Background: The nematophagous fungus Pochonia chlamydosporia can degrade ascarid (e.g. Ascaridia galli) eggs in agar and soil in vitro. However, it has not been investigated how this translates to reduced infection levels in naturally exposed chickens. We thus tested the infectivity of soil artificially contaminated with A. galli (and a few Heterakis gallinarum) eggs and treated with P. chlamydosporia. Sterilised and non-sterilised soils were used to examine any influence of natural soil biota.
Methods: Unembryonated eggs were mixed with sterilised (S)/non-sterilised (N) soil, either treated with the fungus (F) or left as untreated controls (C) and incubated (22 °C, 35 days) to allow eggs to embryonate and fungus to grow. Egg number in soil was estimated on days 0 and 35 post-incubation. Hens were exposed to the soil (SC/SF/NC/NF) four times over 12 days by mixing soil into the feed. On day 42 post-first-exposure (p.f.e.), the hens were euthanized and parasites were recovered. Serum A. galli IgY level and ascarid eggs per gram of faeces (EPG) were examined on days -1 and 36 (IgY) or 40 p.f.e. (EPG).
Results: Egg recovery in SF soil was substantially lower than in SC soil, but recovery was not significantly different between NF and NC soils. SF hens had a mean worm count of 76 whereas the other groups had means of 355-453. Early mature/mature A. galli were recovered from SF hens whereas hens in the other groups harboured mainly immature A. galli. Heterakis gallinarum counts were low overall, especially in SF. The SF post-exposure IgY response was significantly lower while EPG was significantly higher compared to the other groups.
Conclusions: Pochonia chlamydosporia was very effective in reducing ascarid egg numbers in sterilised soil and thus worm burdens in the exposed hens. However, reduced exposure of hens shifted A. galli populations toward a higher proportion of mature worms and resulted in a higher faecal egg excretion within the study period. This highlights a fundamental problem in ascarid control: if not all eggs in the farm environment are inactivated, the resulting low level infections may result in higher contamination levels with associated negative long-term consequences.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5975387 | PMC |
http://dx.doi.org/10.1186/s13071-018-2898-1 | DOI Listing |
Front Vet Sci
January 2025
Rui Pu Agricultural Technology Co., Ltd., Hohhot, China.
Introduction: The control of parasites infections in livestock is an ongoing concern, with parasites developing resistance to commonly used antiparasitic drugs. The current study investigated the destructive effect of the fungus Pochonia chlamydosporia on the eggs and oocysts of several equine parasites, as well as assessing the safety of the fungus in mice.
Methods: , , Anoplocephala spp eggs and spp.
Sci Rep
January 2025
Division of Microbiology, Indian Agricultural Research Institute, New Delhi, 110012, India.
Root-knot nematodes (Meloidogyne spp.) are significant pests that cause considerable damage to crops, prompting a need for sustainable control methods. This study evaluated the nematicidal potential of fungal culture filtrates and botanicals as eco-friendly alternatives.
View Article and Find Full Text PDFVet Parasitol
December 2024
College of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot, Inner Mongolia, China; Key Laboratory of Clinical Diagnosis and Treatment of Animal Diseases, Ministry of Agriculture, National Animal Medicine Experimental Teaching Center, China. Electronic address:
To address the economic burden caused by livestock parasitic diseases, particularly gastrointestinal nematodes (GIN) and liver flukes, which are exacerbated by growing anthelmintic resistance, researchers are increasingly focusing on biological control strategies as a promising solution. Among these, the fungus Pochonia chlamydosporia has demonstrated promising helminth control properties. This study explored the potential of P.
View Article and Find Full Text PDFFront Plant Sci
September 2024
Institute for Sustainable Agriculture (IAS), Spanish National Research Council (CSIC), Cordoba, Spain.
Front Microbiol
April 2024
State Key Laboratory of Vegetable Biobreeding, Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences, Beijing, China.
Chemical study of the nematicidal biocontrol fungus PC-170 led to discovery of six resorcylic acid lactones (RALs), including three nematicidal glycosylated RALs, monocillin VI glycoside , colletogloeolactone A and monocillin II glycoside , and three antibacterial non-glycosylated RALs, monocillin VI , monocillin IV and monocillin II . The planar structure of the new compound monocillin VI glycoside was elucidated using HRESIMS and NMR data, and its monosaccharide configuration was further determined through sugar hydrolysis experiment and GC-MS analysis method. Furthermore, their two biosynthetic-related PKS genes, and , were identified through the gene knockout experiment.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!