Wikipedia

Perivitellins

Perivitellins are egg proteins found in the perivitelline fluid of many gastropods. They are multifunctional complexes providing the developing embryo with nutrition, protection from the environment, and defense against predators.[1]

Despite the central role perivitellins play in reproduction and development, there is little information about their role in gastropod Molluscs. Most studies of perivitellins have been performed in eggs of Ampullaridae, a family of freshwater snails (Caenogastropoda), notably the Pomacea genus, mostly those of Pomacea canaliculata, Pomacea scalaris and Pomacea maculata.[2][3]

Synthesis

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Perivitellins are almost exclusively synthesized in the albumen gland (also known as albumen gland-capsule gland complex or uterine gland), an accessory gland from the female reproductive system of gastropods.[4][5] This has been experimentally confirmed for the perivitellins ovorubin (PcOvo) and PcPV2, which were only found in the albumen gland with no extra-gland synthesis, circulation or storage.[6][7][8] During the reproductive season, these perivitellins are transferred to eggs. After oviposition, they are rapidly restored in the albumen gland, decreasing their total amount in the gland only after repeated ovipositions.[4][9] In Pomacea canaliculata snails, perivitellins would act, together with the polysaccharide galactogen, as a limiting factor of the reproductive effort during reproduction.[4]

Types of perivitellins

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The first studies performed in Pomacea canaliculata identified two proteins named perivitellin-1, PV1 or ovorubin (now called PcOvo) and perivitellin-2 or PV2 massively accumulated in eggs, comprising 60-70% of total protein, respectively, and a heterogeneous fraction dubbed perivitellin-3 or PV3 fraction.[10] Recent proteomic analyses of perivitelline fluids, however, identified a total of 34 proteins from Pomacea canaliculata, 38 in Pomacea maculata, and 32 in Pomacea diffusa.[11][12][13][14]

Perivitellin-1 or PcOvo (former ovorubin) and perivitellin-2 or PcPV2 are probably the best characterized from snails.[5][8][10][15][16][17][18][19] Both perivitellins are multimeric and glycosylated proteins with remarkable thermal stability up to 100°C and 60°C, respectively, and over a wide range of pH.[20][21] They are also highly resistant to the combined action of pepsin and trypsin proteases.[17][18][21]

The perivitelline fluid of Pomacea scalaris and Pomacea diffusa contain one major perivitellin, PsSC (also named scalarin) and PdPV1, respectively, which are structurally and phylogenetically related to PcOvo.[19][22][23][24] The perivitelline fluid of P. maculata is also similar, with two major perivitellins, PmPV1 and PmPV2, structurally and functionally similar to PcOvo and PcPV2, respectively.[25][26][27]

The rest of Pomacea perivitellins (over 25) have been characterized at the transcriptomic and proteomic levels, but biochemical studies are still largely missing.[28]

Perivitellin functions

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Perivitellins provide nutrition, energy storage, defense against predation, and protection from the environment to the developing embryo.

A functional classification of the perivitellin aminoacid sequences based on the Kyoto Encyclopedia of Genes and Genomes (KEGG), classified them in "environmental information processing", among which several immune proteins are included, "metabolism", "organismal systems", "cellular processes", "other", and a considerable number of "unknown" proteins.

The first functional studies performed in Pomacea canaliculata, considered them mostly as storage proteins that provided energetic and structural precursors for the embryos, since they are consumed during development.[16]

Later research on PV1s (PcOvo, PmPV1, and PsSC) reported that their carotenoid cofactor, notably astaxanthin, serves as a potent antioxidant and provides the reddish color to the eggs.[1][20][25][29] These carotenoproteins are also highly resistant to gastrointestinal digestion, and withstand the passage through the digestive system without significant modifications; this characteristic was related to embryo defenses, deterring predators by lowering the nutritional value of the eggs.[8][22][26] PcOvo and PsSC also carry phosphate groups attached to serine residues that may serve as a phosphorus reserve for the embryo.[19] Unlike PcOvo and PmPV1, PsSC is also an active lectin that agglutinates bacteria and alters the gastrointestinal mucosa of rats, functions associated with embryo protection against both pathogens and predators.[19][23]

PV2s are toxins only found in Pomacea canaliculata (PcPV2) and Pomacea maculata (PmPV2) perivitelline fluid.[25][30][31] They are potent neurotoxins when intraperitoneally injected to mice, while exerting enterotoxic functions when ingested.[27][30][32] Each of the two dimeric units of either PcPV2 or PmPV2 consists of a carbohydrate-binding protein of the tachylectin family (acting as a targeting module) disulfide-linked to a pore-forming subunit of the Membrane Attack Complex and Perforin (MACPF) subfamily (toxic module).[18][27] These toxins bear a structural resemblance to botulinic and ricin heterodimeric toxins, the so-called "AB toxins" previously known only in bacteria and plants. Perivitellin-2 is also resistant to gastrointestinal digestion, which contributes to lowering the egg nutritional value.[18][32]

Finally, a recent study of Pomacea canaliculata PV3 fraction identified and characterized two protease inhibitors from the Kunitz and Kazal families, a function also related to an antipredator defense since it would prevent predators to digest proteins from the eggs when ingested.[28]

References

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  1. ^ a b Heras H, Dreon MS, Ituarte S, Pollero RJ (2007-07-01). "Egg carotenoproteins in neotropical Ampullariidae (Gastropoda: Arquitaenioglossa)". Comparative Biochemistry and Physiology. Toxicology & Pharmacology. 146 (1–2): 158–67. doi:10.1016/j.cbpc.2006.10.013. PMID 17320485.
  2. ^ Hayes KA, Burks RL, Castro-Vazquez A, Darby PC, Heras H, Martín PR, Qiu JW, Thiengo SC, Vega IA, Wada T, Yusa Y (2015). "Insights from an Integrated View of the Biology of Apple Snails (Caenogastropoda: Ampullariidae)". Malacologia. 58 (1–2): 245–302. doi:10.4002/040.058.0209. hdl:11336/7919. S2CID 85707576.
  3. ^ Heras H, Dreon MS, Ituarte S, Pasquevich MY, Cadierno MP, Joshi RC, Cowie RH, Sebastian LS (2017). Apple snail perivitellins, multifunctional egg proteins. Philippine Rice Research Institute. ISBN 978-621-8022-25-6.
  4. ^ a b c Cadierno MP, Saveanu L, Dreon MS, Martín PR, Heras H (August 2018). "Biosynthesis in the Albumen Gland-Capsule Gland Complex Limits Reproductive Effort in the Invasive Apple Snail Pomacea canaliculata". The Biological Bulletin. 235 (1): 1–11. doi:10.1086/699200. hdl:11336/101954. PMID 30160995. S2CID 52135669.
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  6. ^ Dreon M, Lavarias S, Garin CF, Heras H, Pollero RJ (February 2002). "Synthesis, distribution, and levels of an egg lipoprotein from the apple snail Pomacea canaliculata (Mollusca: Gastropoda)". The Journal of Experimental Zoology. 292 (3): 323–30. doi:10.1002/jez.10043. PMID 11857466.
  7. ^ Dreon MS, Heras H, Pollero RJ (January 2003). "Metabolism of ovorubin, the major egg lipoprotein from the apple snail". Molecular and Cellular Biochemistry. 243 (1–2): 9–14. doi:10.1023/a:1021616610241. PMID 12619883. S2CID 6345962.
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  15. ^ Cheesman DF (December 1958). "Ovorubin, a chromoprotein from the eggs of the gastropod mollusc Pomacea canaliculata". Proceedings of the Royal Society of London. Series B, Biological Sciences. 149 (937): 571–87. Bibcode:1958RSPSB.149..571C. doi:10.1098/rspb.1958.0093. PMID 13623805. S2CID 44905224.
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  17. ^ a b Dreon MS, Ituarte S, Heras H (December 2010). "The role of the proteinase inhibitor ovorubin in apple snail eggs resembles plant embryo defense against predation". PLOS ONE. 5 (12): e15059. Bibcode:2010PLoSO...515059D. doi:10.1371/journal.pone.0015059. PMC 2997075. PMID 21151935.
  18. ^ a b c d Dreon MS, Frassa MV, Ceolín M, Ituarte S, Qiu JW, Sun J, et al. (2013-05-30). "Novel animal defenses against predation: a snail egg neurotoxin combining lectin and pore-forming chains that resembles plant defense and bacteria attack toxins". PLOS ONE. 8 (5): e63782. Bibcode:2013PLoSO...863782D. doi:10.1371/journal.pone.0063782. PMC 3667788. PMID 23737950.
  19. ^ a b c d Ituarte S, Dreon MS, Pasquevich MY, Fernández PE, Heras H (September 2010). "Carbohydrates and glycoforms of the major egg perivitellins from Pomacea apple snails (Architaenioglossa: Ampullariidae)". Comparative Biochemistry and Physiology. Part B, Biochemistry & Molecular Biology. 157 (1): 66–72. doi:10.1016/j.cbpb.2010.05.004. PMID 20471490.
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  23. ^ a b Ituarte S, Brola TR, Fernández PE, Mu H, Qiu JW, Heras H, Dreon MS (2018-06-01). "A lectin of a non-invasive apple snail as an egg defense against predation alters the rat gut morphophysiology". PLOS ONE. 13 (6): e0198361. Bibcode:2018PLoSO..1398361I. doi:10.1371/journal.pone.0198361. PMC 5983499. PMID 29856808.
  24. ^ Brola, T. R.; Dreon, M. S.; Qiu, J. W.; Heras, H. (2020-01-01). "A highly stable, nondigestible lectin from Pomacea diffusa unveils clade-related protection systems in apple snail eggs". Journal of Experimental Biology. 223 (19): jeb.231878. doi:10.1242/jeb.231878. hdl:11336/144003. ISSN 0022-0949. PMID 32719049. S2CID 220841934.
  25. ^ a b c Pasquevich MY, Dreon MS, Heras H (March 2014). "The major egg reserve protein from the invasive apple snail Pomacea maculata is a complex carotenoprotein related to those of Pomacea canaliculata and Pomacea scalaris". Comparative Biochemistry and Physiology. Part B, Biochemistry & Molecular Biology. 169: 63–71. doi:10.1016/j.cbpb.2013.11.008. hdl:11336/100510. PMID 24291422.
  26. ^ a b Pasquevich MY, Dreon MS, Qiu JW, Mu H, Heras H (November 2017). "Convergent evolution of plant and animal embryo defences by hyperstable non-digestible storage proteins". Scientific Reports. 7 (1): 15848. Bibcode:2017NatSR...715848P. doi:10.1038/s41598-017-16185-9. PMC 5696525. PMID 29158565.
  27. ^ a b c Giglio ML, Ituarte S, Milesi V, Dreon MS, Brola TR, Caramelo J, et al. (August 2020). "Exaptation of two ancient immune proteins into a new dimeric pore-forming toxin in snails". Journal of Structural Biology. 211 (2): 107531. doi:10.1016/j.jsb.2020.107531. hdl:11336/143650. PMID 32446810. S2CID 218873723.
  28. ^ a b tuarte S, Brola TR, Dreon MS, Sun J, Qiu JW, Heras H (2019-02-01). "Non-digestible proteins and protease inhibitors: implications for defense of the colored eggs of the freshwater apple snail Pomacea canaliculata". Canadian Journal of Zoology. 97 (6): 558–566. doi:10.1139/cjz-2018-0210. hdl:1807/95364. ISSN 0008-4301. S2CID 92566772.
  29. ^ Dreon MS, Schinella G, Heras H, Pollero RJ (February 2004). "Antioxidant defense system in the apple snail eggs, the role of ovorubin". Archives of Biochemistry and Biophysics. 422 (1): 1–8. doi:10.1016/j.abb.2003.11.018. PMID 14725852.
  30. ^ a b Heras H, Frassa MV, Fernández PE, Galosi CM, Gimeno EJ, Dreon MS (September 2008). "First egg protein with a neurotoxic effect on mice". Toxicon. 52 (3): 481–8. doi:10.1016/j.toxicon.2008.06.022. PMID 18640143.
  31. ^ Giglio ML, Ituarte S, Pasquevich MY, Heras H (2016-09-12). "The eggs of the apple snail Pomacea maculata are defended by indigestible polysaccharides and toxic proteins". Canadian Journal of Zoology. 94 (11): 777–785. doi:10.1139/cjz-2016-0049. hdl:1807/74381.
  32. ^ a b Giglio ML, Ituarte S, Ibañez AE, Dreon MS, Prieto E, Fernández PE, Heras H (2020). "Novel Role for Animal Innate Immune Molecules: Enterotoxic Activity of a Snail Egg MACPF-Toxin". Frontiers in Immunology. 11: 428. doi:10.3389/fimmu.2020.00428. PMC 7082926. PMID 32231667.
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