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疫霉菌引起的马铃薯晚疫病在阿拉斯加马铃薯和番茄上的发生情况。

Occurrence of Late Blight Caused by Phytophthora infestans on Potato and Tomato in Alaska.

作者信息

Winton L M, Leiner R H, Krohn A L, Deahl K L

机构信息

USDA-ARS Subarctic Agricultural Research Unit, University of Alaska-Fairbanks, Fairbanks 99775.

Palmer Research and Extension Center, University of Alaska-Fairbanks, Palmer, AK 99645.

出版信息

Plant Dis. 2007 May;91(5):634. doi: 10.1094/PDIS-91-5-0634A.

Abstract

Phytophthora infestans, causal agent of late blight, was included in a list of plant pathogens found in Alaska in 1934 (1). No notes of symptoms, extent of disease, or dates were recorded. The only reference to the location was given as Wrangell, a town in southeast Alaska with subsistence gardening. Neither P. infestans nor late blight was noted again in the state for another 59 years. Late blight first appeared in Alaska's major potato-growing region in south-central Alaska's Matanuska Valley in 1995. Subsequent outbreaks have been sporadic, occurring only in 1998, 2005, and 2006. Each of these outbreaks was identified from rapidly enlarging brown foliar lesions with branched sporangiophores and lemon-shaped sporangia (~25 × 30 μm). The 1995 and 1998 potato late blight outbreaks in Alaska were not sampled extensively nor have they previously been formally reported. We recovered single isolates of P. infestans from symptomatic potato foliage in the 1995 and 1998 outbreaks. In 2005, symptomatic foliage was collected from individual potato plants in 10 commercial fields and from tomato plants in greenhouses at two locations. Sporulating stem and leaf tissue were used to inoculate semiselective rye medium and 147 isolates from potato and six from tomato were recovered. The isolates from the 1995, 1998, and 2005 outbreaks were analyzed to determine genotype at the allozyme loci GPI and PEP (3), mitochondrial haplotype (4), mating type, and metalaxyl sensitivity (2). The 1998 and 2005 outbreaks were similar because both were caused by the relatively aggressive US-11 allozyme genotype and had significant economic impact for commercial potato growers. All 153 isolates from potato and tomato in 2005 displayed the same allozyme pattern as the US-11 genotype, possessed the IIB mitochondrial haplotype, and were mating type A1. Of the 16 isolates tested, all were determined to be metalaxyl resistant because isolates grown on 5 and 100 μg/ml metalaxyl exhibited growth greater than 40% of the unamended control. The 1995 outbreak was caused by the relatively rare US-7 genotype and started so late during the season that economic impact was minimal. Similarly, the 2006 outbreak was noted from only one commercial potato field at the time of harvest in September 2006. However, the genotype of the 2006 isolate has not been determined because the patch was destroyed before adequate samples could be collected. Because the disease occurs so sporadically in Alaska, fungicides are not routinely in use, but it is unlikely that the pathogen has persisted locally between outbreaks. The source of P. infestans is unknown for each of the occurrences in Alaska. However, possible routes include seed potatoes for home gardens or commercial farms, tomato transplants, and retail vegetables shipped to Alaska from out of state. While potato is Alaska's main vegetable crop, there are less than 405 ha (1,000 acres) of potatoes planted in the state, with the majority planted in the Matanuska Valley. To our knowledge, this is the first formal report of P. infestans on both tomato and commercial potato in Alaska. References: (1) E. K. Cash. Plant Dis. Rep. 20:121, 1936. (2) D. E. L. Cooke et al. Plant Pathol. 52:181, 2003. (3) S. B. Goodwin et al. Plant Dis. 79:1181, 1995. (4) G. W. Griffith and D. S. Shaw. Appl. Environ. Microbiol. 64:4007, 1998.

摘要

致病疫霉是晚疫病的病原体,于1934年被列入阿拉斯加发现的植物病原体名单中(1)。当时未记录症状、病害程度或日期。唯一提到的地点是兰格尔,阿拉斯加东南部一个有自给自足园艺的城镇。在该州,致病疫霉和晚疫病在接下来的59年里都未再被提及。1995年,晚疫病首次出现在阿拉斯加中南部马塔努斯卡山谷的主要马铃薯种植区。随后的疫情呈零星发生,仅在1998年、2005年和2006年出现。每次疫情都通过迅速扩大的褐色叶片病斑、具分枝的孢囊梗和柠檬形孢子囊(约25×30μm)得以确认。1995年和1998年阿拉斯加马铃薯晚疫病疫情未进行广泛采样,此前也未正式报道过。我们从1995年和1998年疫情中有症状的马铃薯叶片中分离出了致病疫霉的单个菌株。2005年,从10个商业田地的单个马铃薯植株以及两个地点温室中的番茄植株上采集了有症状的叶片。用产生孢子的茎和叶组织接种半选择性黑麦培养基,从马铃薯中分离出147个菌株,从番茄中分离出6个菌株。对1995年、1998年和2005年疫情分离出的菌株进行分析,以确定其在等位酶位点GPI和PEP(3)、线粒体单倍型(4)、交配型和甲霜灵敏感性(2)方面的基因型。1998年和2005年的疫情相似,因为两者均由相对具有侵袭性的US - 11等位酶基因型引起,对商业马铃薯种植者造成了重大经济影响。2005年从马铃薯和番茄中分离出的所有153个菌株都显示出与US - 11基因型相同的等位酶模式,具有IIB线粒体单倍型,交配型为A1。在测试的16个菌株中,所有菌株都被确定为对甲霜灵耐药,因为在含有5μg/ml和100μg/ml甲霜灵的培养基上生长的菌株,其生长量大于未添加甲霜灵对照的40%。1995年的疫情由相对罕见的US - 7基因型引起,且在生长季后期才开始,因此经济影响最小。同样,2006年的疫情仅在2006年9月收获时在一个商业马铃薯田被发现。然而,由于在采集到足够样本之前该地块已被破坏,2006年分离菌株的基因型尚未确定。由于该病在阿拉斯加发生极为零星,杀菌剂未常规使用,但病原体在疫情爆发之间在当地持续存在的可能性不大。阿拉斯加每次致病疫霉出现的来源不明。然而,可能的传播途径包括家庭菜园或商业农场的种薯、番茄秧苗以及从州外运到阿拉斯加的零售蔬菜。虽然马铃薯是阿拉斯加的主要蔬菜作物,但该州种植的马铃薯面积不足405公顷(1000英亩),大部分种植在马塔努斯卡山谷。据我们所知,这是阿拉斯加关于致病疫霉在番茄和商业马铃薯上的首次正式报道。参考文献:(1)E. K. Cash。植物病害报告20:121,1936年。(2)D. E. L. Cooke等人。植物病理学52:181,2003年。(3)S. B. Goodwin等人。植物病害79:1181,1995年。(4)G. W. Griffith和D. S. Shaw。应用与环境微生物学64:4007,1998年。

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