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Relationship: 1742
Title
Inhibition, CHS-1 leads to Decrease, Cuticular chitin content
Upstream event
Downstream event
AOPs Referencing Relationship
| AOP Name | Adjacency | Weight of Evidence | Quantitative Understanding | Point of Contact | Author Status | OECD Status |
|---|---|---|---|---|---|---|
| S-adenosylmethionine depletion leading to population decline (1) | adjacent | Agnes Aggy (send email) | Under development: Not open for comment. Do not cite | |||
| Chitin synthase 1 inhibition leading to mortality | adjacent | Moderate | Low | Brendan Ferreri-Hanberry (send email) | Open for citation & comment | WPHA/WNT Endorsed |
Taxonomic Applicability
Sex Applicability
| Sex | Evidence |
|---|---|
| Unspecific | Moderate |
Life Stage Applicability
| Term | Evidence |
|---|---|
| Larvae | High |
| Juvenile | High |
| Adult | Moderate |
Chitin in the arthropod cuticle is synthesized by the chitin synthase isoform 1 (CHS-1) which spans the plasma membrane on the apical plasma membrane of epithelial cells (Locke and Huie 1979; Binnington 1985; Merzendorfer and Zimoch 2003; Merzendorfer 2006). Since CHS-1 is the enzyme to polymerize chitin from UDP-N-Acetylglucosamine (UDP-GlcNAc) (Merzendorfer 2006), it is solely responsible for the content of chitin in the exoskeleton. Consequently, the inhibition of CHS-1 leads to a decrease in chitin content in the arthropod cuticle.
| ID | Experimental Design | Species | Upstream Observation | Downstream Observation | Citation (first author, year) | Notes |
|---|
| Title | First Author | Biological Plausibility |
Dose Concordance |
Temporal Concordance |
Incidence Concordance |
|---|
Biological Plausibility
Dose Concordance Evidence
Temporal Concordance Evidence
Incidence Concordance Evidence
Uncertainties and Inconsistencies
The major uncertainty in this KER is the absence of studies which assess both endpoints, the inhibition of the chitin synthase and the decrease in cuticular chitin content after exposure to specific stressors.
CHS is dependent on bivalent ions as cofactor such as Mg2+ or Mn2+ (Merzendorfer 2006). Both low and high levels of Mg2+ inhibited CHS activity in vitro (Zhang and Yan Zhu 2013).
Response-response Relationship
Due to the lack of studies linking the inhibition of CHS-1 to the decrease in cuticular chitin content, it is not possible to describe the nature of the response-response relationship.
Time-scale
Due to the lack of studies assessing the inhibition of CHS-1 and the decrease in cuticular chitin content, it is not possible to make a statement on the timescale of the relationship. However, the expression of CHS-1 peaks at the time of ecdysis (Ampasala et al. 2011; Wang et al. 2012), indicating the highest rate of chitin synthesis at this timepoint. Hence it can be assumed that a decrease in chitin content in the newly synthesized cuticle should become apparent shortly after. In studies where CHS-1 was knocked down, chitin contents were assessed after 3 and 7 days and found to be decreased (Arakane et al. 2005, Li et al. 2017, Zhang X. et al. 2010).
Known Feedforward/Feedback loops influencing this KER
Upon knockdown of CHS-1 in the salmon louse Lepeophtheirus salmonis, upregulation of the UDP-GlcNAc pyrophosphorylase (UAP), which catalyzes the conversion of GlcNAc to UDP-GlcNAc, was observed (Braden et al. 2020). The knockdown of UAP also led to upregulation of CHS-1 demonstrating a clear dependence of the two enzymes. Most likely, the upregulation of UAP is a compensatory mechanism with the goal to restore homeostasis in absence of CHS-1. The exact regulation of the feedback, however, remains to be investigated.
Taxonomic: Likely, this KER is likely applicable to the whole phylum of arthropods as they all depend on the synthesis of chitin.
Life stage: This KER is applicable for organisms synthesizing chitin in order to grow and develop, namely larval stages of insects and all life stages of crustaceans and arachnids.
Sex: This KER is applicable to all sexes.
Chemical: Substances inducing both, the inhibition of CHS-1 and the decrease in cuticular chitin content are of the family of pyrimidine nucleosides (e.g. polyoxin D, polyoxin B and nikkomycin Z) (Gijswijt et al. 1979; Cohen and Casida 1982; Turnbull and Howells 1982; Calcott and Fatig 1984; Kuwano and Cohen 1984; Cohen and Casida 1990; Zhang and Yan Zhu 2013; Zhuo et al. 2014; Osada 2019). The phthalimide captan was also shown to induce CHS-1 inhibition and a decrease in cuticular chitin content (Cohen and Casida 1982; Gelman and Borkovec 1986). However, studies assessing both endpoints in sequence are lacking.