An In-depth Proteomic Map of Leishmania donovani Isolate from Post Kala-azar Dermal Leishmaniasis (PKDL) Patient.


Journal

Acta parasitologica
ISSN: 1896-1851
Titre abrégé: Acta Parasitol
Pays: Switzerland
ID NLM: 9301947

Informations de publication

Date de publication:
Jun 2022
Historique:
received: 10 08 2021
accepted: 09 12 2021
pubmed: 13 1 2022
medline: 26 5 2022
entrez: 12 1 2022
Statut: ppublish

Résumé

The trypanosomatid protozoan parasite Leishmania donovani is the etiological agent of visceral leishmaniasis (VL) or kala-azar. The patients that have undergone treatment may still harbor the parasite and in a small fraction of the patients the disease re-erupts in the form of post kala-azar dermal leishmaniasis (PKDL). PKDL is a pathological condition found to be intermediate between VL and complete cure of VL. The PKDL disease progression is determined by the host immune response to L. donovani. The majority of the proteomic studies on L. donovani till date have been undertaken on parasites either isolated from kala-azar patients or on established laboratory strains of L. donovani. However, no proteomic information is available on the cutaneous localized isolates of L. donovani from PKDL patients. The promastigote stage of L. donovani isolate from PKDL patient was cultured and harvested. The cell lysates were trypsin digested, followed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis. The LC-MS/MS raw data were analyzed on Proteome Discoverer. Further bioinformatics analysis was carried out. In the present, we have used high-resolution mass spectrometry to map the global proteome of a L. donovani isolate from PKDL patient. This in-depth study resulted in the identification of 5537 unique proteins from PKDL isolate of L. donovani which covered 64% of its proteome. This study also identified proteins previously shown to be upregulated in PKDL L. donovani. This is the most in-depth proteome of Leishmania donovani parasite till date.

Sections du résumé

BACKGROUND BACKGROUND
The trypanosomatid protozoan parasite Leishmania donovani is the etiological agent of visceral leishmaniasis (VL) or kala-azar. The patients that have undergone treatment may still harbor the parasite and in a small fraction of the patients the disease re-erupts in the form of post kala-azar dermal leishmaniasis (PKDL). PKDL is a pathological condition found to be intermediate between VL and complete cure of VL. The PKDL disease progression is determined by the host immune response to L. donovani. The majority of the proteomic studies on L. donovani till date have been undertaken on parasites either isolated from kala-azar patients or on established laboratory strains of L. donovani. However, no proteomic information is available on the cutaneous localized isolates of L. donovani from PKDL patients.
METHODS METHODS
The promastigote stage of L. donovani isolate from PKDL patient was cultured and harvested. The cell lysates were trypsin digested, followed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis. The LC-MS/MS raw data were analyzed on Proteome Discoverer. Further bioinformatics analysis was carried out.
RESULTS RESULTS
In the present, we have used high-resolution mass spectrometry to map the global proteome of a L. donovani isolate from PKDL patient. This in-depth study resulted in the identification of 5537 unique proteins from PKDL isolate of L. donovani which covered 64% of its proteome.
OUTCOME RESULTS
This study also identified proteins previously shown to be upregulated in PKDL L. donovani. This is the most in-depth proteome of Leishmania donovani parasite till date.

Identifiants

pubmed: 35020128
doi: 10.1007/s11686-021-00511-3
pii: 10.1007/s11686-021-00511-3
doi:

Substances chimiques

Proteome 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

687-696

Subventions

Organisme : Department of Science and Technology, Ministry of Science and Technology
ID : DST-WOS-A

Informations de copyright

© 2022. The Author(s) under exclusive licence to Witold Stefański Institute of Parasitology, Polish Academy of Sciences.

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Auteurs

Chinmayee Bar Routaray (CB)

Department of Zoology, Centre for Advanced Study, Savitribai Phule Pune University, Pune, 411007, India.

Avishek Kumar (A)

INNODx Solutions Pvt Ltd, Biotech Bioincubator (BBB), Regional Centre for Biotechnology, NCR Biotech Science Cluster, Faridabad, Haryana, 1221001, India.

Shyam Sundar (S)

Institute of Medical Sciences, Banaras Hindu University, Varanasi, 221005, India.

Gajanan Sathe (G)

Institute of Bioinformatics, International Technology Park, Bangalore, 560066, India. gajanan@ibioinformatics.org.
Manipal Academy of Higher Education, Manipal, India. gajanan@ibioinformatics.org.

Harsh Pawar (H)

Faculty of Biology, Technion-Israel Institute of Technology, 3200003, Haifa, Israel. harshpawar@campus.technion.ac.il.
Division of Biomedical & Life Sciences, Faculty of Health & Medicine, Lancaster University, Lancaster, UK. harshpawar@campus.technion.ac.il.

Kalpana Pai (K)

Department of Zoology, Centre for Advanced Study, Savitribai Phule Pune University, Pune, 411007, India. drkalpanapai@gmail.com.

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