2019
DOI: 10.1016/j.pmpp.2018.08.004
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Diversity of Meloidogyne spp. from peri-urban areas of sub-Saharan Africa and their genetic similarity with populations from the Latin America

Abstract: A B S T R A C TIn Africa, peri-urban vegetable production systems supply perishable vegetables to the rapidly expanding urban centers. These highly intensive systems are characterized by high levels of pests and diseases and an excessive use of synthetic pesticides to reduce their population densities. Root-knot nematodes (RKN) are especially prevalent in these systems but are often not recognized, or diagnosed correctly. The limited ability to accurately identify these pathogens likely results in the inapprop… Show more

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Cited by 15 publications
(7 citation statements)
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“…In the current study, the Meloidogyne spp. were not identified to species level, although it is likely that M. javanica and/or M. incognita were present, both of which are common to the region [ 33 ] and are the two most commonly occurring Meloidogyne spp. found infecting cassava [ 23 ].…”
Section: Discussionmentioning
confidence: 99%
“…In the current study, the Meloidogyne spp. were not identified to species level, although it is likely that M. javanica and/or M. incognita were present, both of which are common to the region [ 33 ] and are the two most commonly occurring Meloidogyne spp. found infecting cassava [ 23 ].…”
Section: Discussionmentioning
confidence: 99%
“…A population of M. incognita originally isolated from tomato in Nigeria and identified using perineal pattern and isozyme techniques (dos Santos et al, 2019) was used in the study. Pure cultures, derived from a single egg mass population, were maintained in the screenhouse on cockscomb (Celosia argentea) and tomato (Solanum lycopersicum).…”
Section: Meloidogyne Incognita Inoculummentioning
confidence: 99%
“…A promising approach for molecular identification of M. luci and other tropical RKN species was demonstrated by [34], using a DNA barcoding approach with six mtDNA genes, but the method has so far not been adopted in diagnostic laboratories. A species-specific SCAR marker was developed for M. ethiopica, a sister species of M. luci [35], but this diagnostic method was not shown to be reliable and reproducible [36,37]. In contrast, M. luci can be detected with a PCR method using a primer pair specific for the Meloidogyne ethiopica group (MEG), i.e., for the three closely related and similar species M. ethiopica, M. luci, and M. inornata.…”
Section: Introductionmentioning
confidence: 99%