亚洲免费av电影一区二区三区,日韩爱爱视频,51精品视频一区二区三区,91视频爱爱,日韩欧美在线播放视频,中文字幕少妇AV,亚洲电影中文字幕,久久久久亚洲av成人网址,久久综合视频网站,国产在线不卡免费播放

        ?

        紅江橙可培養(yǎng)內(nèi)生真菌生物多樣性和種群結(jié)構(gòu)分析

        2024-05-29 05:00:47孫鵬王蕓盧冬梅袁紅旭王鋰韞

        孫鵬 王蕓 盧冬梅 袁紅旭 王鋰韞

        摘 要 為探究紅江橙內(nèi)生真菌種群多樣性和群落結(jié)構(gòu),比較紅江橙健株和患黃龍病病株內(nèi)生真菌群落的差異, 采用組織塊分離法從紅江橙的根、莖、葉中分離內(nèi)生真菌,以形態(tài)學(xué)結(jié)合ITS-rDNA 序列分析法進(jìn)行菌株分類(lèi)鑒定,根據(jù)Shannon-Wiener 多樣性指數(shù)、菌株分離的相對(duì)頻率和相似性指數(shù)分析紅江橙內(nèi)生真菌的菌群分布及多樣性。結(jié)果表明,從紅江橙根、莖、葉中分離得到內(nèi)生真菌117株,鑒定歸屬為3綱11目15科18屬,其中炭疽菌屬(Colletotrichum spp.)、鐮刀菌屬(Fusarium spp.)、葉點(diǎn)霉屬(Phyllosticta spp.)、黑孢霉屬 (Nigrospora spp.)和青霉菌屬(Penicillium spp.)為優(yōu)勢(shì)菌群,其相對(duì)分離率分別為58.97%、8.55%、? 8.55%、4.27%、3.42%。植株總體內(nèi)生真菌Shannon-Wiener 多樣性指數(shù)為1.68,總均勻度指數(shù)為0.30,莖與葉、根與葉及根與莖的相似性指數(shù)分別為0.48、0.33、0.32。黃龍病病株與健株內(nèi)生真菌Shannon-Wiener 多樣性指數(shù)有較大差異,健株多樣性指數(shù)除根部略低于病株外,總多樣性指數(shù)和莖、葉的多樣性指數(shù)分別是病株的1.73倍、2.07倍和5.54倍。健株和病株內(nèi)生真菌菌落相似性指數(shù)為0.43,在根、莖、葉部位健病株相似性指數(shù)根部較高為0.75,其次是葉為0.44,莖的最低為0.35。分離得到的內(nèi)生真菌中炭疽菌屬在病株莖、葉中的相對(duì)分離率為77.78%、92.86%,遠(yuǎn)高于其在健株中的相對(duì)分離率54.05%、54.17%。結(jié)果顯示紅江橙內(nèi)生真菌屬類(lèi)豐富,但分布不均勻,其內(nèi)生真菌類(lèi)群分布具有組織特異性?;键S龍病的紅江橙內(nèi)生真菌群落與健株的顯著不同,其內(nèi)生真菌群落總多樣性指數(shù)顯著低于健株,其中葉部降低最顯著,其次為莖部。

        關(guān)鍵詞 紅江橙; 內(nèi)生真菌; 多樣性;黃龍病

        植物內(nèi)生真菌是一類(lèi)生活在植物體內(nèi),不引起宿主明顯病害的真菌[1]。植物內(nèi)生真菌能與植物病原菌產(chǎn)生營(yíng)養(yǎng)競(jìng)爭(zhēng),并產(chǎn)生各種抗菌次級(jí)代謝物質(zhì)[2] 從而提高寄主植株的抗病能力[3],也能提高寄主植株耐鹽、耐干旱或?qū)I(yíng)養(yǎng)不良的抵抗能力[4],促進(jìn)植株的健康生長(zhǎng)[5-8]。反之植株的健康狀況也會(huì)影響內(nèi)生真菌的種群分布和數(shù)量,有研究指出植物內(nèi)生真菌可能在生命周期的某個(gè)階段成為寄主的致病菌[9-13]。因此,了解植物內(nèi)生真菌的種群分布特別是對(duì)應(yīng)健株和病株內(nèi)生真菌的種群分布,對(duì)認(rèn)識(shí)內(nèi)生真菌與寄主生長(zhǎng)的關(guān)系有重要幫助。

        紅江橙是湛江地方特色紅橙品種,具有多汁化渣、酸甜適口的特點(diǎn),在湛江地區(qū)已廣泛種植,但近年來(lái)黃龍病導(dǎo)致紅江橙減產(chǎn)甚至品種退化的情況越來(lái)越嚴(yán)重。黃龍病改變植株根際微生物群落的結(jié)構(gòu)和功能多樣性[14],從而使受根際微生物影響的養(yǎng)分獲取、氮循環(huán)、碳循環(huán)發(fā)生改變[15-16],這種改變將影響到植物內(nèi)生真菌的多樣性及種群結(jié)構(gòu)[17-19] 。本研究擬從紅江橙各組織部位分離純化內(nèi)生真菌,通過(guò)分子生物學(xué)方法進(jìn)行鑒定,系統(tǒng)分析紅江橙各組織部位內(nèi)生真菌的種群分布及多樣性,并對(duì)健株、黃龍病病株不同部位內(nèi)生真菌的種群分布及多樣性進(jìn)行分析,為后續(xù)研究紅江橙內(nèi)生真菌與寄主相互作用及發(fā)現(xiàn)潛在的具備產(chǎn)生抑菌物質(zhì)的菌株提供參考。

        1 材料與方法

        1.1 試驗(yàn)材料

        樣品從廣東省湛江市紅江農(nóng)場(chǎng)(21°62′ N,109°86′E)采集,采用隨機(jī)采樣法,從果園中隨機(jī)挑選8 a以上樹(shù)齡的健康紅江橙植株和典型的黃龍病癥狀植株各15株,取根、莖、葉若干,放入無(wú)菌袋內(nèi)貼上標(biāo)簽,4 ℃存放,并在48 h內(nèi)進(jìn)行菌體分離。

        1.2 內(nèi)生真菌的分離與純化

        樣品的分離方法參考文獻(xiàn)[20]中的方法,將采集的樣品在自來(lái)水下沖洗,除去表面泥土,依次用次氯酸鈉和乙醇進(jìn)行表面消毒,用無(wú)菌水沖洗3遍,最后一次沖洗的無(wú)菌水進(jìn)行表面消毒效果檢查。以無(wú)菌濾紙吸干水分,將根和莖(上部嫩莖)剪成2~3 mm的小段,葉剪成約5 mm×? 5 mm 的小片,剪碎的根、莖、葉樣品分別混合均勻后,隨機(jī)各取50個(gè)于加有鏈霉素(50 mg/L)的 PDA平板上封口28 ℃恒溫培養(yǎng),待長(zhǎng)出菌體后純化至純種。

        1.3 內(nèi)生真菌的鑒定

        采用分子生物學(xué)的方法結(jié)合形態(tài)學(xué)對(duì)純化后的內(nèi)生真菌進(jìn)行鑒定。其中形態(tài)學(xué)鑒定參考《真菌鑒定手冊(cè)》[21] ,分子鑒定中采用通用引物ITS1、 ITS4[22]以直接PCR擴(kuò)增法[23] 參照MightyAmp DNA Polymerase說(shuō)明擴(kuò)增內(nèi)轉(zhuǎn)錄間隔區(qū)序列(Internal transcribed spacer,ITS),擴(kuò)增成功的樣品送上海生工生物工程股份有限公司進(jìn)行序列測(cè)定,測(cè)序成功的序列利用 NCBI 數(shù)據(jù)庫(kù) BLAST 對(duì)序列進(jìn)行相似性分析,同時(shí)使用 ClustalW 進(jìn)行序列比對(duì)、切除, 采用MEGA 7.0構(gòu)建系統(tǒng)發(fā)育樹(shù)。

        1.4 數(shù)據(jù)統(tǒng)計(jì)分析

        用Shannon-Wiener多樣性指數(shù)(H′)來(lái)反映江紅橙內(nèi)生真菌物種多樣性,用相對(duì)分離頻率(RF)衡量某種內(nèi)生真菌的優(yōu)勢(shì)度,用均勻度指數(shù)(E)分析內(nèi)生真菌種群在各部位分布的均勻程度,用相似性指數(shù)(Cs)分析不同部位內(nèi)生真菌組成的相似性程度。具體計(jì)算分別如下式所示。

        H′=-∑kipi×lnpi

        RF=分離到的某種內(nèi)生菌的菌株數(shù)/分離到的內(nèi)生真菌的總株數(shù)

        E= H′/ln(S); Cs=2j/(a+b)

        其中,Pi指第i種內(nèi)生真菌的菌株數(shù)占分離到內(nèi)生真菌菌株總數(shù)的比值;S 為菌株屬數(shù),N 為內(nèi)生真菌總數(shù);j 為兩部位共有的內(nèi)生真菌屬數(shù);a、b是兩個(gè)部位各自有的內(nèi)生真菌屬數(shù)。多樣性指數(shù)和均勻度指數(shù)采用past 3軟件計(jì)算。

        2 結(jié)果與分析

        2.1 紅江橙內(nèi)生真菌種類(lèi)

        從紅江橙樹(shù)不同部位共分離得到內(nèi)生真菌117株(NCBI登錄號(hào)MK399689-399805),對(duì)所有菌株在形態(tài)學(xué)分類(lèi)的基礎(chǔ)上,將其ITS序列與模式菌株ITS序列一起構(gòu)建系統(tǒng)樹(shù)確定其分類(lèi)地位。結(jié)果表明紅江橙內(nèi)生真菌分有3綱11目15科18屬(表1),其中子囊菌綱(Sordariomycetes)6目8科8屬,散囊菌綱(Eurotiomycetes)1目1科2屬,座囊菌綱(Dothideomycetes)4目6科8屬。在分離得到的真菌屬中炭疽菌屬(Colletotrichum spp.)、鐮刀菌屬(Fusarium spp.)、葉點(diǎn)霉屬(Phyllosticta spp.)、黑孢霉屬 (Nigrospora spp.)和青霉菌屬(Penicillium spp.)為優(yōu)勢(shì)菌群,其相對(duì)分離率分別為58.97%、? 8.55%、8.55%、4.27%、3.42%(圖1),其他分離率較高的屬為枝孢屬(Cladosporium spp.)? 2.56%、毛殼菌屬(Arcopilus spp.)1.71% 、曲霉菌屬(Aspergillus spp.)1.71% 、彎孢屬(Curvularia spp.) 1.71%、平臍疣孢屬(Zasmidium spp.)1.71%,而擬莖點(diǎn)霉屬(Phomopsis spp.)、粘帚霉屬(Clonostachys spp.)、木霉屬(Trichoderma spp.)、擬盤(pán)多毛孢屬(Pestalotiopsis spp.)、離蠕孢屬(Bipolaris spp.)、棺孢腔菌屬(Cophinforma spp.)、葡萄座腔菌屬(Botryosphaeria spp.)、短梗霉屬(Aureobasidium spp.)的分離率均為0.85%。

        2.2 紅江橙不同組織部位內(nèi)生真菌的多樣性

        由表2可知,從紅江橙根、莖、葉分別分離出內(nèi)生真菌5、14、7屬,紅江橙內(nèi)生真菌總體Shannon-Wiener 多樣性指數(shù)(H′)1.68,總均勻度指數(shù)0.30,由此可知,紅江橙內(nèi)生真菌種類(lèi)豐富但分布不均勻。根、莖、葉各部位內(nèi)生真菌的Shannon-Wiener多樣性指數(shù)分別為1.32、1.50、1.12,均勻度指數(shù)(E)分別為0.75、0.32、0.44。3個(gè)部位中莖的內(nèi)生真菌屬類(lèi)最豐富,但均勻度指數(shù)最低。莖與葉、根與葉及根與莖的相似性指數(shù)(Cs)分別為0.48、0.33、0.32,3個(gè)部位中內(nèi)生真菌屬的類(lèi)別差異較大。

        2.3 紅江橙健株和黃龍病病株內(nèi)生真菌種類(lèi)和多樣性

        由表3可知,紅江橙中分離得到的炭疽菌屬在健株和病株中的相對(duì)分離率有明顯差別,其在病株的相對(duì)分離率72.92%比健株的相對(duì)分離率49.28%高出23.64%;在病株的根、莖和葉部位炭疽菌屬的相對(duì)分離率分別為14.29%、 77.78%、92.86%,均高于其在健株中各部位的相對(duì)分離率,高出的幅度分別為1.79%、23.73%、38.69%。鐮刀菌屬、葉點(diǎn)霉屬在紅江橙中表現(xiàn)出一定的組織部位寄生性,鐮刀菌屬主要出現(xiàn)在根部,莖葉中僅少量分布,且其在健株的相對(duì)分離率高于病株;葉點(diǎn)霉屬只在莖、葉分離得到,且其在健株和病株中的相對(duì)分離率沒(méi)有明顯差異,根部未分離出。

        由表4可知,紅江橙健株內(nèi)生真菌H′為? 1.87,黃龍病病株內(nèi)生真菌H′為1.08,健株為病株的1.73倍。健株和病株中分離得到的內(nèi)生真菌屬種類(lèi)數(shù)分別為15、8,健株中內(nèi)生真菌種類(lèi)較病株內(nèi)生真菌豐富。病株與健株內(nèi)生真菌種類(lèi)和多樣性在莖和葉中有明顯差別,其中健莖中H′為1.72、健葉中H′為1.44,病莖中H′為0.83、病葉中H′為0.26,健株的莖和葉中內(nèi)生真菌Shannon-Wiener 多樣性指數(shù)是病株的莖和葉中內(nèi)生真菌Shannon-Wiener多樣性指數(shù)的2.07倍和5.54倍。另外,健株內(nèi)生真菌的分布均勻性(E=0.43)優(yōu)于病株(E=0.37),但在根、莖和葉部位僅莖中內(nèi)生真菌的均勻性表現(xiàn)為健株大于? 病株。

        紅江橙健株和病株內(nèi)生真菌種類(lèi)存在差別,總體相似性指數(shù)為0.43中等,在根、莖和葉部位,健病株內(nèi)生真菌相似性指數(shù)分別為0.75、0.35和 0.44。健病株中內(nèi)生真菌種類(lèi)差異性最大的為莖部,其次為葉部,根部差異性最小。

        3 討? 論

        本研究從紅江橙中分離得到的內(nèi)生真菌中炭疽菌屬、鐮刀菌屬、葉點(diǎn)霉屬、黑孢霉屬和青霉菌屬為優(yōu)勢(shì)菌群,毛殼菌屬、 枝孢屬、擬莖點(diǎn)霉屬、曲霉菌屬、彎孢屬、平臍疣孢屬為常見(jiàn)菌群,粘帚霉屬、木霉屬、擬盤(pán)多毛孢屬、離蠕孢屬、棺孢腔菌屬、葡萄座腔菌屬、葡萄座腔菌屬為稀有菌群。紅江橙中炭疽菌屬主要出現(xiàn)于莖和葉,根部出現(xiàn)頻率極低;鐮刀菌屬在根、莖和葉中均有出現(xiàn),但僅根部中相對(duì)分離率高;葉點(diǎn)霉屬只在莖和葉中分離得到,根部未分離到。黑孢霉屬只在莖和葉中出現(xiàn),根部未出現(xiàn);青霉菌屬只在根和莖中分離得到,葉中未出現(xiàn)。羅永蘭等[24]從溫州蜜柑、甜橙、文旦柚中分離得到的內(nèi)生真菌中炭疽菌屬、鐮刀菌屬、青霉菌屬、鏈格孢屬(Alterneria spp.)為優(yōu)勢(shì)菌群;曲霉菌屬、盤(pán)多毛孢霉屬、木霉屬、派倫霉屬(Peyronellaea spp.)、葡萄孢屬(Botrytis spp.)、莖點(diǎn)霉屬(Phoma spp.)、卵孢霉屬(Oospora spp.)、共頭霉屬(Syncephalastrum spp.)、毛霉菌屬(Mucor spp.)、輪枝菌屬(Verticillium spp.)為較常見(jiàn)菌群;彎孢屬、Cephalosprium spp.、枝孢屬、疣孢霉屬(Mycogone spp.)、Rhzoctonia spp.、Glioclasium spp.、地絲菌屬(Geotrichum spp.)、鏈核盤(pán)菌屬(Monilinia spp.)、疫霉屬(Phytophtora spp.)為稀有菌群。其中炭疽菌屬在莖和葉中出現(xiàn),根部未出現(xiàn);鐮刀菌屬在根、莖和葉中均有出現(xiàn),根部出現(xiàn)頻率高;青霉菌屬在根、莖和葉中都有出現(xiàn),但葉中出現(xiàn)頻率極低。由此可知炭疽菌屬、鐮刀菌屬和青霉菌屬在柑橘類(lèi)植物中普遍存在,是柑橘類(lèi)植物常見(jiàn)的優(yōu)勢(shì)種群。這3類(lèi)優(yōu)勢(shì)菌群在不同類(lèi)柑橘中寄生的位置也有共同的特點(diǎn),炭疽菌屬主要分布于柑橘的葉片中其次在莖中,根部?jī)H有少量分布;鐮刀菌屬在根、莖和葉均有分布,但主要分布于根部;青霉菌屬主要分布于根和莖中,葉中分布極少。除炭疽菌屬、鐮刀菌屬和青霉菌屬3類(lèi)優(yōu)勢(shì)菌群在紅江橙、溫州蜜柑、甜橙、文旦柚均分離得到外,曲霉菌屬、彎孢屬、枝孢屬、木霉屬也都在上述柑橘類(lèi)植株中分離得到,但除曲霉菌屬外,其他屬分離率極低。紅江橙中分離得到的18個(gè)屬的內(nèi)生真菌中僅上述7個(gè)屬的內(nèi)生真菌在其他柑橘種類(lèi)中分離得到外,其余11屬未在其他柑橘類(lèi)植物種分離得到,可見(jiàn)內(nèi)生真菌的種類(lèi)與柑橘類(lèi)品種有較大關(guān)系。

        現(xiàn)階段對(duì)患柑橘黃龍病的植株內(nèi)生菌群落的研究主要針對(duì)內(nèi)生細(xì)菌,研究的方面有患黃龍病的病株內(nèi)生細(xì)菌菌落種類(lèi)及多樣性[14,25-27],黃龍病病株和健株內(nèi)生細(xì)菌種群異同及多樣性變化,黃龍病病株內(nèi)生細(xì)菌的種類(lèi)及內(nèi)生細(xì)菌與罹患黃龍病的相關(guān)性[28-30],但對(duì)黃龍病病株和健株內(nèi)生真菌種類(lèi)及多樣性變化報(bào)道較少。本論文研究紅江橙中黃龍病病株與健株內(nèi)生真菌種類(lèi)及群落多樣性,并比較健株和病株根、莖、葉部位內(nèi)生真菌種群差異,研究發(fā)現(xiàn)木霉屬、擬莖點(diǎn)霉屬、黑孢霉屬、擬盤(pán)多毛孢屬、離蠕孢屬、 枝孢屬、平臍疣孢屬、短梗霉屬、棺孢腔菌屬、葡萄座腔菌屬只在健株中出現(xiàn),其中黑孢霉屬、枝孢屬在健株的莖、葉部位均分離得到,其他幾個(gè)屬只在植株某一部位出現(xiàn)且分離率極低。Kim等[31] 發(fā)現(xiàn)黑孢霉對(duì)9種植物病原菌有抑制作用,對(duì)致病疫霉(Phytophthora infestans)孢子囊和游動(dòng)孢子的萌發(fā)有抑制作用。Zhu等[32]篩選出的內(nèi)生黑胞屬菌具有較強(qiáng)的抑制α -葡萄糖苷酶效果,并強(qiáng)烈抑制蘋(píng)果炭疽菌。Yang等[33]篩選出的枝孢屬海洋內(nèi)生真菌對(duì)耐藥性金黃色葡萄球菌有較好的抑制效果。因此,僅在紅江橙健株中篩選出的黑胞屬和枝孢屬內(nèi)生真菌可以去探究其對(duì)黃龍病的抑制效果或者延緩效果。

        4 結(jié) 論

        紅江橙內(nèi)生真菌種類(lèi)豐富,但分布不均勻,其根、莖、葉間內(nèi)生真菌種類(lèi)差異較大。紅江橙健株內(nèi)生真菌種類(lèi)較黃龍病病株的內(nèi)生真菌種類(lèi)豐富,健株內(nèi)生真菌分布也較黃龍病病株內(nèi)生真菌均勻,在莖和葉部位紅江橙健株內(nèi)生真菌與黃龍病病株內(nèi)生真菌種類(lèi)差異明顯。

        參考文獻(xiàn) Reference:

        [1] ZHAO? J,SHAN T,MOU Y,et al. Plant-derived bioactive compounds produced by endophytic fungi[J].Mini-Reviews in Medicinal Chemistry,2011,11 (2):159-168.

        [2] ZHENG R,LI S,ZHANG X,et al.Biological activities of some new secondary metabolites isolated from endophytic fungi:a review study[J].International Journal of Molecular Sciences,2021,22(2):959.

        [3] HACQUARD S,SPAEPEN S,GARRIDO R,et al.Interplay Between Innate Immunity and the Plant Microbiota[J].Annual Review of Phytopathology,2017,55(1),565-589.

        [4] MANJUNATHA N,MANJUNATHA N,LI H,et al.Fungal endophytes from salt-adapted plants confer salt tolerance and promote growth in wheat (Triticum aestivum L.) at early seedling stage[J].Microbiology,2022,168(8):1225.

        [5] KHALMURATOVA I,CHOI D H,KIM J G,et al.Endophytic fungi of salt-tolerant plants:diversity and ability to promote plant growth[J].Journal of Microbiology and Biotechnology,2021,31(11):1526-1532.

        [6] AVERILL C,TURNER B L,F(xiàn)INZI A C.Mycorrhiza-mediated competition between plants and decomposers drives soil carbon storage[J].Nature,2014,505,543-545.

        [7] MARTINO E,MORIN E,GRELET G A,et al.Comparative genomics and transcriptomics depict ericoid mycorrhizal fungi as versatile saprotrophs and plant mutualists[J].New Phytologist,2018,217(3):1213-1229.

        [8] AAMIR M,KASHYAP S P,ZEHRA A,et al.Trichoderma erinaceum bio-priming modulates the WRKYs defense programming in tomato against the Fusarium oxysporum f.sp.lycopersici (Fol) challenged condition[J].Frontiers in Plant Science,2019,10:911.

        [9] TADYCH M,BERGEN MS,JOHNSON-CICALESE J,? et al.Endophytic and pathogenic fungi of developing cranberry ovaries from flower to mature fruit:diversity and succession[J].Fungal Diversity,2012,54(1):101-116.

        [10] GHIMIRE S R,CHARLTON N D,BELL J D,et al.Biodiversity of fungal endophyte communities inhabiting switchgrass (Panicum virgatum L.) growing in the?? native tallgrass prairie of northern Oklahoma[J].Fungal Diversity,2011,47(1):19-27.

        [11] HAMILTON C E,BAUERLE T L.A new currency for mutualism Fungal endophytes alter antioxidant activity in hosts responding to drought[J].Fungal Diversity,2012,54(1):39-49.

        [12] LARKIN B G,HUNT L S,RAMSEY P W.Foliar nutrients shape fungal endophyte communities in Western white pine (Pinus monticola) with implications for white-tailed deer herbivory[J].Fungal Ecology,2012,5(2):252-260.

        [13] SLIPPERS B,WINGFIELD M J.Botryosphaeriaceae as endophytes and latent pathogens of woody plants:diversity,ecology and impact[J].Fungal Biology Review,2007,21(2):90-106.

        [14] TRIVEDI P,HE Z,NOSTRAND J,et al.Huanglongbing alters the structure and functional diversity of microbial communities associated with citrus rhizosphere [J].The Isme Journal,2012,6(2):363-383.

        [15] NANNIPIERI P,ASCHER J,CECCHERINI M T,et al.Microbial diversity and soil functions[J].European Journal of Soil Science,2017,68(1):12-26.

        [16] FITTER A H,GILLIGAN C A,HOLLINGWORTH K,et al.Biodiversity and ecosystem function in soil[J].Functional Ecology,2005,19(3):369-377.

        [17] BASTIANEL G,GARNIER-SEMANCIK M,RNAUDIN J,et al.Diversity of “Candidatus liberibacter asiaticus”,based on the omp gene sequence[J].Applied and Environmental Microbiology,2005,71(11):6473-6478.

        [18] WANG X,CHEN G,HUANG F,et al.Phyllosticta species associated with citrus diseases in China[J].Fungal Diversity,2012,52(1):209-224.

        [19] KRIEL W M,SWART W J,CROUS P W.Foliar endophytes and their interactions with host plants,with specific reference to the Gymnospermae [J].Advances in Botanical Research,2000,33:1-34.

        [20] 高曉霞,王 磊,周偉平,等.假鷹爪莖、葉組織內(nèi)生真菌的分布和rDNA ITS序列系統(tǒng)發(fā)育分析[J].中國(guó)藥學(xué)雜志,2013,48 (24):2102-2106.

        GAO X X,WANG L,ZHOU W P,et al.Distribution and phylogenetic analysis of endophytic fungi in stems and leaves of Desmos chinensis based on histochemistry and rDNA ITS sequence[J].Chinese Pharmaceutical Journal,2013,48 (24):2102-2106.

        [21] 魏景超.真菌鑒定手冊(cè)[M].上海:上??茖W(xué)技術(shù)出版社,1979:24-608.

        WEI J CH,Manual of Determinative Fungi[M].Shanghai:Shanghai Scientific and Technical Publishers,1979:24-608.

        [22] INNIS M A,GELFAND D H,SNINSKY J J,et al.PCR Protocols:a Guide to Methods and Applications[M].New York:Academic Press Inc,1990:315-322.

        [23] GUSSOW D,CLACKSON T.Direct clone characterization from plaques and colonies by the polymerase chain-reaction[J].Nucleic Acids Research,1989,17(10):4000.

        [24] 羅永蘭,張志元,冉國(guó)華.柑橘內(nèi)生真菌的分離與鑒定[J].湖南農(nóng)業(yè)大學(xué)學(xué)報(bào)(自然科學(xué)版),2005,31(4):418-421.

        LUO? Y L,ZHANG? ZH Y,RAN G H.Isolation and identification of endophytic fungi in Citrus[J].Journal of Hunan Agricultural University(Natural Sciences),2005,31(4):418-421.

        [25] 王 芳,殷幼平,孫麗琴,等.柑橘黃龍病罹病植株顯癥差異組織內(nèi)生細(xì)菌群落結(jié)構(gòu)分析[J].微生物學(xué)報(bào),2014,? 54(8):868-875.

        WANG F,YIN Y P,SUN L Q,et al.Endophytic bacterial community in the symptoms and symptomless tissues of HLB-affected citrus plant[J].Acta Microbiologica Sinica,2014,54(8):868-875

        [26] 熊大維,金丹鳳,顧斌濤,等.柑橘黃龍病贛南臍橙內(nèi)生菌種群結(jié)構(gòu)分析[J].微生物學(xué)通報(bào),2017,44(3):631-638.

        XIONG? D W,JIN D F,GU B T,et al.Endophytic bacterial community in Gannan navel orange affected by huanglongbing[J].Microbiology China,2017,44(3):631-638.

        [27] LI C B,GAO F Y,ZHANG M,et al.Analysis of 16S rDNA sequences of endophytic bacteria associated with Huanglong disease of citrus plants in Guangning county,China[J].New Biotechnology,2014,31:181

        [28] YUN S W,LI J Z,XIAO Y Y,et al.Transcriptome profiling of Huanglongbing (HLB) tolerant and susceptible citrus plants reveals the role of basal resistance in HLB tolerance[J].Frontiers in Plant Science,2016,7:933.

        [29] MARTINELLI F,REAGAN R L,DOLAN D,et al.Proteomic analysis highlights the role of detoxification pathways in increased tolerance to Huanglongbing disease[J].BMC Plant Biology,2016,16(1):167-181.

        [30] TRIVEDI P,SPANN T,WANG N.Isolation and characterization of beneficial bacteria associated with citrus roots in Florida[J].Microbiology Ecology,2011,62(2):324-336.

        [31] KIM J C,CHOI G J,PARK J H,et al.Activity against plant pathogenic fungi of phomalactone isolated from Nigrospora sphaerica[J].Pest Management Science,2001,57(6):554-559.

        [32] ZHU X W,CHEN J Q,ZHU S R,et al.Two new compounds from Nigrospora sphaerica ZMT05,a fungus derivated from Oxya chinensis Thunber[J].Natural Product Research,2018,32(20):2375-2381.

        [33] YANG G,NENKEP V N,SIWE X N,et al.An acetophenone derivative,clavatol,and a benzodiazepine alkaloid,circumdatin A,from the marine-derived fungus Cladosporium[J].Natural Product Sciences,2009,15(3):130-133.

        Biodiversity and? Community Structure of Culturable Endophytic Fungi in Hongjiang Orange

        SUN Peng,WANG Yun,LU Dongmei,YUAN? Hongxu and WANG Liyun

        (Life Science and Technology School,Lingnan Normal University, Zhanjiang? Guangdong 524048,China )

        Abstract To compare the difference of the endophytic fungal diversity and community composition between healthy? Hongjiang orange plants? and those infected with Candidatus Liberibacter asiaticus, the endophytic fungi were isolated using the method of tissue block culture from roots, stems and leaves.? The result showed? that the endophytic fungal communities were highly diverse and rich, with the total of 117 strains? obtained, and distributed into 3 classes, 11 orders, 15 families and 18 genera. The dominant members belonged to the geuns Colletotrichum, Fusarium, Phyllosticta , Nigrospora? and Penicillium, with relative abundance of 58.97%,8.55%,8.55%,4.27% and 3.42% respectively. The total Shannon-Wiener diversity index (H′) was 1.68, and the total similarity index was?? 0.30. The similarity index between stem and leaf was 0.48, followed by root and leaf at? 0.33 and root and stem at 0.32. The Shannon-Wiener diversity index of endophytic fungi of healthy plants was significantly different from? that in diseased plants. The diversity index of the root in healthy plants was slightly lower than that in the diseased plants, while the total diversity index and the diversity index of the stem and leaf were 1.73, 2.07 and 5.54 times that of? the diseased plants, respectively. The endophytic fungi community similarity index (Cs) between healthy and diseased plants was 0.43, and in the similarity index of the endophytic fungi of healthy and diseased plants in root, stem and leaf, the index of root was higher (Cs=0.75), followed by the index of leaf (Cs=0.44), the index of stem was lowest (Cs=0.35). Colletotrichum species were enriched as dominant populations, with relative abundances of 77.78% and 92.86% in stem and leaves, respectively,? which were significantly higher than those in? healthy plants (54.05%,54.17%). In? summary,? the endophytic fungi community of Hongjiang orange were rich at genus level, but its distribution were uneven,exhibiting tissue specificity. The community structure of endophytic fungi in Hongjiang orange infected with Citrus huanglongbing(HLB) differs significantly from that of? healthy plants.The diversity index of endophytic fungi in diseased plants was significantly lower than that in? healthy plants, especially in leaves and stems.

        Key words Hongjiang orange; Endophytic fungi;Diversity; Huanglongbing

        Received ?2023-01-08??? Returned 2023-04-14

        Foundation item High Value Development and Utilization Innovation Team of Western Guangdong Marine Traditional Chinese Medicine and Southern Medicine, Department of Education of Guangdong Province(No.2021KCXTD039).

        First author SUN Peng, male, lecturer. Research area:application of microorganisms.E-mail:speagle2003@163.com

        Corresponding?? author WANG Liyun, female,professor.Research area:microbial biotechnology.? E-mail:wangliyun714@gmail.com

        (責(zé)任編輯:史亞歌 Responsible editor:SHI Yage)

        久久久久国产精品四虎| 亚洲老妈激情一区二区三区| 精品综合久久久久久97超人| 亚洲中文久久久久无码| 国产精品亚洲在线播放| 成熟了的熟妇毛茸茸 | 在线观看视频日本一区二区| av 日韩 人妻 黑人 综合 无码 | 国产精品刺激好大好爽视频| 婷婷精品国产亚洲av| 男奸女永久免费视频网站| 精品无码av一区二区三区| 玖玖资源站无码专区| 一区二区丝袜美腿视频| 亚洲国产av一区二区三区| 香港三级日本三级a视频| 爱a久久片| 男子把美女裙子脱了摸她内裤 | 亚洲日韩中文字幕无码一区| 欧美精品免费观看二区| 少妇一级aa一区二区三区片| 中文字幕国产亚洲一区| 日韩丰满少妇无码内射| 96免费精品视频在线观看| 日韩av一区二区三区在线观看 | 激情视频国产在线观看| 中国一级特黄真人片久久| 日韩精品无码视频一区二区蜜桃 | 国产一区二区三区我不卡| 欧美寡妇xxxx黑人猛交| 免费成人福利视频| 亚洲伊人伊成久久人综合| 九九在线中文字幕无码| 国产精品久久久久久人妻精品 | 亚洲中文字幕无码爆乳av| 色人阁第四色视频合集网| 亚洲天堂成人av影院| 国产精品免费看久久久8| 日韩av二区三区一区| 亚洲中文字幕一区精品| 免费看av在线网站网址|