109–115.

Chen X M. 2005. Epidemiology and control of stripe rust [Puccinia striiformis f. sp. tritici] on wheat. Canadian Journal of Plant Patholology, 27, 314–337.

Cui S P, Kang Z S, Zhao J, Yu X M. 2006. A method of quickly extracting total RNA from wheat leaves. Acta Botanica Boreali-Occidentalia Sinica, 26, 314–318. (in Chinese)

De Francesco L. 2003. Real-time PCR takes center stage. Analitical Chemistry, 75, 175A–179A.

Filion M, St-Arnaud M, Jabaji-Hare S H. 2003. Direct quantification of fungal DNA from soil substrate using real-time PCR. Journal of Microbiological Method, 53, 67–76.

Kang Z S, Li Z Q, Shang H S, Chong J. 1993. Electron microscope of the formation for urediniospores of Puccinia striiformis f. sp. tritici. Journal of Northwest Sci-Tech University of Agriculture and Forestry, 21(S2), 10–13. (in Chinese)

Leite G M, Magan N, Medina Á. 2012. Comparison of different bead-beating RNA extraction strategies: An optimized method for filamentous fungi. Journal of Microbiological Method, 88, 413–418.

Li Z Q, Shang H S. 1989. Wheat Rusts and Their Control. Shanghai Science and Technology Press, Shanghai. (in Chinese)

Li Z Q, Zeng S M. 2002. Wheat Rust in China. China Agricultural Press, Beijing. (in Chinese)

Luo Y, Ma Z H, Reyes H C, Morgan D M. 2007. Quantification of airborne spores of Monilinia fructicola in stone fruit orchards of California using real-time PCR. European Journal of Plant Patholology, 118, 145–154.

Manning K. 1991. Isolation of nucleic acids from plants by differential solvent precipitation. Analitical Biochemistry, 195, 45–50.

McNeil M, Roberts A M I, Cockerell V, Mulholland V. 2004. Real-time PCR assay for quantification of Tilletia caries contamination of UK wheat seed. Plant Pathology, 53, 741–750.

Pan J J, Luo Y, Huang C, Sun Z Y, Zhao L, Yan J H, Ma Z H. 2010. Quantification of latent infections of wheat stripe rust by using real-time PCR. Acta Phytopathologica Sinica, 40, 504–510. (in Chinese)

Peng L, Meinan W, Chen X M, Garland C K. 2007. Construction and characterization of a full-length cDNA library for the wheat stripe rust pathogen (Puccinia striiformis f. sp. tritici). BMC Genomics, 8, 145.

Shang H S. 2008. Wheat Stripe Rust and Its Control. Jindun Press, Beijing. (in Chinese)

Sharma-Poudyal D, Chen X M. 2009. Prediction models for potential yield losses caused by wheat stripe rust in the US Pacific Northwest. Phytopathology, 99, S111.

Yan J H, Luo Y, Pan J J, Wang H G, Jin S L, Cao S Q, Ma Z H. 2011. Quantification of latent infection of wheat stripe rust in the fields using real-time PCR. Acta Phytopathologica Sinica, 41, 618–625. (in Chinese)

Yin C T, Chen X M, Wang X J, Han Q M, Kang Z S, Hulbert S H. 2009. Generation and analysis of expression sequence tags from haustoria of the wheat stripe rust fungus Puccinia striiformis f. sp. tritici. BMC Genomics, 10, 626.

Yu Y, Wang X J, Han Q M, Kang Z S. 2007. Comparison of different protocols of extracting total RNA from rust induced wheat leaves and LD-PCR amplification. Journal of Triticeae Crops, 27, 471–474. (in Chinese)
[1] FAN Xu-dong, ZHANG meng-yan, ZHANG Zun-ping, REN Fang, HU Guo-jun, DONG Ya-feng. Prevalence and genetic diversity of grapevine fabavirus isolates from different grapevine cultivars and regions in China[J]. >Journal of Integrative Agriculture, 2020, 19(3): 768-774.
[2] LIANG Qiao-lan, WEI Lie-xin, XU Bing-liang, A. Calderón-Urrea, XIANG Dong. Study of viruses co-infecting white clover (Trifolium repens) in China[J]. >Journal of Integrative Agriculture, 2017, 16(09): 1990-1998.
No Suggested Reading articles found!