The life-cycle of Leishmania in the sandfly with special reference to the form infective to the vertebrate host
Ann. Parasitol. Hum. Comp., 65 (1990) 37-42
Published online: 2016-08-15
Articles citing this article
The Citing articles tool gives a list of articles citing the current article.
The citing articles come from EDP Sciences database, as well as other publishers participating in CrossRef Cited-by Linking Program. You can set up your personal account to receive an email alert each time this article is cited by a new article (see the menu on the right-hand side of the abstract page).
Cited article:
This article has been cited by the following article(s):
Current state of the art of gold complexes as antileishmanial agents
Catherine Hemmert, Heinz Gornitzka, Céline Deraeve and Jean-Luc StiglianiCoordination Chemistry Reviews 528 216408 (2025)
https://doi.org/10.1016/j.ccr.2024.216408
(2025)
https://doi.org/10.2139/ssrn.5279706
Comparison of biosynthetic zinc oxide nanoparticle and glucantime cytotoxic effects on Leishmania major (MRHO/IR/75/ER)
Fatemeh Saleh, Farnaz Kheirandish, Mohammad Abbasi, Fatemeh Ahmadpour, Saeed Veiskarami and Atefe MirderikvandJournal of Basic Microbiology 64 (5) (2024)
https://doi.org/10.1002/jobm.202300490
Single-cell atlas of Leishmania development in sandflies reveals the heterogeneity of transmitted parasites and their role in infection
Carolina M. C. Catta-Preta, Kashinath Ghosh, David L. Sacks and Tiago R. FerreiraProceedings of the National Academy of Sciences 121 (52) (2024)
https://doi.org/10.1073/pnas.2406776121
An update on Leishmania martiniquensis infections: Transmission, clinical characteristics, and treatment
Somayyeh Ahmadi, Maryam Hataminejad, Bahman Rahimi Esboei, Seyed Abdollah Hosseini and Mahdi FakharParasite Epidemiology and Control 27 e00386 (2024)
https://doi.org/10.1016/j.parepi.2024.e00386
(2024)
https://doi.org/10.1101/2024.09.13.612636
Sojourn of Nitrogenous Heterocycles as Promising Antileishmanial Agents: Medicinal Perspectives and Structure–Activity Relationship Studies
Bhupender Nehra, Manoj Kumar, Sumitra Singh, Viney Chawla and Pooja A. ChawlaChemistry Africa 7 (7) 3485 (2024)
https://doi.org/10.1007/s42250-024-00944-z
(2024)
https://doi.org/10.21203/rs.3.rs-4022188/v1
(2024)
https://doi.org/10.1007/5584_2024_811
A novel approach to design chimeric multi epitope vaccine against Leishmania exploiting infected host cell proteome
Sooram Banesh, Neharika Gupta, Chethireddy Vihadhar Reddy, Uppuladinne Mallikarjunachari, Nupoor Patil, Sonavane Uddhavesh and Prakash SaudagarHeliyon 10 (10) e31306 (2024)
https://doi.org/10.1016/j.heliyon.2024.e31306
Experimental Susceptibility of Nyssomyia antunesi and Lutzomyia longipalpis (Psychodidae: Phlebotominae) to Leishmania (Viannia) lainsoni and L. (V.) lindenbergi (Trypanosomatidae: Leishmaniinae)
Yetsenia del Valle Sánchez Uzcátegui, Fernando Tobias Silveira, Thais Gouvea de Morais, Rodrigo Ribeiro Furtado, Thiago Vasconcelos dos Santos and Marinete Marins PóvoaMicroorganisms 12 (4) 809 (2024)
https://doi.org/10.3390/microorganisms12040809
Investigating potential sand fly vectors after the first reported outbreak of cutaneous leishmaniasis in Ghana
Dziedzom K. de Souza, Seth Offei Addo, Kwame Desewu, et al.Parasites & Vectors 16 (1) (2023)
https://doi.org/10.1186/s13071-023-05767-4
(2023)
https://doi.org/10.21203/rs.3.rs-2497061/v1
Vector-borne Trypanosoma brucei parasites develop in artificial human skin and persist as skin tissue forms
Christian Reuter, Laura Hauf, Fabian Imdahl, Rituparno Sen, Ehsan Vafadarnejad, Philipp Fey, Tamara Finger, Nicola G. Jones, Heike Walles, Lars Barquist, Antoine-Emmanuel Saliba, Florian Groeber-Becker and Markus EngstlerNature Communications 14 (1) (2023)
https://doi.org/10.1038/s41467-023-43437-2
Evaluation of Hepatotoxicity Effect of Sodium Stibogluconate (Pentostam) in Mice Model
Kaula. A. Saad, Intisar. O. Abdalla, Hanan. A. Alkailani , Ahmed. M. Elbakush and Zena. A. ZreibaAl-Mukhtar Journal of Sciences 37 (1) 22 (2022)
https://doi.org/10.54172/mjsc.v37i1.738
Vaccine Design
Sunil Kumar, Shubhranshu Zutshi, Mukesh Kumar Jha, Prashant Chauhan and Bhaskar SahaMethods in Molecular Biology, Vaccine Design 2410 433 (2022)
https://doi.org/10.1007/978-1-0716-1884-4_23
Seasonal Dynamics of Sand Flies (Diptera, Pshycodidae), Vectors of Cutaneous Leishmaniasis, in the City of Fez, Northern Morocco
Najoua Darkaoui, Abdellatif Janati Idrissi, Fatima Zahra Talbi, et al.The Scientific World Journal 2022 1 (2022)
https://doi.org/10.1155/2022/4095129
Some Scaffolds as Anti-leishmanial Agents: A Review
Thatikayala Mahender, Wadhwa Pankaj, Singh Pankaj Kumar, Vaidya Ankur and Sahu Sanjeev KumarMini-Reviews in Medicinal Chemistry 22 (5) 743 (2022)
https://doi.org/10.2174/1389557521666210913115116
Recent advancements in anti-leishmanial research: Synthetic strategies and structural activity relationships
Ojasvi Gupta, Tathagata Pradhan, Rohit Bhatia and Vikramdeep MongaEuropean Journal of Medicinal Chemistry 223 113606 (2021)
https://doi.org/10.1016/j.ejmech.2021.113606
Development of Various Leishmania (Sauroleishmania) tarentolae Strains in Three Phlebotomus Species
Lucie Ticha, Barbora Kykalova, Jovana Sadlova, Marina Gramiccia, Luigi Gradoni and Petr VolfMicroorganisms 9 (11) 2256 (2021)
https://doi.org/10.3390/microorganisms9112256
Species diversity and spatial distribution of CL/VL vectors: assessing bioclimatic effect on expression plasticity of genes possessing vaccine properties isolated from wild-collected sand flies in endemic areas of Iran
Ali Bordbar and Parviz ParviziBMC Infectious Diseases 21 (1) (2021)
https://doi.org/10.1186/s12879-021-06129-0
Marine Natural Products
Sofia Kokkaliari, Nicole E. Avalon, Kristin Herrera, et al.Topics in Heterocyclic Chemistry, Marine Natural Products 58 209 (2021)
https://doi.org/10.1007/7081_2021_56
Pathogenesis, Treatment and Prevention of Leishmaniasis
Shobha Upreti, Veni Pande, Diksha Joshi, Vinita Gouri and Mukesh SamantPathogenesis, Treatment and Prevention of Leishmaniasis 209 (2021)
https://doi.org/10.1016/B978-0-12-822800-5.00008-1
The lectin pathway of complement and the initial recognition of Leishmania infantum promastigotes
Altair Rogerio Ambrosio, Lorena Bavia, Priscila Mazzocchi Hiraiwa, et al.Life Sciences 282 119793 (2021)
https://doi.org/10.1016/j.lfs.2021.119793
Characterization of an Atypical eIF4E Ortholog in Leishmania, LeishIF4E-6
Nitin Tupperwar, Rohit Shrivastava, Nofar Baron, Orli Korchev, Irit Dahan and Michal ShapiraInternational Journal of Molecular Sciences 22 (23) 12720 (2021)
https://doi.org/10.3390/ijms222312720
Risk Factors of Leishmania Infection among HIV-Infected Patients in Trang Province, Southern Thailand: A Study on Three Prevalent Species
Sakarn Charoensakulchai, Lertwut Bualert, Jipada Manomat, et al.The American Journal of Tropical Medicine and Hygiene 103 (4) 1502 (2020)
https://doi.org/10.4269/ajtmh.20-0332
Medicinal Chemistry
Rebekah N. Duffin, Melissa V. Werrett and Philip C. AndrewsAdvances in Inorganic Chemistry, Medicinal Chemistry 75 207 (2020)
https://doi.org/10.1016/bs.adioch.2019.10.001
An overview of the sandfly fauna (Diptera: Psychodidae) followed by the detection of Leishmania DNA and blood meal identification in the state of Acre, Amazonian Brazil
Thais de Araujo-Pereira, Daniela de Pita-Pereira, Sandylere Moreira Baia-Gomes, et al.Memórias do Instituto Oswaldo Cruz 115 (2020)
https://doi.org/10.1590/0074-02760200157
Casein kinase 1.2 over expression restores stress resistance to Leishmania donovani HSP23 null mutants
Constanze Kröber-Boncardo, Stephan Lorenzen, Christine Brinker and Joachim ClosScientific Reports 10 (1) (2020)
https://doi.org/10.1038/s41598-020-72724-x
Impact of Climatic Factors on the Seasonal Fluctuation of Leishmaniasis Vectors in Central Morocco (Meknes Prefecture)
Hajar El Omari, Abdelkader Chahlaoui, Fatima Zahra Talbi, et al.Canadian Journal of Infectious Diseases and Medical Microbiology 2020 1 (2020)
https://doi.org/10.1155/2020/6098149
Heat Shock Proteins in Inflammatory Diseases
Constanze Kröber-Boncardo, Janne Grünebast and Joachim ClosHeat Shock Proteins, Heat Shock Proteins in Inflammatory Diseases 22 469 (2020)
https://doi.org/10.1007/7515_2020_27
Encyclopedia of Environmental Health
Labrini V. Athanasiou, Sofia G. Boutsini and Marina G. BisiaEncyclopedia of Environmental Health 581 (2019)
https://doi.org/10.1016/B978-0-12-409548-9.11268-0
Functional genomics in sand fly–derived Leishmania promastigotes
Pedro J. Alcolea, Ana Alonso, Ricardo Molina, et al.PLOS Neglected Tropical Diseases 13 (5) e0007288 (2019)
https://doi.org/10.1371/journal.pntd.0007288
In vitro antileishmanial and antioxidant potential, cytotoxicity evaluation and phytochemical analysis of extracts from selected medicinally important plants
Shaila Mehwish, Arshad Islam, Ikram Ullah, et al.Biocatalysis and Agricultural Biotechnology 19 101117 (2019)
https://doi.org/10.1016/j.bcab.2019.101117
43 (2018)
https://doi.org/10.1002/9783527802883.ch3
An update on small molecule strategies targeting leishmaniasis
Swati Kapil, Pankaj Kumar Singh and Om SilakariEuropean Journal of Medicinal Chemistry 157 339 (2018)
https://doi.org/10.1016/j.ejmech.2018.08.012
The vector competence of Phlebotomus perniciosus for Leishmania infantum zymodemes of Tunisia
Latifa Remadi, Maribel Jiménez, Najla Chargui, et al.Parasitology Research 117 (8) 2499 (2018)
https://doi.org/10.1007/s00436-018-5939-y
ROS regulate differentiation of visceralizingLeishmaniaspecies into the virulent amastigote form
Yousuf A. Khan, Norma W. Andrews and Bidyottam MittraParasitology Open 4 (2018)
https://doi.org/10.1017/pao.2018.15
Metabolic regulation of infection and inflammation
Prashant Chauhan and Bhaskar SahaCytokine 112 1 (2018)
https://doi.org/10.1016/j.cyto.2018.11.016
Leishmaniases as Re-emerging Diseases
M. Magdalena Aguirre-Garcia, Alma R. Escalona-Montaño, Arturo A. Wilkins-Rodríguez and Laila Gutiérrez-KobehLeishmaniases as Re-emerging Diseases (2018)
https://doi.org/10.5772/intechopen.75169
Redox Biology of Leishmania and Macrophage Targeted Nanoparticles for Therapy
Hafiz Shoaib Sarwar, Sohail Akhtar, Muhammad Farhan Sohail, Zaeema Naveed, Muhammad Rafay, Akhtar Nadhman, Masoom Yasinzai and Gul ShahnazNanomedicine 12 (14) 1713 (2017)
https://doi.org/10.2217/nnm-2017-0049
Leishmaniases in Ecuador: Comprehensive review and current status
Yoshihisa Hashiguchi, Lenin N. Velez, Nancy V. Villegas, et al.Acta Tropica 166 299 (2017)
https://doi.org/10.1016/j.actatropica.2016.11.039
Blocking transmission of vector-borne diseases
Sandra Schorderet-Weber, Sandra Noack, Paul M. Selzer and Ronald KaminskyInternational Journal for Parasitology: Drugs and Drug Resistance 7 (1) 90 (2017)
https://doi.org/10.1016/j.ijpddr.2017.01.004
Febrifugine analogues as Leishmania donovani trypanothione reductase inhibitors: binding energy analysis assisted by molecular docking, ADMET and molecular dynamics simulation
Rajan Kumar Pandey, Bajarang Vasant Kumbhar, Shubham Srivastava, et al.Journal of Biomolecular Structure and Dynamics 35 (1) 141 (2017)
https://doi.org/10.1080/07391102.2015.1135298
Redundant and regulatory roles for Toll-like receptors in Leishmania infection
P Chauhan, D Shukla, D Chattopadhyay and B SahaClinical and Experimental Immunology 190 (2) 167 (2017)
https://doi.org/10.1111/cei.13014
ALTERAÇÕES DA MATRIZ EXTRACELULAR ESPLÊNICA EM CÃES NATURALMENTE INFECTADOS COM Leishmania (Leishmania) infantum chagasi
Nathálya dos Santos Martins, Glaucia Barbosa Coelho, Larissa Sarmento dos Santos, et al.Ciência Animal Brasileira 16 (1) 103 (2015)
https://doi.org/10.1590/1089-68916i123500
In silico work flow for scaffold hopping in Leishmania
Barnali Waugh, Ambarnil Ghosh, Dhananjay Bhattacharyya, Nanda Ghoshal and Rahul BanerjeeBMC Research Notes 7 (1) (2014)
https://doi.org/10.1186/1756-0500-7-802
Emerging Infections 3
James H. MaguireEmerging Infections 3 99 (2014)
https://doi.org/10.1128/9781555818418.ch7
217 (2013)
https://doi.org/10.1002/9783527675401.ch11
Topley & Wilson's Microbiology and Microbial Infections
Paul A. Bates and R.W. AshfordTopley & Wilson's Microbiology and Microbial Infections (2010)
https://doi.org/10.1002/9780470688618.taw0181
Low and high-dose intradermal infection with Leishmania majorand Leishmania amazonensis in C57BL/6 mice
Denise Fonseca Côrtes, Matheus Batista Heitor Carneiro, Liliane Martins Santos, et al.Memórias do Instituto Oswaldo Cruz 105 (6) 736 (2010)
https://doi.org/10.1590/S0074-02762010000600002
Leishmania actin binds and nicks kDNA as well as inhibits decatenation activity of type II topoisomerase
Prabodh Kapoor, Ashutosh Kumar, Rangeetha Naik, et al.Nucleic Acids Research 38 (10) 3308 (2010)
https://doi.org/10.1093/nar/gkq051
An Unconventional Form of Actin in Protozoan Hemoflagellate, Leishmania
Prabodh Kapoor, Amogh A. Sahasrabuddhe, Ashutosh Kumar, et al.Journal of Biological Chemistry 283 (33) 22760 (2008)
https://doi.org/10.1074/jbc.M800213200
Natural Sesquiterpene Lactones are Active Against Leishmania mexicana
Patricia A. Barrera, Verónica Jimenez-Ortiz, Carlos Tonn, et al.Journal of Parasitology 94 (5) 1143 (2008)
https://doi.org/10.1645/GE-1501.1
A MATHEMATICAL MODEL OF IMMUNE RESPONSE IN CUTANEOUS LEISHMANIASIS
MARCOS C. DE ALMEIDA and HELMAR N. MOREIRAJournal of Biological Systems 15 (03) 313 (2007)
https://doi.org/10.1142/S0218339007002209
Amastin Peptide-Binding Antibodies as Biomarkers of Active Human Visceral Leishmaniasis
Sima Rafati, Nafiseh Hassani, Yasaman Taslimi, Hesam Movassagh, Annie Rochette and Barbara PapadopoulouClinical and Vaccine Immunology 13 (10) 1104 (2006)
https://doi.org/10.1128/CVI.00188-06
Mapping the Antigenicity of the Parasites in Leishmania donovani Infection by Proteome Serology
Michael Forgber, Rajatava Basu, Kaushik Roychoudhury, et al.PLoS ONE 1 (1) e40 (2006)
https://doi.org/10.1371/journal.pone.0000040
Leishmania (Viannia) braziliensis: Interaction of mannose‐binding lectin with surface glycoconjugates and complement activation. An antibody‐independent defence mechanism
A. R. AMBROSIO and I. J. T. DE MESSIAS‐REASONParasite Immunology 27 (9) 333 (2005)
https://doi.org/10.1111/j.1365-3024.2005.00782.x
Medical Entomology
Phillip G. Lawyer and Peter V. PerkinsMedical Entomology 231 (2004)
https://doi.org/10.1007/978-94-007-1009-2_8
Leishmaniose tegumentar americana
Bernardo Gontijo and Maria de Lourdes Ribeiro de CarvalhoRevista da Sociedade Brasileira de Medicina Tropical 36 (1) 71 (2003)
https://doi.org/10.1590/S0037-86822003000100011
Two separate growth phases during the development of Leishmania in sand flies: implications for understanding the life cycle
Sharon M Gossage, Matthew E Rogers and Paul A BatesInternational Journal for Parasitology 33 (10) 1027 (2003)
https://doi.org/10.1016/S0020-7519(03)00142-5
Leishmanial infection: analysis of its first steps. A review
MC de Almeida, V Vilhena, A Barral and M Barral-NettoMemórias do Instituto Oswaldo Cruz 98 (7) 861 (2003)
https://doi.org/10.1590/S0074-02762003000700001
Medical and Veterinary Entomology
LOUIS C. RUTLEDGE and RAJ K. GUPTAMedical and Veterinary Entomology 147 (2002)
https://doi.org/10.1016/B978-012510451-7/50011-6
Leishmaniasis and other dermatozoonoses in Brazil
Marcia Ramos-E-Silva and Claudio De Moura Castro JacquesClinics in Dermatology 20 (2) 122 (2002)
https://doi.org/10.1016/S0738-081X(01)00251-6
Inhibition of HSP90 in Trypanosoma cruzi Induces a Stress Response but No Stage Differentiation
Sebastian E. B. Graefe, Martina Wiesgigl, Iris Gaworski, Andrea Macdonald and Joachim ClosEukaryotic Cell 1 (6) 936 (2002)
https://doi.org/10.1128/EC.1.6.936-943.2002
Phospholipase D (PLD) is Present in Leishmania donovani and its Activity Increases in Response to Acute Osmotic Stress
J. JOSEPH BLUM, JASON A. LEHMAN, JEFF M. HORN and JULIAN GOMEZ‐CAMBRONEROJournal of Eukaryotic Microbiology 48 (1) 102 (2001)
https://doi.org/10.1111/j.1550-7408.2001.tb00421.x
Leishmania-sand fly interactions controlling species-specific vector competence. Microreview
David L. SacksCellular Microbiology 3 (4) 189 (2001)
https://doi.org/10.1046/j.1462-5822.2001.00115.x
Canine experimental infection: intradermal inoculation of Leishmania infantum promastigotes
Gabriela M Santos-Gomes, Lenea Campino and Pedro AbranchesMemórias do Instituto Oswaldo Cruz 95 (2) 193 (2000)
https://doi.org/10.1590/S0074-02762000000200010
Medical Entomology
Phillip G. Lawyer and Peter V. PerkinsMedical Entomology 231 (2000)
https://doi.org/10.1007/978-94-011-6472-6_8
A Sensitive Method for Assaying Chemotaxic Responses of Leishmania Promastigotes
Jamil S. Oliveira, Maria N. Melo and Nelder F. GontijoExperimental Parasitology 96 (3) 187 (2000)
https://doi.org/10.1006/expr.2000.4569
Advances in Parasitology Volume 44
Emanuela HandmanAdvances in Parasitology, Advances in Parasitology Volume 44 44 1 (1999)
https://doi.org/10.1016/S0065-308X(08)60229-8
Investigations on the in vitro metacyclogenesis of a visceral and a cutaneous human strain of Leishmania infantum1This paper is dedicated to the memory of Prof. Dr. José L. González Castro recently deceased.1
Mostafa Louassini, Francisco Javier Adroher, Marı́a Remedios Foulquié and Rocı́o Benı́tezActa Tropica 70 (3) 355 (1998)
https://doi.org/10.1016/S0001-706X(98)00041-2
Differential sensitivity of New World Leishmania spp. promastigotes to complement-mediated lysis: Correlation with the expression of three parasite polypeptides
Fátima S.M. Noronha, Álvaro C. Nunes, Kátia T. Souza, M. Norma Melo and F.Juarez Ramalho-PintoActa Tropica 69 (1) 17 (1998)
https://doi.org/10.1016/S0001-706X(97)00108-3
A Physical Map of the Leishmania majorFriedlin Genome
Alasdair C. Ivens, Sharon M. Lewis, Azadeh Bagherzadeh, et al.Genome Research 8 (2) 135 (1998)
https://doi.org/10.1101/gr.8.2.135
Leishmania mexicana:Binding of Promastigotes to Type I Collagen
Rosalia Lira, Jose Luis Rosales-Encina and Carlos ArgüelloExperimental Parasitology 85 (2) 149 (1997)
https://doi.org/10.1006/expr.1996.4127
Presencia de nectomonadas metaciclicas de L. pifanoi en la hipofaringe de Lutzomyia youngi y la ingestion de azúcares
Elina Rojas and José V. ScorzaRevista de Saúde Pública 30 (3) 240 (1996)
https://doi.org/10.1590/S0034-89101996000300006
Parasitic Protozoa
Lionel F. Schnur and Charles L. GreenblattParasitic Protozoa 1 (1995)
https://doi.org/10.1016/B978-0-12-426020-7.50006-2
Haemoglobin inhibits the development of infective promastigotes and chitinase secretion inLeishmania majorcultures
Y. Schlein and R. L. JacobsonParasitology 109 (1) 23 (1994)
https://doi.org/10.1017/S0031182000077726
Expression of Cysteine Proteinases by Metacyclic Promastigotes of Leishmania mexicana
PAUL A. BATES, COLIN D. ROBERTSON and GRAHAM H. COOMBSJournal of Eukaryotic Microbiology 41 (3) 199 (1994)
https://doi.org/10.1111/j.1550-7408.1994.tb01497.x
Vector competence of some Neotropical sandflies for the Leishmania (Viannia) braziliensis complex
CONSUELO JARAMILLO, BRUNO L. TRAVI and JAMES MONTOYAMedical and Veterinary Entomology 8 (1) 1 (1994)
https://doi.org/10.1111/j.1365-2915.1994.tb00375.x
Development ofLeishmania chagasi (Kinetoplastida: Trypanosomatidae) in the second blood-meal of its vectorLutzomyia longipalpis (Diptera: Psychodidae)
D. A. Elnaiem, R. D. Ward and P. E. YoungParasitology Research 80 (5) 414 (1994)
https://doi.org/10.1007/BF00932379
Complete developmental cycle ofLeishmania mexicanain axenic culture
P. A. BatesParasitology 108 (1) 1 (1994)
https://doi.org/10.1017/S0031182000078458
Leishmania Differentiation in Natural and Unnatural Sand Fly Hosts1
LAUREL L. WALTERSJournal of Eukaryotic Microbiology 40 (2) 196 (1993)
https://doi.org/10.1111/j.1550-7408.1993.tb04904.x
Advances in Parasitology Volume 31
James Alexander and David G. RussellAdvances in Parasitology, Advances in Parasitology Volume 31 31 175 (1992)
https://doi.org/10.1016/S0065-308X(08)60022-6
Leishmania tropica infection in hamsters and a review of the animal pathogenicity of this species
Patrick Bastien and Robert Killick-KendrickExperimental Parasitology 75 (4) 433 (1992)
https://doi.org/10.1016/0014-4894(92)90256-A
Advances in Disease Vector Research
Peter J. HamAdvances in Disease Vector Research, Advances in Disease Vector Research 9 101 (1992)
https://doi.org/10.1007/978-1-4612-2910-0_4