{"title":"蓝金银花(Lonicera caerulea L.)采后果实腐病病原菌研究初报水果在中国。","authors":"Haohao Yan, Yuxuan Li, Zijian Man, Yusheng Lv, Xin Zhao, Zexu Chen, Liangchuan Guo, Junwei Huo, Mingyu Sang, Chunyan Li, Yi Cheng, Hailian Zang","doi":"10.1094/PDIS-12-24-2557-PDN","DOIUrl":null,"url":null,"abstract":"<p><p>Blue honeysuckle (Lonicera caerulea L.) plants produce small fruit that are used as food and medicine. In September 2024, 100 kg of blue honeysuckle 'Lanjingling' (China National Plant Variety Protection (CNPVP) 20200389) fruits were harvested in Harbin, China (126.48°E, 45.87°N), and 20% of the fruits showed postharvest fruit rot symptoms, leading to whole-fruit rotting with skin browning and necrotic lesions (Fig. 1. A). Small (1 to 2 mm) samples of infected tissue were obtained from five randomly selected fruits. Samples were surface sterilized with 75% ethanol for 30 s and 5% sodium hypochlorite (NaClO) for 3 min, rinsed three times with sterile distilled water, dried with paper towel, and plated on 9 cm Petri dishes containing potato dextrose agar (PDA). Purified cultures were obtained using the single-spore technique. After 5 d at 28°C, the colonies displayed yellow brown aerial mycelium on the PDA plates (Fig. 1. B, C). Conidiophores were transparent and smooth, while conidial heads were brown and nearly spherical (Fig. 1. D). The entire surface was fertile, producing mostly spherical to subglobose conidia with diameters of 2.12 to 3.24 μm (n = 50) (Fig. 1. E). The internal transcribed spacer region (ITS, included ITS1+5.8S +ITS2, GenBank PQ606583), β-tubulin (TUB, GenBank PQ611757), and nuclear large subunit rRNA (LSU, GenBank PQ620103) genes were partially amplified with their respective primers (ITS1/ITS4 (White et al. 1990), Btub2Fd/Btub4Rd (Glass and Donaldson, 1995) and LROR/LR7 (Rehner and Samuels, 1994). BLAST analysis revealed that the sequences of the three genes showed 99.30 to 100% homology (526/526 nt, 141/142 nt, and 882/882 nt) with the MH859926, AY819971, and MH876373 sequences for isolates of Aspergillus ochraceus. In a phylogenetic tree constructed by Maximum likelihood method based on ITS and TUB sequences, the isolate LDGS-6 was located in the same clade with A. ochraceus (Fig. 2). For pathogenicity, twenty healthy blue honeysuckle 'Lanjingling' fruits were superficially sterilized with 75% ethanol and washed with distilled water. Ten fruits were inoculated with a 10 μL conidial suspension of isolate LDGS-6 (106 spores/mL) and ten with sterile distilled water (control). After fruits were incubated in 9 cm Petri dishes at 28°C and 75% relative humidity in the dark for 7 d, inoculated fruits displayed rot symptoms while control fruits did not (Fig. 1. F and G). The experiment was replicated three times. The causal agent was isolated from inoculated fruits, and it was identified as the original isolate based on morphological traits and ITS, TUB, and LSU sequencing, whereas no Aspergillus-like strains were isolated from control fruits, thus confirming Koch's postulates. In conclusion, based on molecular, morphological, and pathogenic analysis, A. ochraceus is the causal agent of the fruit rot disease on blue honeysuckle fruits (Ou et al. 2024). A. ochraceus was previously reported in China in Shengzhou nane (on Prunus salicina var. taoxingli) (Ou et al. 2024). To our knowledge, this is the first report of postharvest fruit rot caused by A. ochraceus on blue honeysuckle fruits in China. The annual fruit yield production of trees over 5 years old can reach about 40,000 tons during the high-yielding years in China (Sun et al. 2024), but its storage is challenged by pathogen infection. Future work should focus on monitoring its occurrence and spread and developing effective control strategies.</p>","PeriodicalId":20063,"journal":{"name":"Plant disease","volume":" ","pages":""},"PeriodicalIF":4.4000,"publicationDate":"2025-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"First Report of Postharvest Fruit Rot Caused by <i>Aspergillus ochraceus</i> on Blue Honeysuckle (<i>Lonicera caerulea</i> L.) Fruit in China.\",\"authors\":\"Haohao Yan, Yuxuan Li, Zijian Man, Yusheng Lv, Xin Zhao, Zexu Chen, Liangchuan Guo, Junwei Huo, Mingyu Sang, Chunyan Li, Yi Cheng, Hailian Zang\",\"doi\":\"10.1094/PDIS-12-24-2557-PDN\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Blue honeysuckle (Lonicera caerulea L.) plants produce small fruit that are used as food and medicine. In September 2024, 100 kg of blue honeysuckle 'Lanjingling' (China National Plant Variety Protection (CNPVP) 20200389) fruits were harvested in Harbin, China (126.48°E, 45.87°N), and 20% of the fruits showed postharvest fruit rot symptoms, leading to whole-fruit rotting with skin browning and necrotic lesions (Fig. 1. A). Small (1 to 2 mm) samples of infected tissue were obtained from five randomly selected fruits. Samples were surface sterilized with 75% ethanol for 30 s and 5% sodium hypochlorite (NaClO) for 3 min, rinsed three times with sterile distilled water, dried with paper towel, and plated on 9 cm Petri dishes containing potato dextrose agar (PDA). Purified cultures were obtained using the single-spore technique. After 5 d at 28°C, the colonies displayed yellow brown aerial mycelium on the PDA plates (Fig. 1. B, C). Conidiophores were transparent and smooth, while conidial heads were brown and nearly spherical (Fig. 1. D). The entire surface was fertile, producing mostly spherical to subglobose conidia with diameters of 2.12 to 3.24 μm (n = 50) (Fig. 1. E). The internal transcribed spacer region (ITS, included ITS1+5.8S +ITS2, GenBank PQ606583), β-tubulin (TUB, GenBank PQ611757), and nuclear large subunit rRNA (LSU, GenBank PQ620103) genes were partially amplified with their respective primers (ITS1/ITS4 (White et al. 1990), Btub2Fd/Btub4Rd (Glass and Donaldson, 1995) and LROR/LR7 (Rehner and Samuels, 1994). BLAST analysis revealed that the sequences of the three genes showed 99.30 to 100% homology (526/526 nt, 141/142 nt, and 882/882 nt) with the MH859926, AY819971, and MH876373 sequences for isolates of Aspergillus ochraceus. In a phylogenetic tree constructed by Maximum likelihood method based on ITS and TUB sequences, the isolate LDGS-6 was located in the same clade with A. ochraceus (Fig. 2). For pathogenicity, twenty healthy blue honeysuckle 'Lanjingling' fruits were superficially sterilized with 75% ethanol and washed with distilled water. Ten fruits were inoculated with a 10 μL conidial suspension of isolate LDGS-6 (106 spores/mL) and ten with sterile distilled water (control). After fruits were incubated in 9 cm Petri dishes at 28°C and 75% relative humidity in the dark for 7 d, inoculated fruits displayed rot symptoms while control fruits did not (Fig. 1. F and G). The experiment was replicated three times. The causal agent was isolated from inoculated fruits, and it was identified as the original isolate based on morphological traits and ITS, TUB, and LSU sequencing, whereas no Aspergillus-like strains were isolated from control fruits, thus confirming Koch's postulates. In conclusion, based on molecular, morphological, and pathogenic analysis, A. ochraceus is the causal agent of the fruit rot disease on blue honeysuckle fruits (Ou et al. 2024). A. ochraceus was previously reported in China in Shengzhou nane (on Prunus salicina var. taoxingli) (Ou et al. 2024). To our knowledge, this is the first report of postharvest fruit rot caused by A. ochraceus on blue honeysuckle fruits in China. The annual fruit yield production of trees over 5 years old can reach about 40,000 tons during the high-yielding years in China (Sun et al. 2024), but its storage is challenged by pathogen infection. Future work should focus on monitoring its occurrence and spread and developing effective control strategies.</p>\",\"PeriodicalId\":20063,\"journal\":{\"name\":\"Plant disease\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2025-02-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant disease\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1094/PDIS-12-24-2557-PDN\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant disease","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1094/PDIS-12-24-2557-PDN","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
摘要
蓝金银花(Lonicera caerulea L.)植物结出的小果实可用作食物和药物。2024年9月,在中国哈尔滨(126.48°E, 45.87°N)收获了100公斤蓝金银花‘蓝景岭’(中国国家植物品种保护(CNPVP) 20200389)果实,20%的果实出现采后腐果症状,导致整个果实腐烂,果皮褐变和坏死(图1)。A).从随机选择的五个水果中获得了小的(1至2毫米)感染组织样本。样品表面用75%乙醇消毒30 s, 5%次氯酸钠(NaClO)消毒3 min,用无菌蒸馏水冲洗3次,用纸巾擦干,然后镀在含有马铃薯葡萄糖琼脂(PDA)的9 cm培养皿上。采用单孢子技术获得纯化培养物。28℃下培养5 d后,菌落在PDA平板上呈现黄褐色气生菌丝(图1)。B, C)。分生孢子孔透明光滑,分生孢子头呈棕色,近球形(图1)。D)。整个表面肥沃,产生的分生孢子大多为球形至亚球形,直径为2.12至3.24 μm (n = 50)(图1)。E)。内部转录间隔区(ITS,包括ITS1+5.8S +ITS2, GenBank PQ606583)、β-微管蛋白(TUB, GenBank PQ611757)和核大亚基rRNA (LSU, GenBank PQ620103)基因用各自的引物(ITS1/ITS4 (White et al. 1990)、Btub2Fd/Btub4Rd (Glass and Donaldson, 1995)和LROR/LR7 (Rehner and Samuels, 1994)部分扩增。BLAST分析结果显示,3个基因序列与ochraceus Aspergillus分离株MH859926、AY819971和MH876373序列的同源性(526/526 nt、141/142 nt和882/882 nt)为99.30% ~ 100%。在基于ITS和TUB序列的最大似然法构建的系统发育树中,分离物LDGS-6与a . ochraceus位于同一进化支(图2)。为了确定致病性,我们用75%乙醇对20个健康的蓝金银花果实进行表面消毒,然后用蒸馏水清洗。10个果实接种10 μL LDGS-6分生孢子悬浮液(106个孢子/mL), 10个果实接种无菌蒸馏水(对照)。果实在28℃、75%相对湿度的9 cm培养皿中黑暗培养7 d后,接种的果实出现腐烂症状,而对照果实则没有(图1)。实验重复了三次。从接种的果实中分离出致病因子,并根据形态特征和ITS、TUB和LSU测序确定其为原始分离物,而从对照果实中未分离出曲霉样菌株,从而证实了Koch的假设。综上所述,从分子、形态和病原分析来看,A. ochraceus是蓝金银花果实腐病的致病因子(Ou et al. 2024)。国内曾有报道称,在嵊州名(on Prunus salicina var. taoxingli) (Ou et al. 2024)。据我们所知,这是中国首次报道蓝金银花果实采后腐烂病。中国5年以上果树高产年份的年产量可达4万吨左右(Sun et al. 2024),但贮藏受到病原菌感染的挑战。今后的工作重点是监测其发生和传播,制定有效的控制策略。
First Report of Postharvest Fruit Rot Caused by Aspergillus ochraceus on Blue Honeysuckle (Lonicera caerulea L.) Fruit in China.
Blue honeysuckle (Lonicera caerulea L.) plants produce small fruit that are used as food and medicine. In September 2024, 100 kg of blue honeysuckle 'Lanjingling' (China National Plant Variety Protection (CNPVP) 20200389) fruits were harvested in Harbin, China (126.48°E, 45.87°N), and 20% of the fruits showed postharvest fruit rot symptoms, leading to whole-fruit rotting with skin browning and necrotic lesions (Fig. 1. A). Small (1 to 2 mm) samples of infected tissue were obtained from five randomly selected fruits. Samples were surface sterilized with 75% ethanol for 30 s and 5% sodium hypochlorite (NaClO) for 3 min, rinsed three times with sterile distilled water, dried with paper towel, and plated on 9 cm Petri dishes containing potato dextrose agar (PDA). Purified cultures were obtained using the single-spore technique. After 5 d at 28°C, the colonies displayed yellow brown aerial mycelium on the PDA plates (Fig. 1. B, C). Conidiophores were transparent and smooth, while conidial heads were brown and nearly spherical (Fig. 1. D). The entire surface was fertile, producing mostly spherical to subglobose conidia with diameters of 2.12 to 3.24 μm (n = 50) (Fig. 1. E). The internal transcribed spacer region (ITS, included ITS1+5.8S +ITS2, GenBank PQ606583), β-tubulin (TUB, GenBank PQ611757), and nuclear large subunit rRNA (LSU, GenBank PQ620103) genes were partially amplified with their respective primers (ITS1/ITS4 (White et al. 1990), Btub2Fd/Btub4Rd (Glass and Donaldson, 1995) and LROR/LR7 (Rehner and Samuels, 1994). BLAST analysis revealed that the sequences of the three genes showed 99.30 to 100% homology (526/526 nt, 141/142 nt, and 882/882 nt) with the MH859926, AY819971, and MH876373 sequences for isolates of Aspergillus ochraceus. In a phylogenetic tree constructed by Maximum likelihood method based on ITS and TUB sequences, the isolate LDGS-6 was located in the same clade with A. ochraceus (Fig. 2). For pathogenicity, twenty healthy blue honeysuckle 'Lanjingling' fruits were superficially sterilized with 75% ethanol and washed with distilled water. Ten fruits were inoculated with a 10 μL conidial suspension of isolate LDGS-6 (106 spores/mL) and ten with sterile distilled water (control). After fruits were incubated in 9 cm Petri dishes at 28°C and 75% relative humidity in the dark for 7 d, inoculated fruits displayed rot symptoms while control fruits did not (Fig. 1. F and G). The experiment was replicated three times. The causal agent was isolated from inoculated fruits, and it was identified as the original isolate based on morphological traits and ITS, TUB, and LSU sequencing, whereas no Aspergillus-like strains were isolated from control fruits, thus confirming Koch's postulates. In conclusion, based on molecular, morphological, and pathogenic analysis, A. ochraceus is the causal agent of the fruit rot disease on blue honeysuckle fruits (Ou et al. 2024). A. ochraceus was previously reported in China in Shengzhou nane (on Prunus salicina var. taoxingli) (Ou et al. 2024). To our knowledge, this is the first report of postharvest fruit rot caused by A. ochraceus on blue honeysuckle fruits in China. The annual fruit yield production of trees over 5 years old can reach about 40,000 tons during the high-yielding years in China (Sun et al. 2024), but its storage is challenged by pathogen infection. Future work should focus on monitoring its occurrence and spread and developing effective control strategies.
期刊介绍:
Plant Disease is the leading international journal for rapid reporting of research on new, emerging, and established plant diseases. The journal publishes papers that describe basic and applied research focusing on practical aspects of disease diagnosis, development, and management.