Andrew Kiggundu

Andrew Kiggundu

Biotechnology, National Agricultural Research Organisation (NARO), Entebbe, Wakiso, Uganda

Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

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

Representative Publications

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1 November 2019 in Phytopathology®
Verified
Journal Article
Open access
AAAbdulwahab Abdurahman
Abdulwahab Abdurahman
MPMonica L. Parker
Monica L. Parker
JKJan Kreuze
Jan Kreuze
JEJohn G. Elphinstone
John G. Elphinstone
Paul C. StruikPaul C. Struik
Paul C. Struik
KSKalpana Sharma
Kalpana Sharma
Bacterial wilt (BW) caused by the Ralstonia solanacearum species complex (RSSC) is a serious threat to potato production in Uganda. However, little is known about the extent of the disease and the type of the pathogen strains involved. A nationwide survey was conducted to study BW prevalence and incidence in potato, and potato tuber and stem samples of potential alternative hosts were collected for pathogen isolation. DNA was extracted from pure cultures for genetic diversity studies. The pathogen was phylotyped by multiplex PCR; then, a subset of isolates was typed at sequevar level. Isolates of the same sequevar were then haplotyped using multilocus tandem repeat sequence typing (TRST) schemes. BW prevalence and incidence in potato farms were 81.4 and 1.7%, respectively. Three RSSC phylotypes were identified, with the majority of the strains belonging to Phylotype II (80%) followed by Phylotype I (18.5%) and III (1.5%). Phylotype I strains belonged to Sequevar 31, and Phylotype II strains belonged to Sequevar 1. Potato-associated Phylotype II Sequevar 1 strains were more diverse (27 TRST haplotypes) than nonpotato Phylotype I (5 TRST haplotypes). Mapping of TRST haplotypes revealed that three TRST haplotypes of Phylotype II Sequevar 1 strains play an important epidemiological role in BW of potato in Uganda being disseminated via latently infected seed. [ ] Copyright © 2019 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license .

16 July 2019 in BMC Research Notes
Verified
Journal Article
Open access
PDF file
STSamuel Tuhaise
Samuel Tuhaise
JNJesca L. Nakavuma
Jesca L. Nakavuma
JAJohn Adriko
John Adriko
KSKenneth Ssekatawa
Kenneth Ssekatawa
Andrew KiggunduAndrew Kiggundu
Andrew Kiggundu
ObjectivePassion fruit improvement efforts by conventional breeding have had limited success calling for research into alternative approaches such as tissue culture and genetic engineering. An efficient and reproducible regeneration system is a prerequisite for successful genetic engineering. Currently, there is no reliable regeneration system for Uganda's passion fruit varieties owing to the high heterogeneity of the Passiflora genus. Therefore, this study aimed at establishing an efficient and reproducible regeneration system for Uganda's Passiflora edulis f. flavicarpa (yellow passion fruit) and Passiflora edulis f. edulis (purple passion fruit) for routine utilization with an ultimate goal of improving its agronomic value.ResultsThe study successfully induced shoots by both direct and indirect organogenesis for the yellow passion fruit variety. Highest shoot induction frequency (14.85%) was achieved on 8.9 mu M BAP while 7.9 mu M BAP did not initiate any shoots. Optimal shoot elongation and rooting was achieved on 0.44 mu M BAP and 5.37 mu M alpha-naphthaleneacetic (NAA) respectively. Rooted yellow passion fruit plantlets were successfully weaned with over 65% survival rates. It took approximately 6months to produce a weaned healthy passion fruit plant. The purple passion fruit variety proved to be recalcitrant to tissue culture with no successful shoot or callus induction.