Towards a formal microsporidian taxonomy

20 - 21 April 2026 09:00 - 17:00 Holiday Inn Manchester - City Centre Free
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Theo Murphy meeting organised by Dr Jamie Bojko, Dr Jonathan Snow, Dr Bryony Williams and Dr Aaron Reinke.

The Microsporidia are spore-forming obligate parasites, whose taxonomic history has fluctuated for over a century. Morphological and genetic methods have created a plethora of taxa, but the formality of these taxa is questionable. By bringing together experts in microsporidian taxonomy, and representatives from fields in which microsporidians are pervasive (eg Agriculture, Aquaculture), we will develop agreeable Microsporidia Taxonomic Criteria (MTCs), which taxonomists can use as the foundation of new discoveries.

Programme

The programme, including the speaker biographies and abstracts, will be available soon. Please note the programme may be subject to change.

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Enquiries: contact the Scientific Programmes team.

Organisers

  • Dr Jamie Bojko, Teesside University, UK

    Dr Jamie Bojko

    Dr Jamie Bojko is an Associate Professor in Disease Ecology at Teesside University's National Horizons Centre, and part of the Biodiscovery team. Jamie's research includes the taxonomic understanding of the Microsporidia - a group of obligate spore-forming pathogens with a wide host range. Jamie employs classic pathology tools (histology/electron microscopy) and experimental designs, coupled with the latest in genomic and bioinformatic techniques, to characterise novel pathogens across marine and terrestrial ecosystems. His focus has largely involved biological invasions, but the basis to all of his work resides in taxonomy.

  • Dr Jonathan Snow, Barnard College, USA

    Dr Jonathan Snow

    Jonathan Snow is currently Professor and Chair of the Department of Biology of Barnard College, Columbia University. Dr Snow received his PhD in Biomedical Sciences from the University of California, San Francisco, and completed a postdoctoral fellowship at Children's Hospital Boston and Harvard Medical School. His graduate and postgraduate work focused on signal transduction, regulation of gene expression, and organismal stress responses in blood development of mammals. He subsequently became fascinated with the honey bee and changed his research focus to the study molecular mechanisms of disease in the key pollinator. Our current focus is on the biology, diagnosis, and treatment of the honey bee microsporidia parasite Vairimorpha (Nosema) ceranae. He continues his avocation as a beekeeper while teaching and maintaining an active research laboratory.

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    Dr Bryony Williams

  • Dr Aaron Reinke, University of Toronto, Canada

    Dr Aaron Reinke

    Dr Reinke is an expert in studying microsporidia, which are widespread parasites that cause death and disease in humans and other animals. Dr Reinke started his independent research career in September 2017 in the Department of Molecular Genetics at the University of Toronto. Recent work from his lab includes identifying molecules that inhibit microsporidia infection, discovering a host protein necessary for microsporidia invasion, characterising a novel intergenerational immune response to microsporidia infection, and elucidating how the microbiome influences microsporidia infection. The lab has also studied microsporidia genomic evolution and host specificity, examining the extensive ecological and phenotypic diversity of microsporidia, analysing the genomic and phenotypic evolution of nematode-infecting microsporidia, finding conserved gene expression between related microsporidia and hosts, and demonstrating widespread functional loss of microsporidia proteins. Dr Reinke has also received several young investigator awards including a Sloan Research Fellowship in Computational & Evolutionary Molecular Biology.

Schedule

Chair

Dr Jamie Bojko, Teesside University, UK

Dr Jamie Bojko

Teesside University, UK

09:00-09:05 Welcome by the lead organiser
09:05-09:30 Towards a formal microsporidian taxonomy: a history and a future

The 'Microsporidia' is currently considered a sub-phylum within the Rozellomycota, which contains 'long-branch' and 'short-branch' taxa, as defined by phylogenetic inference. These organisms are obligate parasites, requiring either a host cytoplasm or nucleus to be able to proliferate. Their initial discovery in the 1800s, beginning with Nosema bombycis from silkworm, has brought us to today's long list of candidates. Over 1000 putative microsporidium species are represented by only morphological data, where around 300 'formal' species are support by combined morphological and molecular data, and a further undefined number have been observed using molecular data alone. The availability of genomes has expanded greatly in recent years, including high quality telomere to telomere constructs, which give the field a new view of potential taxonomic value.

In this talk, I will provide an outline of the Microsporidia through history, using key examples to explore how a new committee, focal to the Microsporidia, may better define species, genes, family, and higher taxonomic criteria and delineation methods. This talk will kick off the two-day debate around rules and regulations that we might choose to employ when characterising a new microsporidium. Through better definition and regulation of microsporidian taxa, studies into pathology, evolution, and impact will all become more feasible, with clear benefits for health care, veterinary sciences, and ecological (One Health) understanding.

Dr Jamie Bojko

Dr Jamie Bojko

Teesside University, UK

09:30-10:00 Where do Microsporidia sit in the tree of life
Professor David Bass

Professor David Bass

Centre for Environment, Fisheries and Aquatic Sciences, UK

10:00-10:30 Break
10:30-11:00 Microsporidia hiding in the sequence read archive

Microsporidia, a vast phylum of obligate intracellular parasites classified as early branching Fungi, exhibit a remarkable ability to infect a wide variety of hosts, including over 220 genera of both vertebrates and invertebrates. To get an idea of the extent of the vastness of microsporidian diversity, we employed a data mining strategy to extract valuable insights from publicly available Panarthropod transcriptomic assembly projects. In total, more than 300 species across over 200 genera and 25 orders of panarthropod hosts were retrieved as 'potentially infected' with expected infection patterns. This not only underscores the ubiquity of these parasites across the Panarthropoda phylum, but also reveals environmental density with globally distributed host samples ranging from the wild to laboratory settings, including an insect cell line. Furthermore, we used a novel approach to to construct a multi-protein phylogeny using proteins extracted from the 'parasitised' assemblies and reference genomes. The resulting phylogenetic analysis not only confirmed the existence of established microsporidia clades and their typical hosts, but also unveiled potential novel clades. This study underscores the significance of data mining approaches in conjunction with traditional field studies, offering a promising avenue to elucidate the ecology and host spectrum of these often-overlooked parasites.

Dr Sam Edwards

Dr Sam Edwards

Wageningen University, The Netherlands

11:00-11:30 Microsporidian genomics

Microsporidia are of growing importance to public health and agriculture, yet many aspects of their biology and evolution remain poorly understood, in part due to their obligately intracellular lifestyle. Large-scale biodiversity genomics projects are transforming microsporidian research by incidentally generating parasite genomes when infected host individuals are sequenced. Using 40 such microsporidian genome assemblies that I have recently released, along with additional genomes assembled since, I will explore what these unexpected resources reveal about microsporidian biology and evolution. In particular, I discuss polyploidy in Microsporidia, how it can be reconciled with the life cycle, and patterns of genome evolution in the group. I also examine the microsporidian phylogeny from a whole-genome perspective and explore how genome-scale data can inform species delineation for these parasites.

Mr Amjad Khalaf

Mr Amjad Khalaf

Wellcome Sanger Institute, UK

11:30-12:00 Early Microsporidia: from morphology to phylogeny
Dr Elena Nassonova

Dr Elena Nassonova

Institute of Cytology, Russia

12:00-12:30 “Grades” versus “Clades” in taxonomy of the Microsporidia: lessons from two lineages: “Paranosema - Antonospora” and “Nosema - Vairimorpha”

"Clades," defined as monophyletic groups sharing derived characters, and "grades," based on common morphological or functional traits, represent two distinct yet potentially complementary taxonomic approaches. The rise of sequence-based cladistics has often conflicted with traditional morphology-based taxonomy across many organisational groups, including the Microsporidia. This presentation examines how such conflicts have influenced practical taxonomy, focusing on two notable cases: Paranosema vs. Antonospora and Nosema vs. Vairimorpha (referring to honeybee microsporidia). Both cases are related to my research, and, besides, Nosema locustae, N apis and N. ceranae are famous for their applied and scientific importance. My points in brief: (i) Paranosema locustae, P grylli and P whitei, belong to one clade with solitary bee microsporidium Antonospora scoticae, but not to the genus Antonospora, (ii) Vairimorpha, like Nosema, remains a "holding" genus and a clade, and both honeybee microsporidia belong to this clade but not to the genus Vairimorpha. (iii) Given that the prime goal of taxonomy is to reflect biodiversity, in my view, Vairimorpha clade comprises several genera: Vairimorpha sensus stricto, Oligosporium and Rugispora to be retained, and more to be described. (iv) Our recent ultrastructural analysis justifies establishing a new genus for N apis. (v) In practical taxonomy I suggest following a golden rule: "create new genera for those lineages that do not correspond to the type taxon" (Bojko et al, 2022). (vi) Clades are not equivalent to taxa, and for now I advocate for a dual system indicating both the clade and formal taxon, thereby integrating phylogenetic insight with traditional classification.

Dr Yuliya Sokolova

Dr Yuliya Sokolova

National Institute on Deafness and Other Communication Disorders, USA

Chair

Dr Jonathan Snow, Barnard College, USA

Dr Jonathan Snow

Barnard College, USA

13:30-14:00 Genomics and species delineation
Dr Bryony Williams

Dr Bryony Williams

University of Exeter, UK

14:00-14:30 Development of baculovirus taxonomy and the functioning of the respective ICTV study group

Viruses of four families of arthropod-specific, large dsDNA viruses share a number of features. The viruses in these families are rod-shaped, have large, circular double-stranded DNA genomes and replicate in the nucleus of infected invertebrate cells. These shared characteristics and the presence of homologs encoding per os infectivity factors (pif genes), along with their absence from other viruses, suggest a common origin for the viruses in these families. Therefore, the class Naldaviricetes was recently proposed and later established by the International Committee on Taxonomy of Viruses (ICTV), accommodating these four families. Within this class of the ICTV approved the creation of the order Lefavirales for three of the four families, whose members carry homologs of the baculovirus genes for viral RNA polymerase subunits (late essential factors or lef genes), required for late gene expression. We further established a system for the binomial naming of the virus species in this order, in accordance with the 2019 ICTV decision to adopt a standardised nomenclature for all virus species. In this presentation, I will illustrate the history of baculovirus taxonomy and nomenclature, and use this example to show how ICTV study groups function and interact with the Executive Committee of ICTV.

Professor Monique van Oers

Professor Monique van Oers

Wageningen University and Research, The Netherlands

14:30-15:00 Challenges, pitfalls, and horrors of establishing and maintaining novel biological taxonomies
Dr Jens H Kuhn

Dr Jens H Kuhn

Independent Researcher, USA

15:00-15:15 Break
15:15-17:00 Microsporidian systematics discussion

Chair

Dr Yuliya Sokolova, National Institute on Deafness and Other Communication Disorders, USA

Dr Yuliya Sokolova

National Institute on Deafness and Other Communication Disorders, USA

09:00-09:30 Probing microsporidian parasite dynamics using live cell imaging and scRNA-seq

Studying the dynamics of microsporidian replication in the host is challenging due the the lack of genetic tools, limitations on imaging in live animals, and the speed and stochastic nature of the invasion process. We have recently stumbled upon a strategy for live cell imaging of parasites in mammalian cultured cells, which bypasses some of the challenges described above, and allows us to track a single parasite from entry through replication in the host cell, and its ultimate spread to neighboring cells. Combined with other imaging techniques, such as ultrastructure expansion microscopy, we are gaining new insights into parasite replication and cell biology. In parallel, we have been using scRNA-seq to characterize the transcriptional landscape of microsporidian parasites throughout the lifecycle, and heterogeneity in host cell responses to infection. I will present our latest work in these areas, and discuss how these dynamics may differ between cell types and between microsporidian species.

Professor Damian Ekiert

Professor Damian Ekiert

John Hopkins University, USA

09:30-10:00 A multiscale imaging approach to studying the invasion organelle from microsporidia pathogens

Microsporidia are tiny, single-celled parasites similar to fungi that infect a wide range of animal species, from worms and honey bees to humans. In humans, these opportunistic pathogens can cause life-threatening infections in immunocompromised individuals. To initiate an infection, microsporidia harness a specialized harpoon-like invasion apparatus called the polar tube (PT) to gain entry into host cells. The PT is tightly coiled within the transmissible extracellular spore, and is about 20 times the length of the spore. Once triggered, the PT is rapidly ejected, within milliseconds, and is thought to penetrate the host cell, acting as a conduit for the transfer of infectious cargo into the host, to initiate infection. Once inside host cells, microsporidia create a niche which is permissive to their development. We combine optical microscopy, Volume electron microscopy and structural cell biology to decipher the 3-dimensional organization, dynamics, and mechanism of the polar tube, parasite development, and host-parasite interactions.

Dr Gira Bhabha

Dr Gira Bhabha

John Hopkins University, USA

10:00-10:30 Break
10:30-11:00 Talk title TBC
Dr Naomi Fast

Dr Naomi Fast

University of British Columbia, Canada

11:00-11:30 Development of forward genetics in microsporidia using drug resistance screens

The study of microsporidia gene function has been hindered by a lack of genetic techniques. We have developed methods in C. elegans infected with its natural microsporidian parasite Nematocida parisii to perform genetic screens to select for drug resistance. We perform large-scale liquid cultures of C. elegans infected with N. parisii for multiple generations using increasing concentrations of two drugs, albendazole and dexrazoxane, with different mechanisms of action. We have isolated six isolates of N. parisii resistant to albendazole and three isolates resistant to dexrazoxane. Half of the albendazole-resistant isolates have genetic variants in beta-tubulin, the likely target of albendazole, and are resistant to multiple benzimidazole analogs, whereas the other three albendazole-resistant isolates show partial or no resistance to other benzimidazole analogs tested. We are currently analysing whole-genome sequencing data to identify potential causative genes for resistance in albendazole-resistant isolates without beta-tubulin mutations and in dexrazoxane-resistant isolates. The albendazole-resistant mutants with beta-tubulin mutations appear to be homozygous, suggesting that recombination occurred during selection. We are currently using albendazole- and dexrazoxane-resistant mutants to determine if sexual recombination between N. parisii can occur in a laboratory setting. Together, these genetic approaches will aid in characterizing gene function in N. parisii and are likely applicable to the study of other microsporidia species.

Dr Aaron Reinke

Dr Aaron Reinke

University of Toronto, Canada

11:30-12:00 Talk title TBC
Dr Louis Weiss

Dr Louis Weiss

Albert Einstein College, USA

Chair

Dr Judy Chen

Dr Judy Chen

USDA Agricultural Research Service’s Bee Research Laboratory (BRL), USA

13:00-13:30 Talk title TBC
Professor Tian Li

Professor Tian Li

Southwest University, China

13:30-14:00 Non-antibiotic treatments for honey bee diseases in the era of omics

Honey bees provide essential pollination services for approximately 35% of global food crop production, yet their populations continue to decline worldwide due to the combined impacts of pathogens, parasites, and environmental stressors. The microsporidian parasite Vairimorpha (Nosema) ceranae is a major contributor to honey bee morbidity and has been strongly implicated in widespread colony losses. For more than five decades, fumagillin-B has been the only antibiotic available for Nosema control in North America; however, concerns over resistance, off-target effects, and environmental impacts have led to its restriction or ban in many regions, underscoring the urgent need for non-antibiotic alternatives.

Using integrated genomic, comparative genomic, and transcriptomic approaches, we identified key parasite virulence factors required for host invasion and intracellular replication, as well as host pathways involved in V. ceranae–honey bee interactions. These omics-driven insights enabled the identification of molecular targets for novel disease-control strategies. We evaluated the therapeutic potential of RNA interference (RNAi) through two complementary approaches. First, parasite-derived virulence genes, including polar tube protein 3 (PTP3) and spore wall proteins (SWP8 and SWP12), were targeted using orally delivered double-stranded RNA (dsRNA), resulting in suppressed gene expression and significantly reduced Nosema spore loads. Second, RNAi was used to downregulate honey bee genes encoding negative regulators of immune and physiological functions, including naked cuticle (nkd), transferrin, and Suppressors of Cytokine Signaling 5 (SOCS5). Knockdown of these host genes enhanced immune responses, suppressed parasite reproduction, reduced infection intensity, and extended honey bee lifespan. Together, these results demonstrate that RNAi-based, omics-guided therapeutics represent a promising, targeted, and sustainable alternative to antibiotics for honey bee disease management, with broad implications for improving pollinator health and agricultural resilience.

Dr Judy Chen

Dr Judy Chen

USDA Agricultural Research Service’s Bee Research Laboratory (BRL), USA

14:00-14:30 Talk title TBC
Professor Pattana Jaroenlak

Professor Pattana Jaroenlak

Chulalongkorn University, Thailand

14:30-14:45 Break
14:45-17:00 Working groups and panel discussion