Article 59 – ‘New diseases’ 1.
Hi welcome to Taiga Bonzai, in this post we discuss the outbreak of new diseases recently found in 2024.
Introduction – according to Wiley on behalf of the British Society for Plant Pathology. New Disease Reports provide a platform for publication of significant new and emerging plant disease outbreaks. These, cover diseases caused by bacteria, fungi, nematodes, oomycetes, phytoplasmas, viruses and viroids.
They state that “We aim to provide a repository for such records to support the work of field advisers, diagnosticians, researchers, and plant health policy makers. We are proud to be a fully open access journal, published by Wiley on behalf of the British Society for Plant Pathology.“
https://bsppjournals.onlinelibrary.wiley.com/journal/20440588
According to P. Kong, R. Ioos and C. X. Hong in their New Disease Reports Volume 49, Issue 2 e12278. ‘First report of ‘Calonectria henricotiae’ that causes ‘box blight’ in Spain first published: 02 May 2024 https://doi.org/10.1002/ndr2.12278.
Box blight – is caused by two closely related fungi, Calonectria pseudonaviculata (Cps) and/or C. henricotiae (Che) (Gehesquière et al., 2016). Cps is widespread globally (Daughtrey, 2019) while Che is limited to eight central European countries. (Hong, 2023) To determine whether Che is present in southern Europe, we visited ten large boxwood gardens and street plantings in Madrid and Toledo, Spain and in Bordeaux, Lyon and Sainte-Foy-la-Grande, France.
Boxwood Buxus spp. twigs with black streaks were only observed in Madrid, Toledo, and Sainte-Foy-la-Grande. Diseased twigs were collected in sealed triple bags and brought to the laboratory under the USDA permit. (P526P-21-05960)
After surface sterilization with 10% bleach for two minutes and three rinses in deionised water, twigs were placed on a mesh with wet paper towels underneath in closed plastic containers at 23°C. They were sprayed with sterile distilled water every two days until white mould appeared on leaves. The mould was suspended in 15 µL sterile distilled water then transferred onto a glass slide for microscopy.
Following observations of rod-shaped conidia, typical of Calonectria spp., 1-µL drops of the suspensions were pipetted from slides onto acidified potato dextrose agar (PDA) for isolation (Kong et al., 2023). Clean colonies were only obtained from the Madrid and Sainte-Foy-la-Grande samples and were sub-cultured on regular PDA.


Colony PCR (Kong et al., 2005) was performed from a total of 159 colonies grown from three-day PDA cultures, using Cps– and Che-specific primers (Guo & Pooler, 2021). Also included in the PCR were three French isolates from the ANSES collection: LSVM0960 collected by Department Île-de-France in 2013, LSVM1007 by Department Meurthe-et-Moselle in 2014, and LSVM1235 by Department Finistère in 2015.
All 99 isolates from Spain were identified as Che while 63 isolates from France were Cps. Seven Spanish and nine French isolates were sub-cultured in potato dextrose broth for DNA extraction. Their identities were confirmed by PCR of the DNA and PCR product sequencing (GenBank Accession Nos. PP632113-19 For Che isolates and PP632120-28 for Cps isolates) with the same primer pairs.
The same isolates were tested for temperature tolerance. The Spanish isolates had an average colony diameter of 1.6 cm in PDA at 28.5°C for 10 days, while the French isolates did not grow under the same conditions, further confirming their identities (Gehesquière et al., 2016)
To our knowledge, this is the first report of Calonectria henricotiae causing box blight in Spain. Knowing the actual distribution of the fungus is critical to preventing its further spreading to other countries and areas currently not affected by this pathogen, promoting safe plant trade.
This work was funded by the USDA National Institute of Food and Agriculture – Specialty Crop Research Initiative (2020-51181-32135).
New Disease Reports – Volume 49, Issue 2 e12265 ‘Current epidemiological situation of mealybug wilt of pineapple disease in Ecuador’. J. F. Cornejo-Franco, A. Olmedo-Velarde, D. F. Quito-Avila. First published 02 April 2024.
https://doi.org/10.1002/ndr2.12265
Mealybug wilt of pineapple (MWP) is the most important virus-associated syndrome affecting pineapple worldwide. The wide range of symptoms including bronze-to-red colouring of leaves, tip dieback, leaf downward-curving and wilting has obscured the aetiology of MWP. (Dey et al., 2018) At least five ampeloviruses (family Closteroviridae), Pineapple mealybug wilt-associated virus 1 (PMWaV-1), PMWaV -2, -3, -5 and -6 have been associated with MWP.
Recently, additional viruses have been reported in pineapple including, Pineapple secovirus A (PSV-A), PSV-B, -C, and -D, all members of the Sadwavirus genus (family Secoviridae), Pineapple bacilliform CO virus (PBCOV) and Pineapple bacilliform ER virus. (PBERV)
These are both members of the Badnavirus genus family Caulimoviridae (Larrea-Sarmiento et al., 2022). In Ecuador, PMWaV-1 is the only virus reported from plants showing MWP-like symptoms. (Alvarez-Quinto et al., 2015) This study aimed to determine the prevalence of MWP and the viruses potentially associated with the disease in the largest pineapple-producing area of Ecuador.
In 2023, a total of 400 pineapple MD-2 hybrid plants were randomly sampled and inspected for disease symptoms to estimate the prevalence of MWP in a planting located in Santo Domingo, Ecuador (Figure. 1). Sampling was done in 36-week-old fields. Only 30 plants (8%) showed the typical tip dieback symptoms characteristic of MWP and these were found on the edge of plantations. Virus testing was done on all symptomatic plants (n = 30) and also on 30 symptomless plants.
Total RNA extraction and RT-PCR for virus testing was done as described by Cornejo-Franco et al. (2023) using primers and PCR conditions detailed by Larrea-Sarmiento et al. (2022) and Alvarez-Quinto et al. (2015). Virus identity was confirmed by Sanger sequencing of cloned amplicons (GenBank Accession Nos. PP479943, PP479944, PP489387-PP489390)

Virus indexing showed a strong association between the observed MWP symptoms and co-infections of PMWaV-2 and PMWaV-1 (73%), while single infections of these two viruses were also found (<53%) in symptomless plants. PMWaV-3 and PSV-B were found in both symptomatic and symptomless plants in similar proportions, while PSV-A was detected in one third of symptomatic and 13% of symptomless plants.
PBCOV was found in 20% of symptomatic plants. All viruses showed high nucleotide identity (>95%) with Hawaiian homologs, except for PSV-A and -B which showed <88% nucleotide identity. No clear association was observed between the occurrence of PMWaV-3, PSV-A, PSV-B, or PBCOV and MWP PMWaV-5 and -6, PSV-C and -D and PBERV were not detected during this study.
Pineapple mealybugs (Dysmicoccus spp.) were present in all pineapple plants sampled in this study. Hence, the aetiology of MWP remains to be further studied. These findings are consistent with those previously reported in Hawaii, where PMWaV-2 and mealybugs were present on plants with MWP symptoms. (Sether et al., 2002)
This study was funded by Centro de Investigaciones Biotecnológicas del Ecuador, CIBE, through a seed funding call, under project code CIBE-0004-2023. The authors would like to thank Mr. Jhonny España from Cibe for field assistance.
As we have often stated pests and disease are not only spread via wind and wing they are distributed by mankind as well. Now the globe has shrunk due to the various modes of transportation, which is a free ‘ticket’ to ride, pests and diseases are on the increase. This problem is getting worse with no way to sustain or permanently eradicate it’s onslaught.
Plants that are vulnerable will quickly perish, because their defence mechanisms are inadequate moreover, countless pests and disease are immune to many pesticides and fungicides and other chemical compounds. In the next article we look at some more diseases of 2024, until next time, BW, Nik.


