Carstens E, Linde C C, Slabbert R, Miles A K, Donovan N J, Li H, Zhang K, Dewdney M M, Rollins J A, Glienke C, Schutte G C, Fourie P H, McLeod A
First, twelfth, and thirteenth authors: Department of Plant Pathology, Stellenbosch University, Private Bag X1, Matieland, 7601, South Africa; first, eleventh, and twelfth authors: Citrus Research International, PO Box 28, Nelspruit, 1200, South Africa; second author: Evolution, Ecology and Genetics, Research School of Biology, Building 116, Daley Rd, Australian National University, Canberra, ACT 2601, Australia; third author: Central Analytical Facilities, Stellenbosch University, Private Bag X1, Matieland, 7601, South Africa; fourth author: Centre for Plant Science, Queensland Alliance for Agricultural and Food Innovation, The University of Queensland, Brisbane, Queensland 4072, Australia; fifth author: New South Wales Department of Primary Industries, Elizabeth Macarthur Agricultural Institute, Private Bag 4008, Narellan, NSW 2567, Australia; sixth author: Biotechnology Institute, Zhejiang University, Hangzhou 310058, China; seventh and eighth authors: Citrus Research and Education Center, University of Florida, Lake Alfred 33850; ninth author: Department of Plant Pathology, University of Florida, Gainesville; and tenth author: Department of Genetics, Universidade Federal do Paraná, Curitiba, Paraná, Brazil.
Phytopathology. 2017 Jun;107(6):758-768. doi: 10.1094/PHYTO-08-16-0292-R. Epub 2017 Apr 11.
The citrus pathogen Phyllosticta citricarpa was first described 117 years ago in Australia; subsequently, from the summer rainfall citrus-growing regions in China, Africa, and South America; and, recently, the United States. Limited information is available on the pathogen's population structure, mode of reproduction, and introduction pathways, which were investigated by genotyping 383 isolates representing 12 populations from South Africa, the United States, Australia, China, and Brazil. Populations were genotyped using seven published and eight newly developed polymorphic simple-sequence repeat markers. The Chinese and Australian populations had the highest genetic diversities, whereas populations from Brazil, the United States, and South Africa exhibited characteristics of founder populations. The U.S. population was clonal. Based on principal coordinate and minimum spanning network analyses, the Chinese populations were distinct from the other populations. Population differentiation and clustering analyses revealed high connectivity and possibly linked introduction pathways between South Africa, Australia, and Brazil. With the exception of the clonal U.S. populations that only contained one mating type, all the other populations contained both mating types in a ratio that did not deviate significantly from 1:1. Although most populations exhibited sexual reproduction, linkage disequilibrium analyses indicated that asexual reproduction is important in the pathogen's life cycle.
柑橘病原菌柑桔叶点霉于117年前在澳大利亚首次被描述;随后在中国、非洲和南美洲的夏季降雨柑橘种植区被发现;最近在美国也有发现。关于该病原菌的种群结构、繁殖方式和引入途径的信息有限,为此对代表来自南非、美国、澳大利亚、中国和巴西12个种群的383个分离株进行了基因分型研究。使用7个已发表的和8个新开发的多态性简单序列重复标记对种群进行基因分型。中国和澳大利亚的种群具有最高的遗传多样性,而来自巴西、美国和南非的种群表现出奠基者种群的特征。美国的种群是克隆的。基于主坐标分析和最小生成网络分析,中国的种群与其他种群不同。种群分化和聚类分析显示南非、澳大利亚和巴西之间具有高度的连通性以及可能相关的引入途径。除了仅包含一种交配型的克隆美国种群外,所有其他种群都包含两种交配型,其比例与1:1无显著偏差。虽然大多数种群表现出有性繁殖,但连锁不平衡分析表明无性繁殖在该病原菌的生命周期中也很重要。