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相似文献

1
First Report of Bacterial Canker of Pecan Caused by Pseudomonas syringae pv. syringae in China.丁香假单胞菌丁香致病变种引起的山核桃细菌性溃疡病在中国的首次报道
Plant Dis. 2022 Oct 28. doi: 10.1094/PDIS-08-22-1842-PDN.

丁香假单胞菌丁香致病变种引起的山核桃细菌性溃疡病在中国的首次报道

First Report of Bacterial Canker of Pecan Caused by Pseudomonas syringae pv. syringae in China.

作者信息

Gao Xian, Zhu Cancan, Zhuo Keer, Zhao Wenjun, Na R, Ma Longhai, Lu Xiaomei, Tian Yanli, Hu Baishi, Zhao Yuqiang

机构信息

Nanjing Agricultural University, 70578, Nanjing, Jiangsu, China;

Institute of Botany Jiangsu Province and Chinese Academy of Sciences, 101674, Nanjing, Jiangsu, China;

出版信息

Plant Dis. 2022 Oct 28. doi: 10.1094/PDIS-08-22-1842-PDN.

DOI:10.1094/PDIS-08-22-1842-PDN
PMID:36306441
Abstract

Pecan (Carya illinoinensis) is a world-famous nut tree that is widely cultivated in China, especially in Jiangsu Province (Zhang et al. 2015). In April 2022, cankers on trunks were recorded in pecan (cv. Pawnee) fields located in Taizhou (32°27'58″ N, 120°0'49″ E), Jiangsu. Cankers on the trunks resulted in wilt of the plants. Usually, the color of infected bark on the trunk became darker than the healty bark. When the outer bark was peeled away, the inner tissues were water-soaked, often with reddish streaks. In the surveyed orchards, disease incidence ranged from 10 to 20% among young saplings (about 200 three-year-old trees). While no fungal mycelium or spores were found in the diseased areas by microscope, bacterial colonies were isolated by surface-sterilizing small fragments (25 mm2) of symptomatic tissue in 0.5% NaOCl, rinsing the sections twice in sterilized water, and then streaking them on Luria-Bertani (LB) plates. More than 20 bacterial isolates were obtained and all isolates induced a hypersensitive response on Nicotiana tabacum. All isolates were fluorescent on King's medium B, and were gram-negative based on lysis by KOH. Isolates were positive for levan formation, negative for oxidase and arginine dihydrolase, and did not cause soft rot on potato slices. Based on above information, the isolates thus belonged to Lelliot's LOPAT group 1, P. syringae (Lelliott and Stead 1988). The 16S rRNA sequences of five representative isolates (accession numbers OP175939-OP175943) were amplified by PCR, sequenced, and compared with the NCBI GenBank database (Weisburg et al. 1991; Sarkar and Guttman 2004), finding a 99.92% genetic similarity with a previously reported 16S rRNA sequence of a Pseudomonas syringae pv. syringae (Pss) isolate (accession numbers NW389777). Additional housekeeping genes gap1(accession numbers OP186937-OP186941), rpoD (accession numbers OP186952-OP186956), gyrB (accession numbers OP186947-OP186951), and gltA (accession numbers OP186942-OP186946) were PCR-amplified and sequenced as reported by Hwang et al. (2005), followed by multilocus sequence typing analysis (MLSA). Molecular phylogenetic trees (MEGA vesion 6.0, maximum likelihood with Jukes-Cantor model, 1,000 bootstraps) were generated based on each of these five DNA regions and revealed that all five isolates were clustered together with the strains in P. syringae genomospecies 2, and grouped these isolates with Pss in the PAMDB database (Hwang et al. 2005). As a result, these isolates were identified as Pss. Pathogenicity on pecan (cv. Pawnee) was confirmed by cutting the trunks of two-year-old pecan trees with sterilized blades dipped in cell suspensions containing 107 CFU/ml of each isolate. Plants inoculated in a similar manner with sterile water served as negative controls. The inoculated plants were incubated in a greenhouse maintained at 25°C and 80% relative humidity. After 7 to 8 days, all inoculated plants showed the symptoms of necrosis previously described for the original field plants, while the control plants did not show symptoms. The bacteria reisolated from the inoculated plants were identified as Pss using the LOPAT tests. These results and the sequence analysis of the 16S rRNA and four housekeeping genes described above, fulfilled Koch's postulates. No target bacteria were isolated from the control plants. To our knowledge, this is the first report of Pseudomonas syringae pv. syringaecausing bacterial canker of pecan worldwide. The identification of this pathogen will allow the study of strategies for managing the disease. References: Hwang, M. S., et al. 2005. Applied and Environmental Microbiology, 71:5182-5191. Lelliott, R. A., and Stead, D. E. 1988. Blackwell Scientific, Sussex, UK. Sarkar, S. F., and Guttman, D. S. 2004. Applied and Environmental Microbiology, 70:1999. Weisburg, W. G., et al. 1991. Journal of Bacteriology, 173: 697. Zhang, R., et al. 2015. Scientia Horticulturae, 197: 719-727. The author(s) declare no conflict of interest. Keywords: Carya illinoinensis, Pseudomonas syringae, Canker, Identification †Indicates the corresponding author.Y. Q. Zhao; zhaoyuqiang123@126.com.

摘要

山核桃(Carya illinoinensis)是一种世界著名的坚果类树木,在中国广泛种植,尤其是在江苏省(Zhang等人,2015年)。2022年4月,在江苏省泰州市(北纬32°27′58″,东经120°0′49″)的山核桃(品种:波尼)果园中,记录到树干上出现溃疡病。树干上的溃疡导致植株枯萎。通常,树干上受感染树皮的颜色比健康树皮更深。当剥去外层树皮时,内部组织呈水渍状,常有红色条纹。在调查的果园中,幼树(约200棵三年生树)的发病率在10%至20%之间。虽然在患病区域通过显微镜未发现真菌菌丝体或孢子,但通过将有症状组织的小片段(25平方毫米)在0.5%次氯酸钠中进行表面消毒、在无菌水中冲洗两次,然后在Luria-Bertani(LB)平板上划线,分离出了细菌菌落。获得了20多个细菌分离株,所有分离株在烟草上均引发过敏反应。所有分离株在King氏培养基B上呈荧光,基于氢氧化钾裂解试验为革兰氏阴性。分离株在形成果聚糖方面呈阳性,氧化酶和精氨酸双水解酶呈阴性,并且在土豆片上不引起软腐。基于上述信息,这些分离株属于Lelliot的LOPAT第1组,丁香假单胞菌(Lelliott和Stead,1988年)。通过PCR扩增了五个代表性分离株(登录号OP175939 - OP175943)的16S rRNA序列,进行测序,并与NCBI GenBank数据库进行比较(Weisburg等人,1991年;Sarkar和Guttman,2004年),发现与先前报道的丁香假单胞菌丁香致病变种(Pss)分离株的16S rRNA序列(登录号NW389777)有99.92%的遗传相似性。按照Hwang等人(2005年)的方法,PCR扩增并测序了另外一些管家基因gap1(登录号OP186937 - OP186941)、rpoD(登录号OP186952 - OP186956)、gyrB(登录号OP186947 - OP186951)和gltA(登录号OP186942 - OP186946),随后进行多位点序列分型分析(MLSA)。基于这五个DNA区域中的每一个生成了分子系统发育树(MEGA版本6.0,采用Jukes - Cantor模型的最大似然法,1000次重复抽样),结果显示所有五个分离株与丁香假单胞菌基因组种2中的菌株聚集在一起,并在PAMDB数据库中将这些分离株与Pss归为一组(Hwang等人,2005年)。因此,这些分离株被鉴定为Pss。通过用蘸有含每种分离株10⁷CFU/ml细胞悬液的无菌刀片切割两年生山核桃树的树干,证实了其对山核桃(品种:波尼)的致病性。以类似方式用无菌水接种的植株作为阴性对照。将接种的植株在保持在25°C和80%相对湿度的温室中培养。7至8天后,所有接种的植株均表现出先前在田间原始植株中描述的坏死症状,而对照植株未表现出症状。从接种植株中重新分离出的细菌通过LOPAT试验鉴定为Pss。上述结果以及16S rRNA和四个管家基因的序列分析,满足了柯赫法则。对照植株未分离到目标细菌。据我们所知,这是世界上首次报道丁香假单胞菌丁香致病变种引起山核桃细菌性溃疡病。该病原菌的鉴定将有助于研究该病的防治策略。参考文献:Hwang, M. S.,等人,2005年。《应用与环境微生物学》,71:5182 - 5191。Lelliott, R. A.,和Stead, D.E.,1988年。英国苏塞克斯布莱克韦尔科学出版社。Sarkar, S.F.,和Guttman, D.S.,2004年。《应用与环境微生物学》,70:1999。Weisburg, W.G.,等人,1991年。《细菌学杂志》,173: 697。Zhang, R.,等人,2015年。《园艺学报》,197: 719 - 727。作者声明无利益冲突。关键词:山核桃、丁香假单胞菌、溃疡病、鉴定 †表示通讯作者。Y.Q. Zhao;zhaoyuqiang123@126.com