期刊
BIOLOGY-BASEL
卷 11, 期 9, 页码 -出版社
MDPI
DOI: 10.3390/biology11091344
关键词
schistosomiasis; Schistosoma mansoni; cercariae; putative neuropeptide; behavioural bioassay; parasite-host interaction
类别
资金
- Australian Research Council [ARC DP180103694, ARC LE170100192]
This study investigates the effect of potential neuropeptides derived from cercariae on cercarial behavior. It identifies several neuropeptide precursor proteins specific to Schistosoma and characterizes their interactions with structural proteins in cercariae. The study finds that certain neuropeptides can stimulate behavioral changes in cercariae and suggests their potential use in biocontrol strategies against human schistosomiasis.
Elucidating the infectivity of Schistosoma mansoni, one of the main etiological agents of human schistosomiasis, requires an improved understanding of the behavioural mechanisms of cercariae, the non-feeding mammalian infective stage. This study investigated the presence and effect of cercariae-derived putative neuropeptides on cercarial behaviour when applied externally. Cercariae were peptidomically analysed and 11 neuropeptide precursor proteins, all of which were specific to the Schistosoma genus and most of which highly expressed in the cercarial stage, were identified in cercariae for the first time. Protein-protein interaction analysis predicted the interaction of various neuropeptide precursors (e.g., Sm-npp-30, Sm-npp-33, Sm-npp-35) with cercarial structural proteins (e.g., myosin heavy chain and titin). In total, nine putative neuropeptides, selected based on their high hydrophobicity and small size (similar to 1 kilodalton), were tested on cercariae (3 mg/mL) in acute exposure (1 min) and prolonged exposure (360 min) behavioural bioassays. The peptides AAYMDLPW-NH2, NRKIDQSFYSYY-NH2, FLLALPSP-OH, and NYLWDTRL-NH2 stimulated acute increases in cercarial spinning, stopping, and directional change during active states. However, only NRKIDQSFYSYY-NH2 caused the same behavioural changes at a lower concentration (0.1 mg/mL). After prolonged exposure, AAYMDLPW-NH2 and NYLWDTRL-NH2 caused increasing passive behaviour and NRKIDQSFYSYY-NH2 caused increasing body-first and head-pulling movements. These findings characterise behaviour-altering novel putative neuropeptides, which may inform future biocontrol innovations to prevent human schistosomiasis.
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