A UPR-independent infection-specific role for a BiP/GRP78 protein in the control of antimicrobial peptide expression in C. elegans epidermis.

The nematode C. elegans responds to infection by the fungus Drechmeria coniospora with a rapid increase in the expression of antimicrobial peptide genes. To investigate further the molecular basis of this innate immune response, we took a two-dimensional difference in-gel electrophoresis (2D-DIGE) approach to characterize the changes in host protein that accompany infection. We identified a total of 68 proteins from differentially represented spots and their corresponding genes. Through class testing, we identified functional categories that were enriched in our proteomic data set. One of these was "protein processing in endoplasmic reticulum," pointing to a potential link between innate immunity and endoplasmic reticulum function. This class included HSP-3, a chaperone of the BiP/GRP78 family known to act coordinately in the endoplasmic reticulum with its paralog HSP-4 to regulate the unfolded protein response (UPR). Other studies have shown that infection of C. elegans can provoke a UPR. We observed, however, that in adult C. elegans infection with D. coniospora did not induce a UPR, and conversely, triggering a UPR did not lead to an increase in expression of the well-characterized antimicrobial peptide gene nlp-29. On the other hand, we demonstrated a specific role for hsp-3 in the regulation of nlp-29 after infection that is not shared with hsp-4. Epistasis analysis allowed us to place hsp-3 genetically between the Tribbles-like kinase gene nipi-3 and the protein kinase C delta gene tpa-1. The precise function of hsp-3 has yet to be determined, but these results uncover a hitherto unsuspected link between a BiP/GRP78 family protein and innate immune signaling.

Introduction

The nematophagous fungus Drechmeria coniospora infects various species of nematodes. Its spores adhere to the surface of a worm, germinate and perforate the cuticle. The worm’s body is then totally invaded by the fungus, rapidly causing death (reviewed by Engelmann and Pujol). When D. coniospora infects Caenorhabditis elegans this triggers the expression of a large number of genes including those encoding antimicrobial peptides (AMPs) of the NLP family.- The induction of several nlp genes is dependent upon a protein kinase C delta (PKC∂)/p38 MAPK pathway that can be activated in the epidermis either by infection or by sterile wounding. In both cases, signaling passes via TPA-1, a PKC∂ that acts upstream of TIR-1, the nematode ortholog of SARM, and a MAPK cassette constituted of a MAP3K (NSY-1), MAP2K (SEK-1) and the p38 MAPK PMK-1. This then acts upstream of the STAT-like transcription factor STA-2 to regulate nlp gene expression. The elements that contribute to signaling upstream of TPA-1 have only been partially characterized. Wounding and infection require G-protein signaling upstream of TPA-1, while infection specifically involves the Tribbles-like kinase NIPI-3.,

Part of the innate defenses against intestinal pathogens and toxins are also mediated by a p38 MAPK cascade that shares many but not all of the elements that act in the epidermis;- reviewed by Partridge et al. and Coleman and Mylonakis. Intestinal infection or exposure to bacterial toxins can also induce an unfolded protein response (UPR); this too is linked to the p38 pathway.,

The UPR in C. elegans is divided into constitutive and inducible pathways, the former being essential during development., Part of the UPR involves activation of the endoribonuclease IRE-1 that leads to the production of an alternatively spliced isoform of the mRNA of the transcription factor XBP-1. Compounds such as thapsigargin, dithiothreitol and tunicamycin that perturb endoplasmic reticulum (ER) homeostasis trigger a UPR and lead to IRE-1 activation. The subsequent production of the specific form of XBP-1 then leads to the expression throughout the organism of a large number of genes, many involved in metabolism, or the secretory pathway, including chaperones.- Feeding worms the bacterial pore-forming toxin Cry5B also activates IRE-1 and upregulates chaperone expression specifically in the intestine. This requires the p38 MAPK signaling cassette. The Gram-negative bacterial pathogen Pseudomonas aeruginosa also induces IRE-1-mediated splicing of xbp-1 mRNA in larvae and consequent chaperone gene expression, in a p38 MAPK-dependent manner. As the UPR-deficient xbp-1 mutants arrest as larvae when cultured on P. aeruginosa, in this case, it was suggested that the ER cannot cope with the combined developmental and defense demands placed upon it (reviewed in Ewbank and Pujol).

In addition to the UPR-mediated changes in protein maturation, turnover and trafficking, the innate immune response may also affect the activity, post-translational modification and subcellular localization of signal transduction proteins. These can be analyzed at a global level through proteomic approaches. Indeed, there have already been a number of informative studies addressing the changes in the proteome that accompany infection of C. elegans by several different bacterial pathogens.-

To extend our characterization of the response of C. elegans to D. coniospora we have now compared the proteomes of infected and control worms using two-dimensional difference gel electrophoresis (2D-DIGE). This fluorescence-based method allows two different protein samples tagged with two distinct fluorescent dyes to be run on the same gel, thereby improving comparative quantitation. We decided to focus on a single time point, early in the infection, with the hope of detecting changes in proteins involved in signal transduction, rather than finding proteins altered by the pathophysiological consequences of infection. We found that few changes were detected in whole extracts, but after fractionation we detected changes in many proteins. For one of these candidates, a C. elegans BiP/GRP78 homolog, we defined a novel role in the regulation of AMP gene expression.

Results

Protein fractionation reveals changes in the proteome induced by fungal infection

The infection of C. elegans by D. coniospora induces significant changes in gene expression within a matter of hours (and unpublished data). We used a standard 2D-DIGE approach to identify alterations at the protein level in C. elegans after 5 h of infection with D. coniospora. As with any 2D gel approach, with DIGE it is appropriate to refer to changes in representation, rather than stating that a protein is more or less abundant, unless all protein spots are identified and quantified. With whole animal extracts (FT), when we used a narrow-range pH gradient for isoelectric focusing, although 890 protein spots were detected, we observed no differences between extracts of infected and control worms. With a broad-range pH gradient that allowed 1,478 spots to be resolved, just three differentially represented proteins were detected. Only one of these was present in sufficient quantities to allow identification; it corresponded to the galectin LEC-6 (see Materials and Methods for access to data). We therefore adopted a more laborious approach, separating the extracts into four fractions (F1, F2, F3 and FNS), and performing DIGE as above for each one. The fractionation allowed many more spots to be detected (9,246 in total), and revealed differences in intensity for 67 and 103 spots in the narrow- and broad-range pH gradient gels, respectively. All these spots were excised and analyzed by mass-spectrometry, leading to an identification of a protein from 98 spots (Tables 1 and 2). This clearly illustrates the interest of combining DIGE with a prior protein fractionation approach.

Table 1. Protein identification from narrow pH (4–7) gel

Fractions	F1	F2	F3	FNS	FT	Total
Number of detected spots	867	933	883	1,016	890	4,589
Number of differentially represented spots	12	14	13	28	0	67
Number of identified spots	4	6	7	26	0	43

Table 2. Protein identification from broad pH (3–10) gel

Fraction	F1	F2	F3	FNS	FT	Total
Number of detected spots	1,588	1,238	1,083	1,638	1,478	7,025
Number of differentially represented spots	35	13	7	45	3	103
Number of identified spots	20	1	0	33	1	55

Classification of differentially represented proteins

In some cases, the same protein was identified from more than one spot, either within the same fraction on the same gel, or from different fractions and/or gels. As a consequence, the 98 characterized spots corresponded to 67 individual proteins that were differentially-represented between infected and control worms (Table 3). We used WormMart (WS220) to match each of the 68 identified proteins (LEC-6 and the 67 others) with its corresponding C. elegans gene (Table 3). They fall into many different structural and functional classes (). We therefore performed two complementary bioinformatic analyses to find common themes. We first used the KEGG database to determine whether there was an over-representation of higher-level systemic functions within the list of 68 genes. The most populated categories (Table 3) were “implicated in a metabolic pathway” (13 genes), and “protein processing in endoplasmic reticulum” (8 genes). We then used EASE, with our extensive in-house annotations culled from the C. elegans literature and referenced to WS220. There were 24 functional classes identified as significantly enriched (p < 0.001, Fisher exact test; see Materials and Methods). Among these classes, 6 were related to the response of C. elegans to infection, with a further 10 linked to aging and stress-resistance, including to the insulin/DAF-2 pathway (Tables 4). Given the intimate connection between stress-resistance and susceptibility to infection, a part of the observed protein changes could thus be directly or indirectly associated with an innate immune response. The EASE analysis also revealed a potential connection with protein processing in the endoplasmic reticulum, as had been seen with KEGG.

Table 3. List of identified proteins from spots with different intensities

Spot N°Range pH 4–7	Spot N°Range pH 3–10	Wormpep name	Worm base ID	Gene name
	F1-740	ZK455.1	WBGene00000040	aco-1*
F2-401; FNS-17	FNS-677	C34E10.6	WBGene00000229	atp-2*
FNS-489	FNS-1706	F47B10.1	WBGene00009812	F47B10.1*
	FNS-1926	K10B3.7	WBGene00001685	gpd-3*
	FNS-1965	F33H1.2	WBGene00001686	gpd-4*
	FNS-1717	H28O16.1	WBGene00010419	H28O16.1*
FNS-228		Y45G12B.1	WBGene00021562	nuo-5*
F3-516		K12G11.3	WBGene00010790	sodh-1*
FNS-455		Y49A3A.2	WBGene00013025	vha-13*
F3-516		Y39G8B.1	WBGene00012722	Y39G8B.1*
F2-821	F2-1119	Y69A2AR.18	WBGene00022089	Y69A2AR.18*
FNS-401	FNS-1522	ZK829.4	WBGene00014095	ZK829.4*
FNS-198		F40F9.6	WBGene00009583	aagr-3*†
FNS-463		Y38A10A.5	WBGene00000802	crt-1†
FNS-315		C15H9.6	WBGene00002007	hsp-3†
FNS-411		C07A12.4	WBGene00003963	pdi-2†
	F1-776	Y113G7A.3	WBGene00004754	sec-23†
FNS-239		T05E11.3	WBGene00011480	T05E11.3†
F3-142		T14G8.3	WBGene00011771	T14G8.3†
FNS-157		T24H7.2	WBGene00020781	T24H7.2†
F1-463	F1-1375; F1-1389;FNS-739; FNS-1617	M03F4.2	WBGene00000066	act-4
F1-460		T25C8.2	WBGene00000067	act-5
	FNS-1450	B0334.3	WBGene00007143	B0334.3
F2-100		C08H9.2	WBGene00007463	C08H9.2
	F1-1246; FNS1717	C44B7.10	WBGene00016630	C44B7.10
	F1-1234	C07H6.5	WBGene00000479	cgh-1
	FNS-2317	T03E6.7	WBGene00000776	cpl-1
	FNS-2295	F58G1.4	WBGene00010266	dct-18
F3-526; F3-531	FNS-1996	C18A11.7	WBGene00001000	dim-1
FNS-684		F54H12.6	WBGene00018846	eef-1B.1
FNS-684		Y41E3.10	WBGene00012768	eef-1B.2
FNS-209	FNS-996; FNS-1002;FNS-1018; FNS-1019; FNS-1055	F25H5.4	WBGene00001167	eef-2
		F09B12.3	WBGene00008607	F09B12.3
		F57F4.4	WBGene00019017	F57F4.4
FNS-285; FNS-286;FNS-287; FNS-288		T21G5.3	WBGene00001598	glh-1
FNS-489		C26D10.2	WBGene00001840	hel-1
FNS-390		Y22D7AL.5	WBGene00002025	hsp-60
	F1-1012	F10C1.2	WBGene00002053	ifb-1
FNS-401		M6.1	WBGene00002056	ifc-2
	FNS-1051	C43C3.1	WBGene00002067	ifp-1
FNS-503		F57B9.6	WBGene00002083	inf-1
	F1-553; F1-579	K08H10.2	WBGene00010695	K08H10.2
	FNS-1284	Y71H2AM.19	WBGene00002244	laf-1
	F1-533; F1-579	K08H10.1	WBGene00002263	lea-1
	FT-1877	Y55B1AR.1	WBGene00002269	lec-6
	F1–1012	DY3.2	WBGene00003052	lmn-1
	FNS-1051	Y48C3A.7	WBGene00003119	mac-1
F2-821		Y69A2AR.30	WBGene00003161	mdf-2
F3-731		C36E6.3	WBGene00003369	mlc-1
	F1-362; F1-367	R07G3.3	WBGene00019940	npp-21
FNS-134	FNS-739	F54F2.1	WBGene00003929	pat-2
	F2-1199	R05G6.7	WBGene00019900	R05G6.7
F2-564; F3-516		F25H2.10	WBGene00004408	rla-0
F2-584		B0041.4	WBGene00004415	rpl-4
	F1-741	T22F3.3	WBGene00020696	T22F3.3
F2-456; FNS-463	F1-1115; FNS1669	K01G5.7	WBGene00006536	tbb-1
F2-401; FNS-455		C36E8.5	WBGene00006537	tbb-2
	FNS-1567	Y71H2AM.23	WBGene00007000	tufm-1
FNS-784		F40G9.3	WBGene00006715	ubc-20
F1-114; F3-97	F1-463; FNS-373	F11C3.3	WBGene00006789	unc-54
	F1-1234; F1-1246	F08B6.4	WBGene00006819	unc-87
	F1-908	Y54E10A.9	WBGene00006888	vbh-1
	FNS-534	K09F5.2	WBGene00006925	vit-1
	FNS-501; FNS-517; FNS-518	C42D8.2	WBGene00006926	vit-2
	FNS-518; FNS-532	F59D8.1	WBGene00006927	vit-3
	FNS-531; FNS-534	F59D8.2	WBGene00006928	vit-4
	FNS-1126; FNS-1129	K07H8.6	WBGene00006930	vit-6
FNS-831		Y48A6B.3	WBGene00012964	Y48A6B.3

* Proteins implicated in a metabolic pathway. Protein processing in endoplasmic reticulum.

Table 4. Functional classification by EASE of differentially represented proteins

Gene category	Infection	Stress	List hits	Population hits	Probability
Down ≥ 2x daf-2 (D6); Halaschek-Wiener 2005		X	25	234	7.6E-31
Proteome changes S. aureus; Bogaerts 2010	X		17	109	7.2E-24
Differentially expressed proteins in crt-1;cnx-1 vs N2 at 20°C; Lee 2006			7	13	9.0E-15
Protein expression; Kim 2001			14	446	4.7E-10
Proteome changes Aeromonas h.; Bogaerts 2010	X		7	64	2.8E-09
Down ≥ 2x dauer; Halaschek-Wiener 2005		X	6	36	2.9E-09
Differentially expressed proteins in crt-1;cnx-1 vs N2 at 25°C; Lee 2006			4	12	7.2E-08
Up > 1.75x in M. luteus vs. Pseudomonas sp; Coolon 2009	X		6	69	1.7E-07
Glycoproteins GaL6 binding; Kaji 2007			9	287	8.0E-07
Heat shock; Kim 2001		X	4	25	1.8E-06
Cell structural, muscle; Kim 2001			9	332	2.6E-06
Down after organophosphorus pesticide chlorpyrifos + diazinon; Vinuela 2010		X	5	65	3.5E-06
Regulated down_daf-2 mutant and RNAi,Class2,-IGF1; Murphy 2003		X	7	222	1.4E-05
Down > 1.75x in Pseudomonas spp vs E. coli; Coolon 2009	X		4	44	1.8E-05
Down after organophosphorus pesticide diazinon; Vinuela 2010		X	5	121	7.2E-05
Regulated down_Bt toxin, Cry5B; Huffman 2004		X	8	442	0.00017
Differentially expressed proteins in crt-1 vs N2 at 20°C; Lee 2006			2	7	0.00026
Regulated down_Cadmium; Huffman 2004		X	7	388	0.00046
Energy generation; Kim 2001			4	104	0.00052
Up > 1.75x in B. megaterium vs. Pseudomonas sp; Coolon 2009	X		3	45	0.00055
Down ≥ 2x oxidative stress; Park 2009		X	2	13	0.00095
DNA synthesis; Kim 2001			7	440	0.00096
Up ≥ 2x by PA14 8h; Troemel 2006	X		5	233	0.00146
Overlap Between oxidative stress and aging—downregulated genes by oxidative stress; Park 2009		X	3	66	0.00169

Fungal infection in adults does not provoke the UPR

The proteins linked to protein processing in the endoplasmic reticulum included the calreticulin CRT-1, the protein disulphide isomerase PDI-2 and HSP-3. HSP-3 and the closely related HSP-4 represent the worm’s BiP/GRP78 homologs. All these proteins function in the ER to ensure the correct folding of nascent polypeptides and are important components of the UPR. Given the reported link between the UPR and resistance to bacterial toxins and infection,,,,, we decided to investigate whether the UPR is involved in the host response to D. coniospora infection.

A direct measure of the activation of the UPR is provided by the detection of a specific UPR-associated alternatively spliced isoform of the transcription factor XBP-1. In contrast to the splicing of xbp-1 observed when young adult worms were treated with the UPR-inducing drug tunicamycin, the alternatively spliced isoform of xbp-1 was not detected following D. coniospora infection (Fig. 1A). Another indicator of the UPR is an increased expression of hsp-3 and hsp-4. In C. elegans, the UPR is often monitored in vivo using a phsp-4::GFP transgene reporter, which has a lower constitutive expression and higher level of induction during a UPR than phsp-3::GFP. In contrast to tunicamycin-treated worms, there was neither induction of an phsp-4::GFP transgene reporter after infection (Fig. 1B), nor increase of the hsp-4 transcript as measured by qRT-PCR (data not shown). This is consistent with previous genome-wide transcriptome studies that found that the expression of hsp-4 (and hsp-3) was not significantly altered following infection with D. coniospora., When worms carrying a pnlp-29::GFP transgene reporter were exposed to tunicamycin, strong GFP expression was observed in young larvae. This is consistent with a previous microarray study that reported the induction of a number of epidermal AMP genes, including nlp-29, in L2 larvae treated with tunicamycin. A marked increase in reporter gene expression was also seen in young larvae carrying a pnlp-30::GFP reporter transgene. On the other hand, no induction of either of these reporters was seen in L4 or adult worms (Fig. 1B and data not shown). Similar results were obtained using the UPR-inducing agents dithiothreitol and thapsigargin (data not shown).

Figure 1. Fungal infection of adult worms does not induce a UPR. (A) RT-PCR analysis of xbp-1 splicing. Under standard culture conditions (control), a 220 bp amplicon from an unspliced (us) xbp-1 transcript is detected, together with very low levels of a 197 bp amplicon from a spliced (s) transcript. The abundance of this smaller band does not increase after infection with D. coniospora (infection) or PMA treatment (PMA), but is clearly increased upon UPR-induction with tunicamycin (Tu). (B) The green fluorescence in transgenic worms carrying a pnlp-29::GFP (strain IG274; left column) or a phsp-4::GFP (IG1320; right column) reporter was observed after infection, exposure to tunicamycin, or high salt. While infection and osmotic stress induced high level of pnlp-29::GFP expression, tunicamycin induced phsp-4::GFP.

We also tested whether direct activation of effector genes in the epidermis would trigger a UPR. PMA activates the PKCδ TPA-1 that controls multiple AMP genes, including nlp-29. It provokes very high levels of AMP gene expression within 4 h (unpublished results). Treating worms with PMA for 5 h did not lead to splicing of xbp-1 nor to induction of hsp-4 or the phsp-4::GFP transgene reporter (Fig. 1A, data not shown). The expression of many epidermal genes, including some AMPs, is strongly upregulated by osmotic stress., Although exposure to high salt did induce a pnlp-29::GFP transgene reporter as expected, it did not cause a measurable increase in phsp-4::GFP expression (Fig. 1B). Thus, neither fungal infection nor the strong induction of gene expression by PMA or salt provokes a UPR, and conversely a UPR does not trigger the expression of anti-fungal immune effectors in adult C. elegans.

hsp-3 regulates nlp-29 AMP gene expression

While the results described above suggested that the UPR did not play a direct role in the antifungal innate immune response, the representation of a number of ER-resident proteins is modulated by infection. This led us to assay directly the role of the corresponding genes in the regulation of nlp-29 by RNAi. While several of the tested genes had an effect (results not shown), hsp-3 stood out for its strong effect, essentially totally blocking the induction of pnlp-29::GFP normally observed upon infection in adult worms (Fig. 2A). A similar abrogation of reporter gene expression was seen in an atf-6 mutant, but not in a pek-1 mutant background ().

Figure 2. A specific role for hsp-3 in the regulation of nlp-29. (A) Quantification of the effect of control (K04G11.3), GFP, hsp-3 and sta-2 RNAi on pnlp-29::GFP expression in a wild-type or daf-16(mu86) mutant background. For reasons given elsewhere, in this and the subsequent graphs, error bars are not shown. Data are representative of three independent experiments. (B) Quantification of pnlp-29::GFP expression in hsp-3(ok1083) and hsp-4(gk514) mutant backgrounds following different treatments. In all cases, quantification was with the COPAS Biosort. The normalized average ratio of green to red fluorescence is shown. The analysis was restricted to worms with a TOF above 450. The number of worms analyzed here and in subsequent figures is given in the .

The mRNA sequence of the second BiP/GRP78 gene in C. elegans, hsp-4, is highly similar to that of hsp-3 (1472/1873 nucleotides identical, including several contiguous stretches of more than 21 nucleotides) and would thus be predicted to be targeted by the hsp-3 RNAi construct. At the same time, there is a reciprocal control of hsp-3 and hsp-4, such that a decrease in hsp-3 expression normally leads to an increase in the level of hsp-4, and vice versa. As RNAi with hsp-4 did block pnlp-29::GFP induction upon infection in adult worms (data not shown), we sought to discriminate between the two genes using available null mutants. We observed a strong reduction in pnlp-29::GFP expression only in an hsp-3 mutant, not in an hsp-4 mutant background (Fig. 2B). Attempts to establish a hsp-3;hsp-4 strain were confounded by the fact that homozygous double mutants were sterile. When we inactivated hsp-3 by RNAi in the hsp-4 mutant background, the adult worms were sterile, and the induction of pnlp-29::GFP expression upon infection was blocked (data not shown).

In C. elegans, fertility and pathogen resistance are interlinked, via the FOXO transcription factor DAF-16,, which also plays a role in the UPR. We therefore assayed the effect of hsp-3 RNAi on pnlp-29::GFP expression in a daf-16 mutant background. Loss of daf-16 had no effect on the abrogation of pnlp-29::GFP expression provoked by hsp-3 RNAi, or by RNAi with the STAT-like transcription factor sta-2, previously characterized for its role in nlp-29 expression (Fig. 2A), indicating that the effect of hsp-3, and of sta-2, is independent of daf-16.

We then determined the specificity of the effect of hsp-3 on reporter gene expression. In clear contrast to the near-complete block of pnlp-29::GFP expression after infection, in an hsp-3 mutant the induction of the reporter gene was at least as strong as in the wild-type background when triggered by PMA, salt or wounding. In the hsp-4 mutant, however, no effect was seen under any of the experimental conditions (Fig. 2B). These results underline the specific role hsp-3 plays in regulating pnlp-29::GFP only after infection, and place hsp-3 genetically upstream of, or parallel to, the PKCδ TPA-1.

hsp-3 acts downstream of nipi-3 to regulate nlp-29 AMP gene expression

The only previously known component of the innate immune signaling pathways that regulates nlp-29 expression specifically upon infection is the Tribbles-like kinase nipi-3. Overexpression of nipi-3 leads to an induction of pnlp-29::GFP. This induction was blocked in the hsp-3 mutant background, placing hsp-3 genetically downstream of nipi-3 (Fig. 3A). Consistent with this result, hsp-3 did not block the increased expression of pnlp-29::GFP provoked by an activated form of GPA-12 that triggers TPA-1 independently of NIPI-3 (Fig. 3B). Together these results indicate that hsp-3 acts between nipi-3 and tpa-1 to control the expression of nlp-29 upon fungal infection (Fig. 4).

Figure 3.hsp-3 acts genetically downstream of nipi-3 but not of gpa-12. (A) pnlp-29::GFP reporter expression was quantified in wt and hsp-3(ok1083) mutant worms with (black bars) or without (blue bars) copies of a transgene containing nipi-3 under the control of its own promoter. (B) Quantification of pnlp-29::GFP reporter expression in wt, tpa-1(k530), nipi-3(fr4) and hsp-3(ok1083) mutant worms with (green bars) or without (blue bars) copies of a transgene containing a gain-of-function (*) allele of gpa-12 under the control of the epidermis-specific col-19 promoter. Both pnipi-3::NIPI-3 and pcol-19::GPA-12* transgenes provoke a robust nlp-29 upregulation in the absence of infection in adult worms. Quantification was with the COPAS Biosort. The normalized average ratio of green fluorescence to time of flight (TOF) is shown. The analysis was restricted to worms with a TOF between 450 and 650.

Figure 4. Model of the control of nlp-29 expression. Signals perceived upon D. coniospora infection and injury are transduced by a PKCδ - p38 MAPK pathway to regulate the expression of nlp-29. HSP-3 functions between NIPI-3 and the PKCδ TPA-1. Many other known regulatory elements, including the OSM-11/WNK-1/GCK-3 pathway and the recently described pseudokinase NIPI-4 have been omitted for the sake of clarity.

Discussion

Much of our previous characterization of the innate immune response of C. elegans to D. coniospora has been focused on the host transcriptional changes that accompany infection. In Drosophila, the expression of many components of immune signaling pathways are themselves highly regulated upon infection., In contrast, none of 18 genes known to influence nlp-29 expression, including the p38 MAPK cascade components nsy-1, sek-1 and pmk-1, show a marked change in their expression level after infection. In a previous DIGE-based pilot study, we identified RACK-1 as a factor involved in the regulation of anti-fungal defenses. In an attempt to identify additional candidates, we extended the approach and undertook a comprehensive proteomic study of the changes that accompany fungal infection.

A number of other comparative gel-based proteomic studies have been performed using C. elegans, including two looking at protein changes upon bacterial infection of the intestine., It is striking that certain proteins, such as ACT-4, SODH-1, VHA-13 and PDI-2, appear in almost every published list. This may reflect an intrinsic bias in the approach, since the measured expression level for the genes corresponding to the proteins that we identified as differentially represented was very significantly higher than that of genes in general, (71.7% > 5 dcpm vs. 6.6% for all transcripts; p < 0.001 binomial test). It may also result from the fact that all these analyses used whole-animal extracts, potentially masking tissue-specific biologically relevant variations in protein abundance, and underlines the interest for developing efficient and simple methods to allow protein extraction from a specific C. elegans tissue.

If a particular spot on a gel increases or decreases in intensity, one cannot always infer that the total level of the corresponding protein was changed. For example, post-translational modifications may render a protein more difficult to extract, so that spot intensity does not reflect protein abundance. Similarly, post-translational modifications may also lead to an alteration of the sub-cellular localization of a protein, which may cause a protein to be found in different extraction fractions, and thereby affect spot intensity. As many proteins give rise to multiple spots, generally because of post-translational modifications, only if all the spots for a given protein were identified and quantified from each fraction would one be able to quantitate protein abundance. The development of alternative methods, such as metabolic labeling coupled to mass spectrometry holds considerable promise for profiling changes during pathogenic challenge in C. elegans. In the meantime, caution needs to be exercised when analyzing gel-based proteomic results. For this reason, until we have further functional evidence for a role in innate immunity for the various candidate proteins we identified, any discussion of a putative role would be premature.

The exception is HSP-3, which clearly has a specific function in regulating AMP gene expression. The hsp-3 gene is expressed at a high-level and is unchanged by infection, so the total level of HSP-3 may not change upon infection. We have not established the change in HSP-3 (e.g., degradation, phosphorylation, etc.) that leads to a change in intensity of the corresponding spot. It is noteworthy that in an atf-6 mutant background there is a marked reduction of pnlp-29::GFP expression after infection. This may reflect a role for ATF-6 in regulating HSP-3 levels.

During development, hsp-3 has an unambiguous role in the UPR., The data presented here indicate that the immune function of hsp-3 is independent of its function in the UPR. There is, however, evidence for a link between the UPR and AMP gene regulation in larvae. As mentioned above, a number of genes, including cnc-4, fipr-26, nlp-28 and nlp-29 are induced in L2 larvae after treatment with tunicamycin, apparently independently of xbp-1. But although tunicamycin does provoke upregulation of pnlp-29::GFP in larvae, D. coniospora infection does not induce phsp-4::GFP expression either in larvae or adults. Further, this UPR-induced expression of pnlp-29::GFP is independent of the p38 MAPK pathway, as it is observed in pmk-1 mutant background, as well as in a tpa-1 and nipi-3 mutant backgrounds (data not shown), and overall, there is only a minimal overlap between the genes upregulated by tunicamycin and D. coniospora infection., So the relationship between anti-fungal innate immunity and the UPR is not straightforward.

It is interesting, nonetheless, to speculate on how HSP-3 might exert its influence on AMP expression. There are several plausible models that are based on the idea that although genetically hsp-3 is positioned between nipi-3 and tpa-1, it seems unlikely that it plays a direct role in signal transduction. HSP-3 might be needed to ensure the correct intracellular localization of NIPI-3, itself, or of a protein that acts downstream of NIPI-3 and upstream of TPA-1. It may therefore be worthwhile to look at NIPI-3 localization in wild-type and hsp-3 mutant worms. The presence of two almost identical BiP/GRP78 proteins in the nematode is intriguing, as mammals, for example, only have one. It is conceivable that HSP-3 has a UPR-independent function outside the ER. Interestingly, one of the areas of sequence divergence between the two proteins is at the C-terminus; where HSP-3 has the ER retention signal KDEL sequence, HSP-4 has HDEL.

There are many examples of heat shock proteins playing a more or less direct role in innate immune responses. For example, they can function as endogenous danger signals to indicate cell stress and tissue damage to the immune system. As another example, the conserved SGT1/HSP90 complex binds NLR proteins, and modulates innate immune signaling in plants and animals, although it should be noted that there are no obvious NLR proteins in C. elegans. A study of the intracellular localization of HSP-3, and of the consequences of artificially expressing it in the cytoplasm could be merited. It is interesting to note that in an hsp-3 mutant there is some residual induction of the nlp-29 reporter gene, but this is fully abolished if the mutants are subject to RNAi against hsp-4 (C.C., unpublished observations). On the other hand, we have shown that loss of hsp-4 function alone has no effect on nlp-29 reporter gene expression. This suggests that hsp-4 can partially compensate for the absence of hsp-3.

It has been shown that during C. elegans development, the activation of a p38 MAPK pathway that follows intestinal infection with the P. aeruginosa strain PA14 causes a UPR. This is believed to be a consequence of the increased expression of innate immune effectors that overload the protein folding machinery in the ER. The results we have presented here show that infection of adult C. elegans by D. coniospora and the resultant induction of a large number of defense proteins in the epidermis does not provoke a UPR. This might reflect a relatively low constitutive activity of the secretory pathway in the epidermis, and therefore a buffering capacity in adult animals to cope with the consequences of infection. It will be interesting to dissect further the complex interplay between developmental, physiological (e.g., production of digestive enzymes in the intestine) and induced processes that put stress on the ER, both in C. elegans and other organisms. Additional study is also required to understand fully the UPR-independent role of BiP/GRP78 in innate immunity in C. elegans and to determine whether it might play any such role in other organisms.

Materials and Methods

Strains and culture condition

Worms were grown and maintained on nematode growth medium (NGM) and cultured with the E. coli strain OP50, as described. The hsp-3(ok1083), hsp-4(gk514), daf-16(mu86), tpa-1(k530), atf-6(ok551), pek-1(ok275) mutants were obtained from the Caenorhabditis Genetics Center (CGC). The strain SJ17 (xbp-1(zs12) III; zsIs4[phsp-4::GFP] V) was the kind gift of Dr Eric Chevet.

Reporter gene constructs and transgenic lines

IG274 (wt; frIs7[pnlp-29::GFP, pcol-12::DsRed] IV) is described elsewhere. IG981 [hsp-3(ok1083) X; frIs7 IV], IG982 [hsp-4(gk514) II; frIs7 IV] and IG1161 [daf-16(mu86) I; frIs7 IV], IG983 [atf-6(ok551) II; frIs7 IV], IG1424 [pek-1(ok275) II; frIs7 IV], were obtained by crossing the mutants hsp-3(ok1083), hsp-4(gk514), daf-16(mu86), atf-6(ok551) and pek-1(ok275) with IG274. The strain IG1320 (wt; zsIs4[phsp-4::GFP] V) was obtained by backcrossing the strain SJ17 with N2. The strain IG1363 (wt; frEx486[(pcol-19::GPA-12*), pNP21(pBunc-53::GFP)]) was the kind gift of Dr Nathalie Pujol. The strains IG1361 [tpa-1(k530) frIs7 IV; frEx486], IG1364 [hsp-3(ok1083) X; frIs7 IV; frEx486] and IG1365 [nipi-3(fr4) X; frIs7 IV; frEx486] were obtained by crossing respectively tpa-1(k530), hsp-3(ok1083) and nipi-3(fr4) with IG1363.

Splicing of xbp-1

N2 worms were grown and maintained on NGM plates with OP50. When they reached the young adult stage, worms were infected with D. coniospora by transferring them to NGM/OP50 plates previously spread with a dense suspension of spores. These had been freshly harvested in M9 buffer. Otherwise uninfected young adult worms were tranferred onto NGM/OP50 plates containing 10 µg/mL or 20 µg/mL tunicamycin (Sigma) or 1 µg/mL PMA (Sigma). After 5 h worms were harvested and RNA extracted with Trizol as described. Reverse transcription used High-Capacity cDNA Reverse Transcription Kit (Applied Biosystems) and PCR analyses were performed as described. Samples were normalized by Q-PCR as described with eft-217 as an internal control.

RNAi

All RNAi feeding experiments were performed essentially as described, using clones from the Ahringer library. All RNAi clones were sequence verified before use. The experiments were performed with worms cultured on OP50 until the L2 stage.

Infection, wounding, osmotic stress, PMA stress

Infection, and wounding were performed as described. For exposure to osmotic stress, PMA and tunicamycin, compounds were added to NGM plates to a final concentration of 300 mM for NaCl, 1 µg/mL for PMA and 10 or 20 µg/mL for tunicamycin. Worms were grown and maintained on NGM plates with OP50. When they reached the young adult stage, worms were transferred onto the appropriate modified NGM/OP50 plates. Similar conditions were used to assay the induction of GFP expression in the strains IG274 and IG1320 (shown in Fig. 1B), except images were taken after only 5 h.

Biosorter

The quantification of fluorescent reporter gene (GFP) expression was performed with the COPAS Biosort (Union Biometrica), essentially as described. Generally, animals were analyzed for length (time of flight), optical density (extinction), green fluorescence, and red fluorescence (if appropriate).

Protein extraction

A synchronized population of L4 IG274 worms was infected with D. coniospora. After 5 h, when there was a clear induction of GFP, indicative of the innate immune response to a productive infection, worms were harvested by washing plates with M9 buffer. Worms were pelleted by decantation, washed twice in the M9 buffer, then twice with PBS buffer. Proteins were extracted from a pellet of 500 µL of worms either by sonication in 8 M urea, 2 M thiourea, 4% (w/v) CHAPS, pH 8.5, containing a phosphatase inhibitor cocktail (Roche), or using the 2D fractionation kit (Amersham) according to the manufacturer’s instructions.

Protein fractionation, labeling, gel electrophoresis and identification

Full experimental details are publically available at http://miapegeldb.expasy.org/experiment/118. The comprehensive set of analytical data from this study is available at the World-2DPAGE database http://world-2dpage.expasy.org/repository/0042.