Cultivation of Protozoa Parasites In Vitro: Growth Potential in Conventional Culture Media versus RPMI-PY Medium

被引:5
作者
Castelli, Germano [1 ]
Oliveri, Eugenia [1 ]
Valenza, Viviana [1 ]
Giardina, Susanna [1 ]
Facciponte, Flavia [1 ]
La Russa, Francesco [1 ]
Vitale, Fabrizio [1 ]
Bruno, Federica [1 ]
机构
[1] Ctr Referenza Nazl Leishmaniosi C Re Na L, Ist Zooprofilatt Sperimentale Sicilia, WOAH Leishmania Reference Lab, Via Gino Marinuzzi 3, I-90129 Palermo, Italy
关键词
protozoa parasites; culture media; RPMI-PY medium; Leishmania spp; Trypanosoma cruzi; FETAL CALF SERUM; LEISHMANIA-BRAZILIENSIS; TRYPANOSOMA-CRUZI; LIQUID-MEDIUM; PROMASTIGOTES; DIAGNOSIS;
D O I
10.3390/vetsci10040252
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Simple Summary Many different media have been used to grow protozoa parasites, which can be classified into two main categories: biphasic and liquid. All major biphasic media require blood as an essential component for parasite replication: Evans's modified Tobie and Novy-MacNeal-Nicolle media are the conventional media used for the cultivation of Leishmania and Trypanosoma parasites. These media are time-consuming and often complex, and they are based on relatively expensive reagents and blood components, which complicate immunological and biochemical studies. Our study shows that a new liquid medium, RPMI-PY, can be used for both diagnostic and research purposes since comparable and sometimes better results were found for parasite load compared with the reference media in Leishmania and Trypanosoma. The relative simplicity of RPMI-PY medium, the general availability of its components, and above all, the lack of fresh animal blood requirement renders this medium the best choice for many purposes in protozoa parasites studies. The elimination of fresh blood components is important for economic and ethical aspects, with no need for rabbits' housing and bleeding, as well as to avoid the complication of the blood components of media in immunological and biochemical studies. Our approach allowed us to clearly evaluate the significant changes in the biological parameters of promastigotes in each medium. The in vitro cultivation of Leishmania and Trypanosoma parasites plays an important role in the diagnosis and treatment of parasitic diseases. Although Evans's modified Tobie and Novy-MacNeal-Nicolle media, for Leishmania spp. and Trypanosoma cruzi, respectively, are the two commonly used media for both isolation and maintenance of strains in vitro, their preparation is expensive and laborious and requires fresh rabbit blood from housed animals. The purpose of this study was to evaluate the in vitro growth of both parasites with an alternative monophasic, blood-free, easy, and affordable medium called RPMI-PY, which was previously demonstrated suitable for the in vitro growth of Leishmania infantum. The potential growth of different Leishmania species and Trypanosoma cruzi was evaluated in traditional culture media versus RPMI-PY medium, and we recorded the protozoa parasites' morphology via orange acridine-ethidium bromide staining. The results of our study show that RPMI-PY medium can be used for Trypanosoma cruzi, Leishmania amazonensis, Leishmania major, and Leishmania tropica species since in all the species except Leishmania braziliensis, the exponential growth of the parasite was observed, in many cases higher than conventional media. The staining confirmed not only their growth during the 72 h investigation but also the optimal morphology and viability of the protozoa in the RPMI-PY medium.
引用
收藏
页数:11
相关论文
共 45 条
  • [1] A simple monophasic LGPY medium for routine maintenance of Leishmania donovani promastigotes
    Abhishek, Suman
    Chaturvedi, Sanjay Kumar
    Gupta, Anil Kumar
    Ahmed, Ghufran
    Das, Vidyanand Ravi
    Narayan, Shyam
    [J]. PARASITOLOGY RESEARCH, 2021, 120 (08) : 2969 - 2971
  • [2] A semisynthetic fetal calf serum-free liquid medium for in vitro cultivation of Leishmania promastigotes
    Ali, SA
    Iqbal, J
    Ahmad, B
    Masoom, M
    [J]. AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1998, 59 (01) : 163 - 165
  • [3] Axenic cultivation and partial characterization of Leishmania braziliensis amastigote-like stages
    Balanco, JMF
    Pral, EMF
    da Silva, S
    Bijovsky, AT
    Mortara, RA
    Alfieri, SC
    [J]. PARASITOLOGY, 1998, 116 : 103 - 113
  • [4] SIMPLE MONOPHASIC MEDIUM FOR AXENIC CULTURE OF HEMOFLAGELLATES
    BERENS, RL
    BRUN, R
    KRASSNER, SM
    [J]. JOURNAL OF PARASITOLOGY, 1976, 62 (03) : 360 - 365
  • [5] Trypanosoma cruzi and Chagas' Disease in the United States
    Bern, Caryn
    Kjos, Sonia
    Yabsley, Michael J.
    Montgomery, Susan P.
    [J]. CLINICAL MICROBIOLOGY REVIEWS, 2011, 24 (04) : 655 - 681
  • [6] A novel nanoliposomal formulation of the FDA approved drug Halofantrine causes cell death of Leishmania donovani promastigotes in vitro
    Bhagat, Stuti
    Parikh, Yashvi
    Singh, Sanjay
    Sengupta, Souvik
    [J]. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2019, 582
  • [7] CYTOTOXIC SCREENING AND IN VITRO EVALUATION OF PENTADECANE AGAINST LEISHMANIA INFANTUM PROMASTIGOTES AND AMASTIGOTES
    Bruno, Federica
    Castelli, Germano
    Migliazzo, Antonella
    Piazza, Maria
    Galante, Antonella
    Lo Verde, Vincenza
    Calderone, Simona
    Nucatolo, Giuseppa
    Vitale, Fabrizio
    [J]. JOURNAL OF PARASITOLOGY, 2015, 101 (06) : 701 - 705
  • [8] Carod-Artal Francisco Javier, 2013, Handb Clin Neurol, V114, P103, DOI 10.1016/B978-0-444-53490-3.00007-8
  • [9] Molecular Diagnosis of Leishmaniasis: Quantification of Parasite Load by a Real-Time PCR Assay with High Sensitivity
    Castelli, Germano
    Bruno, Federica
    Reale, Stefano
    Catanzaro, Simone
    Valenza, Viviana
    Vitale, Fabrizio
    [J]. PATHOGENS, 2021, 10 (07):
  • [10] In vitro antileishmanial activity of trans-stilbene and terphenyl compounds
    Castelli, Germano
    Bruno, Federica
    Vitale, Fabrizio
    Roberti, Marinella
    Colomba, Claudia
    Giacomini, Elisa
    Guidotti, Laura
    Cascio, Antonio
    Tolomeo, Manlio
    [J]. EXPERIMENTAL PARASITOLOGY, 2016, 166 : 1 - 9