Laura Morales

Dr. Laura Morales

University of Natural Resources and Life Sciences, Vienna
orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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5 February 2016 in Theoretical and Applied Genetics
Verified
Journal Article
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TJTiffany M. Jamann
Tiffany M. Jamann
XLXingyu Luo
Xingyu Luo
Laura MoralesLaura Morales
Laura Morales
JKJudith M. Kolkman
Judith M. Kolkman
CCChia-Lin Chung
Chia-Lin Chung
RNRebecca J. Nelson
Rebecca J. Nelson

1 April 2017 in Field Crops Research
Verified
Journal Article
Closed access
Samuel K MutigaSamuel K Mutiga
Samuel K Mutiga
Laura MoralesLaura Morales
Laura Morales
SASamuel Angwenyi
Samuel Angwenyi
JWJames Wainaina
James Wainaina
JHJagger Harvey
Jagger Harvey
RNRebecca J Nelson
Rebecca J Nelson

5 August 2016 in African Journal of Food, Agriculture, Nutrition and Development
Verified
Journal Article
Closed access
LSLaura E. Smith
Laura E. Smith
Matthew StasiewiczMatthew Stasiewicz
Matthew Stasiewicz
RHR Hestrin
R Hestrin
Laura MoralesLaura Morales
Laura Morales
Samuel K MutigaSamuel K Mutiga
Samuel K Mutiga
RNR.J. Nelson
R.J. Nelson
Maize, a staple food in most African countries, is prone to contamination by aflatoxins, toxic secondary metabolites mainly produced by Aspergillus flavus and A. parasiticus. Aflatoxins are known to cause liver cancer, and chronic exposure has been linked to other adverse health outcomes including growth faltering in children. To mitigate exposure in maize-dependent populations, there is need to identify the factors associated with aflatoxin contamination. This is difficult, however, because of high sampling cost and lack of affordable and accurate analytical methods. Publicly available, remotely-sensed data on vegetation, precipitation, and soil properties could be useful in predicting locations at risk for aflatoxin contamination in maize. This study investigates the utility of publicly available remotely-sensed data on rainfall, vegetation cover (indicated by normalized difference vegetation index or NDVI), and soil characteristics as potential predictors of aflatoxin contamination in Kenyan maize. Aflatoxin was analyzed in maize samples (n=2466) that were collected in 2009 and 2010 at 243 local hammer mills in eastern and western Kenya. Overall, 60% of maize samples had detectable aflatoxin. Global positioning system coordinates of each mill location were linked to remotely-sensed, spatially explicit indicators of average monthly NDVI, total monthly rainfall, and soil properties. Higher rainfall and vegetation cover during the maize pre-flowering period were significantly associated with higher prevalence of aflatoxin contamination. Conversely, higher rainfall and vegetation cover during the maize flowering and post-flowering periods (not including harvest) were associated with lower prevalence of aflatoxin contamination. Water stress throughout the growing season may cause increased plant susceptibility to fungal colonization and aflatoxin accumulation. Soil organic carbon content, pH, total exchangeable bases, salinity, texture, and soil type were significantly associated with aflatoxin. In conclusion, this study shows that remotely-sensed data can be regressed on available aflatoxin data highlighting important potential predictors that could reduce the cost of data collection and the cost of aflatoxin risk forecasting models.

1 February 2019 in Toxins
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Journal Article
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Laura MoralesLaura Morales
Laura Morales
CZCharles T. Zila
Charles T. Zila
DMDanilo E. Moreta Mejía
Danilo E. Moreta Mejía
MAMelissa Montoya Arbeláez
Melissa Montoya Arbeláez
PBPeter J. Balint-Kurti
Peter J. Balint-Kurti
RNRebecca J Nelson
Rebecca J Nelson
The fungus Fusarium verticillioides can infect maize ears, causing Fusarium ear rot (FER) and contaminating the grain with fumonisins (FUM), which are harmful to humans and animals. Breeding for resistance to FER and FUM and post-harvest sorting of grain are two strategies for reducing FUM in the food system. Kernel and cob tissues have been previously associated with differential FER and FUM. Four recombinant inbred line families from the maize nested associated mapping population were grown and inoculated with F. verticillioides across four environments, and we evaluated the kernels for external and internal infection severity as well as FUM contamination. We also employed publicly available phenotypes on innate ear morphology to explore genetic relationships between ear architecture and resistance to FER and FUM. The four families revealed wide variation in external symptomatology at the phenotypic level. Kernel bulk density under inoculation was an accurate indicator of FUM levels. Genotypes with lower kernel density—under both inoculated and uninoculated conditions—and larger cobs were more susceptible to infection and FUM contamination. Quantitative trait locus (QTL) intervals could be classified as putatively resistance-specific and putatively shared for ear and resistance traits. Both types of QTL mapped in this study had substantial overlap with previously reported loci for resistance to FER and FUM. Ear morphology may be a component of resistance to F. verticillioides infection and FUM accumulation.

29 April 2020 in The Plant Journal
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Journal Article
Closed access
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Laura MoralesLaura Morales
Laura Morales
ARA. C. Repka
A. C. Repka
KSKelly L. Swarts
Kelly L. Swarts
WSWilliam C. Stafstrom
William C. Stafstrom
YHYijian He
Yijian He
PBPeter J. Balint‐Kurti
Peter J. Balint‐Kurti

1 December 2018 in Phytopathology®
Verified
Journal Article
Open access
Laura MoralesLaura Morales
Laura Morales
TMThiago Pablo Marino
Thiago Pablo Marino
AWAnthony Wenndt
Anthony Wenndt
JFJulia Quinn Fouts
Julia Quinn Fouts
JHJames B. Holland
James B. Holland
RNRebecca J Nelson
Rebecca J Nelson
The fungus Fusarium verticillioides can infect maize ears, contaminating the grain with mycotoxins, including fumonisins. This global public health threat can be managed by breeding maize varieties that are resistant to colonization by F. verticillioides and by sorting grain after harvest to reduce fumonisin levels in food systems. Here, we employed two F. verticillioides inoculation techniques representing distinct infection pathways to dissect ear symptomatology and morphological resistance mechanisms in a diverse panel of maize inbred lines. The “point” method involved penetrating the ear with a spore-coated toothpick and the “inundative” method introduced a liquid spore suspension under the husk of the ear. We evaluated quantitative and qualitative indicators of external and internal symptom severity as low-cost proxies for fumonisin contamination, and found that kernel bulk density was predictive of fumonisin levels (78 to 84% sensitivity; 97 to 99% specificity). Inundative inoculation resulted in greater disease severity and fumonisin contamination than point inoculation. We also found that the two inoculation methods implicated different ear tissues in defense, with cob morphology being a more important component of resistance under point inoculation. Across both inoculation methods, traits related to cob size were positively associated with disease severity and fumonisin content. Our work demonstrates that (i) the use of diverse modes of inoculation is necessary for combining complementary mechanisms of genetic resistance, (ii) kernel bulk density can be used effectively as a proxy for fumonisin levels, and (iii) trade-offs may exist between yield potential and resistance to fumonisin contamination.