Blomquist C L, Rooney-Latham S, Nolan P A
California Department of Food and Agriculture, Sacramento 95832.
San Diego County Department of Agriculture, San Diego, CA 92123.
Plant Dis. 2009 Sep;93(9):968. doi: 10.1094/PDIS-93-9-0968A.
Sweet basil (Ocimum basilicum) is a culinary herb grown in fields and greenhouses in California. In August of 2008, samples were submitted to the San Diego County Plant Diagnostic Laboratory with a grayish brown, downy growth that covered areas of the abaxial side of the leaf. Early symptoms included leaf chlorosis followed by the appearance of scattered grayish brown conidia and conidiophores in the chlorotic areas. Conidiophore emergence progressed to a grayish brown, velvety growth with some of the chlorotic areas becoming necrotic. Similarly affected plants were submitted to the laboratory from another field 32 km (20 miles) away in the same county. Both fields were drip irrigated and located in inland valleys. Approximately 50 to 60% of the plants were symptomatic. Conidiophores, on the abaxial side of the leaves that were characteristic of Peronospora, branched dichotomously three to five times and measured 390 to 1,100 × 2.5 to 7.0 μm (675.6 × 4.9 μm average). Light brown, globose to ellipsoidal conidia measured 20 to 34 × 18 to 26 μm (26 × 22 μm average). To confirm pathogenicity, three basil plants in 10.2-cm (4-inch) pots were sprayed with a suspension of 4.5 × 10 conidia/ml and incubated in a dew chamber at 20°C for 48 h in the dark. Three noninoculated plants were sprayed with water. Plants were then placed in a growth chamber at 18°C with a 16-h photoperiod. Relative humidity was maintained near 95% by placing the plants over a tray of water and covering each group with a plastic tent. Signs of grayish brown, downy growth were seen approximately 14 days after inoculation. Pathogenicity experiments were repeated once. No symptoms developed on plants sprayed with water. Sequence of the intergenic spacer regions and 5.8S gene was obtained from a sample collected in one field, through amplification with primers DC6 and ITS4 and sequencing with primers ITS6 and ITS4 (2). The sequence (Accession No. FJ436024) from the field sample was identical to GenBank Accession No. AY884605 that represented a Peronospora sp. from basil in Switzerland. On the basis of morphological and sequence information, the Peronospora sp. from San Diego County is most likely the same Peronospora sp. that was identified from sweet basil in Switzerland, Italy (1), and South Africa (4), as well as coleus in New York and Louisiana (3). The basil Peronospora sp. has been shown to be present in seed (1). Since both growers purchased their seed from the same supplier, seeds could have been a possible inoculum source. To our knowledge, this is the first report of a downy mildew on sweet basil in California. References: (1) L. Belbahri et al. Mycol. Res. 109:1276, 2005. (2) D. E. L. Cooke et al. Fungal Genet. Biol. 30:17, 2000. (3) M. L. Daughtrey et al. Plant Dis. 90:1111, 2006. (4) A. McLeod et al. Plant Dis. 90:1115, 2006.
甜罗勒(Ocimum basilicum)是一种在加利福尼亚州的田地和温室中种植的烹饪用香草。2008年8月,一些带有覆盖叶片背面部分区域的灰棕色、绒毛状生长物的样本被提交至圣地亚哥县植物诊断实验室。早期症状包括叶片黄化,随后在黄化区域出现散生的灰棕色分生孢子和分生孢子梗。分生孢子梗的出现发展为灰棕色、天鹅绒状生长,一些黄化区域变为坏死。来自同一县内32公里(20英里)外另一片田地的类似受影响植株也被提交至该实验室。两块田地均采用滴灌,位于内陆山谷。大约50%至60%的植株出现症状。叶片背面具有霜霉属特征的分生孢子梗二叉分枝三至五次,大小为390至1100×2.5至7.0微米(平均675.6×4.9微米)。浅棕色、球形至椭圆形的分生孢子大小为20至34×18至26微米(平均26×22微米)。为确认致病性,将三株种植在10.2厘米(4英寸)花盆中的罗勒植株用浓度为4.5×10个分生孢子/毫升的悬浮液喷雾处理,并在黑暗中于20°C的保湿箱中培养48小时。三株未接种的植株用水喷雾处理。然后将植株放置在温度为18°C、光周期为16小时的生长室中。通过将植株放置在一盘水上并用塑料帐篷覆盖每组植株,使相对湿度保持在95%左右。接种后约14天可见灰棕色、绒毛状生长的症状。致病性实验重复了一次。用水喷雾处理的植株未出现症状。通过使用引物DC6和ITS4进行扩增以及使用引物ITS6和ITS4进行测序,从一片田地采集的样本中获得了基因间隔区和5.8S基因的序列(2)。来自田间样本的序列(登录号FJ436024)与代表来自瑞士罗勒上的一种霜霉属的GenBank登录号AY884605相同。基于形态学和序列信息,圣地亚哥县的这种霜霉属很可能与在瑞士、意大利(1)和南非(4)的甜罗勒以及纽约和路易斯安那州的彩叶草(3)中鉴定出的是同一种霜霉属。已证明罗勒霜霉属存在于种子中(1)。由于两位种植者都从同一供应商购买种子,种子可能是一个潜在的接种源。据我们所知,这是加利福尼亚州甜罗勒上霜霉病的首次报道。参考文献:(1)L. Belbahri等人,《真菌学研究》109:1276,2005年。(2)D. E. L. Cooke等人,《真菌遗传学与生物学》30:17,2000年。(3)M. L. Daughtrey等人,《植物病害》90:1111,2006年。(4)A. McLeod等人,《植物病害》90:1115,2006年。