key: cord-0015621-y0hh9t1e
authors: Xiong, Qin; Zhang, Linlin; Zheng, Xinyue; Qian, Yulin; Zhang, Yaxin; Zhao, Lijuan; Cheng, Qiang
title: Rapid and Specific Detection of the Poplar Black Spot Disease Caused by Marssonina brunnea Using Loop-Mediated Isothermal Amplification Assay
date: 2021-01-28
journal: Plants (Basel)
DOI: 10.3390/plants10020253
sha: 699803824047034f4aad5abaf1df917b3dba80f9
doc_id: 15621
cord_uid: y0hh9t1e

Marssonina brunnea is the main pathogen that causes poplar black spot disease, which leads to the decrease of the photosynthetic efficiency and significantly affects the production and quality of timber. Currently, no in-field diagnostic exists for M. brunnea. Here, we described a loop-mediated isothermal amplification (LAMP) assay for the rapid and sensitive detection of M. brunnea. A set of six oligonucleotide primers was designed to recognize eight distinct sequences of the internal transcribed spacer (ITS) region of M. brunnea. The LAMP assay was optimized by the combination of high specificity, sensitivity, and rapidity for the detection of less than 10 pg/μL of target genomic DNA in 60 min per reaction at 65 °C, whereas with PCR, there was no amplification of DNA with concentration less than 1 ng/μL. Among the genomic DNA of 20 fungalisolates, only the samples containing the genomic DNA of M. brunnea changed from violet to sky blue (visible to the naked eye) by using hydroxynaphthol blue (HNB) dye. No DNA was amplified from the eight other fungus species, including two other Marssonina pathogens, three other foliar fungi pathogens of poplar, and three common foliar fungal endophytes of poplar. Moreover, the detection rates of M. brunnea from artificially and naturally infected poplar leaves were 10/16 (62.5%) and 6/16 (37.5%) using PCR, respectively, while the positive-sample ratios were both 16/16 (100%) using the LAMP assay. Overall, the ITS LAMP assay established here can be a better alternative to PCR-based techniques for the specific and sensitive detection of M. brunnea in poplar endemic areas with resource-limited settings.

The poplar black spot disease is one of the most destructive foliar diseases that often severely breaks out in poplar plantations all over the world recently [1] [2] [3] [4] [5] [6] . The fungal species Marssonina brunnea (Ellis & Everh.) Magnus is the most pathogenic species, attacking species of the three largest and commercially most important sections of the genus Populus, i.e., Tacamahaca, Aigieros, and Leuce, causing premature defoliation and, ultimately, weakening and dieback of the tree [6] [7] [8] . On the basis of the host range and conidial morphology, research has classified the population of M. brunnea into two specialized forms, M. brunnea f. sp. multigermtubi and M. brunnea f. sp. monogermtubi [9] . The former is hosted on many species of section of Aigieros and their hybrids, as well as hybrids of sections Aigieros and Tacamahaca. The conidia germinate 1-5 (generally 2-3) germtubes, whereas the latter is only pathogenic to poplars of the section Leuce, such as Populus adenopoda and Populus tomentosa, and their hybrids. The conidia germinate one germtube [8, 9] . The germtubes penetrated poplar leaves directly through the cuticle and epidermal wall, and

A successful LAMP reaction with species-specific primers produced many bands of different sizes in a reproducible ladder-like pattern. When the sample tube did not contain selected target DNA or any of the primers F3 (forward outer primer), B3 (backward outer primer), FIP (forward inner primer), and BIP (backward inner primer), no amplification was observed.

In testing of all primers using the nucleotide Basic Local Alignment Search Tool (BLAST) on the NCBI sequence database revealed no significant hits as to August 2020, suggesting high primer specificity for the target sequences. Moreover, the specificity of the M. brunnea ITS amplicons amplified with F3 and B3 primers ( Table 1 ) was checked against the NCBI Nucleotide database using nucleotide BLAST (BLASTn) analysis, which showed a 100% identity with sequences of Marssonina brunnea f. sp. multigermtubi strain HY14 and Marssonina brunnea f. sp. monogermtubi strain BBHB2 (GenBank accession numbers KU508806 and KM246324, respectively) ( Figure 1B ). 

To determine the optimum temperature for efficient amplification by the LAMP assay, we incubated the LAMP reaction mixtures at 60, 62.5, 65, and 67.5 • C for 60 min, using the four basic LAMP primers (F3, B3, FIP, and BIP). A total of 100 pg of genomic DNA of M. brunnea f. sp. multigermtubi strain XY-3 was selected as a template. The results are shown in Figure 2A ,B. The clear DNA ladder-like pattern and color change only appeared at 62.5 • C and 65.0 • C. Nonspecific reactions were not observed at other reaction temperatures ( Figure  2A ,B). Because higher reaction temperatures decrease nonspecific primer annealing [39] , and the amplification products displayed a much clearer DNA ladder-like pattern and color change from violet to sky blue at 65.0 • C than at 62.5 • C, we selected 65.0 • C for further evaluation. Following standardization, optimization of the LAMP assay was also carried out with regard to the effect of two additional loop primers on reaction kinetics and sensitivity. We found that the positive LAMP results (violet-to-blue change and typical DNA ladder-like pattern) could be observed after only 35 min when the forward and backward loop primers were added. Therefore, we used the loop primers in the following tests to accelerate the amplification reaction. (forward outer primer) , F2, F1, B1C, B2C, and B3 (backward outer primer) from the 5' end. As C represents a complementary sequence, F1C and B1C are complementary to F1 and B1, respectively. Two inner primers (FIP (forward inner primer) and BIP (backward inner primer)) and outer primers (F3 and B3) are used in the LAMP method. FIP (BIP) is a hybrid primer consisting of the F1C (B1C) sequence and the F2 (B2) sequence. FL and BL represent forward and backward loop primers, respectively. (B) Nucleotide sequence alignment of ITS sequences from M. brunnea f. sp. multigermtubi, M. brunnea f. sp. monogermtubi, and three closely related species. In the aligned sequences, grey shade indicates a match, and a dash indicates a gap sequence. Polymorphic sites among the five species are highlighted in color. The rectangular boxes with different colors correspond to the different primer sequences of the LAMP primer set shown in A. 

The specificity of the LAMP assay was determined with DNA from 12 M. brunnea isolates, 2 isolates of two other Marssonina species, and 6 isolates of other poplar foliar fungi including three common foliar fungal endophytes of poplar (Alternaria sp., Botryosphaeria sp., and Pseudocercospora sp.) and three other foliar pathogens of poplar (Melampsora larici-populina Kleb., Venturia populina (Vuill.) Fabr., and Elsinoë australis) ( Table 2 ). Positive or negative results were confirmed by adding hydroxynaphthol blue (HNB) to the reaction system prior to amplification. After the reaction, the color of the positive samples changed to sky blue, differing from the violet color in the negative samples. Meanwhile, the LAMP amplification products of the positive samples displayed the typical ladder-like patterns in agarose gel electrophoresis. As shown in Figure 3 , 12 M. brunnea strains, whether isolated from Populus tomentosa Carr., Populus × canadensis Moench, and Populus × euramericana "I-214" in Jiangsu Province, or isolated from Populus simonii Carr. in Liaoning Province, showed positive LAMP reactions, whereas reactions containing two other Marssonina species (Marssonina coronaria and Marssonina rosae) and six other fungal species were negative ( Figure 3A ,B). At least three replicates were analyzed to verify the specificity of the LAMP reactions. PCRs were performed using the same DNA samples and the same result was observed. Amplification products of 193 bp were only observed in the tubes containing M. brunnea DNA as compared to no products in negative control and other fungi ( Figure 3C ). This was indicative of the ribosomal DNA internal transcribed spacer (rDNA-ITS) region being suitable as a target for detecting and identifying M. brunnea. 

To determine the sensitivity of the LAMP assay, we performed reactions using 10-fold serial dilutions of a 100 ng/µL genomic DNA solution (M. brunnea strain XY-3) down to 1 fg/µL. The results are shown in Figure 4A ,B, in which the DNA concentrations decreased from left to right. The minimum concentration detected was 10 pg/µL in the LAMP assay ( Figure 4A ,B). PCRs were performed using the same DNA samples. PCR amplification products of 193 bp were observed in samples ranging from 100 ng/µL to 1 ng/µL ( Figure 4C ). Negative control showed no amplification under the same conditions ( Figure 4A -C). The LAMP and PCR assays were carried out in triplicate for each template DNA. The results suggest that the LAMP assay (10 pg/µL) has a 100-fold greater sensitivity as compared with conventional PCR (1 ng/µL).

Artificially inoculated poplar leaves exhibiting symptoms of black spots in the greenhouse were evaluated by the LAMP and PCR assays. The positive-sample ratios were 16/16 (100%) by the LAMP assay ( Figure 5A ,B) and 10/16 (62.5%) by conventional PCR ( Figure 5C ). By contrast, negative results were obtained in healthy leaves inoculated with liquid water and no DNA sample by both PCR method and LAMP reaction ( Figure 5) . The results showed that the LAMP assay succeeded in detecting M. brunnea in the infected poplar samples. 

The LAMP assay for M. brunnea detection was applied to the diseased poplar leaves collected in the field in the campus of Nanjing Forestry University. As shown in Figure 6 , the presence of M. brunnea could be accurately detected in a total of 16 diseased leaf samples by the LAMP assay ( Figure 6A,B) , while M. brunnea was detected in only 6 out of 16 diseased leaf samples by PCR ( Figure 6C ). No amplification products were observed in the negative control (M. brunnea-free leave sample) or no template (NT) control. These results were consistent between two independent repeats of each assay. These results indicate that the LAMP assay reported here could be successfully applied to field-collected poplars to detect the poplar black pot disease. 

This work successfully established and optimized a rapid and specific diagnostic LAMP assay conducted on the basis of rDNA ITS region of the forest pathogen M. brunnea.

Owing to the unavailable of the complete genome sequences or other traditional genetic markers (i.e., β-tubulin gene, histone H3 gene, and calmodulin gene) of all Marssonina pathogens mentioned in this study, the only choice of the target selection is the rDNA ITS gene. Marssonina coronaria, a devastating plant pathogen causing apple blotch, possesses different detection methods, including optical coherence tomography (OCT)-based technique, hyperspectral imaging system, PCR, quantitative PCR (Q-PCR), and LAMP [40] [41] [42] [43] [44] .

In the literature to date, only the rDNA ITS sequence of M. coronaria has been selected as the target for primer design. The sequence alignment of the ITS region has shown 95 to 100% homology among the different strains of Marssonina from diverse geographical locations ( Figure 1B) . After considering several key factors for designing LAMP primers, such as primer length, GC content, stability, primer secondary structures, melting temperature (Tm), and the distance between primers [45] , we selected one primer set that satisfied all design guidelines, but it showed B3 is only one bp differ from the others, and that F1, B1, and B2 are the same as the other three closely related species. However, the primer set surprisingly had the ability to distinguish the closely related species from each other, suggesting that F3 and F2 primers may play essential roles in avoiding cross homologies during LAMP detection assay of M. brunnea. In the future, maybe the other potential targets for molecular diagnostics could be identified by bioinformatics tools, such as integrated or comparative genomic, transcriptomic, and proteomic approaches. Dai et al. [37] recently applied comparative genomics approaches for the design of LAMP detection assays of Phytophthora cinnamomi.

In this study, the comparative evaluation of LAMP vs. conventional PCR revealed LAMP stands out a preferred diagnostic tool with higher sensitivity, specificity, rapidity, simplicity, and adaptability to field conditions. The LAMP assay was found to be 100-fold more sensitive than PCR with a minimum detection limit of 10 pg/µL template ( Figure 4) . Further, the sensitivity can be significantly improved by multiple endonuclease restriction real-time-LAMP technology [46] , dye-binding Q-PCR [47] , or biosensor assays, making the LAMP assay even more efficient at detecting M. brunnea in poplar. Therefore, it could be a better alternative method for screening samples with minute quantities of M. brunnea that might escape the PCR detection. Moreover, it was markedly faster compared with PCR, requiring just 35 min to complete the reaction rather than at least 90 min for PCR. The high amplification efficiency of LAMP is attributed to the lack of a need to choose complex-variable temperature conditions and set different response procedures [25] . That is to say, the LAMP has great advantage over PCR in terms of rapidity, wherein LAMP allows for immediate diagnosis.

The LAMP assay also demonstrated a higher degree of specificity for detection of M. brunnea in both the artificially inoculated and naturally infested poplar leaves, having no false-positive or false-negative results when compared with PCR assay (Figures 5 and 6 ), indicating that it is highly specific for the target sequence. Specificity of the LAMP and PCR-based assays were also validated by the negative detection results against eight isolates belonging to other species, including two other reported Marssonina pathogens, three common foliar fungal endophytes of poplar, and three other foliar pathogens of poplar with same spot symptom in the early stage as that caused by M. brunnea. Due to the limitation of the currently reported Marssonina pathogens, only two well-known isolates of other Marssonina spp. (Marssonina coronaria and Marssonina rosae) were included, which also need to be further improved. Nevertheless, we had a wider detection range compared with the existing PCR-based and LAMP-based methods for M. coronaria detection [41] [42] [43] , for which none of the other Marssonina species were tested in the specificity assay.

The simplicity of LAMP could also be described in the result visualization. Two formats in this study to judge the reaction results include visual inspection with HNB dye and agarose gel electrophoresis. The common intercalating dyes including calcein, SYBR green I, and HNB [24, 28, 48] , as well as several other existing dyes, such as malachite green [49] , Picogreen [50] , Gelred [51] , SYTO fluorescent [52] , Evagreen [53] , Goldview II [54] , and berberine [55] , were added into the reaction tube for visualization LAMP products. Positive reaction tube will exhibit color change or fluorescence, while for negative controls, this will not occur. Thus, unlike PCR, tedious procedure of gel electrophoresis is not needed. However, adding the dyes often requires the opening of the reaction tubes, therefore increasing the risk of carry-over contamination [56] . To avoid such contamination, we selected HNB dye as a visual indicator that we added to the LAMP reaction tube prior to amplification in our study. A positive reaction was indicated by a color change from violet to sky blue Figure 2A , Figure 3B , Figure 4B , Figure 5B , and Figure 6B ). Moreover, it has been reported that the SYBR green I dye could inhibit LAMP reaction if the dye is added before isothermal incubation [57] . The pre-addition of 192 µM HNB into the LAMP reaction mixture enabled real-time monitoring with no inhibitory effect. Meanwhile, the results of the visual detection with HNB in this study were further verified by 2% agarose gel electrophoresis, as the result of positive tube after amplification will display a ladder-like pattern. The results obtained are perfectly in accordance with that of the visual detection with HNB Figure 2 , Figure 3A ,B, Figure 4A ,B, Figure 5A ,B, and Figure 6A ,B).

In conclusion, the established LAMP assay in this study is rapid, sensitive, specific, simple, and low-cost, which is a promising diagnostic tool to replace conventional PCRbased methods for M. brunnea detection in both plant and environmental samples. This method has the potential for early diagnosis of M. brunnea and for greatly preventing poplar black spot disease in the field.

The LAMP primers ( Figure 1A) were designed on the basis of the rDNA ITS sequences of Marssonina brunnea f. sp. multigermtubi (Genbank accession no. KU508806) and Marssonina brunnea f. sp. monogermtubi (Genbank accession no. KM246324). Other related species (M. mali-EU520097, M. rosae-AY904059, and M. coronariae-JN587494) were retrieved from the GenBank database and aligned to identify highly conserved regions using the BioEdit software V7.2.0 [58] ( Figure 1B) . The LAMP primers were designed using the PRIMER EXPLORER V4 software program (http://primerexplorer.jp/e/) (Eiken Chemical Co., Ltd., Tokyo, Japan) and modified manually in order to increase the concentration of DNA produced during the LAMP reaction. A set of six primers were designed for the detection of M. brunnea, including two outer primers (forward primer F3 and backward primer B3) and two inner primers (forward inner primer FIP and backward inner primer BIP), which recognized six distinct regions of the target DNA, as well as two additional loop primers FL and BL, which can accelerate the LAMP reaction. Positions of primers within the nucleotide sequence of the ITS region are given in Figure 1 . A BLASTn analysis of the target sequence was carried out to evaluate the specificity of the primers. Primers were synthesized and purified by Invitrogen Trading Shanghai Co., Ltd., and all sequences are listed in Table 1 .

The strains used to evaluate the sensitivity and specificity of the primers are listed in Table 2 

The LAMP reaction was prepared in a 25 µL mixture containing 2.5 µL 10× ThermoPol Buffer, 4 µL MgSO 4 (50 mM), 3.5 µL deoxynucleotide triphosphates (dNTPs) (10 mM), 2 µL each internal primer FIP and BIP (20 µM), 0.5 µL each external primer F3 and B3 (10 µM), 1 µL each loop primer FL and BL (10 µM), 4 µL betaine (5 M, Sigma-Aldrich, Saint Louis, MO, USA), 2 µL hydroxy naphthol blue HNB (2.4 mM, Aladdin, China), 1 µL Bst DNA polymerase (8 U/µL, New England BioLabs, Tokyo, Japan), and 1 µL of genomic DNA as the template. Negative controls containing an equivalent volume of nuclease-free water instead of DNA were included in each reaction. The final volume of each reaction was 25 µL. LAMP reactions were then optimized for amplification temperatures and incubation periods. The LAMP amplification mixtures were incubated at a constant temperature ranging from 60 to 67.5 • C for 1 hour, and then heated at 80 • C for 5 min to inactivate the Bst polymerase. Each treatment was replicated 3 times, and the experiment was repeated twice. To determine the optimal incubation periods, we mixed the LAMP amplification mixtures at the optimal temperature for 20 min to 1 h and then heated them at 80 • C for 5 min to stop the reaction. Subsequently, LAMP products were visualized directly by the naked eye. Samples that turned sky blue were considered to be M. brunnea-positive, while those that remained violet were considered to be M. brunnea-negative. The images of the LAMP tubes were captured with a Panasonic digital camera (Model: DMC-FZ28GK). After the visual assessment, the LAMP products were further verified by gel electrophoresis (2% agarose gel for 50 min at 80 V).

For conventional PCR, we used F3 and B3 primers to amplify the same specific region of rDNA ITS region. The PCR reaction mixture was composed of 1.0 µL DNA template, 12.5 µL PrimerSTAR Max Premix (2X; Takara, R045A), and 0.5 µL of each of the primers F3 (10 µM) and B3 (10 µM) ( Table 1) , adding nuclease-free H 2 O to a final volume of 25 µL. The thermal cycling program was 98 • C for 4 min; 31 cycles of 98 • C for 10 s, 56 • C for 5 s, and 72 • C for 5 s; and 72 • C for 5 min. After the amplification, PCR products were examined by 1.5% agarose gel electrophoresis for 30 min at 120 V, stained with ethidium bromide, and visualized by UV translumination. DNA ladder marker II (Tiangen, MD102, Beijing, China) was used for size references.

To evaluate the sensitivity of the LAMP and PCR assays, we tested DNA extracted from a representative isolate of M. brunnea XY-3 in 3 independent 10-fold dilution series ranging from 100 ng/µL to 1 fg/µL. DNA concentrations were estimated using a Nanodrop. In order to investigate the specificity of the LAMP and PCR assays, we tested DNA extracts from cultures of 12 isolates of M. brunnea (target species), 2 isolates of other Marssonina spp. (non-target species most closely related in the genus), and 6 isolates of other fungal species ( Table 2 ). The assays were evaluated on the basis of change in the color of HNB and the appearance of ladder-like pattern for LAMP and on 1.5% agarose gel electrophoresis for PCR. There were 3 replicates for each treatment, and the experiment was repeated twice.

To assess the ability of LAMP method to detect M. brunnea from infected samples, we prepared the artificially inoculated samples as described by Cheng et al. [59] with minor modifications. The pathogen-free branches of P. tomentosa Carr. and Populus euramericana cv. I-214 were cut out in winter and cultured in the greenhouse at 22 • C with a 12-h photoperiod. The cuttings were approximately 0.5-1 m high and produced 20 to 50 leaves after 12 weeks. A total of 8 fully expanded leaves from each poplar clone were collected, rinsed thoroughly with autoclaved water 5 to 6 times, and placed on sterilized 2% water agar culture plates with the abaxial surface of the leaf facing upward.

Conidia of M. brunnea f. sp. multigermtubi strain 214-4 and M. brunnea f. sp. monogermtubi strain QC2 were cultured in PDA medium for 10 days and suspended in sterile water, respectively. The conidia suspensions of strains 214-4 and QC2 were adjusted to 10 5 spores/mL and sprayed onto the abaxial surface of the poplar leaves from clones P. euramericana cv. I-214 and P. tomentosa Carr., respectively. The treated leaves were incubated in an illuminated incubator under 100% relative humidity (RH) at 22 • C with a 12-h photoperiod. After 3 days, visible disease symptoms began to develop. Symptomatic leaves infected by M. brunnea f. sp. multigermtubi strain 214-4 and M. brunnea f. sp. monogermtubi strain QC2 were harvested and then ground in liquid nitrogen immediately for DNA extraction, respectively. Pathogen-free leaves were excised from sterile tissue cultures of P. tomentosa Carr. clone (we could not generate tissue culture of P. euramericana cv. I-214 clone, despite numerous trials), then spray-inoculated with deionized water, which were used as a negative control. Genomic DNA (100 ng) extracted from the mycelium of M. brunnea strain XY-3 was used as a positive control. LAMP and PCR detection of M. brunnea in the inoculated poplar samples were performed using the above-described protocol and repeated at least twice per sample.

To demonstrate the suitability of LAMP as a tool for the detection of M. brunnea in environmental samples, we collected a total of 16 leaves showing classical black spot symptoms from poplar trees (P. tomentosa Carr. and P. euramericana cv. I-214) located in the campus of Nanjing Forestry University (NJFU), where some of M. brunnea f. sp. monogermtubi and M. brunnea f. sp. multigermtubi strains we used in this study were respectively isolated from. Asymptomatic leaves collected from the M. brunnea-free site for several years at NJFU were used as a negative control (NC). For each sample, the purified genomic DNA was extracted by using a Plant DNA Mini Kit (Omega Biotek, China) according to the manufacturer's protocol. The DNA concentration for each sample was determined by NanoDrop (ND-3300 fluorospectrometer, Thermo-Fisher Scientific, Wilmington, DE, USA). Both LAMP and PCR assays were carried out at least twice using 17 extracted DNAs as templates. A positive control (100 ng purified gDNA from mycelium of M. brunnea strain XY-3) and a no template (NT) control were included in each assay. 

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We highly appreciate Qiang Zhuge at Nanjing Forestry University for kindly sharing lab equipment as well as Justin Waletich and Kai Tao at the Oregon State University for their editorial assistance.

The authors declare no conflict of interest.