Baysal-Gurel F, Cinar A
Department of Plant Pathology, The Ohio State University, OARDC, Wooster, OH 4469.
Department of Plant Protection, Faculty of Agriculture, Cukurova University, Balcali, Adana, Turkey 01330.
Plant Dis. 2014 Oct;98(10):1439. doi: 10.1094/PDIS-05-14-0463-PDN.
Citrus rootstocks, Carrizo citrange (Citrus sinensis [L.] Osb. × Poncirus trifoliata [L.] Raf.) and sour orange (C. aurantium L.) grown in containers filled with 5 liters of potting mix of 40% peat and 60% volcanic tuff declined in a 0.2-ha commercial nursery in Adana, Turkey, between 2004 and 2007. Seedlings with symptoms of root rot were found with an average disease incidence of 20% among 1,000 Carrizo citrange seedlings and 10% among 15,000 sour orange seedlings. The potting mixture preparation unit was located next to an oak tree (Quercus sp.) showing symptoms of Armillaria root rot. Six- to 12-month-old seedlings of both rootstocks were stunted and the crowns were necrotic with the presence of white mycelium. Mycelial fans were observed beneath the bark of infected roots and they expanded into the crown. The root systems and nearby potting mix contained rhizomorphs. Thus, Armillaria spp. was suspected as a possible causal agent. Three diseased crowns and three rhizomorphs were surface-sterilized with 1% NaClO for 1 min and cultured on benomyl-dichloran-streptomycin containing selective medium (3) at 25°C in the dark for 1 week. Six isolates transferred to 1.5% malt extract agar at 33°C in the dark for 7 weeks consistently yielded abundant aerial hyphae and mean diameter growth range was 4 to 21 mm and the mycelium margin was regular (1). To confirm pathogen identity, total DNA was extracted using the PowerSoil DNA Isolation Kit (MO BIO Laboratories, Inc., CA) directly from 7-day-old cultures grown in potato dextrose broth (PDB). The ribosomal DNA internal transcribed spacer (ITS) region was amplified by PCR using the primer pair ITS1 and ITS4 (5) and sequenced. The sequences were 99% identical to that of Armillaria mellea isolates from Japan (AB510880) and China (KF032535). This confirmed the identity of the causal agent as A. mellea (Vahl.) P. Kumm. Ten 3-month-old seedlings of Carrizo citrange and sour orange were transplanted into steam-sterilized potting mix and inoculated with wood pieces of oak (Quercus sp.) colonized by the fungus (two pieces for each container) (2). The oak wood pieces were sterilized prior to the colonization by the pathogen. Plants were maintained in a greenhouse (23 to 25°C) until symptoms appeared. Ten non-inoculated seedlings from each rootstock served as controls and were maintained in the same environment. After 4 months, the crowns of the seedlings developed necrotic areas and root systems contained rhizomorphs on all inoculated seedlings and fungus was re-isolated from crowns and rhizomorphs. All control plants remained disease-free and no fungus was re-isolated. A. mellea was reported to infect citrus rootstocks in Spain in 1999 (4). To our knowledge, this is the first report of Armillaria root rot caused by A. mellea infecting Carrizo citrange and sour orange rootstocks in Turkey. This indicates that citrus rootstocks could be at risk for infection and sterilization of the potting mix and good sanitation practices in nurseries are very important. References: (1) J. N. Bruhn et al. Mycopathologia 142:89, 1998. (2) F. M. Grasso et al. Plant Dis. 91:1517, 2007. (3) T. C. Harrington et al. Page 81 in: Methods for Research on Soilborne Phytopathogenic Fungi. APS Press, St. Paul, MN, 1992. (4) J. J. Tuset et al. Bol. San. Veg. Plagas 25: 491, 1999. (5) T. J. White et al. Page 315 in: PCR Protocols: A Guide to Methods and Applications. Academic Press, San Diego, 1990.
2004年至2007年期间,在土耳其阿达纳一个0.2公顷的商业苗圃中,种植在装有5升由40%泥炭和60%火山凝灰岩组成的盆栽混合料容器中的卡里佐枳橙(Citrus sinensis [L.] Osb. × Poncirus trifoliata [L.] Raf.)和酸橙(C. aurantium L.)柑橘砧木出现衰退。在1000株卡里佐枳橙幼苗中,发现有根腐症状的幼苗,平均发病率为20%;在15000株酸橙幼苗中,发病率为10%。盆栽混合料制备单元位于一棵显示蜜环菌根腐症状的橡树(Quercus sp.)旁边。两种砧木6至12个月大的幼苗生长受阻,树冠坏死,有白色菌丝体。在受感染根部的树皮下方观察到菌丝扇,并延伸到树冠。根系和附近的盆栽混合料中含有菌索。因此,怀疑蜜环菌属是可能的致病因子。将三个患病树冠和三个菌索用1%次氯酸钠进行表面消毒1分钟,并在含有苯菌灵-敌菌丹-链霉素的选择性培养基(3)上于25°C黑暗条件下培养1周。将六个分离物转移到1.5%麦芽提取物琼脂上,于33°C黑暗条件下培养7周,始终产生丰富的气生菌丝,平均直径生长范围为4至21毫米,菌丝边缘规则(1)。为了确认病原体身份,使用PowerSoil DNA提取试剂盒(MO BIO Laboratories, Inc., CA)直接从在马铃薯葡萄糖肉汤(PDB)中培养7天的培养物中提取总DNA。使用引物对ITS1和ITS4(5)通过PCR扩增核糖体DNA内部转录间隔区(ITS)区域并进行测序。这些序列与来自日本(AB510880)和中国(KF032535)的蜜环菌分离物的序列99%相同。这证实了致病因子为蜜环菌(Vahl.)P. Kumm。将十株3个月大的卡里佐枳橙和酸橙幼苗移植到蒸汽灭菌的盆栽混合料中,并用被该真菌定殖的橡木(Quercus sp.)木块接种(每个容器两块)(2)。橡木木块在被病原体定殖之前进行了消毒。将植物置于温室(23至25°C)中直至出现症状。每种砧木的十株未接种幼苗作为对照,置于相同环境中。4个月后,所有接种幼苗的树冠都出现坏死区域,根系含有菌索,并且从树冠和菌索中再次分离出真菌。所有对照植物均未发病,也未再次分离出真菌。1999年在西班牙报道蜜环菌感染柑橘砧木(4)。据我们所知,这是土耳其首次报道由蜜环菌引起的蜜环菌根腐病感染卡里佐枳橙和酸橙砧木。这表明柑橘砧木可能有感染风险,盆栽混合料的灭菌以及苗圃中的良好卫生措施非常重要。参考文献:(1)J. N. Bruhn等人,《真菌病理学》142:89,1998年。(2)F. M. Grasso等人,《植物病害》91:1517,2007年。(3)T. C. Harrington等人,载于《土传植物病原真菌研究方法》第81页。APS出版社,明尼苏达州圣保罗,1992年。(4)J. J. Tuset等人,《植物病虫害防治通报》25:491,1999年。(5)T. J. White等人,载于《PCR协议:方法与应用指南》第315页。学术出版社,圣地亚哥,1990年。