<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>42(9)</volume><submitter>Pratlong F</submitter><pubmed_abstract>In the south of France, leishmaniasis due to Leishmania infantum occurs in the following five foci of endemicity (from west to east): Pyrénées-Orientales, Cévennes, Provence, Côte d'Azur, and Corsica. Between 1981 and 2002, 712 Leishmania strains obtained from humans, dogs, cats, and sand flies were studied by isoenzyme analysis. In total, seven zymodemes were identified: MON-1, MON-11, MON-24, MON-29, MON-33, MON-34, and MON-108. The Pyrénées-Orientales focus is characterized by a predominance of human cutaneous leishmaniasis and a high enzymatic polymorphism (five zymodemes). In the other foci, where human visceral leishmaniasis is predominant, only two zymodemes are present. L. infantum MON-1 is the parasite most frequently found, in patients both with and without concomitant human immunodeficiency virus infection. MON-1 is the only zymodeme present in dogs, which act as the reservoir host in all of the foci. In Cévennes, where the complete life cycle of zymodeme MON-1 has been identified, Phlebotomus perniciosus and Phlebotomus ariasi are vectors. The enzymatic polymorphism is compared to that of neighboring countries (Spain and Italy). In Pyrénées-Orientales, small variant zymodemes with electromorphs of heterozygote-like and homozygotic patterns can be explained by different genetic hypotheses.</pubmed_abstract><journal>Journal of clinical microbiology</journal><pagination>4077-82</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC516332</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Isoenzymatic analysis of 712 strains of Leishmania infantum in the south of France and relationship of enzymatic polymorphism to clinical and epidemiological features.</pubmed_title><pmcid>PMC516332</pmcid><pubmed_authors>Marty P</pubmed_authors><pubmed_authors>Dereure J</pubmed_authors><pubmed_authors>Lanotte G</pubmed_authors><pubmed_authors>Dedet JP</pubmed_authors><pubmed_authors>Pratlong F</pubmed_authors><pubmed_authors>Rioux JA</pubmed_authors><pubmed_authors>Faraut-Gambarelli F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Isoenzymatic analysis of 712 strains of Leishmania infantum in the south of France and relationship of enzymatic polymorphism to clinical and epidemiological features.</name><description>In the south of France, leishmaniasis due to Leishmania infantum occurs in the following five foci of endemicity (from west to east): Pyrénées-Orientales, Cévennes, Provence, Côte d'Azur, and Corsica. Between 1981 and 2002, 712 Leishmania strains obtained from humans, dogs, cats, and sand flies were studied by isoenzyme analysis. In total, seven zymodemes were identified: MON-1, MON-11, MON-24, MON-29, MON-33, MON-34, and MON-108. The Pyrénées-Orientales focus is characterized by a predominance of human cutaneous leishmaniasis and a high enzymatic polymorphism (five zymodemes). In the other foci, where human visceral leishmaniasis is predominant, only two zymodemes are present. L. infantum MON-1 is the parasite most frequently found, in patients both with and without concomitant human immunodeficiency virus infection. MON-1 is the only zymodeme present in dogs, which act as the reservoir host in all of the foci. In Cévennes, where the complete life cycle of zymodeme MON-1 has been identified, Phlebotomus perniciosus and Phlebotomus ariasi are vectors. The enzymatic polymorphism is compared to that of neighboring countries (Spain and Italy). In Pyrénées-Orientales, small variant zymodemes with electromorphs of heterozygote-like and homozygotic patterns can be explained by different genetic hypotheses.</description><dates><release>2004-01-01T00:00:00Z</release><publication>2004 Sep</publication><modification>2025-05-29T19:16:29.389Z</modification><creation>2024-11-05T20:18:15.19Z</creation></dates><accession>S-EPMC516332</accession><cross_references><pubmed>15364993</pubmed><doi>10.1128/jcm.42.9.4077-4082.2004</doi><doi>10.1128/JCM.42.9.4077-4082.2004</doi></cross_references></HashMap>