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Interactions between free-living amoebae and Cryptosporidium parvum: an experimental study

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Free-Living Amebae (FLA) and Cryptosporidium oocysts occasionally share the same environment. From 2004 to 2016, Cryptosporidium was responsible for 60% of 905 worldwide waterborne outbreaks caused by protozoan parasites. The aim of this study was to evaluate interactions between C. parvum oocysts and two common FLAs (Acanthamoeba castellanii and Vermamoeba vermiformis) in a water environment. Encystment and survival of FLAs were evaluated by microscopy using trypan blue vital coloration. Oocysts were numerated on microscopy. Interactions were studied over time in conditions both unfavorable and favorable to phagocytosis. Potential phagocytosis was directly evaluated by several microscopic approaches and indirectly by numeration of microorganisms and oocyst infectivity evaluation. Occasional phagocytosis of C. parvum by FLAs was documented. However, oocyst concentrations did not decrease significantly, suggesting resistance of oocysts to phagocytosis. A temporary decrease of oocyst infectivity was observed in the presence of A. castellanii. The effect of these interactions on C. parvum infectivity is particularly interesting. The biofilm condition could favor the persistence or even the proliferation of oocysts over time. This study demonstrated interactions between C. parvum and FLAs. Further knowledge of the mechanisms involved in the decrease of oocyst infectivity in the presence of A. castellanii could facilitate the development of new therapeutic approaches.
Title: Interactions between free-living amoebae and Cryptosporidium parvum: an experimental study
Description:
Free-Living Amebae (FLA) and Cryptosporidium oocysts occasionally share the same environment.
From 2004 to 2016, Cryptosporidium was responsible for 60% of 905 worldwide waterborne outbreaks caused by protozoan parasites.
The aim of this study was to evaluate interactions between C.
parvum oocysts and two common FLAs (Acanthamoeba castellanii and Vermamoeba vermiformis) in a water environment.
Encystment and survival of FLAs were evaluated by microscopy using trypan blue vital coloration.
Oocysts were numerated on microscopy.
Interactions were studied over time in conditions both unfavorable and favorable to phagocytosis.
Potential phagocytosis was directly evaluated by several microscopic approaches and indirectly by numeration of microorganisms and oocyst infectivity evaluation.
Occasional phagocytosis of C.
parvum by FLAs was documented.
However, oocyst concentrations did not decrease significantly, suggesting resistance of oocysts to phagocytosis.
A temporary decrease of oocyst infectivity was observed in the presence of A.
castellanii.
The effect of these interactions on C.
parvum infectivity is particularly interesting.
The biofilm condition could favor the persistence or even the proliferation of oocysts over time.
This study demonstrated interactions between C.
parvum and FLAs.
Further knowledge of the mechanisms involved in the decrease of oocyst infectivity in the presence of A.
castellanii could facilitate the development of new therapeutic approaches.

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