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Influence of Leishmania infection on blood-meal digestion in the sandfliesPhlebotomus papatasi andP. langeroni

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Influence of Leishmania infection on blood-meal digestion in the sandfliesPhlebotomus papatasi andP. langeroni. / Dillon, R. J. ; Lane, R. P. .
In: Parasitology Research, Vol. 79, No. 6, 06.1993, p. 492-496.

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Dillon RJ, Lane RP. Influence of Leishmania infection on blood-meal digestion in the sandfliesPhlebotomus papatasi andP. langeroni. Parasitology Research. 1993 Jun;79(6):492-496. doi: 10.1007/BF00931590

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@article{76c9861251bf4bc5b6b5b540b71f8bd1,
title = "Influence of Leishmania infection on blood-meal digestion in the sandfliesPhlebotomus papatasi andP. langeroni",
abstract = "The presence of amastigote-initiated infections of Leishmania major parasites caused a significant suppression in alkaline protease, trypsin and aminopeptidase activity during the first 30 h after ingestion of the infected bloodmeal in Phlebotomus papatasi, the natural vector of L. major. Protease levels were significantly higher in infected flies after 72 h than in the control group, where digestion had ceased. Evidence for the suppression of protease activity in infected P. langeroni, a sympatric but un-natural vector of L. major, was less clear; there was no difference in alkaline protease activity between control and infected groups in the first 24 h. However, protease, trypsin and aminopeptidase activities were elevated after 72 h in infected P. langeroni, indicating a delay in the time to the end of digestion and passage of the bloodmeal. The potential advantages for parasite development in suppressing protease activity and extending the period of bloodmeal digestion are discussed.",
author = "Dillon, {R. J.} and Lane, {R. P.}",
year = "1993",
month = jun,
doi = "10.1007/BF00931590",
language = "English",
volume = "79",
pages = "492--496",
journal = "Parasitology Research",
issn = "0044-3255",
publisher = "Springer Verlag",
number = "6",

}

RIS

TY - JOUR

T1 - Influence of Leishmania infection on blood-meal digestion in the sandfliesPhlebotomus papatasi andP. langeroni

AU - Dillon, R. J.

AU - Lane, R. P.

PY - 1993/6

Y1 - 1993/6

N2 - The presence of amastigote-initiated infections of Leishmania major parasites caused a significant suppression in alkaline protease, trypsin and aminopeptidase activity during the first 30 h after ingestion of the infected bloodmeal in Phlebotomus papatasi, the natural vector of L. major. Protease levels were significantly higher in infected flies after 72 h than in the control group, where digestion had ceased. Evidence for the suppression of protease activity in infected P. langeroni, a sympatric but un-natural vector of L. major, was less clear; there was no difference in alkaline protease activity between control and infected groups in the first 24 h. However, protease, trypsin and aminopeptidase activities were elevated after 72 h in infected P. langeroni, indicating a delay in the time to the end of digestion and passage of the bloodmeal. The potential advantages for parasite development in suppressing protease activity and extending the period of bloodmeal digestion are discussed.

AB - The presence of amastigote-initiated infections of Leishmania major parasites caused a significant suppression in alkaline protease, trypsin and aminopeptidase activity during the first 30 h after ingestion of the infected bloodmeal in Phlebotomus papatasi, the natural vector of L. major. Protease levels were significantly higher in infected flies after 72 h than in the control group, where digestion had ceased. Evidence for the suppression of protease activity in infected P. langeroni, a sympatric but un-natural vector of L. major, was less clear; there was no difference in alkaline protease activity between control and infected groups in the first 24 h. However, protease, trypsin and aminopeptidase activities were elevated after 72 h in infected P. langeroni, indicating a delay in the time to the end of digestion and passage of the bloodmeal. The potential advantages for parasite development in suppressing protease activity and extending the period of bloodmeal digestion are discussed.

U2 - 10.1007/BF00931590

DO - 10.1007/BF00931590

M3 - Journal article

VL - 79

SP - 492

EP - 496

JO - Parasitology Research

JF - Parasitology Research

SN - 0044-3255

IS - 6

ER -