山东小麦白粉病菌的毒性监测及遗传多样性分析

<正>小麦白粉病在山东各麦区均有发生,一般造成减产10%~50%,严重制约小麦高产。小麦白粉菌群体的研究常采用毒性鉴定法,通过病原菌对不同抗病基因的毒性频率来监测群体毒性的变异(段霞瑜等,1998)。但寄主对相应毒性基因具有选择性,仅凭毒性频率揭示病菌群体结构存在局限性,而ISSR标记可快速高效地检测出基因组DNA的多态性。贾少锋等(2007)首次构建了小麦白粉菌的IS-     

25份北欧小麦抗白粉性评价及抗白粉病基因标记鉴定

采用苗期人工接菌的方法鉴定了25份北欧小麦对河南省7个不同地区小麦白粉病菌分离物的抗性,同时利用与已知抗白粉病基因Pm2、Pm3f、Pm4、Pm6、Pm13、Pm16、Pm21和Pm24连锁的分子标记对其中抗性优良的材料进行基因检测。结果表明,8份材料对所有接种的白粉病菌菌株表现高抗或免疫;其中NGB7476和NGB7809携带Pm4a和Pm16基因, NGB7481和NGB9954携带Pm6和Pm16基因,NGB9955和NGB9956同时携带Pm4a、Pm6和Pm16基因,8份材料均不携带Pm2、Pm3f、Pm4b、Pm13、Pm21 和Pm24基因。     

大麦白粉菌种群毒性监测及抗性材料鉴定

2005和2006年从我国冬大麦区采集和分离大麦白粉菌单胞菌株729个,利用Pallas近等基因系进行致病型鉴定和群体毒性频率分析.同时,利用分离得到的不同致病型菌株,通过抗谱分析的方法鉴定了328份大麦品种(系)的白粉病抗性和抗病基因.结果显示:大麦白粉菌群体对抗病基因Mlal Mla(A12)、Mla3、Mla6 Mla14、Mla7 Mla(No3)、Mla7 Ml(Lg2)、Mla9 Mlk、Mla9、Mlal3 MlaRu3、Mlpl、Mlg(Cp)和mlo5的毒性频率为0;对Mla12 MlaEm2、Mla7 Mlk、Mlat Mla8、Mla10MlaDu2和Mlk1的毒性频率很低,分别为0.1%、0.4%、0.9%、2.8%和4.2%.两年共鉴定出不同的致病型21个,致病型000、001和003在两个年度皆为优势致病型.所鉴定的328份材料绝大多数感病,仅37份抗病材料,能明确推导出抗白粉病基因的品种(品系)很少,这些品种(品系)含有的抗白粉病基因为Mr(Bw)Mla8、Mlg、Mira Mla8、Mla9 Mla1、Mla Mla(A12)和mlo5.     

橡胶树白粉菌Oidium heveae侵染寄主拟南芥的筛选

为筛选出橡胶树白粉菌Oidium heveae Steimnann新的寄主载体,通过接种野生型拟南芥Col-0、突变体Sr1-4D及eds1,观察了橡胶树白粉菌侵染不同拟南芥突变体的过程,PCR扩增测序法验证相关致病基因,构建橡胶树白粉菌-拟南芥互作体系。结果表明,在Col-0、Sr1-4D叶片上面,橡胶树白粉菌产生部分菌丝后停止生长,不能形成典型的橡胶树白粉病症状;但能成功侵染eds1叶片,在叶片的正、背面有银白色辐射状菌丝,后期在病斑上出现一层粉层,表现橡胶树白粉病的典型症状。组织染色和显微观察结果显示,在突变体eds1叶片上橡胶树白粉菌完成了侵染过程。PCR扩增测序结果表明接种后突变体eds1叶片上及组织中病菌均为橡胶树白粉菌;使用橡胶树白粉菌3个致病相关基因作为靶标,验证了eds1和橡胶树上白粉菌基因组中的3个致病相关基因相似度均达到99%~100%。表明橡胶树白粉菌可侵染拟南芥突变体eds1。     

云南省燕麦白粉病病原鉴定及致病力测定

为明确云南省燕麦白粉病病原菌种类及其致病力,结合形态学和分子生物学对其进行鉴定分析,并测定了该病原菌对21个燕麦品种的致病力。结果表明,燕麦白粉病病原菌孢子梗不分支、无色、基部呈球形膨大,顶端生有成串的分生孢子,分生孢子无色,呈长卵圆形、单胞,大小为18.84~29.12μm×6.53~10.71μm,初步鉴定为禾本科布氏白粉菌Blumeria graminis(DC.)Speer;分子生物学鉴定结果表明病原菌rDNA-ITS区序列与禾本科布氏白粉菌燕麦专化型Blumeria graminis f.sp.avenae的同源性为100%,结合形态特征与分子鉴定最终将云南燕麦白粉病菌鉴定为禾本科布氏白粉菌燕麦白粉病菌专化型。致病力测定结果显示,21个供试燕麦品种发病株率为100.00%,病情指数为91.73~100.00,发病初期平均发病株率和病情指数分别为14.56%和1.75,35 d后发病株率和病情指数分别增长了85.44%和95.74%,表明云南省燕麦白粉病菌的致病力强。     

种植模式、种植密度及施肥水平对小麦白粉病发生的影响

小麦白粉病是由布氏白粉菌Blumeria graminis (DC.) Speer.f.sp.tritici Marchal.引起的我国小麦生产上的重要病害。近年来,受品种、病原变异、气候、耕作制度及栽培条件等因素影响,其危害呈逐年加重的趋势,一般可减产5~10%,重病田减产20%以上,已成为制约小麦高产的重要因素^[1]。研究表明,该病菌是一种专性寄生的子囊菌,分生孢子萌发温度范围为0.5~30 ℃,以10~20 ℃最适宜。小麦白粉病流行没有明显的周期性,一般中度或重度流行年后2~5年轻度流行。目前在我国广大小麦产区常采用含三唑酮成分的单剂或混剂进行防治,小麦白粉病菌产生了较为严重的抗药性。本试验在四川雅安小麦产区研究了小麦种植模式、密度及施肥水平对小麦白粉病发生及小麦产量的影响。     

小麦小GTP结合蛋白基因TaRop3克隆及其表达分析

利用同源克隆法从小麦抗条锈病基因Yr5近等基因系（Taichung29*6/Yr5）克隆到编码Rop蛋白基因的全长cDNA序列,并将基因命名为TaRop3（Triticum aestivum Rop3）,聚类分析其所在Rop蛋白家族中的亚组,并利用半定量RT-PCR方法分析其组织表达特异性和不同诱导条件下表达动态。序列分析表明,TaRop3开放阅读框为639 bp,预测编码含213个氨基酸残基Ⅱ型Rop蛋白,C末端具有膜定位基序,与大麦HvRop4和水稻OsRac4聚类在同一亚组。TaRop3基因在小麦幼苗和成株根、茎、叶片和茎节、柱头及花药中均有表达,其中在幼苗及成株茎部表达水平较高。非亲和条锈菌小种CYR17侵染和水杨酸处理诱导TaRop3表达增强,而干旱、高温胁迫以及脱落酸、乙烯利和茉莉酸甲酯处理均降低该基因表达水平。     

华南水稻白叶枯病菌致病性分化检测与分析

为了解华南稻区水稻白叶枯病菌的致病性分化和变异动态,采集华南地区水稻白叶枯病病叶标样分离病原菌,应用中国鉴别寄主IR26、南粳15、爪哇14、特特普、金刚30和国际水稻已知抗病基因的近等基因系IRBB5、IRBB13、IRBB3、IRBB14、IRBB2、IR24两套鉴别寄主,在水稻孕穗期采用剪叶法接种,依据寄主和菌株的互作反应检测病菌的致病性分化。结果显示,参试菌株可划分为Ⅰ、Ⅱ、Ⅲ、Ⅳ、Ⅴ、Ⅸ六个致病型和R1、R2、R3、R4、R5、R8、R10七个致病小种。Ⅴ、Ⅳ致病型和R8、R5小种出现频率分别为27.40%、19.30%和44.67%、15.34%,为华南稻区优势种群。Ⅸ、Ⅴ、Ⅳ致病型和R8、R5小种对500份华南稻区品种资源的致病率依次为96.40%、95.00%、50.40%、62.00%和42.60%;Ⅸ致病型毒性最强且发展很快;强致病菌系Ⅴ型已替代Ⅳ型发展为华南优势致病菌系。     

小麦品种——白粉病菌小种群体互作的研究

 本研究首次采用小麦白粉病菌的一个白色菌株,以其菌落纯白色作为形态标记、对白粉病菌毒性与寄主抗性群体互作进行了研究,在此基础上组建了多小种——多品种群体互作模型,目的在于预测病原菌小种或毒性的消长,为抗病育种和病害的管理提供必要的信息。     

用基因芯片技术分析水稻白叶枯病菌侵染过程的基因表达图谱

水稻白叶枯病是由水稻黄单胞细菌(Xan- thomonas oryzae pv．oryzae,简称Xoo)侵染引起的。对Xoo致病机理的研究已从传统生物学、生理生化学逐渐向分子生物学以及新近发展起来的基因组学方向发展。已经从Xoo中克隆和定性了 vir、avr、hrp等几十个致病相关基因,对这些基因结构和功能的研究,在一定程度上增加了对Xoo 与水稻互作分子基础的认识。然而,病原菌致病过程是一个极其复杂的过程,病原菌需要侵入寄主, 避开寄主的防卫反应,摄取营养,形成有效定殖。这一过程不是一个或几个基因产物所能完成的,而是需要大量的毒性因子在特定的时间、空间进行特异水平的表达,才能实现成功的侵染。为了全面认清病菌的致病机理,仅仅对单个基因的功能进行研究显然是不够的,还需要从整个基因组水平上了解     

Virulence phenotypes in powdery mildew (Blumeria graminis) populations and resistance genes in triticale (x Triticosecale)

Triticale (xTriticosecale) is a new host for powdery mildew (Blumeria graminis) being not infected by this pathogen in Germany before 2001. To evaluate population structure of the pathogen and race-specific resistances in the host, 694 isolates were collected in 12 states of Germany in the years 2007 to 2009 on triticale. They were tested by a newly developed initial differential set of 20 triticale cultivars. Corresponding virulences were found for all differentials except for cultivar Grenado. In total, 272 different virulence phenotypes (=pathotypes) were detected. The virulence complexity of the isolates ranged from 6 to 19 of 20 possible virulences with a mean of 15. In all years, a high level of diversity of the powdery mildew populations was observed with Simpson indices in the range 0.95 to 0.97. The distribution of the pathotypes was even across Germany with an Evenness index in the range 0.82 to 0.88. A set of 19 isolates with different virulence pathotypes and 10 cultivars were selected to be used to identify race-specific resistances of triticale cultivars and breeding lines. Some cultivars susceptible to most of the isolates in seedling stage were moderately resistant in adult-plant stage. The high diversity and complexity of the pathotypes found in German powdery mildew populations as well as an increasing acreage of only a few dominating triticale cultivars accelerate the adaptation of the pathogen to race-specific host resistances suggesting restricted durability only. More durable resistance might be achieved by combining new effective race-specific (qualitative) resistance genes with race-nonspecific (quantitative) resistances effective in the adult-plant stage that are already available.     

2009—2010年河南省小麦白粉菌群体毒性及其遗传多样性分析

利用40个鉴别寄主对河南省5个小麦产区的44个单孢子堆纯化分离的小麦白粉病菌进行毒性鉴定分析,并采用多基因家系法进行了遗传多样性分析。结果显示,供试群体对Pm8、Pm1、Pm3a、Pm3b、Pm3c、Pm3f、Pm3e、Pm5、Pm6、Pm7、Pm17、Pm19、Pm34等抗病基因的毒性频率分别达到90%以上,已不能再作为抗源利用;对Pm12、Pm16、Pm21、Pm18、Pm2、Pm2＋6、Pm2＋MLD、Pm5（Mli）、Pm23、Pm30、Pm4a等基因的毒性频率低于15%,仍可以在抗病育种中加以利用;河南省的小麦白粉病菌存在地理之间的差异,同时病菌在地区之间有自西南向东北/东方向的传播。表明省内群体中存在着丰富的遗传多样性。     

Virulence structure of the <Emphasis Type="Italic">Blumeria graminis</Emphasis> DC.f. sp. <Emphasis Type="Italic">avenae</Emphasis> populations occurring in Poland across 2010–2013

The aim of the present study was to determine the virulence structure of powdery mildew of oats (Blumeria graminis DC.f. sp. avena) in Poland in the years 2010–2013. For this purpose, powdery mildew isolates were collected from three experimental stations in Poland. To assess the virulence of the isolates, eight oat varieties with different responses to the pathogen were used. The results showed that a significant proportion of powdery mildew isolates found in Poland overcame the resistance genes of varieties Bruno (Pm6), Jumbo (Pm1) and Mostyn (Pm3). In contrast, lines Av1860 (Pm4), Am27 (Pm5) and Cc3678 (Pm2) were completely resistant to all pathogen isolates involved in the experiment. Changes constantly occurring in the powdery mildew population perfectly reflect diversity indexes, which were the smallest in the first year of observation, where in the following years these parameters were significantly higher. It is worth noting that the presence of powdery mildew is seasonal and local, which is reflected in the prevalence of the disease in a defined area of the country.     

Racial diversity and complexity in regional populations of Erysiphe graminis f.sp. hordei in France over a 5-year period

The evolution of race patterns in three French regional populations of the barley powdery mildew pathogen Erysiphe graminis f.sp. hordei over a 5-year period showed rapid adaptation to newly introduced host resistance genes. In all three regions, the main change consisted of the replacement of initially abundant races by pathotypes differing markedly from them by their virulence gene combinations. This explained the increase in diversity during the first 3 years of the survey, when the second group of pathotypes became more common in the populations, and its subsequent decrease due to the decline of the first group of races. The mean number of virulence genes per isolate did not vary noticeably over time in the three populations, remaining at about four out of 12 genes tested. However, the distribution of the isolates into virulence complexity classes was greatly modified, fitting a binomial distribution by the end of the study, although significant deviations were apparent in the first 2 years (1986 and 1987). The data indicate that selection, migration and recombination are the most important factors shaping race structure and evolution in powdery mildew populations, and that mutation is of limited significance. No convincing evidence was obtained for the existence of stabilizing selection sensu Vanderplank as the mechanism limiting virulence complexity. Implications regarding spatial and temporal deployment of race-specific resistance genes to control powdery mildew are discussed.     

Virulence phenotypes of Blumeria graminis f. sp. hordei in South Africa

Virulence analysis of 224 isolates of Blumeria graminis f. sp. hordei (barley powdery mildew) from South Africa was performed. The isolates were collected from eight fields and a greenhouse in 2004 and 2007. The isolates were tested for virulence on a set of 20 differential varieties. All isolates were virulent on the resistance genes Mla8 and Ml(Ch) and avirulent for the resistance genes Mla3, Mla6, Mla7, Mla9, Mla13, Mla23, Mlp1 and MlaN81. Virulence frequencies of field isolates for the resistance genes Mla12 + MlaEm2, Mlat, Mla22, Mlk1 and Mlh were 52.9–99.5 % and for Mla1 + MlaAl2, MlLa, Mlra, Mlg + MlCP and Ml(Ru2) were 0.5–23.5 %. In total, 46 pathotypes were detected in the field and seven other pathotypes in the greenhouse. Only nine pathotypes were found in both years, but they included 61.8 % of the isolates. The predominant pathotype represented 15.9 % of the isolates, and was the only one common to all three field populations. The average relative virulence complexity per field isolate increased from 0.405 in 2004 to 0.486 in 2007. Two powdery mildew metapopulations in geographically distant and separated areas (North West and Western Cape) were deduced. The South African population of Blumeria graminis f. sp. hordei had unique virulence frequencies and virulence associations when compared to populations from other parts of the world.     

Gene expression profile and physiological and biochemical characterization of hexaploid wheat inoculated with Blumeria graminis f. sp. tritici

Wheat (Triticum aestivum L.) powdery mildew has direct effects on photosynthesis- and energy-related pathways. Because it is prevalent in Sichuan Province, China, knowledge concerning Pm40-mediated wheat powdery mildew resistance is important for understanding host–pathogen interactions. The aim of this study was to understand physiological changes during the host–pathogen interaction, including gene expression, photosynthetic and chlorophyll fluorescence parameters, chlorophyll content, and antioxidant activity, specific to the resistance response to powdery mildew. The Pm40-expressing L693 and Pm40-deficient L1095 wheat lines were employed for comparison analyses. Fifty-eight and 26 expressed sequence tags (ESTs) were obtained from forward and reverse suppression subtractive hybridization cDNA libraries constructed from Bgt-infected L693 and L1095 leaves, respectively, and 69% of the ESTs in the forward library were related to photosynthesis- and energy metabolism-related pathways. Our data indicate that photosynthesis and carbon metabolism as well as nitrogen metabolism related to photosynthesis are the main pathways involved in Pm40-mediated wheat powdery mildew resistance and that an acetyl CoA-like gene might be a key regulatory factor in these pathways. This study provides new insight into the physiological and genetic mechanisms of resistance to wheat powdery mildew.     

苦瓜白粉病病原菌和生理小种的鉴定及苦瓜对白粉病的抗性遗传分析

为明确海南省苦瓜白粉病的病原菌、生理小种及苦瓜对白粉病的抗性遗传规律,结合形态学鉴定和分子鉴定解析白粉病菌及生理小种种类,通过显微镜观察白粉病菌侵染过程,并应用主基因+多基因混合遗传模型分析法探讨苦瓜对白粉病的主要抗性遗传规律。结果表明:采集自海南省6个市(县)的苦瓜白粉病病原菌均为单囊壳白粉菌Sphaerotheca fuliginea,属生理小种2F,该菌在侵染苦瓜叶片时有4个关键时期:接种后4 h为分生孢子萌发高峰期,8 h为附着孢形成高峰期,16～24 h为次生菌丝形成高峰期,5 d为分生孢子梗形成高峰期。将其接种于苦瓜抗、感品系,对白粉病的抗性符合2对加性-显性-上位性主基因+加性-显性多基因模型,主基因和多基因共同控制苦瓜对白粉病的抗性,其中以主基因遗传为主,且会受到环境变异的影响。根据苦瓜抗性遗传规律,F2代主基因遗传率最高,受环境影响最小,在苦瓜的白粉病抗性育种中,以早期世代F2代作为有效选择世代。研究表明白粉病菌侵染叶片的前2 d是白粉病防治的最佳时期,所以在白粉病易发的物候期,可将防治时间提前1～2 d。     

The Hordeum vulgare subsp. spontaneum–Blumeria graminis f. sp. hordei pathosystem: its position in resistance research and breeding applications

Barley (Hordeum vulgare L.) is an important cereal crop and powdery mildew, caused by Blumeria graminis f. sp. hordei, is one of the most serious diseases that occurs on barley throughout the world. In the Middle East, which is the centre of diversity for barley and its pathogens, the wild barley–powdery mildew pathosystem co-evolves resulting in many specific resistances in the host as well as corresponding virulences in the pathogen. Many specific resistances have been used in European breeding programmes and a centre of pathogen diversity has arisen also especially in central Europe. This short review briefly summarizes the use of host resistances derived from wild barley and land races including the durable resistance gene mlo. The use of powdery mildew pathogenicity for studying new and unknown specific resistances and for identifying resistances in commercial varieties is described. However, highly heterogeneous wild barley is also characterized as a valuable source of minor genes for powdery mildew resistance. These might be exploited by barley breeders especially for winter barley improvement where the non-specific resistance gene mlo cannot be used.     

Is virulence phenotype evolution driven exclusively by Lr gene deployment in French Puccinia triticina populations?

Puccinia triticina is a highly damaging wheat pathogen. The efficacy of leaf rust control by genetic resistance is mitigated by the adaptive capacity of the pathogen, expressed as changes in its virulence combinations (pathotypes). An extensive P. triticina population survey has been carried out in France over the last 30 years, describing the evolutionary dynamics of this pathogen in response to cultivar deployment. We analysed the data set for the 2006–2016 period to determine the relationship between the Lr genes in the cultivars and virulence in the pathotypes. Rust populations were dominated by a small number of pathotypes, with variations in most of the virulence frequencies related to the corresponding Lr gene frequencies in the cultivated landscape. Furthermore, the emergence and spread of a new virulence matched the introduction and use of the corresponding Lr gene (Lr28), confirming that the deployment of qualitative resistance genes is an essential driver of evolution in P. triticina populations. However, principal component analysis (PCA) revealed that certain pathotype–cultivar associations cannot be explained solely by the distribution of Lr genes in the landscape. This conclusion is supported by the predominance of a few pathotypes on some cultivars, with the persistence of several other compatible pathotypes at low frequencies. Specific interactions are not, therefore, sufficient to explain the distribution of virulence in rust populations. The hypothesis that quantitative interactions between P. triticina populations and bread wheat cultivars—based on differences in aggressiveness—is also a driver of changes in pathotype frequencies deserves further investigation.