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Identification of loci controlling restriction of parasite growth in experimental Taenia crassiceps cysticercosis.
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PMID:  22206032     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Human neurocysticercosis (NC) caused by Taenia solium is a parasitic disease of the central nervous system that is endemic in many developing countries. In this study, a genetic approach using the murine intraperitoneal cysticercosis caused by the related cestode Taenia crassiceps was employed to identify host factors that regulate the establishment and proliferation of the parasite. A/J mice are permissive to T. crassiceps infection while C57BL/6J mice (B6) are comparatively restrictive, with a 10-fold difference in numbers of peritoneal cysticerci recovered 30 days after infection. The genetic basis of this inter-strain difference was explored using 34 AcB/BcA recombinant congenic strains derived from A/J and B6 progenitors, that were phenotyped for T. crassiceps replication. In agreement with their genetic background, most AcB strains (A/J-derived) were found to be permissive to infection while most BcA strains (B6-derived) were restrictive with the exception of a few discordant strains, together suggesting a possible simple genetic control. Initial haplotype association mapping using >1200 informative SNPs pointed to linkages on chromosomes 2 (proximal) and 6 as controlling parasite replication in the AcB/BcA panel. Additional linkage analysis by genome scan in informative [AcB55xDBA/2]F1 and F2 mice (derived from the discordant AcB55 strain), confirmed the effect of chromosome 2 on parasite replication, and further delineated a major locus (LOD = 4.76, p<0.01; peak marker D2Mit295, 29.7 Mb) that we designate Tccr1 (T. crassiceps cysticercosis restrictive locus 1). Resistance alleles at Tccr1 are derived from AcB55 and are inherited in a dominant fashion. Scrutiny of the minimal genetic interval reveals overlap of Tccr1 with other host resistance loci mapped to this region, most notably the defective Hc/C5 allele which segregates both in the AcB/BcA set and in the AcB55xDBA/2 cross. These results strongly suggest that the complement component 5 (C5) plays a critical role in early protective inflammatory response to infection with T. crassiceps.
Authors:
Ruben Ramirez-Aquino; Irena Radovanovic; Anny Fortin; Edda Sciutto-Conde; Gladis Fragoso-González; Philippe Gros; Irma Aguilar-Delfin
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2011-12-20
Journal Detail:
Title:  PLoS neglected tropical diseases     Volume:  5     ISSN:  1935-2735     ISO Abbreviation:  PLoS Negl Trop Dis     Publication Date:  2011 Dec 
Date Detail:
Created Date:  2011-12-29     Completed Date:  2012-04-19     Revised Date:  2013-06-26    
Medline Journal Info:
Nlm Unique ID:  101291488     Medline TA:  PLoS Negl Trop Dis     Country:  United States    
Other Details:
Languages:  eng     Pagination:  e1435     Citation Subset:  IM    
Affiliation:
Departament of Immunology, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México, México.
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MeSH Terms
Descriptor/Qualifier:
Animals
Complement C5 / genetics*,  immunology*
Crosses, Genetic
Cysticercosis / genetics*,  immunology*
Disease Models, Animal
Female
Genetic Association Studies
Haplotypes
Mice
Mice, Inbred A
Mice, Inbred C57BL
Polymorphism, Single Nucleotide
Taenia / immunology*
Chemical
Reg. No./Substance:
0/Complement C5
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Journal ID (nlm-ta): PLoS Negl Trop Dis
Journal ID (publisher-id): plos
Journal ID (pmc): plosntds
ISSN: 1935-2727
ISSN: 1935-2735
Publisher: Public Library of Science, San Francisco, USA
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Ramirez-Aquino et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Received Day: 30 Month: 8 Year: 2011
Accepted Day: 2 Month: 11 Year: 2011
collection publication date: Month: 12 Year: 2011
Electronic publication date: Day: 20 Month: 12 Year: 2011
Volume: 5 Issue: 12
E-location ID: e1435
ID: 3243719
PubMed Id: 22206032
Publisher Id: PNTD-D-11-00873
DOI: 10.1371/journal.pntd.0001435

Identification of Loci Controlling Restriction of Parasite Growth in Experimental Taenia crassiceps Cysticercosis Alternate Title:Tccr1 Restricts Taenia crassiceps Replication
Ruben Ramirez-Aquino1
Irena Radovanovic2
Anny Fortin2
Edda Sciutto-Conde1
Gladis Fragoso-González1
Philippe Gros2*
Irma Aguilar-Delfin3
Wendy Elizabeth Harrisonedit1 Role: Editor
1Departament of Immunology, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México, México
2Department of Biochemistry, McGill University, Montreal, Canada
3Laboratory of Immunogenomics and Metabolic Diseases, Instituto Nacional de Medicina Genómica (INMEGEN), Ciudad de México, México
Imperial College, United Kingdom
Correspondence: * E-mail: philippe.gros@mcgill.ca
Contributed by footnote: Conceived and designed the experiments: RRA IR AF ESC GFG PG IAD. Performed the experiments: RRA IR IAD. Analyzed the data: RRA IR AF IAD. Contributed reagents/materials/analysis tools: ESC GFG PG IAD. Wrote the paper: IR RRA PG AF GF ESC IAD.
[other] ¶ These authors also contributed equally to this work.

Introduction

Taenia solium seriously affects human health in many countries of Latin America, Asia and Africa [1]. The life cycle of T. solium includes a larval phase (cysticercus), which develops in both pigs and humans from ingested eggs contaminating the environment. When humans ingest improperly cooked pork meat infected with live cysticerci, the cysticerci develop to the stage of an adult intestinal tapeworm, which produces millions of eggs that are then shed to the environment in human faeces [2]. In rural communities where the disease is endemic, unsanitary conditions and presence of free-roaming pigs result in up to 9% of the human open population of these areas to be infected. Despite this high infection rate, only a small fraction of carriers become symptomatic and develop NC, suggesting intrinsic differences in host susceptibility to infection and pathogenesis of the disease [3]. Indeed, several reports have pointed at possible genetic effects in response to cysticercosis in human and pigs. In humans, multi-case families were identified in areas of highly endemic disease, favoring the idea of the participation of multiple genes in NC causality [3]. In a case-control study, resistance to NC was found associated to HLA [4]. Also, a three to five fold difference in parasite load was detected in a genetically heterogeneous pig cohort experimentally challenged with T. solium eggs [5].

Taenia crassiceps is a tapeworm of wild and domestic animals, which does not cause clinical disease in non-immunocompromised humans [6]. T. crassiceps has been used as an experimental model for cysticercosis due to its ability to proliferate by budding [7] and colonize the peritoneal cavity of the murine host [7], where its replication can be measured over time by enumeration of recovered metacestodes. Although the T. crassiceps ORF strain is unable to develop into adult tapeworms [8], its property to rapidly multiply in the peritoneal cavity of infected mice has been extensively used to explore the relevance of biological factors in host-parasite interactions [9], and to identify protective antigens of interest for vaccine development [9], [10]. The mechanisms involved in the protective immunity against T. crassiceps cysticercosis have been extensively studied, but are not fully understood. Studies in inbred mouse strains (growth permissive H2d-bearing BALB/c; growth restrictive H2b-bearing C57BL/6J) initially pointed at the importance of the major histocompatibility locus (MHC) and MHC-linked genes in regulating intraperitoneal growth of the parasite [11]. This was confirmed by additional studies of H2 congenic BALB/c substrains, where BALB/cJ mice express the Qa2 protein and are significantly more resistant than the BALB/cAnN mice [12], [13]. This differential susceptibility may be explained in part by activation of antigen presenting cells, and production of pro-inflammatory cytokine and modulatory chemokines both early and late during T. crassiceps infection [14]. Furthermore, phenotyping of different inbred strains has suggested that an additional, non-MHC linked genetic component may contribute to regulation of T. crassiceps replication [15]. Finally, clear differences between the parasite load of male and female have been noted in inbred mouse strains [16]. Females show higher numbers of cysticerci compared to males due to a significant effect of sex hormones on response to infection [17], [18].

With the aim of further characterizing the host genetic factors that affect host response to T. crassiceps cysticercosis, the differential susceptibility of A/J (permissive) and C57BL/6J (restrictive) mouse strains was studied. For this, a set of 34 reciprocal AcB/BcA recombinant congenic strains (RCS) derived by systematic inbreeding from a double backcross (N3) between A/J and C57BL/6J parents [19] was phenotyped for response to T. crassiceps infection. In the breeding scheme used to derive the AcB/BcA strains set, each of the strains harbors 12.5% of its genome from either A/J or B6, fixed as a set of discrete congenic segments onto 87.5% of the reciprocal parental background. The vast range of permissiveness to T. crassiceps growth in 34 RCS, as measured by the parasite load 30 days post-infection, along with haplotype association mapping suggested that response to T. crassiceps cestode is under complex genetic control, with identifiable contributions of chromosomes 2 and 6. Subsequent genetic linkage analysis in informative crosses validated the chromosome 2 locus, and established the regional position of the regulating locus.


Materials and Methods
Mice

The AcB/BcA set of recombinant congenic strains (RCS) were derived from a double backcross (N3) between A/J and C57BL/6J parents at McGill University and were provided by Emerillon Therapeutics. The breeding, genetic characteristics and genotype of RCS have been described earlier [19]. Inbred strains A/J, B6, and DBA/2 were obtained as pathogen-free mice at 7–8 weeks of age from the Jackson Laboratory (Bar Harbor, ME) and maintained as breeding colonies at UNAM. [AcB55xDBA/2] F2 progeny were bred by systematic brother-sister mating of [AcB55xDBA/2] F1 mice.

Ethics statement

The study protocol (register number 021) was approved by the ethics committee of the Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México (UNAM). All housing and experimental procedures were performed according to the principles set forth in the Guide for the Care and Use of Laboratory Animals, Institute of Laboratory Animal Resources, National Council, Washington, D.C. 1996.

Infection with Taenia crassiceps

The fast growing ORF strain of T. crassiceps, originally isolated by R. S. Freeman [7], was maintained by serial intraperitoneal (i. p.) passage in female BALB/cAnN mice, as previously described [13]. All experimental mice were inoculated intraperitoneally with 10 small (<2 mm) non-budding T. crassiceps larvae, re-suspended in sterile isotonic saline. Thirty days following infection, parasites were harvested from the peritoneal cavity and counted using a stereoscopic microscope [20] to determine the parasite burden. Organs inside the abdominal cavity were removed and carefully inspected for any remaining T. crassiceps larvae.

Genotyping

Genomic DNA was isolated from tail clips of individual F2 mice collected at the time of sacrifice, as previously described [19]. A total of 185 female [AcB55xDBA/2]F2 mice were genotyped at the Centre for Applied Genomics (The Hospital for Sick Children, Toronto, Canada) using the Illumina Mouse Low Density Linkage panel containing 377 SNPs distributed across the genome, out of which 161 were polymorphic between AcB55 and DBA/2 strains. Additional microsatellite markers were obtained from the Mouse Genome Informatics Database (www.informatics.jax.org) and used for gap filling and fine mapping by a standard PCR-based method employing (α-32P) dATP labeling and separation on denaturing 6% polyacrylamide gels.

C5 status in the F2 mice was confirmed by RFLP analysis, as previously described [21]. Briefly, C5 fragment was amplified by PCR and digested with Bsg I, which recognizes a novel restriction site introduced by the 2-bp deletion in exon 6 of the Hc gene [21], [22]. The fragments were resolved on 2% agarose gel; the expected size for wild-type C5 was 446 bp, while the sizes for the samples containing the deletion were 318 and 126 bp.

Linkage and association mapping

QTL mapping was performed using Haley-Knott multiple regression analysis [23] and the two-dimensional scan was performed using the two-QTL model. Empirical genome-wide significance was calculated by permutation testing (1000 tests). All linkage analysis was performed using R/qtl [24]. The detailed algorithm underlying the efficient mixed-model for association mapping has been previously published [25]. The EMMA algorithm is based on the mixed-model association where a kinship matrix accounting for genetic relatedness between inbred mouse strains is estimated and then fitted to the vector of the phenotype, thereby reducing false positive rates. EMMA is publically available as an R package implementation.

Statistical analysis

An unpaired, two-tailed Student's t-test was used to establish significance of differences in mean parasite burden between mouse Tccr1 and C5 genotypes. These data were analyzed using GraphPad Prism 4.0 statistical software. P-values<0.05 were considered significant.


Results
Response to T. crassiceps infection in recombinant congenic strains

A/J and C57BL/6J (B6) mice show differential permissiveness to cysticercosis [16], following the intra-peritoneal inoculation of 10 small (<2 mm diameter) non-budding T. crassiceps larvae (Figure 1). In A/J mice, there is rapid parasite reproduction in the peritoneal cavity, which is detectable by visual and histological examination of the mice (Figure 1A, 1B), and by quantification of parasite load (Figure 1C, magnification in 1D). Enumeration of the parasites recovered 30 days following infection (Figure 2) indicates a 10-fold difference in parasite replication between A/J (200–250) and C57BL/6J (15–30). To study the genetic control of differential replication of T. crassiceps in restrictive B6 and permissive A/J strains, we phenotyped a set of 34 AcB/BcA recombinant congenic strains [19]. The breeding scheme used to generate the reciprocal AcB/BcA strains set results in individual strains harboring 12.5% of its genome donated from either A/J (in BcA strains) or B6 (in AcB strains), fixed as a set of discrete congenic segments onto 87.5% of the reciprocal parental background [19]. The AcB/BcA strain set has previously been used to characterize different genetic traits that control phenotypic differences between B6 versus A/J, including mapping of major monogenic trait [19], and dissection of complex genetic traits into several simple genetic effects [26], [27]. Between 5–10 animals from each strain were infected with T. crassiceps and the total parasite burden was determined 30 days later (Figure 2A and 2B). We segregated AcB/BcA strains according to the predominant genetic background (left and right panels in Figure 2), and further grouped them into permissive or restrictive categories based on the overall mean parasitic load, whereby strains harboring an average of >66 parasites were deemed permissive while those showing <66 were termed restrictive (determined as two standard deviations from the parasite load of restrictive B6 parental group). According to this arbitrary segregation, the majority of BcA strains were parasite growth restrictive, with the notable exception of strains BcA73, 70, 72 and 83 that showed parasite loads similar to those detected in the A/J controls (Figure 2B). Conversely, AcB strains were found to be generally permissive for parasite growth, with the notable exception of strains AcB55 and AcB60 that displayed an average of 12 and 31 cysticerci, respectively. The presence of such discordant strains in both sets of RCS suggests the possibility that the restrictiveness/permissiveness trait is under simple genetic control, and that transfer of a single congenic fragments onto the opposite strain background strongly influences the phenotype of the recipient strain. Such a situation would be similar to the segregation of the Ccs3 (colorectal cancer) [28], Ity (susceptibility to Salmonella) [29] and Lgn1 loci (susceptibility to Legionella) [19] we previously reported in these strains.

Chromosomes 2 and 6 are associated with response to T. crassiceps infection in AcB/BcA strains

To explore the nature and complexity of the genetic control of parasite replication in the AcB/BcA strains set, we performed haplotype association mapping using parasite load as the primary phenotype and 1200 informative polymorphic genetic markers. We applied a statistical model EMMA [25] that corrects for genetic relatedness and population structure of the RCS by computing a kinship matrix in a manner analogous to an inbred mouse strain analysis, as we previously described [30]. Using this approach, we detected suggestive association of chromosome 2 (proximal region) and chromosome 6 alleles with T. crassiceps permissiveness (Figure 3). In the case of chromosome 6, both proximal (weaker) and distal (stronger) portions of the chromosome showed association. Also, for both chromosomes 2 and 6, A/J alleles are associated with permissiveness while B6 alleles are associated with restrictiveness, as expected. Additional strength for these associations is provided by some of the phenodeviant strains; for example, for the proximal part of chromosome 2 (∼35 Mb), susceptible BcA70, 72, and 73 harbor A/J haplotypes, while resistant AcB55 and AcB60 harbor B6-derived haplotypes (Figure S1). Likewise, for distal chromosome 6, BcA72, 73 and 83 have A/J alleles, while AcB55 and 60 have B6 alleles (Figure S1). Nevertheless, the imperfect correlation for both chromosomes requires validation in secondary crosses. It also suggests presence of additional genetic effects controlling T. crassiceps permissiveness in the strain set.

Linkage analysis in [AcB55xDBA/2]F2 cross validates association of chromosome 2 locus with response to T. crassiceps

The genetic control of host response to T. crassiceps was further investigated in strain AcB55. This strain consistently showed the lowest parasite burden in the AcB set (Figure 2, mean parasite load = 11.7), despite ∼87.5% of its background being inherited from the highly susceptible A/J parent (mean parasite load = 256). Therefore, we hypothesized that AcB55 is likely to carry B6-derived chromosomal segments responsible for restrictiveness in both AcB55 and B6. To map such segments, AcB55 was crossed to the permissive strain DBA/2 (Figure 4A, mean parasite load = 108) to produce an [AcB55xDBA/2] F2 population in which individual animals would be informative for the entire genome in linkage analyses. [AcB55xDBA/2] F1 hybrids and 379 [AcB55xDBA/2] F2 animals were infected intraperitoneally with 10 non-budding T. crassiceps larvae in three separate infections, and parasite burden was measured 30 days later (Figure 4A). Due to the previously reported gender-associated differential permissiveness to T. crassiceps, where higher concentrations of estrogen and estradiol are concomitant with increased parasite burdens [17], [18] typically occurring in female mice, we segregated males and females in the analysis (Figure 4A). Both male and female [AcB55xDBA/2] F1 hybrids were fully resistant with parasite load similar to the AcB55 controls (Figure 4A), suggesting that resistance to T. crassiceps is inherited in a dominant fashion. The parasite load of [AcB55xDBA/2] F2 mice followed a continuous distribution between highly permissive and highly restrictive animals, with a clustering of F2 animals in the resistant range. This suggests both a complex genetic control of permissiveness to infection, with a dominant pattern of inheritance of restrictiveness more apparent in the female population (Figure 4A). Interestingly, we observed an identical pattern of inheritance of restrictiveness (dominant) in a distinct F2 population, where the AcB55 strain was crossed to the permissive A/J founder (Figure S2). However, due to limited genetic diversity in the [AcB55xA/J] F2 progeny (∼12.5% due to B6 genomic segments), we conducted genetic linkage analysis by whole genome scanning in the [AcB55xDBA/2] F2 population. Because the frequency distribution of parasite load in F2 females was skewed, we applied a log2 correction to normalize the distribution, followed by regression to an experiment-specific mean (set at 0) (Figure 4B).

A total of 185 [AcB55xDBA/2] F2 female mice were genotyped with the Illumina Mouse Low Density Linkage Panel consisting of 161 informative polymorphic markers with 10 additional microsatellite markers to complete genome coverage. Whole-genome multiple regression linkage analysis in R/qtl (Figure 4C) identified a highly significant locus associated with parasite burden on chromosome 2 (LOD = 4.76, P<0.01) and an additional suggestive linkage on chromosome 19 (LOD = 4.03, P<0.05) (Figure 4C and S3). These loci contributing restrictiveness to T. crassiceps in the AcB55 strain were given a temporary appellation Tccr1 (Taenia crassiceps cysticercosis restrictiveness 1) for chromosome 2 QTL and Tccr2, for chromosome 19 QTL. The Bayesian 95% credible intervals were determined to be 13.1–44.1 Mb for Tccr1 (Figure 5A) and the entire chromosome 19 for Tccr2 (Figure S3), whereas the peak LOD scores were identified at 29.7 Mb (peak marker: D2Mit295) and 46.7 Mb (peak SNP: rs13483650), respectively.

To examine the effect of the most significant Tccr1 locus on parasite load, F2 mice were segregated according to genotype at the most significant chromosome 2 marker D2Mit295 (Figure 5B). Mice carrying the DBA/2 alleles at Tccr1 have significantly higher number of cysticerci (P = 0.0009; Student's t-test) than those harboring one or two AcB55 alleles. This indicates that restrictiveness alleles at Tccr1 are inherited in a strictly dominant fashion. We also examined the LOD score trace for chromosome 19 and the inheritance of parental alleles underlying Tccr2 at the peak marker (rs13483650) (Figure S3). We observed two prominent peaks, suggesting that Tccr2 may be due to multiple genetic effects contributing to lower parasite loads in the AcB55 strain. However, once we segregated the female F2 mice according to their genotype (Figure S3B), we observed that the Tccr2 QTL is driven by heterozygosity, with homozygosity for neither the AcB55- nor the DBA/2-derived alleles having a significant effect on the parasite burden. To determine whether Tccr1 and Tccr2 acted in an additive or epistatic manner, a two-dimensional Haley-Knott multiple regression analysis was carried out, followed by simulation of an overall QTL model using R/qtl. This analysis revealed that, although Tccr1 and Tccr2 are non-interacting loci, their individual and joint contribution to the full QTL model raises the LOD score to 11.26 and explains 25% of observed phenotypic variance.

Interestingly, linkage analysis in the AcB55xDBA/2 cross was successful in validating the chromosome 2 association initially detected by EMMA analysis in 34 RCS (Figure 3), but not the more significant chromosome 6 association. In fact, detailed examination of the region underlying chromosome 6 indicated that both AcB55 and DBA/2 strains harbor similar haplotype blocks at the proximal and distal regions of chromosome 6 (data not shown) and would therefore not segregate in the analyzed F2 cross. Together, haplotype association mapping in 34 RCS along with linkage analysis in an informative F2 cross strongly suggest that T. crassiceps replication in the murine host is controlled by multiple genetic factors, amongst which Tccr1 strongly contributes to the noted resistance of AcB55 mice.

Hemolytic complement (Hc/C5) underlies Tccr1

Maximum linkage for Tccr1 locus is coupled to the D2Mit295 marker, which lies at 29.7 Mb and was previously associated to the gene coding for hemolytic complement (Hc/C5) [21] located approximately 5 Mb further downstream (34.8–34.9 Mb). Since C5 was mapped in an F2 cross derived from A/J and B6 strains and its deficiency correlated to high susceptibility to the fungal pathogen Candida albicans in the majority of RCS [21], we examined the involvement of C5 in the context of T. crassiceps infection. We genotyped the parental AcB55 and DBA/2 strains for the deficiency-causing 2-bp deletion in the C5 gene and confirmed that DBA/2 is C5-deficient [22], while AcB55 is wild type for C5 and does not harbor the deletion [21]. C5 status was also determined in 185 female [AcB55xDBA/2] F2 mice and the parasite replication permissiveness was associated with C5-deficiency (Figure 5C) in a recessive manner, where mice harboring at least one functional copy of the gene are fully resistant. In addition, classifying the set of 34 RCS according to permissiveness to infection and C5 status further corroborates the association of wild-type C5 alleles with increased protection against T. crassiceps (Table 1).

Taken together our results suggest a critical role for the complement component 5 in restricting proliferation of T. crassiceps in mice.


Discussion

The panel of 34 reciprocal AcB/BcA RCS has been used to map major monogenic traits [19], [28] or to facilitate identification of multiple loci involved in complex trait diseases [26], [27]. This approach is based on the premise that unique small congenic fragments derived from the donor strain are fixed and delineated for each strain, which may allow for detection of causative haplotype by the sole study of the strain distribution pattern in relation to the phenotype of interest [19]. Here, we have phenotyped the set of 34 RCS to study the genetic control of susceptibility to T. crassiceps cysticercosis (Figure 2), where the majority of AcB strains were found to be permissive for parasite replication and conversely, most of the BcA strains were deemed restrictive, similarly to progenitor strains A/J and B6, respectively. The presence of phenodeviant strains allowed us to conduct haplotype association mapping and identify significant genomic regions associated with response to infection on chromosomes 2 and 6 (Figure 3). Subsequent genome scan in informative F2 mice generated between resistant AcB55 and susceptible DBA/2 progenitors (fixed for chromosome 6 locus) identified a highly significant linkage on chromosome 2 (Tccr1, LOD score = 4.76, P value<0.01) as conferring resistance to AcB55 in a dominant fashion along with an additional heterozygous-driven effect observed on chromosome 19 (Tccr2, LOD score = 4.03, P value = 0.05) (Figure 4 and Figure 5).

Interestingly, the Tccr1 locus was analogous to a previously identified susceptibility locus for the fungal pathogen Candida albicans attributable to the complement component 5 gene (Hc/C5) [21]. The complement pathway represents the initial line of defense of the innate immune system and elicits an inflammatory response to the site of infection [31], [32]. Activation of the complement cascade is triggered by microbial products via several pathways, which ultimately results in the activation of C3 convertase, cleavage of C5, release of chemotactic factors (C3a and C5a), and generation of the membrane attack complex (MAC) [31]. Similarly to T. crassiceps infection, inbred mouse strains display various degrees of susceptibility to C. albicans, where A/J is highly susceptible and B6 resistant [21]. This differential susceptibility was attributed to the major gene C5, where a single allele of the wild-type C5 confers complete resistance to infection [21]. As previously described [22], C5-deficiency is caused by a 2-bp deletion in the exon 6, leading to a premature stop codon and a product that is not secreted in the serum [33]. We have confirmed that AcB55 carries the B6 allele at C5 and is therefore C5-suficient and resistant to T. crassiceps, whereas DBA/2 is C5-deficient and susceptible. C5 status was also determined in 185 [AcB55xDBA/2]F2 progeny (Figure 5C), where resistance segregated with one or two copies of the wild-type C5 indicating that C5 exerts an early dominant protective effect upon T. crassiceps infection.

In the mouse model of T. crassiceps infection, although the extent of parasite replication depends on the orchestration of immune and hormonal responses, the parasite restriction is initiated by the early immunological response, which was shown to destroy the peritoneal larvae [34] and involve the complement system in innate resistance to T. taeniaeformis[35]. Earlier studies demonstrated that C3 along with IgG is deposited on larval T. taeniaeformis[35], [36] as early as 2 days post infection, but that it is not directly involved in lytic activity through formation of the MAC. Rather, the complement system indirectly triggers host cell recognition and/or activation [35], leading to parasite elimination. Inhibition of complement by cobra venom factor administration to the resistant BALB/cByJ mice prior to T. taeniaformis infection results in decreased parasite mortality, indicating that complement component deposition and activation is necessary in host defense against taenid infection [35]. More precisely, the role of complement component 5 (C5) was established in the mouse model of hyatid disease, caused by the Echinococcus granulosus cestode. C5-deficiency in B10.D2 o/SnJ mice infected with E. granulosus was associated with poor eosinophil infiltration and increased growth of established cysts [37], indicating that C5-mediated mechanisms are detrimental for parasite growth.

The immunopathology of T. crassiceps cysticercosis in mice is that of an initial non-permissive Th1 type, which shifts to a parasite permissive Th2 type during chronic stage of infection and is accompanied by an increase in IL-4, IL-6 and IL-10 cytokines [38][40]. This transition was also reported in individuals with T. solium neurocysticercosis [41] and more precisely, in the brain granulomas surrounding T. solium parasite [42]. Although A/J mice succumb to C. albicans infection early after infection (48 h), they mount a similar Th2-like cytokine storm consisting of high levels of IL-6, IL-10 and TNFα [43], [44], suggesting a common role for C5 in both pathologies. In addition, animals deficient for the Th1 hallmark cytokine IFNγ or upon its neutralization exhibit increased susceptibility to C. albicans[45] and T. crassiceps[39], respectively. Regarding the role of complement in parasite damage, it is known that cysticerci are able to inhibit both classical and alternative pathways of the complement cascade, through C1q inhibition by parasite's paramyosins [46], but the relevance of the complement component 5 (C5) in the restrictiveness to parasite growth remains to be elucidated, especially considering that C5 is cleaved in two different active forms: C5a, which is a potent anaphylatoxin and chemotactic protein, and C5b, which has a binding site for C6 and is the molecule responsible for promoting the MAC (membrane attack complex) assembling in cell membrane. To assess the importance of C5 and possible involvement of additional genetic effects in the A/J versus B6 differential susceptibility to T. crassiceps, we classified the RCS according to susceptibility and C5 status (Table 1). In the majority of RCS, C5 status was a strong predictor of response to T. crassiceps infection with C5 deficiency causing increased parasite replication permissiveness, even when present on the B6 background as seen in BcA73, BcA70, BcA72 and BcA83 strains. Conversely, the presence of wild-type alleles at C5 on an otherwise permissive A/J background, as seen in AcB55 strain, conferred restrictiveness to infection. We noted the presence of several discordant strains (Table 1, denoted by an asterisk), such as BcA76, AcB60 and AcB63. Although C5 explains 25% of phenotypic variance, discordant strains suggest that additional susceptibility and resistance genetic factors, distinct from the dominant C5 effect, modulate response to T. crassiceps infection. In fact, STAT4 and STAT6 transcription factors were recently involved in modulation of the immune response to T. crassiceps in mice. Permissiveness of BALB/c mice was abrogated in STAT6−/− mice of the same background, as they were able to efficiently mount a strong Th1 response and control the infection [47]. Conversely, Th1 response induced via STAT4-dependent signaling pathway is essential for development of immunity against cysticercosis [48]. Also, macrophage activation and subsequent production of nitric oxide represent additional mechanisms essential for host resistance to T. crassiceps infection [49]. Interestingly, we did not uncover any associations of the MHC with susceptibility in our AcB55xDBA/2 cross where DBA/2 mice carry parasite permissive H2-d [11]. This further suggests that the differential permissiveness observed in BALB/c susbstrains and attributed to H2-d haplotype is in fact, BALB-background specific. Similarly, the Tccr2 locus represents a novel effect that arose upon combination of the AcB55 and DBA/2 genetic backgrounds and further emphasizes the importance of genetic modifiers in T. crassiceps permissiveness. Finally, generation of additional informative crosses will be necessary to validate and study the effect contributed by the chromosome 6 underlying genetic effect(s) in T. crassiceps cysticercosis, independently of C5 or in conjunction.

In conclusion, we have combined haplotype association mapping in 34 recombinant congenic strains and linkage analysis to identify and validate a novel locus that modulates the outcome to T. crassiceps infection in mice. We have demonstrated that C5 underlies the Tccr1 locus and uncovered an important role of the complement pathway in susceptibility to T. crassiceps cysticercosis.


Supporting Information Figure S1

Haplotype maps underlying EMMA-identified chromosome 2 and chromosome 6 associations in RCS. Haplotype maps of permissive and restrictive RCS are depicted for the most significant associations on proximal chromosome 2 along with proximal and distal regions of chromosome 6, illustrating segregation of B6 allele (gray) with restrictiveness and A/J (white) allele with permissiveness to T. crassiceps.

(TIF)


Click here for additional data file (pntd.0001435.s001.png)

Figure S2

Parasite load in the [AcB55xA/J]F2 population. [AcB55xA/J]F2 mice (n = 427) were infected intraperitoneally with 10 non-budding T. crassiceps larvae and parasite number was determined 30 days post-infection. The results from three separate infections are plotted along with A/J, B6, DBA/2, and [AcB55xA/J]F1 controls.

(TIF)


Click here for additional data file (pntd.0001435.s002.png)

Figure S3

Effect of the Tccr2 locus on parasite burden in [AcB55xDBA/2]F2 mice. Detailed LOD score traces are shown for chromosome 19 (Tccr2) locus for [AcB55xDBA/2]F2 females (A). The genome-wide thresholds are indicated at P = 0.01 and P = 0.05. The heterozygous-driven permissiveness to T. crassiceps in F2 mice is illustrated for Tccr2 by segregating the parasite load according to the AcB55 (A), DBA/2 (D) or heterozygous (H) alleles at the rs13483650 peak SNP (B).

(TIF)


Click here for additional data file (pntd.0001435.s003.png)


Notes

The authors have declared that no competing interests exist.

This work was supported by a research grant from the Quebec-Mexico joint working group program of the Quebec Ministry of International Relations to P. Gros and G. Fragoso-González. P. Gros is supported by a James McGill Professorship at McGill University. R. Ramirez-Aquino was supported by a fellowship from CONACyT, México. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

The authors thank Sean Wiltshire and Silvia Vidal for helpful discussions.


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Figures

[Figure ID: pntd-0001435-g001]
doi: 10.1371/journal.pntd.0001435.g001.
Figure 1  Taenia crassiceps intraperitoneal murine cysticercosis.

Aspect of the distended abdomen of a cysticercotic permissive mouse 30 days after intraperitoneal T. crassiceps infection compared to a non-infected littermate (A). Hematoxilin and eosin staining was performed on a cross-sectional slice of the abdomen of a cysticercotic mouse (B). Abdominal organs can be distinguished (O = ovary, K = kidney, SI = small intestine, LI = large intestine, V = vertebral column space), whereas cysticerci (denoted by c) appear as thin dark septa limiting the empty spaces. (C) Aspect of cysticerci recovered from the peritoneal cavity of an infected permissive mouse 30 days post-infection, with and without attached buds (D). Photographs kindly provided by Dr. Carlos Larralde.



[Figure ID: pntd-0001435-g002]
doi: 10.1371/journal.pntd.0001435.g002.
Figure 2  Response of AcB/BcA strains to T. crassiceps infection.

Parasite load recovered from female A/J, C57BL/6J (B6) and 34 recombinant congenic AcB/BcA mice 30 days after infection. 4–10 mice per strain were intraperitoneally infected with 10 non-budding T. crassiceps larvae. The average number of parasites is shown (B) along with raw data (A) where each dot represents a single mouse. Bars represent strain mean ± SD. Horizontal line corresponds to two standard deviations from the mean parasite load of resistant B6 strain, which was used to stratify strains into susceptible (black bars), or resistant (white bars) categories.



[Figure ID: pntd-0001435-g003]
doi: 10.1371/journal.pntd.0001435.g003.
Figure 3  Genome-wide association mapping in 34 AcB/BcA strains using EMMA.

Using the R package implementation of EMMA, genome-wide association mapping was conducted across 34 RCS as well as the original parental A/J and B6 inbred strains. The genotyping data consisted of ∼1200 SNPs and informative dinucleotide repeats and was correlated with the parasite load, yielding −log10 transformed P values indicating genome-wide association significance for each SNP. Each line represents a single SNP or marker.



[Figure ID: pntd-0001435-g004]
doi: 10.1371/journal.pntd.0001435.g004.
Figure 4  Linkage analysis in the informative [AcB55xDBA/2]F2 population.

[AcB55xDBA/2]F2 mice (n = 379) were infected intraperitoneally with 10 non-budding T. crassiceps larvae and parasite number was determined 30 days post-infection. The results from three separate infections are plotted along with A/J, B6, DBA/2, and [AcB55xDBA/2]F1 controls (A). Each dot represents a single mouse. Distribution of parasite load is shown in the female [AcB55xDBA/2]F2 population (B), after regression of log2(parasite load) to an experiment-specific mean (set at 0). Mice were genotyped at 171 SNPs and dinucleotide repeats across the genome and interval mapping was carried out using the R/qtl software package. Whole genome LOD score trace is shown for genetic effects controlling parasite burden in female [AcB55xDBA/2]F2 mice (n = 185) (C), identifying linkage to chromosome 2 (LOD = 4.75) and chromosome 19 (LOD = 4.0), designated Tccr1 and Tccr2, respectively. Marker positions are indicated on the x-axis and genome-wide thresholds at P = 0.01 and 0.05 were identified by permutation testing (1000 tests).



[Figure ID: pntd-0001435-g005]
doi: 10.1371/journal.pntd.0001435.g005.
Figure 5  Effect of the Tccr1 locus on parasite burden in [AcB55xDBA/2]F2 mice.

Detailed LOD score traces are shown for chromosome 2 (Tccr1) locus for [AcB55xDBA/2]F2 females (A). The shaded area designates the Bayesian 95% confidence interval and the genome-wide thresholds are indicated at P = 0.01 and P = 0.05. The effect of the AcB55 (A), DBA/2 (D) or heterozygous (H) allele on parasite load is depicted for Tccr1 (B) at the D2Mit295 peak marker and for the underlying C5 gene (C).



Tables
[TableWrap ID: pntd-0001435-t001] doi: 10.1371/journal.pntd.0001435.t001.
Table 1  Phenotypic response of RCS to T. crassiceps infection, with respect to the C5 status.
RCS Hc allelea Parasite load(mean ± s. d.) Phenotypeb
BcA83 0 271.5±56.6 P
BcA73 0 80.1±14.2 P
BcA72 0 119.6±39.1 P
BcA70 0 84.6±23.2 P
AcB65 0 216.9±57.5 P
AcB64 0 66.9±10.8 P
AcB63* 1 136.5±42.4 P
AcB62 0 253.6±61.1 P
AcB61 0 239.1±75.5 P
AcB58 0 129.0±40.2 P
AcB56 0 148.7±32.4 P
AcB54 0 84.7±24.7 P
AcB52 0 96.4±28.0 P
AcB51 0 70.8±8.8 P
A/J 0 256.1±42.5 P
BcA87 1 6.6±10.0 R
BcA86 1 4.5±12.6 R
BcA85 1 0.3±0.7 R
BcA84 1 0.8±1.3 R
BcA82 1 38.1±47.2 R
BcA81 1 0.5±1.6 R
BcA80 1 35.8±48.3 R
BcA79 1 0.4±1.3 R
BcA78 1 22.9±36.1 R
BcA77 1 12.6±36.6 R
BcA76* 0 15.1±15.7 R
BcA75 1 0.2±0.6 R
BcA74 1 7.8±16.9 R
BcA71 1 1.0±1.8 R
BcA69 1 45.9±25.0 R
BcA68 1 1.0±2.0 R
BcA67 1 0.0±0.0 R
BcA66 1 13.0±15.4 R
B6 1 22.8±21.9 R
AcB60* 0 31.2±31.1 R
AcB55 1 11.7±6.4 R

34 RCS along with A/J and B6 controls are classified as permissive (P) or restrictive (R) to T. crassiceps infection. Discordant strains are denoted by *.

a0-C5 deficient; 1-C5 sufficient.

bR-restrictive; P-permissive.

*Discordant strains.



Article Categories:
  • Research Article
Article Categories:
  • Biology
    • Genetics
      • Heredity
        • Linkage (Genetics)
        • Phenotypes
        • Quantitative Traits
        • Trait Locus
      • Animal Genetics
    • Immunology
      • Immune System
        • Complement System
      • Immune Response
    • Microbiology
      • Host-Pathogen Interaction
    • Model Organisms
      • Animal Models
        • Mouse
Article Categories:
  • Medicine
    • Infectious Diseases
      • Neglected Tropical Diseases
        • Cysticercosis
        • Neurocysticercosis
      • Parasitic Diseases
        • Taeniasis
      • Zoonoses
        • Taeniasis


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