Gamete Collection and In Vitro Fertilization of Astyanax mexicanus

Podsumowanie

In vitro fertilization is a commonly used technique with a variety of model organisms to maintain lab populations and produce synchronized embryos for downstream applications. Here, we present a protocol that implements this technique for different populations of the Mexican tetra fish, Astyanax mexicanus.

Streszczenie

Astyanax mexicanus is emerging as a model organism for a variety of research fields in biological science. Part of the recent success of this teleost fish species is that it possesses interfertile cave and river-dwelling populations. This enables the genetic mapping of heritable traits that were fixed during adaptation to the different environments of these populations. While this species can be maintained and bred in the lab, it is challenging to both obtain embryos during the daytime and create hybrid embryos between strains. In vitro fertilization (IVF) has been used with a variety of different model organisms to successfully and repeatedly breed animals in the lab. In this protocol, we show how, by acclimatizing A. mexicanus to different light cycles coupled with changes in water temperature, we can shift breeding cycles to a chosen time of the day. Subsequently, we show how to identify suitable parental fish, collect healthy gametes from males and females, and produce viable offspring using IVF. This enables related procedures such as the injection of genetic constructs or developmental analysis to occur during normal working hours. Furthermore, this technique can be used to create hybrids between the cave and surface-dwelling populations, and thereby enable the study of the genetic basis of phenotypic adaptations to different environments.

Wprowadzenie

In recent years, Astyanax mexicanus has become a model organism in different fields such as developmental biology, evolutionary biology, behavioral biology, and physiology^1,2,3,4. The uniqueness of this system comes from this species having several morphotypes that have adapted to very different environments. The surface dwelling morphotype lives in rivers where there is high biodiversity and plenty of food sources for the fish. In contrast, the cave morphotypes of A. mexicanus, the cavefish, live in caves where biodiversity, food sources, and oxygen are drastically diminished¹. Cavefish differ from the surface fish in a variety of phenotypes such as the absence of eyes and pigmentation, insulin resistance, and the ability to store fat^2,3,4. However, surface fish and cavefish still belong to the same species and are, therefore, interfertile.

For both morphotypes, a set of conditions has been defined to allow routine maintenance and breeding under laboratory conditions^5,6. However, genetic modifications, proper embryonic developmental studies, and creation of hybrids are still challenging for several reasons. A. mexicanus primarily spawn during night hours which is inconvenient for subsequent experiments on early embryonic stages such as injection of genetic constructs or monitoring of early embryonic developmental processes. In addition, generation of surface and cave hybrids is challenging using natural spawning, since the cave morphotypes have an altered circadian rhythm⁷ that ultimately affects the production of viable ova. Successful, yet invasive, IVF procedures have been described for other Astyanax species, where gamete production and spawning behavior was primed using hormonal injections^8,9. Less invasive IVF procedures (i.e., obtaining gametes from manual spawning without the injection of hormonal preparations) have been described but do not consider the differences in the spawning cycle between cave and surface morphotypes of A. mexicanus⁶.

Other fish model organisms, such as the zebrafish, can easily be genetically modified and studied at an embryonic level because the obstacles stated above have been successfully resolved. Implementation of standardized breeding techniques, in vitro fertilization, and sperm cryopreservation have all pushed zebrafish forward and solidified the model's use in the biological sciences¹⁰. Therefore, extending these techniques to A. mexicanus will further strengthen it as a model system.

Here, we present a detailed protocol for IVF that will help to make A. mexicanus more accessible. We will present a breeding setup that enables shifting the light-cycles of the fish from daytime to nighttime so that viable ova can be obtained during day hours without injection of hormonal preparations. We then provide a detailed description of how to obtain the ova and milt used for IVF. This method will enable the production of embryos during normal working hours and make further downstream applications more feasible compared to using embryos from natural spawning.

Protokół

All methods described here have been approved by the Institutional Animal Care and Use Committee (IACUC) of Stowers Institute for Medical Research.

1. Light cycle manipulation

1. Set up fish tanks within an opaque, fully enclosed (light protection), flow-through aquaculture system containing multiple rows of tanks (Figure 1).
   NOTE: The flow-through system as shown in Figure 1 uses system water to flush waste through the back stand pipe of each tank and flows into a sump that empties into a sanitary drain. In this experiment, a water exchange rate of one gallon (US) per hour through a drip emitter was used.
2. Maintain the temperature of each tank with an independent heating element that is used to manually alter the temperature during the priming process.
3. Set up individual rows in a way to enable separate photoperiods in each. Install doors on each row that can be closed to prevent light from entering or escaping.
   NOTE: The automated controller can enable manipulation of all photoperiods with the least disturbance to the fish.
4. Equip the rack with a red work light and blackout curtains for access during dark hours.

2. Adjusting photoperiod and priming fish for gamete collection

1. Remove the desired fish (Figure 2a) from general system racks and place in breeding racks to allow for adjustment of the photoperiod 14 days prior to priming.
   NOTE: This allows the fish to acclimatize to a new environment.
2. Keep the fish at 22.8 °C (73 °F) during this period using the installed aquatic heating system. The normal photoperiod is from 6 a.m. to 8 p.m. light and 8 p.m. to 6 a.m. dark. For the light cycle rack, shift the photoperiod to 10 p.m. to 12 p.m. light and 12 p.m. to 10 p.m. dark by adjusting the timer that powers the light within the rack.
   NOTE: Males and females are housed in the same tank to allow for natural priming behaviors to take place. While spawning may take place in the tank, fish can still be used for in vitro fertilization since gametes are released in stages¹¹.
3. Once the fish are acclimatized, start priming the animals for spawning⁵ as described in steps 2.3.1 to 2.3.5.
   NOTE: This procedure takes six days in total. Over this time, change the temperature to prime the ova production using an installed aquatic heating system. Using the 50W Aquatic Heaters (see Table of Materials), set the heater directly to the temperature (scale on the heater is in Fahrenheit) given in the protocol at each step. Depending on the size of the tank and flow-through rate of the water, time of temperature adjustment may differ. In this experiment, the temperature was adjusted at noon and temperature equilibration took over the next 18 h.
   1. On day 1, raise the temperature from 22.8 °C (73 °F) to 24.4 °C (76 °F).
   2. On day 2, raise the temperature from 24.4 °C (76 °F) to 26.1 °C (79 °F).
   3. On day 3 and 4, keep the temperature at 26.1 °C (79 °F). Fish will be ready to spawn during the day and IVF can be performed.
      NOTE: Depending on the individual fish, females can spawn on day 3 and/or day 4. We recommend trying to obtain ova on day 3 and/or day 4 depending on the success of the ova collection.
   4. On day 5, lower the temperature from 26.1 °C (79 °F) to 24.4 °C (76 °F).
   5. On day 6, lower the temperature from 24.4 °C (76 °F) to 22.8 °C (73 °F).
      NOTE: Provide a 7-day gap before repeating this temperature cycle. It is recommended to continue keeping the fish in this photoperiod since this will reduce the overall time needed by the fish to adjust to this shifted light cycle.

3. Female gamete collection

1. Begin by inserting a moistened tissue wipe into a Petri dish lid and closing the dish to create a humidified chamber and prevent the ova from drying out during the collection process.
2. Next choose a female for collection. Gravid fish with large, protruding abdomens will likely be the best choice for this procedure (Figure 2a).
   NOTE: To differentiate between males and females of adult A. mexicanus, the cotton ball method was used¹².
3. Immobilize a female using chilled water and place her in the supine position in a moistened sponge animal holder. Do so by placing the fish in 4 °C system water for at least 30 s or until the fish is immobilized (i.e., loss of gill movement, see Ross and Ross¹³ for details).
   NOTE: Work quickly and try to avoid warming the fish until the procedure is completed. This may include periodically dipping the gloved tips of the fingers into cold water or offering supplemental anesthesia. Other anesthesia methods (e.g., MS-222¹³) may be used as well. Under the IACUC guidelines of the Stowers Institute for Medical Research, manual collection of ova is considered a non-invasive procedure, which does not require complete anesthesia (e.g., through MS-222).
4. Once positioned, blot the ventral side of the fish with a delicate tissue wipe as contact with water will cause the ova to activate.
5. Hold the female between the thumb and index finger. Gently squeeze against the lateral sides of the coelomic cavity in the direction of the urogenital opening while rolling the fingers slightly. Collect the expressed ova using a disposable spatula.
6. Transfer these ova to the humidified Petri dish.
   NOTE: Several clutches of ova may be combined in the same dish if specific parentage data is not needed. The ova can be stored at 24 °C and are best when used for IVF within 30-60 min after collection.
7. After collection, gently return the fish to a recovery tank filled with system water.
   NOTE: Place the fish back into dark cabinet tank for future ova collection when necessary.

4. Male gamete collection

1. Choose a male for collection.
   NOTE: There are no outwardly visible signs of male gamete quality. However, fish should appear healthy in appearance before use in this procedure. To differentiate between males and females of adult A. mexicanus, the cotton ball method was used¹².
2. Immobilize a male using chilled water and place him in the supine position in a moistened sponge animal holder. Immobilize by placing the fish in 4 °C system water for at least 30 seconds or until the fish is immobilized (i.e., loss of gill movement, see Ross and Ross¹³ for details).
   NOTE: Work quickly and try to avoid warming the fish until the procedure is completed. This may include periodically dipping the gloved tips of the fingers into cold water or offering supplemental anesthesia. Other anesthesia methods (e.g., MS-222¹³) may be used here as well. Under the IACUC guidelines of the Stowers Institute for Medical Research, manual collection of sperm is considered a non-invasive procedure, which does not require complete anesthesia (e.g., through MS-222).
3. Blot the ventral side of the fish with a delicate tissue wipe as contact with water will activate the milt.
4. Gently place the end of a capillary tube at the urogenital opening.
5. Expel milt by applying gentle pressure on the sides of the fish with the thumb and forefinger. Start distal to the gills, moving towards the urogenital opening.
6. Collect the milt in the end of a capillary tube. Gentle suction may be necessary by use of an aspirator tube. Avoid any feces that may be expelled with the milt.
7. Dispense the milt into an empty 1.5 mL centrifuge tube and dilute with twice the volume of Sperm Extender E400 (see Table of Materials). Keep on ice.
   NOTE: Milt from multiple males may be pooled together if specific parentage data is not needed. This step can be used to extend the working time of the milt for several hours, but it is not required for immediate fertilization.
8. After collection, gently return the fish to a recovery tank filled with system water.
   NOTE: Place fish back into dark cabinet tank for future sperm collection when necessary.

5. In vitro fertilization

1. Using a new pipette for each stock, mix the sperm by pipetting and/or agitating the side of the tube before fertilizing as sperm in milt can settle in the E400 solution over time.
2. Dispense the milt or extended milt solution into the freshly collected ova.
3. Quickly add 1 mL of system water to the clutch to activate the sperm and eggs for fertilization. Avoid mixing or agitating the dish contents and allow 2 min for fertilization to occur.
   NOTE: Mixing and agitating greatly reduces the fertilization rates and should, therefore, be avoided¹⁴.
4. Add E2 Embryo Media to fill the dish 2/3^rd full.
   NOTE: Depending on the subsequent procedure, embryos can be either used right away (e.g., for injection of genetic constructs as described before¹⁵) or embryos can be incubated in E2 Embryo Media at 23 °C until they reach 5 dpf. At this point transfer embryos to the main recirculating housing system using system water.

Wyniki

The protocol presented here is mainly based on a previously published protocol⁶. However, since A. mexicanus spawns during night hours, we designed a housing rack for fish breeding that can change the photoperiod independent of working hours (Figure 1). The fish light cycle is altered within a fully enclosed, flow-through aquaculture system containing three rows of tanks (Figure 1). Each tank cont...

Dyskusje

While IVF is a standardized method for many different model organisms such as zebrafish, existing protocols for A. mexicanus do not take into account that this species naturally spawns during night hours⁶. Given that cavefish and surface fish differ quite drastically in their circadian rhythms, the maturation cycle of the ova also differs between the cave and surface morphotypes. While the staging temperatures and times for surface A. mexicanus are well studied^1...

Materiały

Name	Company	Catalog Number	Comments
1.5 mL Centrifuge Tube	Eppendorf	#22364111
100 mm Petri Dishes	VWR International	#25384-302
Aspirator Tube	Drummond	#2-000-000
Calibrated 1-5 µL Capillary Tubes	Drummond	#2-000-001
Dispolable Spatulas	VWR International	#80081-188
HMA-50S  50W Aquatic Heaters	Finnex	HMA-50S
P1000 Pipette	Eppendorf	#3123000063
P1000 Pipette Tips	Thermo Scientific	#2079E
Sanyo MIR-554 incubator	Panasonic Health Care	MIR-554-PA
Sperm Extender E400			130 mM KCl, 50 mM NaCl, 2 mM CaCl2 (2H2O), 1 mM MgSO4 (7H2O), 10 mM D (+)-Glucose, 30 mM HEPES Adjust to pH 7.9 with  5M KOH and filter sterilize. Solution can be stored at 4 ?C for up to 6 months.
Sponge Animal Holder			Made from scrap foam
System Water			Deionized water supplemented with Instant Ocean Sea Salt [Blacksburg, VA] to reach a specific conductance of 800 µS/cm.  Water quality parameters are maintained within safe limits (Upper limit of total ammonia nitrogen range, 1 mg/L; upper limit of nitrite range, 0.5 mg/L; upper limit of nitrate range, 60 mg/L; temperature, 22 °C; pH, 7.65; dissolved oxygen 100 %)
Tissue Wipes	Kimberly-Clark Professional	#21905-026
ZIRC E2 Embryo Media			15 mM NaCl, 0.5 mM KCl, 1.0 mM MgSO4, 150 µM KH2PO4, 50 µM Na2HPO4, 1.0 mM CaCl2, 0.7 mM NaHCO3. Adjust pH to 7.2 to 7.4 using 2 N hydrochloric acid. Filter sterilize. Stored at room temperature for a maximum of two weeks.