Analyzing the safety of the parasiticide fungus Mucor circinelloides : first insights on its virulence profile and interactions with the avian gut microbial community

Author:

Lozano João12ORCID,Cunha Eva12,Almeida Cristina3,Nunes Mónica4,Dias Ricardo4,Vicente Eduardo5,Sebastião Daniela5,Henriques Sérgio6,Madeira de Carvalho Luís12ORCID,Paz-Silva Adolfo7,Oliveira Manuela1289

Affiliation:

1. CIISA – Centre for Interdisciplinary Research in Animal Health, Faculty of Veterinary Medicine, University of Lisbon, Lisbon, Portugal

2. Associate Laboratory for Animal and Veterinary Sciences (AL4AnimalS), Lisbon, Portugal

3. Exoclinic – Clínica Veterinária de Aves e Exóticos, Miraflores, Portugal

4. Biosystems and Integrative Sciences Institute, Faculty of Sciences, University of Lisbon, Lisbon, Portugal

5. Castelo de São Jorge, EGEAC – Empresa de Gestão de Equipamentos e Animação Cultural, Lisbon, Portugal

6. Quinta da Galeana, Ovinos do Futuro, Lda., Nadrupe, Portugal

7. Control of Parasites Research Group (COPAR, GI-2120), Department of Animal Pathology, Faculty of Veterinary, University of Santiago de Compostela, Lugo, Spain

8. cE3c – Centre for Ecology, Evolution and Environmental Changes, Faculdade de Ciências, Universidade de Lisboa, Lisbon, Portugal

9. CHANGE – Global Change and Sustainability Institute, Faculdade de Ciências, Universidade de Lisboa, Lisbon, Portugal

Abstract

ABSTRACT Parasiticide fungi are considered an accurate, sustainable, and safe solution for the biocontrol of animal gastrointestinal (GI) parasites. This research provides an initial characterization of the virulence of the native parasiticide fungus Mucor circinelloides (FMV-FR1) and an assessment of its impact on birds’ gut microbes. The genome of this fungus was sequenced to identify the genes coding for virulence factors. Also, this fungus was checked for the phenotypic expression of proteinase, lecithinase, DNase, gelatinase, hemolysin, and biofilm production. Finally, an in vivo trial was developed based on feeding M. circinelloides spores to laying hens and peacocks three times a week. Bird feces were collected for 3 months, with total genomic DNA being extracted and subjected to long-read 16S and 25S-28S sequencing. Genes coding for an iron permease (FTR1), iron receptors (FOB1 and FOB2), ADP-ribosylation factors (ARFs) (ARF2 and ARF6), and a GTPase (CDC42) were identified in this M. circinelloides genome. Also, this fungus was positive only for lecithinase activity. The field trial revealed a fecal microbiome dominated by Firmicutes and Proteobacteria in laying hens, and Firmicutes and Bacteroidetes in peacocks, whereas the fecal mycobiome of both bird species was mainly composed of Ascomycetes and Basidiomycetes fungi. Bacterial and fungal alpha-diversities did not differ between sampling time points after M. circinelloides administrations ( P = 0.62 and P = 0.15, respectively). Although findings from this research suggest the lack of virulence of this M. circinelloides parasiticide isolate, more complementary in vitro and in vivo research is needed to conclude about the safety of its administration to birds, aiming at controlling their GI parasites. IMPORTANCE A previous study revealed that the native Mucor circinelloides isolate (FMV-FR1) can develop parasiticide activity toward coccidia oocysts, one of the most pathogenic GI parasites in birds. However, ensuring its safety for birds is of utmost importance, namely by studying its virulence profile and potential effect on commensal gut microbes. This initial study revealed that although this M. circinelloides isolate had genes coding for four types of virulence factors—iron permease, iron receptors, ADP-ribosylation factors, and GTPase—and only expressed phenotypically the enzyme lecithinase, the administration of its spores to laying hens and peacocks did not interfere with the abundances and diversities of their gut commensal bacteria and fungi. Although overall results suggest the lack of virulence of this M. circinelloides isolate, more complementary research is needed to conclude about the safety of its administration to birds in the scope of parasite biocontrol programs.

Funder

MEC | Fundação para a Ciência e a Tecnologia

MCINN, Spain; FEDER

AGACAL, Spain

Consellería de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia

Publisher

American Society for Microbiology

Reference48 articles.

1. Madeira de Carvalho L, Bernardo F, Paz-Silva A. 2012. The role of fungi in the control of animal parasites - classification, mode of action and practical applications. In Paz-Silva A, Vázquez M (ed), Fungi: types, environmental impact and role in disease. Nova Science Publishers, Hauppauge, NY, USA.

2. Nematophagous fungi for biological control of gastrointestinal nematodes in domestic animals

3. Analysis of the effect of soil saprophytic fungi on the eggs of Baylisascaris procyonis

4. Isolation of saprophytic filamentous fungi from avian fecal samples and assessment of its predatory activity on coccidian oocysts

5. Controlo integrado da estrongilidose equina com anti-helmínticos associados ao fungo Duddingtonia flagrans. Aspectos da sua utilização em Portugal;Madeira de Carvalho L;Acta Parasitológica Portuguesa,2011

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