Final comments on an interesting taxonomic dilemma: Leishmania infantum versus Leishmania infantum chagasi.
نویسنده
چکیده
It is grateful to see that the new session Readers opinion and discussion created after my comments Leishmania infantum versus Leishmania chagasi: do not forget the law of priority (Dantas-Torres 2006) on the concise review article of Lainson and Rangel (2005) has emerged as the basis of an interesting debate on the aetiological agent of American visceral leishmaniasis, i.e., the taxonomic dilemma concerning its correct nomenclature. Further details of this discussion can be found elsewhere (Dantas-Torres 2006, Lainson & Rangel 2006). Recently, I was surprised (and very happy as well) to see the welcome contribution of Professor Jeffrey Shaw, a world-leading expert in the field of leishmaniasis. Dr Shaw is a respected reference in classification of leishmanial parasites and I must agree with most of his comments. However, I would like to write my last few words on this matter. In fact, as Lainson and Rangel (2006) previously emphasized, the name Leishmania infantum chagasi entirely follows the rules of the International Code of Zoological Nomenclature. That is correct, but the point is: Is this name according to the current criteria used to classify parasites of the genus Leishmania? What are the criteria? Among the techniques currently in use for classification of leishmanial parasites are: isoenzyme electrophoresis (WHO 1990), species-specific monoclonal antibodies, DNA probe and analysis of restriction fragment length polymorphism (RFLP) using different DNA sequences as targets (Macedo et al. 1992, Guizani et al. 1994, Mendonza-Leon et al. 1995). As Shaw (2006) commented, recent studies on the Old World visceral parasites using the internal transcribed spacer (ITS) (Kuhls et al. 2005) and fluorogenic assays (Quispe-Tintaya et al. 2005) suggested the need for a taxonomic revision of Leishmania donovani complex. It is clear that the current status of certain Leishmania species (e.g., Leishmania archibaldi) need to be revised (Mauricio et al. 2006). I have the modest opinion that we should first reestablish (i.e., update) the criteria for the classification of the leishmanial parasites based on the traditional criteria (Lainson & Shaw 1987) and data from recent molecular investigations. Then it would be easier to agree if a given parasite deserves the status of species or subspecies. But what is a subspecies? In the first chapter of the memorable book The Leishmaniases in Biology and Medicine, Lainson and Shaw (1987) defined subspecies as local, geographically isolated populations which show some (usually minor) taxonomic differences from other geographically separated populations of the same species. If we take this definition into account, I should agree that the classification of the aetiological agent of American visceral leishmaniasis as Leishmania infantum chagasi is acceptable. The challenge will be to convince other researchers who do not believe that exist taxonomic differences (even minor) between the aetiological agents of visceral leishmaniasis in the Americas and the Mediterranean basin. Henceforth, I would be happy to see in the current literature the use of a single designation for the aetiological agent of American visceral leishmaniasis. Unfortunately, different names are currently in use, such as Leishmania chagasi (Berman 2006), Leishmania infantum (MoraesSilva et al. 2006), Leishmania infantum chagasi (Lainson & Rangel 2005), Leishmania chagasi/infantum (Feliciangeli et al. 2005), Leishmania infantum (chagasi) (Bern et al. 2005), and even Leishmania (chagasi) infantum (Barrouin-Melo et al. 2006); and this is scientifically unacceptable. I hope this debate initiated by a young leishmaniac and properly complemented by respected experts in the field of leishmaniasis (Dr Lainson, Dr Rangel, and Dr Shaw) will help researchers who are direct or indirectly involved with taxonomy of leishmanial parasites. Finally, I would like to emphasize the importance of assign a single name for the aetiological agent of American visceral leishmaniasis, which appears to be losing its identity but not its virulence (DantasTorres 2005, Dantas-Torres & Brandão-Filho 2006).
منابع مشابه
Complete conservation of an immunogenic gene (lcr1) in Leishmania infantum and Leishmania chagasi isolated from Iran, Spain and Brazil.
BACKGROUND & OBJECTIVES Kala-azar is the visceral and most severe form of leishmaniasis that leads to death if untreated. The causative agents of visceral leishmaniasis (VL) are members of Leishmania (L.) donovani complex which includes L. chagasi and L. infantum. Genome sequences have raised the question whether L. chagasi and L. infantum are synonymous or different. This question has importan...
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Phylogenetic studies on trypanosomatid barcode using V7V8 SSU rRNA and gGAPDH gene sequences have provided support for redefining some trypanosomatid species and positioning new isolates. The genus Leishmania is a slow evolving monophyletic group and including important human pathogens. The phylogenetic relationships of this genus have been determined by the natural history of its vertebrate ho...
متن کاملLeishmania infantum versus Leishmania chagasi: do not forget the law of priority.
Lainson and Rangel (2005) have recently published a consistent review on Lutzomyia longipalpis (Diptera: Psychodidae) and visceral leishmaniasis (VL) in the Americas, with particular attention to the eco-epidemiology of disease in Brazil. In their review, they have discussed with property the taxonomic position and origin of the causal agent of the disease. However, I would like to add some com...
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We report the case of a 66 year-old woman who presented nodular skin lesions on her back and upper extremities. Biopsy revealed amastigotes that were identified as Leishmania infantum-chagasi by PCR. Evaluation also showed hepatomegaly and pulmonary nodules. Treatment with amphotericin B led to complete resolution of skin lesions.
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There are currently no effective vaccines for visceral leishmaniasis, the second most deadly parasitic infection in the world. Here, we describe a novel whole-cell vaccine approach using Leishmania infantum chagasi promastigotes treated with the psoralen compound amotosalen (S-59) and low doses of UV A radiation. This treatment generates permanent, covalent DNA cross-links within parasites and ...
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ورودعنوان ژورنال:
- Memorias do Instituto Oswaldo Cruz
دوره 101 8 شماره
صفحات -
تاریخ انتشار 2006