Skip to main content

Techniques to improve the maintenance of a laboratory colony of Nyssomyia neivai (Diptera: Psychodidae)

Abstract

Background

The most critical phase in sand fly colonization is the high mortality in the larval instars. In this study, we sought out strategies for improving the colonization of Nyssomyia neivai, one of the vectors of cutaneous leishmaniasis agent in South America.

Methods

A colony of Ny. neivai was established in the laboratory from a field population, and the productivity of adults was evaluated considering carrying capacity, diet for larvae and surface for oviposition.

Results

The highest emergency rate of adults was achieved with the fewest couples inside 150 mL rearing chambers on a sterilized diet made of rabbit feces, rabbit food, soil and fish food and with vermiculite as a substrate for oviposition and the development of larvae.

Conclusion

Our data on Ny. neivai colonization showed that the best adult productivities were achieved with fewer couples inside the rearing chambers; smaller rearing containers of 150 mL (due to less fungi growth); sterilized diet made of rabbit feces, rabbit food, soil and fish food; and vermiculite as the substrate for oviposition and development of larvae.

Background

Colonies of insect vectors are suitable for a wide range of investigations, from basic biological aspects to applied research. Despite the importance of laboratory colonies of the vectors of leishmaniasis agent, the difficulty in providing the specific requirements of the more than 900 sand fly species [1] explain why less than 60 species have been successfully reared in the laboratory [2]. The main problem in rearing sand flies is the high mortality during the immature phases. Sand fly larvae are detritivores, and the conventional diet for larvae in laboratory colonies consists of a variety of substrates that are mainly rich in fungal, bacterial and plant material [3]. Although some studies have focused on diets for sand fly larvae, there is not a universal recipe for all species. There have been discussions on whether the different alimentary requirements of phlebotomine larva can contribute to reducing the competition among sand fly species under natural conditions [4].

Nyssomyia neivai is incriminated as one of the vector of cutaneous leishmaniasis agents in South America [58].

The aim of this research was to evaluate the carrying capacity, attraction of the immature stages of Ny. neivai to different diets, survival of the larvae on distinct diets and different rearing surfaces.

Methods

Collection and maintenance of sand flies

Sand flies were collected in Santa Eudóxia, São Paulo state - Brazil (along the edges of the Mogi Guaçu River) on the wall of a house, using a manual aspirator between 18:00 and 23:00 h. In the laboratory, the sand flies were maintained in cages covered with voile (30x30x30 cm) at 26 ± 1 °C, 80–90 % humidity, and a 12:12 (L:D) photoperiod. The sand flies had access to a piece of cotton soaked in a 30 % sucrose solution. The non-bloodfed field-collected females were exposed to BALB/c mice as a blood source. The bloodfed females were individually transferred to vials to oviposition. After oviposition, sand flies were clarified and identified under an optical microscope following the identification key by Galati [9]. Ny. neivai eggs were placed in a 150 mL polystyrene container filled with 2 cm of plaster of Paris on its bottom (oviposition container). The following experiments were carried out in oviposition containers that were kept in the dark at 26 ± 1 °C, 80–90 % humidity.

Ny. neivai carrying capacity in rearing containers of different sizes

Groups of bloodfed females and an equal number of males were selected and transferred to 250 mL and 150 mL polystyrene oviposition chambers. Pairs of male and female sand flies were placed in 250 mL containers in groups of 5, 10, 15, 20, 25 and 30. For the 150 mL containers, 5, 10 and 15 bloodfed females were placed to verify the carrying capacity. The experiments were repeated four times. The chambers were observed daily to check the humidity levels, the mortality of gravid females and the number of eggs. The sucrose solution was changed daily. At the end of the experiments, the productivity of adults was evaluated for each group.

Attractiveness of different diets for Ny. neivai larvae

In the laboratory, we use diets made of rabbit feces, rabbit food from Evialis®, fish food from Alcon® Colours and soil (modified from a personal communication with José Carlos Miranda). We tried other combinations to evaluate their attractiveness for larvae.

Fifty eggs of Ny. neivai were placed in the center of a 250 mL plastic container. The lining of plaster of Paris in the container bottom was divided into four quadrants, and over each of them a specific diet was added on 7th day after oviposition: diet 1 (traditional diet - used in routine rearing of sand flies), diet 2 (rabbit feces and soil), diet 3 (rabbit feces, soil and fish food) and diet 4 (soil and mud – Barretto, 1942). The number of larvae on each quadrant was observed and counted daily until the pupal phase. The experiments were repeated four times.

Diet preparation: rabbit feces were collected from the Veterinary Institute of Universidade de São Paulo (USP) and dried by solar heat for 3 days. The feces, rabbit food, fish food and soil were triturated and sieved through 0.297 mm, 0.125 mm and 0.074 mm meshes. All of the components, except the fish food, were sterilized in an autoclave.

Attractiveness and development of Ny. neivai larvae on two different diets

One hundred eggs were placed in the center of each container (250 mL). The plaster of Paris was divided into four quadrants, and over each one, of the two different diets was added: diet 1 (rabbit feces, rabbit food, fish food and soil) and diet 2 (multimixture flour - a food supplement for pregnant women and children to combat malnutrition - containing rice and wheat bran, wheat flour, corn meal, sesame, soybean, linseed, Moringa oleifera leaves, sunflower or pumpkin seeds and cassava leaf powder). Neighbouring quadrants received different diets. The number of larvae on each quadrant was observed and counted daily until the pupal phase.

To analyse which diet was better for the development of the insects, each diet was added in different containers with 100 eggs each. The diet was added according to the needs of the larvae in different instars. Both experiments were repeated four times.

Development of immature stages on non-sterilized and sterilized diets

One hundred eggs were placed in the center of clean containers (150 mL) and Diet 1 (rabbit feces, rabbit food, fish food and soil) was added daily in the following way: non-sterilized and sterilized (by autoclave or tyndallization). The tests were carried out until the adult phase and were replicated five times.

Evaluation of different substrates for rearing the colony

The substrates that were evaluated individually were plaster of Paris and plaster with a fine layer of vermiculite over it. Five engorged females and five males were placed in the oviposition containers (150 mL). A piece of plaster of Paris was put in the center of the container and used as resting spot. A piece of cotton soaked in a 30 % sucrose solution was offered to the couples. Emerged adults were counted, and the results were analysed. The experiments were repeated 10 times.

Statistical analysis

Data were analysed by Analysis of Variance (ANOVA) and Tukey’s tests or t-tests performed using GraphPad Prism version 5.00.

Ethical approval

This study was carried out in accordance with the Ethical Principles of Animal Experimentation, approved by the Committee on the Ethics of Animal Experiments at State University of Campinas (Protocol number 2951–1).

Results

Ny. neivai carrying capacity in rearing containers of different sizes

The female mortality before oviposition was random and was not dependent on the number of couples in the containers (data not shown). The mean number of eggs per female varied between the different sizes of the rearing containers. For the smallest containers (150 mL), five couples presented the highest mean number of eggs per female (67.2 eggs; p < 0.05). For the largest containers (250 mL), there was no statistical difference among the number of couples in the pots (from 47.1 to 56.5 eggs; p > 0.05) (Table 1).

Table 1 Mean number of eggs per females and standard error in rearing chambers of 150 mL (5, 10 and 15 couples) and 250 mL (5, 10, 15, 20, 25, 30 couples)

The number of adults emerged was negatively correlated with the number of eggs per rearing container. Adult emergency rates were over 50 % in the 250 mL containers that contained approximately 400 eggs. For 150 mL containers, the emergency rates were 30 % (around 600 eggs per pot). The best results for both the smaller and larger containers were seen with five to ten insect couples (Fig. 1).

Fig. 1
figure 1

Percentages of adult emerged per number of eggs in different size containers. a five couples, ten couples, ▲fifteen couples, twenty couples, ♦ twenty five couples, * thirty couples in 250 mL and b five couples, ten couples, ▲fifteen couples in 150 mL containers

Attractiveness of different diets to Ny. neivai larvae

According to the results, the most attractive larval food was diet 1, followed by diet 3 (Fig. 2). Both diets contained fish food. Differences were significant among the four diets (p < 0.05), but there were no significant differences between diets 1 and 3 (p > 0.05) or 2 and 4 (p > 0.05). The presence of fish food appears to be an important factor in the attractiveness of a diet to the larval instars of Ny. neivai.

Fig. 2
figure 2

Number of larvae on four different diets over time. Diet 1 (rabbit feces, rabbit food, fish food, and soil); 2 (rabbit feces and soil); 3 (rabbit feces, soil and fish food); and 4 (soil and mud). P < 0.05

Attractiveness and development of Ny. neivai larvae on two different diets

The number of larvae on diet 1 (traditional) was higher than on the multimixture (p < 0.05) (Fig. 3).

Fig. 3
figure 3

Number of larvae on two different diets over time. Traditional diet (rabbit feces, rabbit food, fish food, and soil) and multimixture diet (plants and grains). P < 0.05

The productivity of adults was much higher on diet 1 (164 adults; 41 %) than on the multimixture (19; 9.5 %) (p > 0.05).

Development of immature stages on non-sterilized and sterilized diets

There were no significant differences among the treatments (p > 0.05). However, the means were higher with both of the sterilized methods, autoclave (46.7 insects) and tyndallization (47.8 insects), compared to only 38.4 insects in the non-autoclaved diet (Fig. 4).

Fig. 4
figure 4

Emergency of adults on non-sterilized and sterilized diets. Means with same letters are not significantly different (P>0.05)

Evaluation of different substrates for rearing the colony

There was a significant difference between the plaster of Paris and the vermiculite (p < 0.05). The mean emergence of adults on the vermiculite was 690 insects, compared to 428 insects on the plaster of Paris (Fig. 5).

Fig 5
figure 5

Emergency of adults in containers with two different substrates: plaster of Paris or vermiculite. Means with different letters are significantly different (P<0.05)

Discussion

Rearing sand fly colonies in the laboratory provides the opportunity to improve the techniques for obtaining a large number of insects for basic or applied studies. Many aspects of the rearing process need to be considered for the success of a laboratory colony, such as carrying capacity, the right conditions for the immature stages, diet and substrate.

The concept of evaluating carrying capacity consists of determining the ideal number of individuals for a specific environmental condition [10, 11].

The maximum number of couples used in this work was 30, and with that number, the density of couples did not affect the mortality of females prior to oviposition. For Ny. neivai, our results showed that the carrying capacity was between five and ten couples for both sizes of containers (150 and 250 mL), where the highest number of adults were achieved.

Santamaría et al. studied the carrying capacity of Pintomyia serrana and verified that the density of flies negatively affected the survival of the females prior to oviposition [11]. However, those authors worked with 1 to 50 couples, which is more than the number of pairs used in our experiments. Their best productivity was with 22 females per container. Under those conditions, female mortality was low and the numbers of eggs and adults emerged were the highest. Apart from the different experimental conditions between the studies, it is probable that other specific characteristics could be involved.

A previous study with a colony of Ny. neivai showed a rate of adults emerged of 20.7 % [12]. Our results showed that a lower number of couples inside the rearing container produced a higher number of adults (Fig. 1). This could be explained by the intraspecific competition for food and space among the larvae. When the container is too crowded, the larvae climb the walls and end up dying of dehydration. The same behaviour was observed by Hertig & Johnson, who called this phenomenon a “suicidal mass migration” [13]. Experiments with Culex sitiens showed that when subjected to overcrowding, the larvae compete for space to feed, increasing their mortality [14].

Many authors have been studying diets for the immature stages of different sand fly species. A mixture of aged rabbit feces and rabbit food was used to rear Lutzomyia cruciata, Dampfomyia anthophora, Psathyromyia shannoni, and Micropygomyia vexator under laboratory conditions. This diet was successful in reducing the growth of fungi [15]. Some modifications of this diet have been used in many sand fly colonies: Phlebotomus papatasi, Phlebotomus argentipes, Phlebotomus duboscqi, Lutzomyia longipalpis [16, 17] and Pi. serrana [2].

Industrialized animal food (for rabbits, dogs, hamsters and aquarium fishes) was compared with aged food for larvae of Nyssomyia intermedia and Lu. longipalpis. Both species developed very well with the aged food, but unlike Lu. longipalpis, Ny. intermedia also presented good results with industrialized animal food [4]. It has been suggested that variability in sand fly species dietary preferences can be important in reducing competition under natural conditions [18].

We did not use aged food in this study. Our results showed that diets that were enriched with fish food were more attractive to sand fly larvae compared to ones without this component. This observation is in agreement with the previous experiments of Rangel et al. [19], and this should be investigated in further studies on the possible attractants for larvae. In our experiments, the survival of adults was higher with traditional food (rabbit feces, rabbit food, fish food and soil) than with other diets that were made up only of plants and different grains (multimixture diet). The multimixture also presented a huge growth of fungi, which cause damage to the lifecycle of the insect. The fungi that grew on the multimixture were extremely dense and had to be removed daily during the insect counting. There is a controversy surrounding the relevance of fungus in diets for sand flies. According to some authors, the fungi on the diet could be fatal to the early instar of the larvae by trapping them on fungi hyphae [13, 18, 20]. Otherwise, the fungi can be profitable for the larvae, complementing their nutrition [4].

Considering the disagreement of many authors about fungi growth on sand fly diets, we decided to compare non-sterilized and sterilized diets. Even though our results did not show a significant difference between sterilized and non-sterilized diets, the autoclave and tyndallization methods (sterilized diets) retarded fungal growth for at least three days, giving enough time for the first instar larvae to develop. Under these conditions, the first instar larvae can grow a little more and avoid being trapped by the hyphae.

Some sand fly species of the Phlebotomus genus prefer non-autoclaved food, but for other species, like Lu. longipalpis, the food can be autoclaved [2]. We observed that the larvae of Ny. neivai did not refuse, in any stage, the sterilized diet, which had the advantage of a decrease in fungi growth; thus, we strongly advise the sterilization method for fungal control in Ny. neivai colonies.

The oviposition experiments on different substrates showed that an irregular surface (vermiculite) presented a higher productivity of adults compared to a flat surface (plaster of Paris). The gravid females were able to oviposit among vermiculite grains. The vermiculite also provided a “refuge” from the fungi hyphae among the grains for the first larval instars. Shaking the containers with grains would break the hyphae. Studies on the physical factors showed that temperature and humidity are important factors in the oviposition behaviour of Ny. neivai [21, 22]. Rough and irregular substrates stimulate a thigmotropic response in gravid flies of L. longipalpis and L. migonei and also provide greater protection, higher humidity and possibly more food for newborn larvae than flat surfaces [23, 24].

Conclusion

In conclusion, our data on Ny. neivai colonization showed a variable emergency rate of adults in different tests, depending on larval population density, diet and oviposition surface. The best adult productivities were achieved with fewer couples inside the rearing chambers (400–600 eggs depending on the size of the container); smaller rearing containers of 150 mL (due to less fungi growth); sterilized diet made of rabbit feces, rabbit food, soil and fish food; and vermiculite as the substrate for oviposition and development of larvae.

References

  1. Ready PD. Biology of phlebotomine sand flies as vectors of disease agents. Annu Rev Entomol. 2013;58:227–50.

    Article  CAS  PubMed  Google Scholar 

  2. Volf P, Volfova V. Establishment and maintenance of sand fly colonies. J Vector Ecol. 2011;36 Suppl 1:S1–9.

    Article  PubMed  Google Scholar 

  3. Moraes CS, Lucena SA, Moreira BH, Brazil RP, Gontijo NF, Genta FA. Relationship between digestive enzymes and food habit of Lutzomyia longipalpis (Diptera: Psychodidae) larvae: Characterization of carbohydrases and digestion of microorganisms. J Insect Physiol. 2012;58(8):1136–45.

    Article  CAS  PubMed  Google Scholar 

  4. Wermelinger ED, Zanuncio JC. Development of Lutzomyia intermedia and Lutzomyia longipalpis (Diptera: Psychodidae: Phlebotominae) larvae in different diets. Braz J Biol. 2001;61(3):405–8.

    Article  CAS  PubMed  Google Scholar 

  5. Córdoba-Lanús E, De Grosso ML, Piñero JE, Valladares B, Salomón OD. Natural infection of Lutzomyia neivai with Leishmania spp. in northwestern Argentina. Acta Trop. 2006;98(1):1–5.

    Article  PubMed  Google Scholar 

  6. Casanova C, Natal D, Santos FA. Survival, population size, and gonotrophic cycle duration of Nyssomyia neivai (Diptera: Psychodidae) at an endemic area of American cutaneous leishmaniasis in southeastern Brazil. J Med Entomol. 2009;46(1):42–50.

    Article  CAS  PubMed  Google Scholar 

  7. Marcondes CB, Bittencourt IA, Stoco PH, Eger I, Grisard EC, Steindel M. Natural infection of Nyssomyia neivai (Pinto, 1926) (Diptera: Psychodidae, Phlebotominae) by Leishmania (Viannia) spp. in Brazil. Trans R Soc Trop Med Hyg. 2009;103(11):1093–7.

    Article  PubMed  Google Scholar 

  8. Brazil RP, Rodrigues AAF, Filho JDA. Sand Fly Vectors of Leishmania in the Americas - A Mini Review. Entomol Ornithol Herpetol. 2015;4:144.

    Google Scholar 

  9. Galati EAB. Classificação de Phlebotominae. In: Rangel EF, Lainson R, editors. Flebotomíneos do Brasil. Rio de Janeiro, Brazil: Fiocruz; 2003.

    Google Scholar 

  10. Price WP. Insect Ecology, Second edn. USA: John Wiley & Sons, Inc; 1984.

    Google Scholar 

  11. Santamaría E, Munstermann LE, Ferro C. Estimating carrying capacity in a newly colonized sand fly Lutzomyia serrana (Diptera: Psychodidae). J Econ Entomol. 2002;95(1):149–54.

    Article  PubMed  Google Scholar 

  12. Andrade Filho JD, Galati EA, Falcão AL. Biology of the first generation of a laboratory colony of Nyssomyia intermedia (Lutz & Neiva, 1912) and Nyssomyia neivai (Pinto, 1926) (Diptera: Psychodidae). Mem Inst Oswaldo Cruz. 2004;99(6):597–601.

    Article  PubMed  Google Scholar 

  13. Hertig M, Johnson PT. The rearing of Phlebotomus sandflies (Diptera:Psychodidae). 1 Technique. Ann Entomol Soc Am. 1961;54:753–66.

    Article  Google Scholar 

  14. Roberts D. Overcrowding of Culex sitiens (Diptera: Culicidae) larvae: population regulation by chemical factors or mechanical interference. J Med Entomol. 1998;35(5):665–9.

    Article  CAS  PubMed  Google Scholar 

  15. Young DG, Perkins PV, Endris RG. A Larval diet for rearing Phlebotomine sand flies (Diptera:Psychodidae). J Med Entomol. 1981;18:446.

    Article  Google Scholar 

  16. Modi GB, Tesh RB. A simple technique for mass rearing Lutzomyia longipalpis and Phlebotomus papatasi (Diptera: Psychodidae) in the laboratory. J Med Entomol. 1983;20(5):568–9.

    Article  CAS  PubMed  Google Scholar 

  17. Lawyer PG, Rowton ED, Perkins PV, Johnson RN, Young DG. Recent advances in laboratory mass rearing of phlebotomine sand flies. Parassitologia. 1991;33(Suppl):361–4.

    PubMed  Google Scholar 

  18. Barreto MP. Contribuição para o estudo da biologia dos flebótomos em condições experimentais (Diptera:Psychodidae). São Paulo: Universidade de São Paulo; 1942.

    Google Scholar 

  19. Rangel EF, Souza NA, Wermelinger ED, Barbosa AF, Andrade CA. Biologia de Lutzomyia intermedia Lutz & Neiva, 1912 e Lutzomyia longipalpis Lutz & Neiva, 1912 (Diptera:Psychodidae) em condições experimentais. 1. Aspectos da alimentação de larvas e adultos. Mem Inst Oswaldo Cruz. 1986;81(4):431–8.

    Article  CAS  PubMed  Google Scholar 

  20. Sherlock IA, Sherlock VA. Métodos práticos para a criação de flebotomíneos em laboratório. R Bras Biol. 1972;32:209–17.

    CAS  Google Scholar 

  21. Foster WA, Tesfa-Yohannes TM, Tecle T. Studies on leishmaniasis in Ethiopia. II. Laboratory culture and biology of Phlebotomus longipes (Diptera: Psychodidae). Ann Trop Med Parasitol. 1970;64(4):403–9.

    CAS  PubMed  Google Scholar 

  22. Chaniotis BH. Successful colonization of the sand fly Lutzomyia trapidoi (Diptera: Psychodidae), with enhancement of its gonotrophic activity. J Med Entomol. 1986;23(2):163–6.

    Article  CAS  PubMed  Google Scholar 

  23. Elnaiem DA, Ward RD. The thigmotropic oviposition response of the sandfly Lutzomyia longipalpis (Diptera: Psychodidae) to crevices. Ann Trop Med Parasitol. 1992;86(4):425–30.

    CAS  PubMed  Google Scholar 

  24. Nieves E, Ribeiro A, Brazil R. Physical factors influencing the oviposition of Lutzomyia migonei (Diptera: Psychodidae) in laboratory conditions. Mem Inst Oswaldo Cruz. 1997;92(6):733–7.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We thank financial support of FAPESP (Fundação de Amparo à Pesquisa do Estado de São Paulo – Process 2012/23832–9) and Programa de Apoio ao Desenvolvimento Científico da Faculdade de Ciências Farmacêuticas at UNESP (PADC/FCFAr).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Mara Cristina Pinto.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

MP and TG conceived and executed the study and drafted the manuscript. TG, CC, VM and FS conducted field captures of sandflies and bioassay experiments. All authors read and approved the final manuscript.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Goulart, T.M., de Castro, C.F., Machado, V.E. et al. Techniques to improve the maintenance of a laboratory colony of Nyssomyia neivai (Diptera: Psychodidae). Parasites Vectors 8, 423 (2015). https://doi.org/10.1186/s13071-015-1035-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13071-015-1035-7

Keywords