Sagastume Soledad, Martín-Hernández Raquel, Higes Mariano, Henriques-Gil Nuno
Centro Apícola Regional, Bee Pathology Laboratory, 19180, Marchamalo, Guadalajara, Spain.
Instituto de Recursos Humanos para la Ciencia y la Tecnología (INCRECYT), Parque Científico de Albacete, Spain.
BMC Evol Biol. 2016 Oct 18;16(1):216. doi: 10.1186/s12862-016-0797-7.
There is great controversy as to whether Microsporidia undergo a sexual cycle. In the paradigmatic case of Nosema ceranae, although there is no morphological evidence of sex, some meiosis-specific genes are present in its reduced genome and there is also high intraspecific variability, with incongruent phylogenies having been systematically obtained. The possibility of sexual recombination is important from an epidemiological standpoint, particularly as N. ceranae is considered to be a major factor in the current disquieting epidemic of widespread bee colony losses. This parasite apparently originated in oriental honey bees, spreading out of Asia and Australia to infect honey bees worldwide. This study had three main objectives: i) to obtain genetic markers that are not part of known multi-copy arrays for strain determination; ii) to shed light on the intraspecific variability and recombination of N. ceranae; and iii) to assess the variability in N. ceranae populations. The answers to these questions are critical to understand the capacity of adaptation of microsporidia.
Biallelic polymorphisms were detected at a number of specific points in the five coding loci analyzed from European and Australian isolates of N. ceranae. Heterozygous genotypes were abundant and cloning experiments demonstrate that they reflect the existence of multiple alternative sequences in each isolate. The comparisons of different clones and genotypes clearly indicate that new haplotypes are generated by homologous recombination.
The N. ceranae isolates from honey bees correspond to genotypically distinct populations, revealing that individual honey bees may not be infected by a particular clone but rather, a pool of different strains. Homologous recombination implies the existence of a cryptic sex cycle yet to be described in N. ceranae. There are no diagnostic alleles associated with Australian or European origins, nor are there differences between the two hosts, A. cerana and A. mellifera, supporting the absence of biological barriers for N. ceranae transmission. Diversity is high among microsporidia of both these origins, and the maintenance of a high heterozygosis in the recently invaded European populations, could hypothetically underlie the stronger virulence of N. ceranae observed in A. mellifera.
关于微孢子虫是否经历有性周期存在很大争议。在典型的蜜蜂微孢子虫(Nosema ceranae)案例中,尽管没有性的形态学证据,但其简化的基因组中存在一些减数分裂特异性基因,并且种内变异性也很高,系统地获得了不一致的系统发育树。从流行病学角度来看,有性重组的可能性很重要,特别是因为蜜蜂微孢子虫被认为是当前令人不安的广泛蜂群损失疫情的主要因素。这种寄生虫显然起源于东方蜜蜂,从亚洲和澳大利亚传播开来,感染了全球的蜜蜂。本研究有三个主要目标:i)获得用于菌株鉴定的、不属于已知多拷贝阵列的遗传标记;ii)阐明蜜蜂微孢子虫的种内变异性和重组情况;iii)评估蜜蜂微孢子虫种群的变异性。这些问题的答案对于理解微孢子虫的适应能力至关重要。
在对来自欧洲和澳大利亚的蜜蜂微孢子虫分离株进行分析的五个编码位点的多个特定位置检测到双等位基因多态性。杂合基因型丰富,克隆实验表明它们反映了每个分离株中存在多个替代序列。不同克隆和基因型的比较清楚地表明新的单倍型是通过同源重组产生的。
来自蜜蜂的蜜蜂微孢子虫分离株对应于基因型不同的种群,这表明单个蜜蜂可能不是被特定的克隆感染,而是被不同菌株的集合感染。同源重组意味着在蜜蜂微孢子虫中存在一个尚未描述的隐秘有性周期。没有与澳大利亚或欧洲起源相关的诊断等位基因,两种宿主中华蜜蜂(Apis cerana)和西方蜜蜂(Apis mellifera)之间也没有差异,这支持了蜜蜂微孢子虫传播不存在生物学障碍的观点。这两个起源的微孢子虫多样性都很高,并且在最近入侵的欧洲种群中维持高杂合性,可能是在西方蜜蜂中观察到的蜜蜂微孢子虫更强毒力的潜在原因。