Publications by authors named "M G Mancilla-Montelongo"

Article Synopsis
  • The study analyzes the expression levels of 10 P-glycoprotein (P-gp) genes in two field isolates of the parasitic nematode Haemonchus contortus from Yucatan, Mexico, one resistant to Ivermectin (IVM) and one susceptible.
  • Results indicated that the IVM-resistant isolate (PARAISO) showed significant upregulation of several P-gp genes compared to both the IVM-susceptible isolate (FMVZ-UADY) and a susceptible reference isolate (CENID-SAI).
  • Understanding the relationship between these gene expressions and IVM resistance may aid in identifying molecular markers for diagnosing resistance, while also emphasizing the importance of geographical factors
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This study applied the in vitro rumen exsheathment test (IVRET) to evaluate the exsheathment kinetics of Haemonchus contortus infective larvae (L) incubated in ruminal liquor (RL) containing acetone:water extracts of Acacia pennatula (AP), Gymnopodium floribundum (GF), Havardia albicans (HA) or Lysiloma latisiliquum (LL). The role of polyphenols in the biological activity of the evaluated extracts was also determined. Larvae were incubated in RL either alone or added with a different plant extract (AP, GF, HA, or LL) at 1200 μg/mL.

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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 (L), 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 L were incubated in ruminal liquor (RL), ruminal liquor with PEG (RL+PEG), ruminal liquor with G.

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Ivermectin (IVM) resistance in parasitic nematodes such as Haemonchus contortus has spurred a search for substances that help to recover its efficacy. One potential agent is the natural product curcumin (CUR). In this study, CUR was combined with polyvinylpyrrolidone (PVP) (CUR/PVP) to improve its solubility and biological applicability.

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This study developed and evaluated an in vitro rumen incubation (IVRI) method to describe the exsheathment kinetics of Haemonchus contortus third-stage infective larvae (L) in ruminal liquor (RL). The specific objectives were (i) to standardize the IVRI method to facilitate the contact between L and RL as well as the larval recovery, and (ii) to apply the IVRI method to describe the exsheathment kinetics of H. contortus and to select the best fitting nonlinear model.

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