Abstract:The tomato potato psyllid (TPP) Bactericera cockerelli (Hemiptera Triozidae) was first notified to the New Zealand Ministry of Agriculture and Forestry (MAF) in May 2006 although it has been suggested by several authors to have been present in New Zealand in 2005 MAF undertook an entry pathway analysis during the initial investigation into TPP in 2006 TPP is a vector of the bacteriumlike pathogen Candidatus Liberibacter solanacearum (liberibacter) and MAF further analysed the entry pathway of TPP during the li… Show more
“…The TPP is a phloem feeder, with a wide range of hosts (Wallis, 1951;Martin, 2008;Thomas et al, 2011) within the families Solanaceae, Convolvulaceae, and Laminaceae (Martin, 2008;Thomas et al, 2011). Its feeding on host plants is highly associated with Lso transmission (Butler et al, 2011;Levy et al, 2011).…”
The tomato potato psyllid (TPP), Bactericera cockerelli (Sulc) (Hemiptera: Triozidae), is the main vector of the bacterium Candidatus Liberibacter solanacearum (Lso), a major disease of solanaceous crops. Feeding of TPP is associated with Lso transmission. However, very little is known about the stylet penetration activities linked to acquisition and inoculation of Lso. The electrical penetration graph (EPG)‐DC system was used to monitor stylet penetration activities during acquisition and inoculation of Lso by individual TPP on tomato [Solanum lycopersicum L. (Solanaceae)]. Female TPP from Lso‐free and Lso‐infected colonies were used in acquisition and inoculation tests, respectively. In the acquisition tests, TPP were tested for Lso after EPG recording of their stylet penetration activities on Lso‐infected tomato shoots. In the inoculation tests, samples from the tomato plants on which the stylet penetration of Lso‐infected TPP had been recorded were tested for Lso infection. The relationships between qPCR results and the EPG waveforms (C, G, D, E1, and E2) representing the main stylet penetration activities performed by individual insects in inoculation and acquisition tests were investigated. Results confirmed that a single adult TPP is capable of infecting a plant with Lso. Our data suggest that acquisition of the bacteria occurs during phloem ingestion (E2), and inoculation is likely associated with salivation into the phloem sieve elements (E1). The durations of EPG parameters were not significantly different between Lso‐infected and Lso‐free TPP (later shown by qPCR) in acquisition tests. In inoculation tests, the durations of E1 or E2 recorded from TPP on Lso‐infected and Lso‐free plants that were later shown by qPCR were not significantly different. However, C was shorter on Lso‐infected plants than on Lso‐free plants, where TPP performed phloem activities. The minimum plant access period required for Lso transmission by a single TPP was estimated to be ca. 2 h, with an acquisition threshold of about 36 min.
“…The TPP is a phloem feeder, with a wide range of hosts (Wallis, 1951;Martin, 2008;Thomas et al, 2011) within the families Solanaceae, Convolvulaceae, and Laminaceae (Martin, 2008;Thomas et al, 2011). Its feeding on host plants is highly associated with Lso transmission (Butler et al, 2011;Levy et al, 2011).…”
The tomato potato psyllid (TPP), Bactericera cockerelli (Sulc) (Hemiptera: Triozidae), is the main vector of the bacterium Candidatus Liberibacter solanacearum (Lso), a major disease of solanaceous crops. Feeding of TPP is associated with Lso transmission. However, very little is known about the stylet penetration activities linked to acquisition and inoculation of Lso. The electrical penetration graph (EPG)‐DC system was used to monitor stylet penetration activities during acquisition and inoculation of Lso by individual TPP on tomato [Solanum lycopersicum L. (Solanaceae)]. Female TPP from Lso‐free and Lso‐infected colonies were used in acquisition and inoculation tests, respectively. In the acquisition tests, TPP were tested for Lso after EPG recording of their stylet penetration activities on Lso‐infected tomato shoots. In the inoculation tests, samples from the tomato plants on which the stylet penetration of Lso‐infected TPP had been recorded were tested for Lso infection. The relationships between qPCR results and the EPG waveforms (C, G, D, E1, and E2) representing the main stylet penetration activities performed by individual insects in inoculation and acquisition tests were investigated. Results confirmed that a single adult TPP is capable of infecting a plant with Lso. Our data suggest that acquisition of the bacteria occurs during phloem ingestion (E2), and inoculation is likely associated with salivation into the phloem sieve elements (E1). The durations of EPG parameters were not significantly different between Lso‐infected and Lso‐free TPP (later shown by qPCR) in acquisition tests. In inoculation tests, the durations of E1 or E2 recorded from TPP on Lso‐infected and Lso‐free plants that were later shown by qPCR were not significantly different. However, C was shorter on Lso‐infected plants than on Lso‐free plants, where TPP performed phloem activities. The minimum plant access period required for Lso transmission by a single TPP was estimated to be ca. 2 h, with an acquisition threshold of about 36 min.
“…Long distance transport of different life stages of this insect pest is possible, particularly by commercial trade of plants in the family Solanaceae, which constitute major hosts for B. cockerelli. This insect was introduced into New Zealand, and was proabably transported with plant material from Western USA, possibly as eggs Thomas et al, 2011). Entry on fruit of host species (e.g.…”
“…Bactericera cockerelli most likely entered New Zealand as a result of smuggling psyllid‐infected primary host material (possibly chilli peppers) from the Americas, rather than through the accidental transportation on consignments of fresh produce through regulated pathways (Thomas et al . ). How B. cockerelli arrived in Norfolk Island is presently unknown (Anon.…”
Section: Introductionmentioning
confidence: 97%
“…Given the geographical distance between New Zealand and areas known to be infested with B. cockerelli in the Americas, and lack of records of psyllids established on islands in between, it is unlikely that B. cockerelli entered New Zealand by dispersing on the wind (Thomas et al . ). However, long‐distance migration by a psyllid is not unknown as the leucaeana psyllid ( Heteropsylla cubana Crawford) is thought to have spread naturally from Central America through to Asia and onto eastern Africa on air currents via several islands in between including Hawaii, Western Samoa, Fiji, the Philippines, New Guinea, Indonesia, Mauritius and Reunion (Bray ; Thomas et al .…”
Section: Introductionmentioning
confidence: 97%
“…Current evidence suggests that the B. cockerelli present in New Zealand originated from the western range of the psyllid in North and/or Central America (Thomas et al . ) from the invasive biotype rather than the native biotype.…”
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