Significance of bacteria in oviposition and larval development of the sand fly Lutzomyia longipalpis
© Peterkova-Koci et al.; licensee BioMed Central Ltd. 2012
Received: 23 April 2012
Accepted: 9 July 2012
Published: 24 July 2012
Microbial ecology of phlebotomine sand flies is not well understood although bacteria likely play an important role in the sand fly biology and vector capacity for Leishmania parasites. In this study, we assessed the significance of the microbial community of rabbit feces in oviposition and larval development of Lutzomyia longipalpis as well as bacterial colonization of the gut of freshly emerged flies.
Sterile (by autoclaving) and non-sterile (control) rabbit feces were used in the two-choice assay to determine their oviposition attractiveness to sand fly females. Bacteria were identified by amplification and sequencing of the 16S rRNA gene with universal eubacterial primers. Sterile, control (non-sterile), and sterilized and inoculated rabbit feces were used to assess the significance of bacteria in L. longipalpis development. Newly emerged adult flies were surface-sterilized and screened for the bacterial population size and diversity by the culturing approach. The digestive tract of L4 sterile and control larvae was incubated with Phalloidin to visualize muscle tissues and DAPI to visualize nuclei.
Two-choice behavioural assays revealed a great preference of L. longipalpis to lay eggs on rabbit feces with an active complex bacterial community (control) (85.8 % of eggs) in comparison to that of sterile (autoclaved) rabbit feces (14.2 %). Bioassays demonstrated that L. longipalpis larvae can develop in sterile rabbit feces although development time to adult stage was greatly extended (47 days) and survival of larvae was significantly lower (77.8 %) compared to that of larvae developing in the control rabbit feces (32 days and 91.7 %). Larval survival on sterilized rabbit feces inoculated with the individual bacterial isolates originating from this substrate varied greatly depending on a bacterial strain. Rhizobium radiobacter supported larval development to adult stage into the greatest extent (39 days, 88.0 %) in contrast to that of Bacillus spp. (76 days, 36.0 %). From the complex natural bacterial community of rabbit feces, R. radiobacter survived pupation and colonized the newly emerged females most successfully (82.6 % of all bacteria cultured); however, only 25 % of females were positive for bacteria in the digestive tract upon emergence. Immunohistochemistry did not reveal any obvious differences in anatomy of the digestive tract between control and axenic larvae.
The bacterial community in the sand fly larval habitat affects oviposition and larval development although bacteria are not essential for successful development of L. longipalpis. Different bacteria contribute to larval development to various degrees and some, e.g. Rhizobium radiobacter, survive pupation and colonize the digestive tract of newly emerged females. With the establishment of the axenic rearing system, this study opens new venues to study the effect of bacteria on the gut epithelial immunity and vector competence of sand flies for Leishmania parasites with a goal to develop paratransgenic approaches for Leishmania control.
The phlebotomine sand fly Lutzomyia longipalpis (Diptera: Psychodidae) is an important biological vector of Leishmania infantum (syn. Leishmania chagasi) in Central and South America. Although very little is known about the larval habitat of sand flies, it is generally agreed that organic material is the main food source for larvae . The larval habitat likely includes feces of rabbits and rodents in underground burrows where the proper temperature and humidity are maintained . Rabbit feces contain a large and diverse microbial community [3, 4] that potentially plays an important role in: a) sand fly oviposition behavior as bacterial volatile compounds may be used as semiochemical cues for females to locate the suitable habitat for their offspring; b) sand fly larval development since bacteria may provide essential or additional nutrients; and c) vector competence of sand flies for Leishmania parasites as bacteria surviving pupation and colonizing the gut of newly emerged females may influence development and transmission of the parasites.
It has been demonstrated that animal feces, including that of rabbits, play a role in L. longipalpis oviposition behavior and the active chemicals for the attraction are hexanal and 2-methyl-2-butanol [5, 6]. Additional oviposition attractant and/or stimulant for L. longipalpis includes dodecanoic acid deposited on eggs from the female accessory glands [7–9]. Furthermore, frass of the larvae also positively affected L. longipalpis oviposition . While the bacterial community in animal feces is likely a major player influencing sand fly oviposition behavior, only one study addressed this topic and showed that bacterial isolates from the soil in the natural breeding habitat of Phlebotomus papatasi attracted gravid females .
Virtually nothing is known about the significance of bacteria in the larval development of sand flies. It has been shown for several other Diptera including stable flies , house flies , horn flies , and face flies  that live bacteria are essential for successful larval development although the basis of this dependence on microbes remains unknown.
While bacteria in the lumen of the digestive tract do not typically survive insect pupation, it has been reported that freshly emerged female mosquitoes Anopheles gambiae and A. stephensi and sand flies P. duboscqi and P. argentipes had live bacteria in the digestive tract.
This study was designed to determine the significance of bacteria in rabbit feces in oviposition and larval development of L. longipalpis as well as to assess the extent of bacterial survival during sand fly pupation.
Sand flies and rabbit feces
A laboratory colony of Lutzomyia longipalpis from Jacobina, Brazil was used in this study. Flies were maintained at 27 ± 1 °C and 75 ± 5 % humidity. Adults were given a 20 % sucrose solution ad libitum and females were blood-fed twice a week on anesthetized mouse to produce eggs. For all experiments, fresh (< 24 hrs) rabbit feces from domestic rabbits kept in outdoor pens and fed alfalfa/corn rabbit pellets and grass garden clippings or bromegrass hay, were used for the assays.
In two-choice assays, sterile (by autoclaving) and non-sterile (control) rabbit feces were used to determine their oviposition attractiveness to sand fly females. Individual blood-fed females were placed in the plastic ovipots (ø = 10 cm, height = 7 cm) with plaster on the bottom and 1.0 g of each, sterile and control rabbit feces on opposite sides of the ovipot. Before each assay, humidity of rabbit feces was measured and adjusted to be the same (65-70 %) for both substrates using sterile tap water. Number of eggs on each substrate was recorded after 24 hrs. Nine individual females were used in each bioassay and each assay was replicated five times. At the end of each assay, rabbit feces of each type (control and sterilized) from two ovipots were sampled, diluted in phosphate-buffered saline (PBS) (pH 7.2; MP Biomedicals), and plated on broad spectrum medium, trypticase soy broth agar (TSBA) (BBL, Sparks) to assess the extent of contamination of sterilized feces by the flies during the assay.
Isolation and identification of bacteria
Fresh (< 24 hrs) rabbit feces were brought to the laboratory in a sterile plastic bag and processed immediately. For the isolation of bacteria, 10 g of feces was suspended in 40 ml of PBS, serially diluted in PBS, and dilutions were plated onto TSBA, and two selective and differentiating media, MacConkey agar (MAC) and modified Enterococcus agar (mENT) (BBL, Sparks). Plates were then incubated aerobically at 26 °C (TSBA), 37 °C (MAC) and 42 °C (mENT) for 48–72 h. Morphologically different single colonies were isolated on TSBA and stored at 4 °C until further analysis. Bacteria were identified by amplification and sequencing of the 16S rRNA gene with universal eubacterial primers: 8F (5'-AGAGTTTGATCC TGGCT CAG-3') and 806R (5'- CTACCAGGGTATCTAAT-3')  following the standard protocols. Isolates from mENT (enterococci) were identified by amplification and sequencing of the manganese-dependent superoxide dismutase gene (sodA) . Sequences were manually edited in CodonCode Aligner (version 1.3.4) (CodonCode Corporation) and identified by BLAST (Basic Local Alignment Search Tool)  search of the GenBank database.
Larval development assay
Four day old sand fly eggs were surface-sterilized with 0.05 % sodium hypochlorite and 70 % ethanol  and placed on TSBA plate until hatching to confirm the surface sterility. Newly hatched larvae (five per plate) were transferred by sterile brush in Petri plates with sterile water agar base. Water agar (1.4 %) was used to maintain appropriate moisture in the plates. For the control group, fresh rabbit feces grounded with mortar and pestle were provided ad libitum. For the axenic group, grounded fresh rabbit feces were sterilized by autoclaving and offered ad libitum. To assess the contribution of bacteria to larval development, sterile feces were inoculated with different bacterial isolates suspended in PBS (~ 106 CFU per ml). Humidity of each substrate was measured before assays and adjusted by sterile PBS. Plates were kept at 26 °C and 40 ± 5 % humidity until adult emergence. Mortality and development time to pupation and adult emergence were monitored on a daily basis. Each assay was conducted in 5 replicates (inoculated rabbit feces) or in 12 replicates (sterile and control feces). Three plates with sterile feces were discarded due to microbial contamination. Sterility of the substrate in the axenic system was confirmed by plating (100 μl) of the rabbit feces (1 g suspended in 10 ml PBS) on TSBA at the end of the assay. To assess the fitness of adult flies from the axenic group, they were fed sterile 20 % sucrose solution offered on sterilized filter papers for 3 days.
Survival of bacteria during sand fly pupation
Newly emerged flies were surface-sterilized (as described above), homogenized by hand using pestles in 100 μl PBS and plated on TSBA maintained at 26 °C under aerobic conditions. Bacterial counts (CFU per fly) were determined and bacterial colonies with distinct morphologies were sub-cultured and identified by amplification and sequencing of the 16S rRNA gene as described above. Sterility of axenic females was confirmed by plating the fly homogenate on TSBA and by DNA extraction and amplification of 16S rDNA with universal primers as described above.
The digestive tract of L4 larvae was dissected in PBS and incubated for 10 min in dark with Alexa Fluor 546 Phalloidin (Molecular Probes) to visualize muscle tissues (Actin) and DAPI (4', 6-diamidino-2-phenylindole) (Sigma) to visualize nuclei. Samples were observed under the compound microscope (Nikon Eclipse E800) with epifluorescent UV light and appropriate filters. Four individual digestive tracts from each group (control and axenic) were analyzed.
One-way ANOVA test was used to assess significance of differences in mortality and development time among flies in different treatments using Origin 7 (OriginLab Corp.). If ANOVA revealed significant differences (P ≤ 0.05) among treatments, pairwise comparisons were conducted using Tukey test in Origin 7 to assign groupings.
Results and Discussion
The following seventeen bacterial isolates from fresh rabbit feces with different colony morphology were identified to the species or genus level by sequencing of the 16S rRNA gene (655–698 bp) or the sodA gene (438 bp): Bacillus firmus (98 % identity), Bacillus sp. KK-1 (99 %); Enterococcus avium (99 %); Enterococcus gallinarum (99 %); Curtobacteriun flaccumfaciens (99 %); Microbacterium foliorum (98 %), Arthrobacter bergeri (99 %), Arthrobacter sp. (99 %), Acinetobacter sp. (99 %); Citrobacter freundii (99 %), Morganella morganii (99 %), Escherichia coli (99 %), Klebsiella sp. (99 %), Enterobacter sp. (97 %), Pseudomonas sp. KK-1 (99 %), Pseudomonas sp. KK-2 (99 %), and Rhizobium radiobacter (100 %). Analysis of the isolates from the digestive tract of freshly emerged sand fly females that developed as larvae in control rabbit feces led to identification of two additional bacterial taxa, Mycobacterium phocaicum (99 %) and Acidovorax sp. (99 %). Most of these bacteria are common members of the mammalian gastro-intestinal tract and some likely originate from the rabbit environment (soil) and feed (grass clippings and hay). Several bacterial species reported in our study including Pseudomonas, Citrobacter, Enterobacter, Escherichia, Klebsiella, and Morganella sp. were detected previously by culturing approach in the midgut of wild L. longipalpis collected from three sites in Brazil . A similar bacterial community was also found by culturing of the gut bacteria from P. argentipes in India  although in this study, higher prevalence of Gram-positive taxa (Bacillus, Staphylococcus, Micrococcu s sp.) was found compared to that of Gouveia et al..
Development of L. longipalpis in rabbit feces (RF) with different treatments and prevalence and concentration of bacteria in the gut of newly emerged females
1stinstar larvae (n)
% survival to adult stage (% females)
% newly emerged females with bacteria in the gut
Mean concentration of bacteria (CFU ± SEM) per female#
1.4 ± 0.9 × 101
1.6 ± 1.5 × 103
Pseudomonas sp. KK-2
3.2 ± 2.6 × 102
Pseudomonas sp. KK-1
2.0 ± 1.2 × 103
1.8 ± 1.3 × 103
8.3 × 101
Bacillus sp. KK-1
six bacterial isolates together
2.8 ± 2.3 × 102*
The basis of bacterial contribution to sand fly larval development is unknown; it may include breakdown of the components of rabbit feces to more digestible and absorbable nutrients and/or production of additional nutrients such as vitamins and amino acids. Although bacterial cells may be digestible in the gut of sand fly larvae and may serve as a source of nutrients, the bacterial cells mass alone (no additional food sources) does not support larval development (data not shown). It is important to emphasize that this study focused on the bacterial community only and other microorganisms including fungi and protozoa may also play a role in sand fly oviposition and larval development.
In general, before and during pupation, bacteria in the gut lumen are eliminated due to major changes in the gut content and structure and secretion of antimicrobial compounds . However, transstadial passage of bacteria from larvae to pupae and adult flies has been reported for P. duboscqi and P. argentipes. In P. duboscqi Ochrobactrum sp. AK was recovered in the midgut and hindgut of 64 % of freshly emerged flies and their counts ranged from (102 to 104 CFU per fly). Hurwitz et al. showed that B. subtilis added (107 CFU) to the P. argentipes (L4) larval medium (fermented rabbit food and feces) either sterilized or control (with other live bacteria) survived pupation and was recovered in 75 % of flies in concentration 7.2 x 103 CFU per fly (sterilized medium) and 74 % of flies with 3.9 x 104 CFU per fly (control medium). The prevalence and concentration of bacteria in those two studies was higher compared to ours; this may be due to differences in survivability between bacteria and also differences in the gut structure and pupation between the sand fly species. Furthermore, Hurwitz et al. reported that P. argentipes failed to develop in a sterile substrate, which is in contrast to our study with L. longipalpis. However, so far, we have not been able to raise P. papatasi on sterile rabbit feces (data not shown) and it may be that there is a difference in dependence on bacteria between Old World and New World sand fly species. Preference of Phlebotomus sp. larvae for non-autoclaved food is also indicated in the study of Volf and Volfova  although more data on the significance of microbes in larval development of sand flies in this genus are needed.
Females of the phlebotomine sand fly L. longipalpis use bacteria-mediated cues to locate an appropriate oviposition substrate. In addition, although bacteria contribute to larval development, an axenic system to raise L. longipalpis is reported. Some bacteria such as R. radiobacter and Pseudomonas sp. KK-1 support larval development to the same extent as a complex bacterial community, survive fly pupation, and colonize the digestive tract of newly emerged females. With the establishment of the axenic rearing system, this study opens new venues to study the effect of bacteria on the gut epithelial immunity and vector competence of sand flies for Leishmania parasites.
This study was supported by the NIH grant P20-RR017686 to LZ. MRO was supported with NIH grants R01 AI074691 and R21 AI088051-01. This is contribution no. 13-009-J from the Kansas Agricultural Experiment Station.
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