Description
Entomopathogenic nematodes (EPNs) form species-specific mutualistic symbiotic relationships with their gut bacteria; on the other hand, they are parasitic to insects, which they infect and rapidly kill with the assistance of their symbiotic bacteria (Dillman and Sternberg, 2012). Studies of EPNs can therefore provide useful insight into parasitism and mutualistic symbiosis. Research in this field has been so far limited by the lack of a genetically tractable system on the host side (Cao
et al.
, 2021).
S. hermaphroditum
was first isolated in Indonesia (Griffin
et al.
, 2001); that isolate was subsequently lost, but the species was recently rediscovered in India (Bhat
et al.
, 2019). It is consistently hermaphroditic, and techniques and methods developed to study hermaphroditic
Caenorhabditis elegans
are largely applicable (Cao
et al.
, 2021). Together with its bacterial symbiote
Xenorhabdus griffiniae
it provides a genetically tractable system for the study of symbiosis.
Nematode development consists of four larval/juvenile stages, known as either L1, L2, L3, and L4 (as in
C. elegans
), or as J1, J2, J3, and J4 (as in
S. hermaphroditum
). As an alternative to the third larval stage, nematodes can become a stress-resistant form known as dauers in
C. elegans
and infective juveniles (IJs) in EPNs in response to environmental conditions including limited food. As a crucial part of their life cycle, IJs search, invade, colonize, and subsequently feed on their insect host. Chemosensation is thought to play a major role in EPNs’ host-seeking behavior, and molecules including CO
2
have been identified as attractants for EPNs (Dillman
et al.
, 2012; Gang and Hallem, 2016; Hallem
et al.
, 2011).
The nervous system of the nematodes is highly conserved across species. For example, the tiny (~1mm) free-living nematode
C. elegans
has a neuroanatomy highly similar to that of the much larger (up to 40cm), evolutionary distant, and parasitic
Ascaris
(Schafer, 2016; Stretton
et al.
, 1992; White
et al.
, 1986). The functionality of nematode neurons are at least partially conserved. For example, ablation of the BAG neurons of both
Steinernema
and
Heterorhabditis
EPNs, identified by their conserved anatomy as corresponding to the
C. elegans
neuron responsible for sensing CO
2
eliminated the EPNs’ CO
2
‑dependent attraction by insect hosts and the jumping response of
Steinernema carpocapsae
to CO
2
(Hallem
et al.
, 2011). In
C. elegans
, amphid neurons are known to be important for chemosensation (Bargmann and Horvitz, 1991a), which is required for the decision-making process of entering and exiting the dauer larval state (Bargmann and Horvitz, 1991b). In
C. elegans
and other nematodes, including
Steinernema carpocapsae
, a dye-filling assay has been shown to be an efficient assay to label some of the amphid neurons (Han
et al.
, 2015; Hedgecock
et al.
, 1985; Perkins
et al.
, 1986; Srinivasan
et al.
, 2008; Tong and Burglin, 2010). In this study, we have developed a protocol for the efficient DiI (1,1′-Dioctadecyl-3,3,3′,3′-Tetramethylindocarbocyanine Perchlorate, Invitrogen) staining of
S. hermaphroditum
head sensory neurons.
We adapted the protocol described by Tong and Burglin (2010) for DiI staining, which has been utilized for the staining of the closely related nematode
S. carpocapsae
(Han
et al.
, 2015). We optimized the staining protocol by altering the concentration of the DiI dye (Fig. 1A, top), buffer solution, (Fig. 1A middle) and staining duration (Fig. 1A bottom). We found that a 20µg/ml DiI concentration with 0.5% Triton X-100 in M9 for 5 hours gave us the best results when considering both the staining effectiveness (Fig. 1A) and the health of the worm. In
C. elegans
, head sensory neurons, including amphids- ASI, ADL, ASK, AWB, ASH, ASJ, and inner labials- IL1 and IL2 are known to fill with DiI (Burket
et al.
, 2006; Shaham, 2006; Starich
et al.
, 1995; Tong and Burglin, 2010) (Fig. 1B, C). In
S. hermaphroditum
, we found that neurons identifiable by position as analogs of the amphid neurons ASI, ADL, ASK, ASJ and the inner labial neurons IL1, and IL2 could be labeled using DiI filling (Fig. 1D-G). While amphid neurons are generally labeled in DiI dye-filling assays in
C. elegans
(Tong and Burglin, 2010), they were only intermittently stained in
S. hermaphroditum
(at least 1 putative amphid neuron is stained in roughly 20% of the treated animals). On the other hand, the inner labial neurons are much more accessible (approximately 90% of the treated animals have at least 2 putative IL neurons stained), including the IL1 neuron that is not commonly filled in
C. elegans
(IL1 staining in
C. elegans
is possible as shown in
https://www.wormatlas.org/
). Our observations are consistent with what has been observed in
S. carpocapsae
, in which putative IL2 neuron is dye accessible, and amphid neurons are stained only occasionally (Han
et al.
, 2015). While our observation focused on the head neurons, it is known that in the tail phasmid neurons, PHAs and PHBs can also be labeled using dye-filling in
C. elegans
(Hedgecock
et al.
, 1985; Tong and Burglin, 2010). However, we did not look for phasmid neurons in
S. hermaphroditum
hermaphrodites and it is unclear whether they were stained. As in
S. carpocapsae
(Han
et al.
, 2015), no dye-filling was observed in the stress-resistant IJ animals (Fig. 1J). By contrast, staining is observed in
C. elegans
dauers (Peckol
et al.
, 2001). The mechanism of dye-filling is not well understood, but the difference among species in uptake is likely caused by structural divergences in the cilia opening. Similarly,
Heterorhabditis bacteriophora,
another EPN, despite that it is evolutionarily much closer to
C. elegans
than that of
S. hermaphroditum
, is reported to have a similar staining pattern: their putative amphid neurons are not stained consistently, and their IJs are not stained (Han
et al.
, 2015). Besides dye filling in the head neurons of non-IJ animals, we also observed dye uptake by the excretory pore on the ventral surface of the animal near the head and in the gut of nearly every worm observed (Fig. 1H, I). Overall, we showed that dye-filling assays could be applied in
S. hermaphroditum
, and the
anatomic characterization based on the staining suggests that it has a neuroanatomy similar to that of other characterized nematodes.
Methods
Nematode maintenance
The handling of
C. elegans
and
S. hermaphroditum
was done as described in Brenner (1974) and Cao
et al.
(2021), respectively. Briefly, the wild‑type
C. elegans
strain N2 (Bristol) was cultured on Nematode Growth Medium (NGM) agar in 6 cm Petri dishes with a lawn of
E. coli
strain OP50 at 20°C; the wild‑type
S. hermaphroditum
strain PS9179 was cultured on NGM agar in 10 cm Petri dishes with a lawn of
Xenorhabdus griffiniae
strain HGB2511 at 25°C. OP50 and HGB2511 were cultured at 37°C and 30°C, respectively, before seeding lawns on NGM agar. Infective juveniles were obtained by water trap as previously described (Cao
et al.
, 2021).
Dye filling assay
Dye filling assay was adapted from a previously described method (Tong and Burglin, 2010) with modifications as described in the main text and as described below. Briefly, well-fed
S. hermaphroditum
was washed three times with 0.5% Triton X-100 in M9 and incubated on a shaker with DiI solution with a final concentration of 20µg/ml in M9 containing 0.5% Triton X-100 by volume, unless indicated otherwise. The DiI (1,1′-Dioctadecyl-3,3,3′,3′-Tetramethylindocarbocyanine Perchlorate, Invitrogen D282) was dissolved in dimethylformamide and stored in -20°C as a stock solution at 20 mg/ml. After 5 hours at 25°C, worms were again washed three times with 0.5% Triton X-100 in M9. Worms were then mounted on a 5% agarose pad with a drop of M9 buffer containing 20 mM sodium azide for observation.
Dye filling assay optimization
The staining protocol was optimized in 3 stages. First, we tested the effectiveness of the staining in 3 different buffers (0.5% Triton X-100 in M9, H2O, M9) at 10µg/ml dye concentration and an incubation time of 10 hours. The staining was best with 0.5% Triton X-100 in M9 and thus was used in subsequent experiments. We then tested the dye concentration using the same condition but with the same buffer (0.5% Triton X-100 in M9), in which we found 20 µg/ml to be the most suitable. Finally, we tested the staining duration (15 hours, 10 hours, 5 hours, 2 hours) using the condition mentioned above (0.5% Triton X-100 in M9 and 20 µg/ml dye) and concluded that a 5-10 hr incubation time would be optimal. The experiment presented in figure 1A was done later with the optimized condition except for one of the parameters.
Image acquisition
Photomicrographs were acquired with a Zeiss Imager Z2 microscope equipped with Apotome 2 and Axiocam 506 mono using Zen 2 Blue software.