Weems J D, Ebelhar S A, Chapara V, Pedersen D K, Zhang G R, Bradley C A
Department of Crop Sciences, University of Illinois, Urbana 61801.
Plant Dis. 2011 Oct;95(10):1318. doi: 10.1094/PDIS-02-11-0102.
In September 2009, sunflower (Helianthus annuus L.) plants (cv. Mycogen 8C451) from a University of Illinois field research trial in Fayette County, Illinois exhibited silvery gray girdling lesions on the lower stems and premature death. When lower stems and roots were split open, the pith tissue was compressed into layers. Black microsclerotia (90 to 180 μm) were present on the outside of the lower stem tissue and in the stem vascular tissue. Five pieces (approximately 1 cm long) of symptomatic stem tissue from five different affected plants (25 pieces total) were soaked in a 0.5% solution of NaOCl for 30 s, rinsed with sterile distilled water, and placed on potato dextrose agar (PDA; Becton, Dickinson, and Company, Franklin Lakes, NJ). Gray hyphae grew from all of the stem pieces, which subsequently turned black and formed black microsclerotia (75 to 175 μm). On the basis of plant symptoms and size and color of the microsclerotia, the disease was diagnosed as charcoal rot caused by Macrophomina phaseolina (Tassi) Goid (2). To confirm that the isolated fungus was M. phaseolina, DNA was extracted from the pure culture, and PCR amplification of a subunit rDNA and internal transcribed spacer (ITS) region with primers EF3RCNL and ITS4 was performed (3). The Keck Biotechnology Center at the University of Illinois, Urbana sequenced the PCR product. The resulting nucleotide sequence shared the highest homology (99%) with sequences of M. phaseolina when compared with the subunit rDNA and ITS sequences in the nucleotide database ( http://www.ncbi.nlm.nih.gov ). A greenhouse experiment was conducted to confirm pathogenicity; the greenhouse temperature was approximately 27°C and sunflower plants (cv. Cargill 270) were grown in pots and watered daily to maintain adequate soil moisture for growth. Sterile toothpicks were infested with M. phaseolina and placed through the stems (10 cm above the soil surface) of five 40-day-old sunflower plants that were approximately at growth stage R4 (1,4). Five sterile, noninfested toothpicks were similarly placed through sunflower plants to act as controls. Parafilm was used to hold the toothpick in the stem and seal the stem injury. Thirty-five days after inoculation, the mean lesion length on stems inoculated with M. phaseolina was 595 mm and no lesions developed on the control plants. M. phaseolina-inoculated plants also began to wilt and die. Cultures identical to the original M. phaseolina isolate were reisolated from stem lesions of the M. phaseolina-inoculated plants. This is the first report of charcoal rot on sunflower in Illinois to our knowledge. Sunflower is currently not a major crop grown in Illinois, but on-going research is focused on evaluating sunflower as a potential late-planted crop to follow winter wheat. If sunflower production increases in Illinois, growers may need to take precautions to manage charcoal rot. References: (1) L. K. Edmunds. Phytopathology 54:514, 1964. (2) T. Gulya et al. Page 263 in: Sunflower Technology and Production. American Society of Agronomy, Madison, WI, 1997. (3) N. S. Lord et al. FEMS Microbiol. Ecol. 42:327, 2002. (4) A. A. Schneiter and J. F. Miller. Crop Sci. 21:901, 1981.
2009年9月,伊利诺伊大学在伊利诺伊州费耶特县进行的田间研究试验中的向日葵(Helianthus annuus L.)植株(品种Mycogen 8C451)在茎基部出现银灰色环腐病斑并过早死亡。将茎基部和根部劈开时,髓组织被挤压成层状。在下位茎组织外部和茎维管束组织中存在黑色小菌核(90至180μm)。从五株不同的患病植株上取五片(约1厘米长)有症状的茎组织(共25片),浸泡在0.5%的次氯酸钠溶液中30秒,用无菌蒸馏水冲洗,然后置于马铃薯葡萄糖琼脂(PDA;Becton, Dickinson, and Company, Franklin Lakes, NJ)上。所有茎段均长出灰色菌丝,随后菌丝变黑并形成黑色小菌核(75至175μm)。根据植株症状以及小菌核的大小和颜色,诊断该病为菜豆壳球孢(Macrophomina phaseolina (Tassi) Goid)引起的炭腐病(2)。为确认分离出的真菌是菜豆壳球孢,从纯培养物中提取DNA,并用引物EF3RCNL和ITS4对rDNA亚基和内部转录间隔区(ITS)进行PCR扩增(3)。伊利诺伊大学厄巴纳分校的凯克生物技术中心对PCR产物进行了测序。与核苷酸数据库(http://www.ncbi.nlm.nih.gov)中的菜豆壳球孢亚基rDNA和ITS序列相比,所得核苷酸序列与之具有最高同源性(99%)。进行了温室试验以确认致病性;温室温度约为27°C,向日葵植株(品种Cargill 270)种植在花盆中,每天浇水以保持土壤湿度适宜生长。用无菌牙签接种菜豆壳球孢,插入五株40日龄、处于R4生长阶段(1,4)的向日葵植株的茎中(土壤表面上方10厘米处)。同样将五根无菌、未接种的牙签插入向日葵植株作为对照。用封口膜将牙签固定在茎中并密封茎部伤口。接种后35天,接种菜豆壳球孢的茎上平均病斑长度为595毫米,对照植株未出现病斑。接种菜豆壳球孢的植株也开始枯萎死亡。从接种菜豆壳球孢的植株茎部病斑中重新分离出与原始菜豆壳球孢分离物相同的培养物。据我们所知,这是伊利诺伊州向日葵炭腐病的首次报道。向日葵目前在伊利诺伊州不是主要种植作物,但正在进行的研究重点是评估向日葵作为冬小麦后茬潜在晚播作物的可能性。如果伊利诺伊州向日葵产量增加,种植者可能需要采取预防措施来防治炭腐病。参考文献:(1) L. K. Edmunds. Phytopathology 54:514, 1964. (2) T. Gulya等人。载于:《向日葵技术与生产》第263页。美国农学会,威斯康星州麦迪逊,1997。(3) N. S. Lord等人。FEMS Microbiol. Ecol. 42:327, 2002。(4) A. A. Schneiter和J. F. Miller。作物科学21:901, 1981。