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<title>GENETIC DIVERSITY OF Striga hermonthica (DEL.) BENTH. WEEDS FROM  NIGERIA AND KENYA, AND THE GENETIC RESPONSES OF SELECTED  HOST MAIZE LINES</title>
<link href="http://hdl.handle.net/123456789/1362" rel="alternate"/>
<subtitle/>
<id>http://hdl.handle.net/123456789/1362</id>
<updated>2026-04-21T23:25:48Z</updated>
<dc:date>2026-04-21T23:25:48Z</dc:date>
<entry>
<title>GENETIC DIVERSITY OF Striga hermonthica (DEL.) BENTH. WEEDS FROM  NIGERIA AND KENYA, AND THE GENETIC RESPONSES OF SELECTED  HOST MAIZE LINES</title>
<link href="http://hdl.handle.net/123456789/1363" rel="alternate"/>
<author>
<name>UNACHUKWU, NNANNA NNAMDI</name>
</author>
<id>http://hdl.handle.net/123456789/1363</id>
<updated>2022-02-21T08:07:55Z</updated>
<published>2019-12-01T00:00:00Z</published>
<summary type="text">GENETIC DIVERSITY OF Striga hermonthica (DEL.) BENTH. WEEDS FROM  NIGERIA AND KENYA, AND THE GENETIC RESPONSES OF SELECTED  HOST MAIZE LINES
UNACHUKWU, NNANNA NNAMDI
Striga hermonthica (SH) is a parasitic weed that attacks and significantly reduces the &#13;
yield of maize in Africa. The genetic interactions responsible for resistance or &#13;
susceptibility of hosts to the parasite and the genetic differentiation that exists between &#13;
and within SH populations are not fully known. This study investigated the genetic &#13;
diversity of SH populations in the largest maize producers in Sub-Saharan Africa &#13;
(Kenya and Nigeria) and; the genetic responses of a susceptible (5057) and a resistant &#13;
(ZD05) maize genotype to SH infestation.&#13;
The SH plants were collected from farms across western Kenya (KSH) and northern &#13;
Nigeria (NSH) in October 2012 and authenticated at the Department of Botany, &#13;
University of Ibadan (UIH-22774). The plants (n=1029) were then genotyped with &#13;
1576 single nucleotide polymorphism markers and indices of genetic diversity &#13;
[effective alleles (Ne), Shannon’s information index (I), expected (He) and observed &#13;
heterozygosity (Ho)] were determined. Population structure and fixation index (Fst), &#13;
were assessed to identify genetic differentiation between and within KSH and NSH &#13;
populations. Two maize varieties (5057 and ZD05) were divided into four groups of &#13;
nine plants each and planted in rhizotrons (root observation chambers). Seven days &#13;
after planting, three groups of each maize genotype were infested with pre-germinated &#13;
SH and the fourth was used as uninfested control. Root tissue was taken at 3, 9 and 22&#13;
days post infestation (DPI) and total ribonucleic acid (RNA) was extracted using &#13;
standard method. The root transcriptome was sequenced using next-generation &#13;
sequencing. Gene expression levels of secondary metabolism, defence, and &#13;
antiapoptotic genes were determined by profiling the messenger RNA levels and &#13;
comparing the log2 fold-change (LFC) between the infested and uninfested maize &#13;
plants and between the genotypes. Data were analysed using two-way ANOVA at &#13;
α0.05.&#13;
The two populations of SH displayed high levels of genetic diversity. KSH showed &#13;
higher levels (Ne=1.41±0.01, I=0.38±0.01, Ho=0.28, He=0.25±0.0) than NSH &#13;
iii&#13;
(Ne=1.41±0.01, I=0.332±0.01, Ho=0.21, He=0.20±0.00). Significant genetic &#13;
differentiation (Fst=0.15) was observed between the two populations and between &#13;
three subpopulations detected within the NSH population (Fst =0.053). At 3DPI, &#13;
secondary metabolism and defence genes, benzoxazineless 1 (LFC=2.5) and chalcone &#13;
synthase 2 (LFC=3.2), were upregulated in ZD05, while in 5057, antiapoptotic genes,&#13;
bax inhibitor1 (LFC=1.4) and bcl-2 binding anthanogene-1 (LFC=1.7) were &#13;
upregulated. At 9DPI, secondary metabolism and defence genes, chalcone synthase &#13;
(LFC=-1.7) and cellulose synthase (LFC=-1.7), were downregulated in 5057, while &#13;
secondary metabolism and defence genes, chalcone isomerase (LFC=2.3), cellulose &#13;
synthase (LFC=1.5), chitinase (LFC=1.6) and phenylalanine ammonia-lyase1 &#13;
(LFC=1.8) were upregulated in ZD05. At 22 DPI, secondary metabolism and defence &#13;
genes, chalcone synthase (LFC=-2.9) and phenylalanine ammonia-lyase1 (LFC=-2.9), &#13;
were down regulated in 5057, while in ZD05, secondary metabolism and defence &#13;
genes, bx13 (LFC=1.8), chalcone synthase (LFC=1.8), phenylalanine ammonia-lyase &#13;
(LFC=2.6) and antiapoptotic gene, bax inhibitor1 (LFC=1.8) were upregulated.&#13;
Striga hermonthica populations in Kenya and Nigeria are genetically distinct and &#13;
ecotypes exist within Nigeria. Genes involved in secondary metabolism and defence &#13;
were upregulated in the resistant maize genotype, but down regulated in the &#13;
susceptible genotype. The resistant line mobilized a more comprehensive response to &#13;
the parasite than the susceptible line.
</summary>
<dc:date>2019-12-01T00:00:00Z</dc:date>
</entry>
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