Gaudino Maria, Chiapponi Chiara, Moreno Ana, Zohari Siamak, O'Donovan Tom, Quinless Emma, Sausy Aurélie, Oliva Justine, Salem Elias, Fusade-Boyer Maxime, Meyer Gilles, Hübschen Judith M, Saegerman Claude, Ducatez Mariette F, Snoeck Chantal J
IHAP, Université de Toulouse, INRAE, ENVT, Toulouse 31076, France.
Department of Virology, Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna 'Bruno Ubertini', Brescia 25124, Italy.
Virus Evol. 2022 Sep 1;8(2):veac081. doi: 10.1093/ve/veac081. eCollection 2022.
Influenza D virus (IDV) is an emerging influenza virus that was isolated for the first time in 2011 in the USA from swine with respiratory illness. Since then, IDV has been detected worldwide in different animal species, and it was also reported in humans. Molecular epidemiological studies revealed the circulation of two major clades, named D/OK and D/660. Additional divergent clades have been described but have been limited to specific geographic areas (i.e. Japan and California). In Europe, IDV was detected for the first time in France in 2012 and subsequently also in Italy, Luxembourg, Ireland, the UK, Switzerland, and Denmark. To understand the time of introduction and the evolutionary dynamics of IDV on the continent, molecular screening of bovine and swine clinical samples was carried out in different European countries, and phylogenetic analyses were performed on all available and newly generated sequences. Until recently, D/OK was the only clade detected in this area. Starting from 2019, an increase in D/660 clade detections was observed, accompanied by an increase in the overall viral genetic diversity and genetic reassortments. The time to the most recent common ancestor (tMRCA) of all existing IDV sequences was estimated as 1995-16 years before its discovery, indicating that the virus could have started its global spread in this time frame. Despite the D/OK and D/660 clades having a similar mean tMRCA (2007), the mean tMRCA for European D/OK sequences was estimated as January 2013 compared to July 2014 for European D/660 sequences. This indicated that the two clades were likely introduced on the European continent at different time points, as confirmed by virological screening findings. The mean nucleotide substitution rate of the hemagglutinin-esterase-fusion (HEF) glycoprotein segment was estimated as 1.403 × 10 substitutions/site/year, which is significantly higher than the one of the HEF of human influenza C virus ( < 0.0001). IDV genetic drift, the introduction of new clades on the continent, and multiple reassortment patterns shape the increasing viral diversity observed in the last years. Its elevated substitution rate, diffusion in various animal species, and the growing evidence pointing towards zoonotic potential justify continuous surveillance of this emerging influenza virus.
丁型流感病毒(IDV)是一种新出现的流感病毒,2011年首次在美国从患有呼吸道疾病的猪身上分离出来。从那时起,IDV在全球不同动物物种中被检测到,也有在人类中被报道的情况。分子流行病学研究揭示了两个主要分支的传播情况,分别命名为D/OK和D/660。还描述了其他一些不同的分支,但仅限于特定地理区域(即日本和加利福尼亚)。在欧洲,2012年首次在法国检测到IDV,随后在意大利、卢森堡、爱尔兰、英国、瑞士和丹麦也检测到了。为了解IDV在欧洲大陆的引入时间和进化动态,在欧洲不同国家对牛和猪的临床样本进行了分子筛查,并对所有可用的和新生成的序列进行了系统发育分析。直到最近,D/OK是该地区唯一检测到的分支。从2019年开始,观察到D/660分支的检测数量增加,同时病毒的总体遗传多样性和基因重配也有所增加。所有现有IDV序列的最近共同祖先时间(tMRCA)估计为1995年,即其被发现前16年,这表明该病毒可能在这个时间段开始全球传播。尽管D/OK和D/660分支的平均tMRCA相似(2007年),但欧洲D/OK序列的平均tMRCA估计为2013年1月,而欧洲D/660序列的平均tMRCA为2014年7月。这表明这两个分支可能在不同时间点引入欧洲大陆,病毒学筛查结果证实了这一点。血凝素-酯酶-融合(HEF)糖蛋白片段的平均核苷酸替换率估计为1.403×10^(-3)替换/位点/年,这显著高于人类丙型流感病毒HEF的替换率(<0.0001)。IDV的基因漂移、新分支在欧洲大陆的引入以及多种重配模式塑造了近年来观察到的病毒多样性增加的情况。其较高的替换率、在各种动物物种中的传播以及越来越多指向人畜共患病潜力的证据,证明了对这种新出现的流感病毒进行持续监测的合理性。