Vrandečić K, Jurković D, Ćosić J, Stanković I, Vučurović A, Krstić B, Bulajić A
Faculty of Agriculture, Kralja Petra Svačića 1d, 31000 Osijek, Croatia.
Institute of Plant Protection, Department of Phytopathology, University of Belgrade-Faculty of Agriculture, Nemanjina 6, 11080 Belgrade, Serbia. This research was supported by grants of the Ministry of Science, Education and Sports of the Republic of Croatia and III-43001 of the Ministry of Education and Science, Republic of Serbia.
Plant Dis. 2012 Nov;96(11):1698. doi: 10.1094/PDIS-05-12-0512-PDN.
Sunflower (Helianthus annus L.) is the most important oilseed crop in Croatia. In August 2009, in six localities of eastern Croatia, severe foliar and stem blight symptoms were observed on several genotypes with disease incidence ranging from 10 to 50%. At the initial stage of the infection, irregular to oval, brown spots different in size, surrounded by a chlorotic halo, appeared on the leaves that gradually became enlarged and coalesced, and whole leaves turned yellow and necrotic, followed by defoliation. Lesions on the stems were light to dark brown, randomly distributed, rounded and tapered on the ends; later becoming large and elongated causing stem breakage. Tissue within the lesion was reddish on the cross section. To determine the causal agent, small pieces of symptomatic leaves and stem tissue of sunflower were surface disinfested and placed on potato dextrose agar. A total of 17 isolates from leaves as well as six from stems were obtained and all formed cottony, dark olivaceous to black colonies under 12 h of fluorescent light per day. All isolates formed uniform solitary, pale brown to brown, long ovoid conidia with five to eight transverse and one to two longitudinal septa. The conidia of all isolates were slightly constricted at the transverse septa, measuring 55 to 90 × 14 to 20 μm. Based on the morphological characteristics, the pathogen was identified as Alternaria helianthiinficiens E.G. Simmons, Walcz & R.G. Roberts (4). The pathogenicity was tested with one representative isolate (Alt5) by injection of a conidial suspension (106 conidia/ml) into stems of 20 healthy sunflower seedlings and by spraying 20 non-wounded detached leaves with a suspension of spores. Small necrotic spots on all inoculated seedlings and leaves formed 5 and 9 days after inoculation, respectively. The control sunflower seedlings and detached leaves, inoculated with sterile water, showed no reactions. The identity of isolate Alt5 was futher confirmed by amplification and sequencing of the internal transcribed spacer (ITS) region of rDNA. Because there are no available corresponding ITS sequences of A. helianthiinficiens in the GenBank, reference type strain CBS 208.86 (publicly purchased, CBS, Utrecht, Netherlands) was also sequenced in this study. Total DNA was extracted directly from fungal mycelium and PCR amplification and sequencing were performed with primers ITS1F/ITS4. Sequence analysis of ITS region revealed 100% nucleotide identity between isolate Alt5 (GenBank Accession No. JX101648) and isolate CBS 208.86 (GenBank Accession No. JX101649). The nucleotide identity of both isolates compared with A. helianthi (HM449991), another sunflower pathogenic fungus, was only 80%. A. helianthiinficiens has previously been reported on sunflower in Hungary and the USA (3), Serbia (1), and Korea (2). However, to our knowledge, this is the first report of A. helianthiinficiens occurrence in Croatia as a new and harmful parasite of sunflower, illustrating an expansion of its geographical range and underscoring the need for phytosanitary control because it is a seedborne fungus. References: (3) M. Aćimović and N. Lačok. Helia 14:129, 1991. (4) H. S. Cho and S. H. Yu. Plant Pathol. J. 16:331, 2000. (2) E. G. Simmons. Mycotaxon 25:203, 1986. (1) E. G. Simmons. Alternaria: An Identification Manual. CBS Fungal Biodiversity Centre, Utrecht, the Netherlands, 2007.
向日葵(Helianthus annus L.)是克罗地亚最重要的油料作物。2009年8月,在克罗地亚东部的六个地区,在几种基因型上观察到严重的叶部和茎部枯萎症状,发病率在10%至50%之间。在感染初期,叶片上出现不规则至椭圆形、大小不一的褐色斑点,周围有褪绿晕圈,斑点逐渐扩大并融合,整片叶子变黄坏死,随后落叶。茎上的病斑为浅褐色至深褐色,随机分布,两端圆形且逐渐变细;后来病斑变大并拉长,导致茎折断。病斑内的组织在横切面上呈红色。为了确定病原菌,将向日葵有症状的叶片和茎组织小块进行表面消毒,然后置于马铃薯葡萄糖琼脂上。从叶片上共获得17个分离株,从茎上获得6个分离株,所有分离株在每天12小时荧光灯下均形成棉絮状、深橄榄色至黑色菌落。所有分离株均形成均匀的单个、浅褐色至褐色、长卵形分生孢子,有五至八个横隔和一至两个纵隔。所有分离株的分生孢子在横隔处略有收缩,大小为55至90×14至20μm。根据形态特征,该病原菌被鉴定为向日葵链格孢(Alternaria helianthiinficiens E.G. Simmons, Walcz & R.G. Roberts (4))。用一个代表性分离株(Alt5)进行致病性测试,将分生孢子悬浮液(106个分生孢子/毫升)注射到20株健康向日葵幼苗的茎中,并将孢子悬浮液喷洒到20片未受伤的离体叶片上。接种后5天和9天,所有接种的幼苗和叶片上分别形成小坏死斑。接种无菌水的对照向日葵幼苗和离体叶片无反应。通过对rDNA的内部转录间隔区(ITS)进行扩增和测序,进一步确认了分离株Alt5的身份。由于GenBank中没有向日葵链格孢的相应ITS序列,本研究还对参考模式菌株CBS 208.86(公开购买,CBS,荷兰乌得勒支)进行了测序。直接从真菌菌丝体中提取总DNA,并用引物ITS1F/ITS4进行PCR扩增和测序。ITS区域的序列分析显示,分离株Alt5(GenBank登录号JX101648)与分离株CBS 208.86(GenBank登录号JX101649)之间的核苷酸同一性为100%。与另一种向日葵致病真菌向日葵链格孢(A. helianthi,HM449991)相比,这两个分离株的核苷酸同一性仅为80%。此前在匈牙利、美国(3)、塞尔维亚(1)和韩国(2)的向日葵上已报道过向日葵链格孢。然而,据我们所知,这是向日葵链格孢在克罗地亚作为向日葵新的有害寄生菌出现的首次报道,表明其地理范围在扩大,并强调了进行植物检疫控制的必要性,因为它是一种种传真菌。参考文献:(3)M. Aćimović和N. Lačok。Helia 14:129,1991。(4)H. S. Cho和S. H. Yu。植物病理学杂志16:331,2000。(2)E. G. Simmons。Mycotaxon 25:203,1986。(1)E. G. Simmons。链格孢属:鉴定手册。CBS真菌生物多样性中心,荷兰乌得勒支,2007。