4.5 Article

XENOFOOD-An Autoclaved Feed Supplement Containing Autoclavable Antimicrobial Peptides-Exerts Anticoccidial GI Activity, and Causes Bursa Enlargement, but Has No Detectable Harmful Effects in Broiler Cockerels despite In Vitro Detectable Cytotoxicity on LHM Cells

Journal

PATHOGENS
Volume 12, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/pathogens12030458

Keywords

multidrug resistance; MDR; EPB (entomo-pathogenic bacteria, Xenorhabdus,(X.budapestensis,X.szentirmaii,Z.innexii), and Photorhabdus species); CFCM (cell-free conditioned media); NR-AMP (non-ribosomal-templated antimicrobial peptides); anti-microbial; anti-bacterial; anti-coccidial; anti-protist activity; cytotoxicity; Clostridium CFU-(colony forming unit); in situ (local) bioavailability; XENOFOOD; alternative antibiotics

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Entomopathogenic bacteria are symbionts of entomopathogenic nematodes that produce antimicrobial peptides with broad-spectrum activity. These peptides can neutralize various pathogens. In a feeding experiment with broiler cockerels, a feed supplement containing these peptides showed gastrointestinal activity, reducing the number of Clostridium perfringens units in the lower jejunum. No adverse effects were observed, indicating the safety of this supplement.
Entomopathogenic bacteria are obligate symbionts of entomopathogenic nematode (EPN) species. These bacteria biosynthesize and release non-ribosomal-templated hybrid peptides (NR-AMPs), with strong, and large-spectral antimicrobial potential, capable of inactivating pathogens belonging to different prokaryote, and eukaryote taxa. The cell-free conditioned culture media (CFCM) of Xenorhabdus budapestensis and X. szentirmaii efficiently inactivate poultry pathogens like Clostridium, Histomonas, and Eimeria. To learn whether a bio-preparation containing antimicrobial peptides of Xenorhabdus origin with accompanying (in vitro detectable) cytotoxic effects could be considered a safely applicable preventive feed supplement, we conducted a 42-day feeding experiment on freshly hatched broiler cockerels. XENOFOOD (containing autoclaved X. budapestensis, and X. szentirmaii cultures developed on chicken food) were consumed by the birds. The XENOFOOD exerted detectable gastrointestinal (GI) activity (reducing the numbers of the colony-forming Clostridium perfringens units in the lower jejunum. No animal was lost in the experiment. Neither the body weight, growth rate, feed-conversion ratio, nor organ-weight data differed between the control (C) and treated (T) groups, indicating that the XENOFOOD diet did not result in any detectable adverse effects. We suppose that the parameters indicating a moderate enlargement of bursas of Fabricius (average weight, size, and individual bursa/spleen weight-ratios) in the XENOFOOD-fed group must be an indirect indication that the bursa-controlled humoral immune system neutralized the cytotoxic ingredients of the XENOFOOD in the blood, not allowing to reach their critical cytotoxic concentration in the sensitive tissues.

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