Chinese Journal OF Rice Science ›› 2021, Vol. 35 ›› Issue (1): 1-10.DOI: 10.16819/j.1001-7216.2021.0511
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Zhijuan JI, Yuxiang ZENG, Yan LIANG, YANGChangdeng*()
Received:
2020-05-15
Revised:
2020-07-30
Online:
2021-01-10
Published:
2021-01-10
Contact:
YANGChangdeng
通讯作者:
杨长登
基金资助:
Zhijuan JI, Yuxiang ZENG, Yan LIANG, YANGChangdeng. Research and Progress of Bakanae Disease Resistance in Rice[J]. Chinese Journal OF Rice Science, 2021, 35(1): 1-10.
季芝娟, 曾宇翔, 梁燕, 杨长登. 水稻恶苗病抗性研究进展[J]. 中国水稻科学, 2021, 35(1): 1-10.
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URL: http://www.ricesci.cn/EN/10.16819/j.1001-7216.2021.0511
Fig.1. Symptoms of bakanae disease in the field. a, Excessive growing symptom of rice plants in the field; b, Normal seedling and infected seedling with excessive growth and reduced tillers.
交配种群 Mating population | 无性态 Anamorph | 有性态 Teleomorph | 分泌的毒素 Mycotoxin |
---|---|---|---|
MP-C | Fusarium fujikuroi | Gibberellafujikuroi | 串珠镰刀菌素、白僵菌素和伏马毒素Moniliformin, beauvericin, fumonisins |
MP-A | Fusarium verticillioides | Gibberellamoniliformis | 伏马毒素Fumonisins |
MP-D | Fusarium proliferatum | Gibberella intermedia | 伏马毒素、白僵菌素和二倍半萜烯真菌毒素Fumonisins, beauvericin,fusaproliferin |
Table 1 Three kinds of mating populations for the pathogen of bakanae disease.
交配种群 Mating population | 无性态 Anamorph | 有性态 Teleomorph | 分泌的毒素 Mycotoxin |
---|---|---|---|
MP-C | Fusarium fujikuroi | Gibberellafujikuroi | 串珠镰刀菌素、白僵菌素和伏马毒素Moniliformin, beauvericin, fumonisins |
MP-A | Fusarium verticillioides | Gibberellamoniliformis | 伏马毒素Fumonisins |
MP-D | Fusarium proliferatum | Gibberella intermedia | 伏马毒素、白僵菌素和二倍半萜烯真菌毒素Fumonisins, beauvericin,fusaproliferin |
鉴定方法 Evaluation method | 孢子浓度 Spore concentration | 处理条件 Treatment condition | 抗性衡量指标 Resistance index | 啊啊啊啊 aaaa |
---|---|---|---|---|
芽期浸菌接种 Immersing in spore suspension at germinationstage | 100倍显微镜视野下 2000个孢子左右 | 浸菌接种3h | 根据苗期和成株期发病率进行抗性 分级(1~9级) | [22,26] |
560nm波长下20% 和50%透光率 | 30℃下振荡培养浸菌接种24h | 根据5d后的幼苗徒长比率进行抗性 分级(1~5级) | [24] | |
8.8×106个/mL | 30℃下振荡培养浸菌接种24h | 7d后的幼苗徒长比率和苗重比率 | [31] | |
1×105个/mL | 浸菌接种24h | 4周后的幼苗死亡率 | [32] | |
1×105个/mL | 浸菌接种1h | 3周后根据发病严重程度定级0~3级; 病菌再分离定殖率 | [35] | |
立针期喷雾接种 Spraying with spore suspension at vertical-needle-shaped incomplete leaf growing stage | 100倍显微镜视野下 2000个孢子左右 | 喷雾接种2~3次, 菌液用量为250 mL/m2 | 根据苗期和成株期发病率进行抗性 分级(1~9级) | [22,26] |
铺病节诱发 Laying infected straw after sowing | 100倍显微镜视野下 2000个孢子左右 | 将病稻节切成约1cm长, 浸透水, 于播种覆土后立即在土表均匀撒上一层 | 根据苗期和成株期发病率进行抗性 分级(1~9级) | [22,26] |
穗期喷雾接种 Spraying with spore suspension at heading stage | 100倍显微镜视野下 2000个孢子左右 | 在抽穗开花期喷雾接种3次 | 根据苗期和成株期发病率进行抗性 分级(1~9级) | [22,26] |
自然诱发 Inoculating under natural condition | - | 预浸后高温催芽的种子直接播种 | 根据苗期和成株期发病率进行抗性 分级(1~9级) | [22,26] |
干种子直接浸菌接种 Immersing dried seeds in spore suspension directly | 1×106个/mL | 浸菌接种12h | 5d, 10d, 20d, 30d 和 40d后根据发病 严重程度指数定级(0~4级) | [27] |
1×105个/mL | 室温下浸菌接种16h | 种子发芽率、15d和30d的发病率 | [10] | |
1×106个/mL | 26℃浸菌接种3d,每天轻轻振荡4次 | 一个月后的健康植株率 | [11] | |
1×106个/mL | 室温浸菌振荡接种30 min | 种子发芽率、根据3周后发病率进行 抗性分级(1~5级) | [36] | |
1×106个/mL | 室温浸菌接种24h | 幼苗死亡率和徒长比率 | [30] | |
幼苗浸根接种 Immersingseedling roots in spore suspension | 1×106个/mL | 幼苗根部浸菌接种2h | 幼苗死亡率和徒长比率 | [30] |
Table 2 Methods for evaluation of rice bakanae disease resistance.
鉴定方法 Evaluation method | 孢子浓度 Spore concentration | 处理条件 Treatment condition | 抗性衡量指标 Resistance index | 啊啊啊啊 aaaa |
---|---|---|---|---|
芽期浸菌接种 Immersing in spore suspension at germinationstage | 100倍显微镜视野下 2000个孢子左右 | 浸菌接种3h | 根据苗期和成株期发病率进行抗性 分级(1~9级) | [22,26] |
560nm波长下20% 和50%透光率 | 30℃下振荡培养浸菌接种24h | 根据5d后的幼苗徒长比率进行抗性 分级(1~5级) | [24] | |
8.8×106个/mL | 30℃下振荡培养浸菌接种24h | 7d后的幼苗徒长比率和苗重比率 | [31] | |
1×105个/mL | 浸菌接种24h | 4周后的幼苗死亡率 | [32] | |
1×105个/mL | 浸菌接种1h | 3周后根据发病严重程度定级0~3级; 病菌再分离定殖率 | [35] | |
立针期喷雾接种 Spraying with spore suspension at vertical-needle-shaped incomplete leaf growing stage | 100倍显微镜视野下 2000个孢子左右 | 喷雾接种2~3次, 菌液用量为250 mL/m2 | 根据苗期和成株期发病率进行抗性 分级(1~9级) | [22,26] |
铺病节诱发 Laying infected straw after sowing | 100倍显微镜视野下 2000个孢子左右 | 将病稻节切成约1cm长, 浸透水, 于播种覆土后立即在土表均匀撒上一层 | 根据苗期和成株期发病率进行抗性 分级(1~9级) | [22,26] |
穗期喷雾接种 Spraying with spore suspension at heading stage | 100倍显微镜视野下 2000个孢子左右 | 在抽穗开花期喷雾接种3次 | 根据苗期和成株期发病率进行抗性 分级(1~9级) | [22,26] |
自然诱发 Inoculating under natural condition | - | 预浸后高温催芽的种子直接播种 | 根据苗期和成株期发病率进行抗性 分级(1~9级) | [22,26] |
干种子直接浸菌接种 Immersing dried seeds in spore suspension directly | 1×106个/mL | 浸菌接种12h | 5d, 10d, 20d, 30d 和 40d后根据发病 严重程度指数定级(0~4级) | [27] |
1×105个/mL | 室温下浸菌接种16h | 种子发芽率、15d和30d的发病率 | [10] | |
1×106个/mL | 26℃浸菌接种3d,每天轻轻振荡4次 | 一个月后的健康植株率 | [11] | |
1×106个/mL | 室温浸菌振荡接种30 min | 种子发芽率、根据3周后发病率进行 抗性分级(1~5级) | [36] | |
1×106个/mL | 室温浸菌接种24h | 幼苗死亡率和徒长比率 | [30] | |
幼苗浸根接种 Immersingseedling roots in spore suspension | 1×106个/mL | 幼苗根部浸菌接种2h | 幼苗死亡率和徒长比率 | [30] |
QTL | 染色体Chromosome | QTL区间 QTL region/Mb | 定位群体 Mapping population | 群体大小Population size | 群体父母本或类型 Parents or type of population | 啊啊啊啊 aaaa |
---|---|---|---|---|---|---|
qBE1.2 | 1 | 0.30–4.56 | RIL | 159 | 日本晴(粳)/9311(籼) | [31] |
qBK1.4 | 1 | 0.40–0.43 | GWAS | 76 | 来自RDP1的种质资源 | [35] |
qBW1 | 1 | 0.56–5.62 | RIL | 132 | 培矮64S(籼)/9311(籼) | [31] |
qBK1_628091 | 1 | 0.62–1.04 | GWAS | 138 | 41个热带粳稻、97个温带粳稻 | [47] |
qBK1.5 | 1 | 2.25–2.33 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qBK1.2 | 1 | 3.10–3.36 | RIL | 168 | Pusa 1342(籼)/Pusa Basmati 1121(籼) | [45] |
qBK1.3 | 1 | 4.65–8.41 | RIL | 168 | Pusa 1342(籼)/Pusa Basmati 1121(籼) | [45] |
qBE1.1 | 1 | 11.91–13.71 | RIL | 132 | 培矮64S(籼)/9311(籼) | [31] |
qBK1WD | 1 | 13.54–15.13 | RIL | 200 | Wonseadaesoo(粳)/Junam(粳) | [48] |
qBK1.6 | 1 | 22.09–22.25 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qFfR1 | 1 | 22.56–24.10 | F2:F3 | 180 | Nampyeong(粳)/DongjinAD(粳) | [32] |
qBK1.1 | 1 | 23.32–23.34 | RIL | 168 | Pusa 1342(籼)/Pusa Basmati 1121(籼) | [45] |
qBK1.7 | 1 | 23.63–23.64 | GWAS | 76 | 来自RDP1的种质资源 | [35] |
qBK1 | 1 | 23.64–23.67 | NIL | 168 | YR24982-9-1(籼)/Ilpum(粳) | [44, 46] |
qB1 | 1 | 34.10–34.95 | DH | 120 | 春江06/TN1 | [43] |
qBK3.1 | 3 | 21.43–21.78 | RIL | 168 | Pusa 1342(籼)/Pusa Basmati 1121(籼) | [45] |
qBK3.2 | 3 | 27.48–27.64 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qBE3 | 3 | 28.68–35.77 | RIL | 159 | 日本晴(粳)/9311(籼) | [31] |
qBW3 | 3 | 34.95–35.60 | RIL | 132 | 培矮64S(籼)/9311(籼) | [31] |
qBK4.1 | 4 | 22.37–22.43 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qBK4_31750955 | 4 | 31.16–31.75 | GWAS | 138 | 41个热带粳稻、97个温带粳稻 | [47] |
qBK6.1 | 6 | 3.28–3.64 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qBK6.2 | 6 | 4.87–5.06 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qBW6 | 6 | 24.40–25.88 | RIL | 132 | 培矮64S(籼)/9311(籼) | [31] |
qBK6.3 | 6 | 25.30–25.64 | GWAS | 76 | 来自RDP1的种质资源 | [35] |
qBK8.1 | 8 | 6.14–6.24 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qBE9 | 9 | 6.38–8.28 | RIL | 132 | 培矮64S(籼)/9311(籼) | [31] |
qFfR9 | 9 | 7.24–7.56 | F2:F3 | 188 | Samgwang(粳)/Junam(粳) | [49] |
qBK10.1 | 10 | 5.68–6.02 | GWAS | 76 | 来自RDP1的种质资源 | [35] |
qBK10.2 | 10 | 6.85–6.86 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qBK10.3 | 10 | 9.09–9.34 | GWAS | 76 | 来自RDP1的种质资源 | [35] |
qB10 | 10 | 18.72–19.23 | DH | 120 | 春江06/TN1 | [43] |
qBK11.1 | 11 | 22.577–22.583 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
Table 3 QTLs related to rice bakanae disease resistance.
QTL | 染色体Chromosome | QTL区间 QTL region/Mb | 定位群体 Mapping population | 群体大小Population size | 群体父母本或类型 Parents or type of population | 啊啊啊啊 aaaa |
---|---|---|---|---|---|---|
qBE1.2 | 1 | 0.30–4.56 | RIL | 159 | 日本晴(粳)/9311(籼) | [31] |
qBK1.4 | 1 | 0.40–0.43 | GWAS | 76 | 来自RDP1的种质资源 | [35] |
qBW1 | 1 | 0.56–5.62 | RIL | 132 | 培矮64S(籼)/9311(籼) | [31] |
qBK1_628091 | 1 | 0.62–1.04 | GWAS | 138 | 41个热带粳稻、97个温带粳稻 | [47] |
qBK1.5 | 1 | 2.25–2.33 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qBK1.2 | 1 | 3.10–3.36 | RIL | 168 | Pusa 1342(籼)/Pusa Basmati 1121(籼) | [45] |
qBK1.3 | 1 | 4.65–8.41 | RIL | 168 | Pusa 1342(籼)/Pusa Basmati 1121(籼) | [45] |
qBE1.1 | 1 | 11.91–13.71 | RIL | 132 | 培矮64S(籼)/9311(籼) | [31] |
qBK1WD | 1 | 13.54–15.13 | RIL | 200 | Wonseadaesoo(粳)/Junam(粳) | [48] |
qBK1.6 | 1 | 22.09–22.25 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qFfR1 | 1 | 22.56–24.10 | F2:F3 | 180 | Nampyeong(粳)/DongjinAD(粳) | [32] |
qBK1.1 | 1 | 23.32–23.34 | RIL | 168 | Pusa 1342(籼)/Pusa Basmati 1121(籼) | [45] |
qBK1.7 | 1 | 23.63–23.64 | GWAS | 76 | 来自RDP1的种质资源 | [35] |
qBK1 | 1 | 23.64–23.67 | NIL | 168 | YR24982-9-1(籼)/Ilpum(粳) | [44, 46] |
qB1 | 1 | 34.10–34.95 | DH | 120 | 春江06/TN1 | [43] |
qBK3.1 | 3 | 21.43–21.78 | RIL | 168 | Pusa 1342(籼)/Pusa Basmati 1121(籼) | [45] |
qBK3.2 | 3 | 27.48–27.64 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qBE3 | 3 | 28.68–35.77 | RIL | 159 | 日本晴(粳)/9311(籼) | [31] |
qBW3 | 3 | 34.95–35.60 | RIL | 132 | 培矮64S(籼)/9311(籼) | [31] |
qBK4.1 | 4 | 22.37–22.43 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qBK4_31750955 | 4 | 31.16–31.75 | GWAS | 138 | 41个热带粳稻、97个温带粳稻 | [47] |
qBK6.1 | 6 | 3.28–3.64 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qBK6.2 | 6 | 4.87–5.06 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qBW6 | 6 | 24.40–25.88 | RIL | 132 | 培矮64S(籼)/9311(籼) | [31] |
qBK6.3 | 6 | 25.30–25.64 | GWAS | 76 | 来自RDP1的种质资源 | [35] |
qBK8.1 | 8 | 6.14–6.24 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qBE9 | 9 | 6.38–8.28 | RIL | 132 | 培矮64S(籼)/9311(籼) | [31] |
qFfR9 | 9 | 7.24–7.56 | F2:F3 | 188 | Samgwang(粳)/Junam(粳) | [49] |
qBK10.1 | 10 | 5.68–6.02 | GWAS | 76 | 来自RDP1的种质资源 | [35] |
qBK10.2 | 10 | 6.85–6.86 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
qBK10.3 | 10 | 9.09–9.34 | GWAS | 76 | 来自RDP1的种质资源 | [35] |
qB10 | 10 | 18.72–19.23 | DH | 120 | 春江06/TN1 | [43] |
qBK11.1 | 11 | 22.577–22.583 | GWAS | 231 | 来自RDP1的种质资源 | [35] |
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