The First Large Identification of 3ANX and NX Producing Isolates of Fusarium graminearum in Manitoba, Western Canada.

IF 4 3区 医学 Q2 FOOD SCIENCE & TECHNOLOGY Toxins Pub Date : 2025-01-17 DOI:10.3390/toxins17010045
Maria Antonia Henriquez, Srinivas Sura, Sean Walkowiak, David Kaminski, Anne Kirk, Mark W Sumarah, Parthasarathy Santhanam, Nina Kepeshchuk, Jules Carlson, E RoTimi Ojo, Pam de Rocquigny, Holly Derksen
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Abstract

Fusarium head blight, caused by Fusarium graminearum, continues to be one of the most important and devastating fungal diseases on cereal grains including wheat, barley, and oat crops. F. graminearum produces toxic secondary metabolites that include trichothecene type A and type B mycotoxins. There are many variants of these toxins that are produced, and in the early 2010s, a novel type A trichothecene mycotoxin known as 3ANX (7-α hydroxy,15-deacetylcalonectrin) and its deacetylated product NX (7-α hydroxy, 3,15-dideacetylcalonectrin) were identified in Minnesota, USA. In the current study, a total of 31,500 wheat spikes over a period of 6 years (2015-2020) within Manitoba, Canada, were screened for the F. graminearum pathogen, which accounted for 72.8% (2015), 98.3% (2016), 71.9% (2017), 74.4% (2018), 92.6% (2019), and 66.1% (2020) of isolations. A total of 303 F. graminearum isolates, confirmed through sequencing of the ribosomal intergenic spacer, were further investigated for variation in the gene Tri1, which was previously associated with the production of the NX toxin, as well as the accumulation of mycotoxins. A subset of these isolates, consisting of 73 isolates, which tested positive or negative for the NX-Tri1-F/R assay in this study, were cultured in vitro using rice media. Mycotoxins were quantified in these samples using mass spectrometry. Using the same rice culture, genomic DNA was isolated, and the Tri1 coding sequence along with its flanking regions (upstream and downstream of the Tri1 gene) was amplified and sequenced. Deoxynivalenol (DON) accumulated in 96% of the cultures from these isolates, while 3-acetyl deoxynivalenol (3ADON) and 3ANX mycotoxins accumulated in 66% and 63%, respectively. Nivalenol, 15-acetyl deoxynivalenol, and NX mycotoxins were detected in 62%, 36%, and 19% of samples, respectively. A significant correlation was observed between 3ADON and 3ANX (r2 = 0.87), as well as between DON and 3ANX (r2 = 0.89). This study highlights the first large identification of 3ANX- and NX-producing isolates of F. graminearum in Western Canada. In addition, it is the first identification of 15ADON chemotypes producing 3ANX in Western Canada and the first identification of 3ANX and NX-producing isolates in Manitoba, collected from wheat samples.

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加拿大西部马尼托巴省首次大规模鉴定出产3ANX和NX的禾谷镰刀菌分离株。
由谷草镰刀菌引起的赤霉病是小麦、大麦和燕麦等谷类作物最重要和最具破坏性的真菌病害之一。F. graminearum产生有毒的次生代谢物,包括A型和B型霉菌毒素。这些毒素有许多变体,在2010年代初,在美国明尼苏达州发现了一种新的a型毛霉毒素,称为3ANX (7-α羟基,15-deacetylcalonectrin)及其去乙酰化产物NX (7-α羟基,3,15-dideacetylcalonectrin)。在本研究中,对加拿大马尼托巴省6年(2015-2020年)的31,500个小麦穗进行了F. graminearum病原菌筛选,分离率分别为72.8%(2015年)、98.3%(2016年)、71.9%(2017年)、74.4%(2018年)、92.6%(2019年)和66.1%(2020年)。通过核糖体基因间间隔测序确认的303株F. graminearum分离株进一步研究了基因Tri1的变异,该基因先前与NX毒素的产生以及真菌毒素的积累有关。这些分离物的一个子集,包括73个分离物,在本研究中对NX-Tri1-F/R检测呈阳性或阴性,使用水稻培养基进行体外培养。用质谱法对这些样品中的真菌毒素进行定量分析。利用相同的水稻培养,分离基因组DNA,扩增Tri1编码序列及其两翼区域(Tri1基因的上游和下游)并测序。脱氧雪腐镰刀菌醇(DON)在96%的培养物中积累,而3-乙酰脱氧雪腐镰刀菌醇(3ADON)和3ANX真菌毒素分别在66%和63%的培养物中积累。雪腐镰刀菌醇、15-乙酰脱氧雪腐镰刀菌醇和NX真菌毒素的检出率分别为62%、36%和19%。3ADON与3ANX呈显著相关(r2 = 0.87), DON与3ANX呈显著相关(r2 = 0.89)。这项研究强调了在加拿大西部首次大规模鉴定出产生3ANX和nx的F. graminearum分离株。此外,这是加拿大西部首次鉴定出产生3ANX的15ADON化学型,也是马尼托巴省首次从小麦样本中鉴定出产生3ANX和nx的分离株。
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来源期刊
Toxins
Toxins TOXICOLOGY-
CiteScore
7.50
自引率
16.70%
发文量
765
审稿时长
16.24 days
期刊介绍: Toxins (ISSN 2072-6651) is an international, peer-reviewed open access journal which provides an advanced forum for studies related to toxins and toxinology. It publishes reviews, regular research papers and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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