EA 3800, Université de Rouen, 76031 Rouen, France Laboratoire de Parasitologie-Mycologie, CHU Charles-Nicolle, 76031 Rouen, France.
L'UNAM Université, Université d'Angers, Groupe d'Etude des Interactions Hôte-Pathogène, EA 3142, 49933 Angers, France Department of Biology, Faculty of Sciences, University Moulay Ismail, Meknes, Morocco.
Med Mycol. 2016 May;54(4):409-19. doi: 10.1093/mmy/myv080. Epub 2015 Oct 19.
The Scedosporium apiospermum species complex usually ranks second among the filamentous fungi colonizing the airways of patients with cystic fibrosis (CF), but little is known about the molecular epidemiology of the airway colonization.
Polymerase chain reaction (PCR) amplification of repetitive sequences (rep-PCR) was applied to the retrospective analysis of a panel of isolates already studied by random amplification of polymorphic DNA (RAPD) and comprising 63 isolates recovered from sputa from 9 CF patients. Results were compared to those obtained previously by RAPD, and herein by beta-tubulin (TUB) gene sequencing and Multilocus Sequence Typing (MLST).
Within the panel of isolates studied,S. apiospermum sensu stricto and Scedosporium boydii, as expected, were the predominant species with 21 and 36 isolates, respectively. Four isolates from one patient were identified as Scedosporium aurantiacum, whereas two isolates belonged to the Pseudallescheria ellipsoidea subgroup of S. boydii rep-PCR analysis of these isolates clearly differentiated the three species and P. ellipsoidea isolates, whatever the rep-PCR kit used, and also permitted strain differentiation. When using the mold primer kit, results from rep-PCR were in close agreement with those obtained by MLST. For both S. apiospermum and S. boydii, 8 genotypes were differentiated by rep-PCR and MLST compared to 10 by RAPD. All S. aurantiacum isolates shared the same RAPD genotype and exhibited the same rep-PCR profile and sequence type.
These results illustrate the efficacy of rep-PCR for both species identification within the S. apiospermum complex and genotyping for the two major species of this complex.Abstract presentation: Part of this work was presented during the 18th Congress of the International Society for Human and Animal Mycology, Berlin (Germany), June 2012.S. Giraud, C. Godon, A. Rougeron, J.P. Bouchara and L. Favennec are members of the ECMM/ISHAM working group on Fungal respiratory infections in Cystic Fibrosis(Fri-CF).
棘孢木霉属复合种通常在气道定植的丝状真菌中位居第二,仅次于假单胞菌属,但对气道定植的分子流行病学知之甚少。
采用聚合酶链反应(PCR)扩增重复序列(rep-PCR),对已经通过随机扩增多态性 DNA(RAPD)研究的一组分离物进行回顾性分析,该组分离物由 9 名 CF 患者痰液中分离的 63 株组成。结果与以前通过 RAPD 获得的结果进行了比较,也与β-微管蛋白(TUB)基因测序和多位点序列分型(MLST)获得的结果进行了比较。
在所研究的分离物中,棘孢木霉和棘孢曲霉是预期的主要种,分别有 21 株和 36 株。从一名患者中分离的 4 株被鉴定为棘孢梭孢霉,而 2 株属于棘孢曲霉的拟青霉亚组。 rep-PCR 分析清楚地区分了这三种和拟青霉亚组,无论使用哪种 rep-PCR 试剂盒,也允许进行菌株分化。当使用霉菌引物试剂盒时,rep-PCR 的结果与 MLST 非常吻合。对于棘孢木霉和棘孢曲霉,通过 rep-PCR 和 MLST 可区分 8 种基因型,而通过 RAPD 可区分 10 种。所有的棘孢梭孢霉分离株共享相同的 RAPD 基因型,表现出相同的 rep-PCR 谱和序列型。
这些结果表明 rep-PCR 不仅可用于鉴定棘孢木霉复合种中的种,还可用于该复合种中两种主要种的基因分型。摘要介绍:这项工作的一部分在 2012 年 6 月德国柏林举行的第十八届国际人类和动物真菌学会大会上进行了介绍。S. Giraud、C. Godon、A. Rougeron、J.P. Bouchara 和 L. Favennec 是真菌性呼吸道感染 ECMM/ISHAM 工作组(Fri-CF)的成员。