Animal Molecular Breeding 2015, Vol. 5, No. 1, 1-8
7
current study (OPB04) generated interesting results on
genetic diversity and population differentiation of
A.
marginata
, however all the three (3) primers used could
not amplify the genomic DNA from one of the samples
(that is, A11), perhaps on account of the presence of
polyphenolic compounds or polysaccharide in the
DNA of the said sample.
In conclusion, the genetic and morphometric analysis
of 16 accessions of
A. marginata
collected from three
(3) different locations in southern Nigeria using
RAPD-PCR and average linkage cluster analysis
revealed high level of genetic diversity and
heterogeneity. Of the 84 scorable bands that were
generated in the RAPD analysis using OPB03, OPB04,
and OPB08 primers, 79 of the bands (accounting for
94.04% of the total number of bands) were
polymorphic. The OPB04 primer gave 30 RAPD
fragments exhibiting significant genetic differentiation
across all samples. At the population level, this primer
revealed significant genetic differences between the
samples from Cross River State (albino-bodied form)
and each of the remaining samples from Akwa Ibom
and Edo States (black), respectively. This study is the
first to elucidate genetic diversity in African land snail
species that are prevalent in Nigeria. Given that the
RAPD markers used in this study showed genetic
variability among a small sample of
A. marginata
found in the southern part of the country, it would
mean that with the use of greater resolution markers
including single nucleotide polymorphisms (SNPs)
and simple sequence repeat markers (SSRs) on a
greater number of diverse samples, the full range of
diversity in African land snail accessions in Nigeria
could be determined.
References
Abere S.A., and Lameed G.A., 2008, The medicinal utilization of snails in
some selected states in Nigeria.
In
: Onyekwelu, J.C. Adekunle, V.A.J.
and Oke, D.O. (Eds.). Proceeding of the 1
st
National Conference of the
Forests and Forest Products Society (FFPS) held in Akure, Ondo State,
Nigeria between 11
th
and 18
th
of April, 2008. Pp 233-237
Adeyeye, E.I., 1996, Waste yield, proximate and mineral composition of
three different types of land snails found in Nigeria, International
Journal of Food Science and Nutrition, 42: 111-116
Bartish I., V. N. Jeppsson and D.H. Nybom, 1999, Population genetics
structure in pioneer plant species
Hippophae rhamnoides
investigated
by random amplified polymorphic DNA (RAPD) markers, Molecular
Ecology, 8: 791-802
Craze P.G. and Mauremootoo, J.R., 2002, A test of methods for estimating
population size of the invasive land snail
Achatina fulica
in dense
vegetation, Journal of Applied Ecology, 39: 653-660
Denny, M., 1980, Locomotion: the cost of gastropod crawling, Science, 208:
288-290
Fearnley, R., 1993, Sexual Selection, Dispersal and Reproductive Behaviour
in Hermaphrodite Land Snails, with Particular Reference to
Helix
aspersa Müller (Pulmonata: Gastropoda)
. Ph.D. Thesis, University of
Manchester, Manchester, UK
Hadrys H., M. Balick and B .Sheierwater, 1992, Applications of random
amplified polymorphic DNA (RAPD), Molecular Ecology, 1: 55-63
Jordano P. And J.A. Godboy, 2000, RAPD variation and population genetic
structure in
Prunus mataleb
(Rosaceae), an animal-dispersed tree,
Molecular Ecology, 9: 1293-1305
Lez, S.W., Ledig, F.T. and Johnson, D. R., 2002, Genetic variation of
allozymes and RAPD markers in
Pinus longaeva
(Pinaceae) of the white
mountains, California. J. American Botanical, 89: 566-577
Madec L.and Bellido A., 2007, Spatial variation of shell morphometrics in
sub-Antartic land snail
Notodiscus hookeri
from Crozet and Kerguelen
Islands. Polar Biology, Springer Berlin/Heidelberg
Mead, A.R., 1961, The giant African snail: A problem in economic
malacology. The University of Chicago Press, Chicago, USA
Pattamarnon, 2004) Shell morphological differences and genetic variation of
the giant African snail
Achatina fulica
(Bowdich, 1822) in Thailand.
Ph.D. Thesis,
Suranaree University of Technology, Thailand
Pfenninger, M., Bahl, A., and Streit, B., 1996, Isolation by distance in a
population of a small land snail
Trochoidea geyeri
: evidence from direct
and indirect methods, Proceeding of the Royal Society of London,
263:
1211-1217
Raut, S.K., and Barker G.M., 2002,
Achatina fulica
Bowdich and other
Achatinidaeas Pests in Tropical Agriculture. Barker, G. M. (ed.)., 2004,
Molluscs as Crop Pests
(pp. 55-114). Hamilton: CABI Publishing
Ruckelshaus M. H., 1998, Spatial scale of genetic structure and an indirect
estimate of gene flow in eelgrass (
Zostera marina
), Evolution, 52:
330-343
Saghai-Maroof, M.A., Soliman, K.M., Jorgenson, R.A., Allard, R.W., 1984,
Ribosomal DNA spacer length polymorphism in barley: Mendelian
inheritance, chromosomal location and population dynamics, Proc. Natl.
Acad. Sci. U.S.A, 81: 8014-8018
Schilthuizen M, and M. Lombaerts, 1994, Population structure and levels of
gene flow in the Mediterranean land snail
Albinaria corrugata
(Pulmonata: Clausiliidae), Evolution, 48: 577-586
Smith, J. W., and Fowler, G., 2003, Pathway risk assessment for Achatinidae
with emphasis on the giant African land snail
Achatina fulica
(Bowdich)
and
Lmicolaria aurora
(Jay) from the Caribbean and Brazil, with
comments on related taxa
Achatina achatina
(Linne), and
Archachatina
marginata
(Swainsan) intercepted by PPQ. USDA-APHIS. Internal
Report. Raleigh. NC: Center for Plant Health Science and Technology
Snedecor G. W. and Cochran W.G., 1994, "Statistical Methods," 8th Edition,
Iowa State University Press, Ames, Iowa 50014, USA
Tassanakajon, A., Pongsomboon, S., Jarayabhand, P., Klinbunga, S., and
Boonsaeng, V., 1998, Genetic structure in wild populations of black tiger
shrimp (
Penaeus monodon
) using randomly amplified polymorphic
DNA analysis,
Journal of Marine Biotechnology, 6: 249-254
Thaewnon-ngiw, B., Klinbunga, S., Phanwichian, K., Sangduang, N.,