Adapting the in vitro rumen incubation method to evaluate the effect of a plant extract on the exsheathment inhibition of Haemonchus contortus infective larvae

• Published in: Veterinary parasitology 2024-04, Vol.327, p.110135-110135, Article 110135
• Main Authors: Marin-Tun, Cindy Goretti, Mancilla-Montelongo, María Gabriela, Capetillo-Leal, Concepción Manuela, Sandoval-Castro, Carlos Alfredo, Hoste, Hervé, Borges-Argáez, Rocío, Torres-Acosta, Juan Felipe de Jesús
• Format: Article
• Language: English
• Subjects: Animal biology; Exsheathment; Gastrointestinal nematodes; Life Sciences; Plant secondary compounds; Ruminal liquor; Third-stage infective larvae; Veterinary medicine and animal Health
• ISSN: 0304-4017; 1873-2550; 0304-4017
• DOI: 10.1016/j.vetpar.2024.110135

This study adapted the in vitro rumen incubation (IVRI) method to evaluate the biological activity of a Gymnopodium floribundum leaves extract against the exsheathment of Haemonchus contortus infective larvae (L3), and to determine the role of plant polyphenols on the biological activity. The incubation protocol followed the IVRI method, adding polyethylene glycol (PEG) as a polyphenol-blocking agent. The L3 were incubated in ruminal liquor (RL), ruminal liquor with PEG (RL+PEG), ruminal liquor with G. floribundum extract (RLE), and ruminal liquor with G. floribundum extract and PEG (RLE+PEG). Incubation condition controls included phosphate buffered saline (PBS), PBS with PEG (PBS+PEG), incubation medium (without ruminal liquor) (IM), and incubation medium with PEG (IM+PEG). The L3 were recovered after incubation times of 0, 1, 3, 6, 9, and 24 h (39 °C). The respective L3 exsheathment kinetics were estimated for the different treatments (RL, RL+PEG, RLE, and RLE+PEG) using Log-Logistic models. The parameters of the different models were compared to determine the impact of the extract, with or without PEG, on the L3 exsheathment kinetics. The exsheathment in PBS and PBS+PEG remained