Ultrastructural Alterations of the Human Pathogen Giardia intestinalis after Drug Treatment
Marlene Benchimol1,2,3, Ana Paula Gadelha4, Wanderley de Souza2,3
1BIOTRANS-CAXIAS, Universidade do Grande Rio. UNIGRANRIO, Rio de Janeiro 96200-000, Brazil.
Abstract:
This review presents the main cell characteristics altered after in vitro incubation of the parasite with commercial drugs used to treat the disease caused by Giardia intestinalis. This important intestinal parasite primarily causes diarrhea in children. Metronidazole and albendazole are the primary compounds used in therapy against Giardia intestinalis. However, they provoke significant side effects, and some strains have developed resistance to metronidazole. Benzimidazole carbamates, such as albendazole and mebendazole, have shown the best activity against Giardia. Despite their in vitro efficacy, clinical treatment with benzimidazoles has yielded conflicting results, demonstrating lower cure rates. Recently, nitazoxanide has been suggested as an alternative to these drugs. Therefore, to enhance the quality of chemotherapy against this parasite, it is important to invest in developing other compounds that can interfere with key steps of metabolic pathways or cell structures and organelles. For example, Giardia exhibits a unique cell structure called the ventral disc, which is crucial for host adhesion and pathogenicity. Thus, drugs that can disrupt the adhesion process hold promise for future therapy against Giardia. Additionally, this review discusses new drugs and strategies that can be employed, as well as suggestions for developing novel drugs to control the infection caused by this parasite.
Insights
This review examines how common drugs affect Giardia intestinalis cells. It highlights the need for new treatments due to drug resistance and side effects, focusing on novel strategies targeting parasite adhesion.
Area of Science:
- Parasitology
- Pharmacology
- Infectious Diseases
Background:
- Giardia intestinalis is a significant intestinal parasite causing diarrhea, particularly in children.
- Current treatments like metronidazole and albendazole face challenges including side effects and emerging drug resistance.
- Benzimidazole carbamates show in vitro efficacy, but clinical outcomes are inconsistent, necessitating alternative therapies.
Purpose of the Study:
- To review cellular alterations in Giardia intestinalis upon incubation with existing antigiardial drugs.
- To discuss the limitations of current therapies and explore novel drug targets and strategies.
- To provide insights for developing more effective chemotherapy against Giardiasis.
Main Methods:
- In vitro incubation of Giardia intestinalis with commercial antigiardial drugs.
- Analysis of altered cell characteristics, including structural and metabolic pathways.
- Review of existing literature on drug efficacy, resistance, and emerging therapeutic approaches.
Main Results:
- Metronidazole and albendazole, common treatments, induce specific cellular changes in Giardia.
- Resistance to metronidazole is a growing concern, impacting treatment effectiveness.
- Benzimidazoles exhibit potent in vitro activity, yet clinical efficacy is variable.
Conclusions:
- There is a critical need for novel therapeutic agents against Giardia intestinalis due to resistance and side effects of current drugs.
- Targeting unique parasite structures like the ventral disc, essential for adhesion, presents a promising avenue for new drug development.
- Further research into alternative compounds and therapeutic strategies is essential for improved Giardiasis treatment.
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