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Cryptosporidium species subtypes and associated clinical manifestations in Indian patients

AIM: Present hospital based study was carried out at our tertiary care centre with an aim to study the distribution of Cryptosporidium species subtypes in patients with complaints of diarrhea. BACKGROUND: Cryptosporidium species are one of the important causative agents of parasitic diarrhea, amongs...

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Autores principales: Khalil, Shehla, Mirdha, Bijay Ranjan, Panda, Ashutosh, Singh, Yogita, Makharia, Govind, Paul, Jaishree
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758740/
https://www.ncbi.nlm.nih.gov/pubmed/29379597
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author Khalil, Shehla
Mirdha, Bijay Ranjan
Panda, Ashutosh
Singh, Yogita
Makharia, Govind
Paul, Jaishree
author_facet Khalil, Shehla
Mirdha, Bijay Ranjan
Panda, Ashutosh
Singh, Yogita
Makharia, Govind
Paul, Jaishree
author_sort Khalil, Shehla
collection PubMed
description AIM: Present hospital based study was carried out at our tertiary care centre with an aim to study the distribution of Cryptosporidium species subtypes in patients with complaints of diarrhea. BACKGROUND: Cryptosporidium species are one of the important causative agents of parasitic diarrhea, amongst which Cryptosporidium hominis (C.hominis) and Cryptosporidium parvum (C.parvum) are the two major species that are associated with human cryptosporidiosis. METHODS: Four hundred and fifty (n=450) diarrheic patients complaining of different types of diarrhea were enrolled in the present study. Both microscopic and molecular diagnostic methods were used for the detection as well as for identification of Cryptosporidium species and its speciation and subtyping. RESULTS: Forty one (n=41) and forty three (n=43) patients were positive for Cryptosporidium species by microscopy and Polymerase chain reaction (PCR) assay respectively. Of these 43 cases, 70% (30/43) were identified as C. hominis and 21% (9/43) was as C. parvum, 7% (3/43) was as Cryptosporidium felis (C.felis) and 2% (1/43) as Cryptopsoridium viatorum (C. viatorum) respectively . Upon subtyping of C. hominis and C. parvum, 16 subtypes belonging to 8 different subtype families could be identified. The frequency of different families were Ia (13%, 5/39), Ib (15%, 6/39), Id (18%, 7/39), Ie (30%, 12/39) and IIa (5%, 2/39), IIc (8%, 3/39), IId (8%, 3/39) and IIe (3%, 1/39). CONCLUSION: Our study results strongly suggest and reinforces the fact that most of the human cryptosporidiosis is anthroponotic and we expect that present molecular epidemiological data will provide more insight to unravel the changing clinical paradigm of human cryptosporidiosis at large.
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spelling pubmed-57587402018-01-29 Cryptosporidium species subtypes and associated clinical manifestations in Indian patients Khalil, Shehla Mirdha, Bijay Ranjan Panda, Ashutosh Singh, Yogita Makharia, Govind Paul, Jaishree Gastroenterol Hepatol Bed Bench Original Article AIM: Present hospital based study was carried out at our tertiary care centre with an aim to study the distribution of Cryptosporidium species subtypes in patients with complaints of diarrhea. BACKGROUND: Cryptosporidium species are one of the important causative agents of parasitic diarrhea, amongst which Cryptosporidium hominis (C.hominis) and Cryptosporidium parvum (C.parvum) are the two major species that are associated with human cryptosporidiosis. METHODS: Four hundred and fifty (n=450) diarrheic patients complaining of different types of diarrhea were enrolled in the present study. Both microscopic and molecular diagnostic methods were used for the detection as well as for identification of Cryptosporidium species and its speciation and subtyping. RESULTS: Forty one (n=41) and forty three (n=43) patients were positive for Cryptosporidium species by microscopy and Polymerase chain reaction (PCR) assay respectively. Of these 43 cases, 70% (30/43) were identified as C. hominis and 21% (9/43) was as C. parvum, 7% (3/43) was as Cryptosporidium felis (C.felis) and 2% (1/43) as Cryptopsoridium viatorum (C. viatorum) respectively . Upon subtyping of C. hominis and C. parvum, 16 subtypes belonging to 8 different subtype families could be identified. The frequency of different families were Ia (13%, 5/39), Ib (15%, 6/39), Id (18%, 7/39), Ie (30%, 12/39) and IIa (5%, 2/39), IIc (8%, 3/39), IId (8%, 3/39) and IIe (3%, 1/39). CONCLUSION: Our study results strongly suggest and reinforces the fact that most of the human cryptosporidiosis is anthroponotic and we expect that present molecular epidemiological data will provide more insight to unravel the changing clinical paradigm of human cryptosporidiosis at large. Shaheed Beheshti University of Medical Sciences 2017 /pmc/articles/PMC5758740/ /pubmed/29379597 Text en ©2017 RIGLD, Research Institute for Gastroenterology and Liver Diseases This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Khalil, Shehla
Mirdha, Bijay Ranjan
Panda, Ashutosh
Singh, Yogita
Makharia, Govind
Paul, Jaishree
Cryptosporidium species subtypes and associated clinical manifestations in Indian patients
title Cryptosporidium species subtypes and associated clinical manifestations in Indian patients
title_full Cryptosporidium species subtypes and associated clinical manifestations in Indian patients
title_fullStr Cryptosporidium species subtypes and associated clinical manifestations in Indian patients
title_full_unstemmed Cryptosporidium species subtypes and associated clinical manifestations in Indian patients
title_short Cryptosporidium species subtypes and associated clinical manifestations in Indian patients
title_sort cryptosporidium species subtypes and associated clinical manifestations in indian patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758740/
https://www.ncbi.nlm.nih.gov/pubmed/29379597
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