The genus Meloidogyne is one of the most economically damaging plant parasitic nematodes on a worldwide basis. To date, only the dragon fruits in Brazil were reported infected by M. javanica or M. incognita in previous surveys. From 2019–2021, we conducted our investigation in 62 orchards from 10 counties of Hainan, which are the main producing areas of dragon fruits in China. The collected roots were visually scored by gall index to evaluate the distribution and severity of diseases caused by Meloidogyne. Then, the isolated nematodes were further confirmed by a combination of morphological and molecular analysis. This survey revealed that the root-knot nematodes were widely distributed in red dragon fruit planting areas in Hainan and caused severe symptoms including stunting, wilting, and yellowing of the stems. The nematode populations were identified as M. enterolobii and M. javanica, among which, M. enterolobii accounted for a larger proportion, 93.9%. To our knowledge, this is the first report of M. enterolobii causing diseases on red dragon fruit. The results obtained from this survey will provide an insight into the presence of root-knot nematodes in dragon fruit plants. Also, these results will raise attention for developing effective management strategies to prevent further spread of root-knot nematodes on dragon fruit in Hainan.

Early detection of pathogens before the planting season is valuable to forecast disease occurrence. Therefore, rapid and reliable diagnostic approaches are urgently needed, especially for one of the most aggressive root knot nematodes, Meloidogyne enterolobii. In this study, we developed a novel primer–TaqMan probe set aimed at M. enterolobii. The primer–probe set was successfully applied in the identification and quantification of M. enterolobii via qPCR technology. It was also suitable for improved PCR technology, known as ddPCR analyses, and this work presents the first application of this technology for plant parasitic nematodes. Compared with qPCR, ddPCR exhibited better performance with regard to analytical sensitivity, which can provide a more accurate detection of M. enterolobii concealed in field soil. In addition, we generated standard curves to calculate the number of eggs in soil using the qPCR and ddPCR platforms. Hopefully, the results herein will be helpful for forecasting disease severity of M. enterolobii infection and adopting effective management strategies.

Meloidogyne enterolobii, a highly pathogenic root-knot nematode species, causes serious damage to agricultural production worldwide. Collagen is an important part of the nematode epidermis, which is crucial for nematode shape maintenance, motility, and reproduction. In this study, we report that a novel collagen gene, Me-col-1, from the highly pathogenic root-knot nematode species Meloidogyne enterolobi was required for the egg formation of this pathogen. Me-col-1 encodes a protein with the size of 35 kDa, which is closely related to collagen found in other nematodes. Real-time PCR assays showed that the expression of Me-col-1 was highest in eggs and lowest in pre-parasitic second-stage juveniles (preJ2). Interestingly, knockdown of Me-col-1 did not compromise the survival rate of preJ2 but significantly reduced the egg production and consequentially caused 35.79% lower multiplication rate (Pf/Pi) compared with control. Our study provides valuable information for better understanding the function of collagen genes in the nematode life cycle, which can be used in the development of effective approaches for nematode control.

In November 2015, an unknown leaf spot was observed during a survey of Capsicum frutescens L.var.longum Bailey growing in Tanniu town of Wenchang City. Small water-soaked grayish spots were present on the infected leaves initially. Typical symptoms showed irregular dark-brown lesions surrounded by a black halo between veins. The infected leaves eventually became wilted and dry. Symptomatic tissues from the junction of diseased and healthy leaf tissue were surface sterilized in 70% ethanol for 30 s, 0.1% mercuric chloride solution for 1 min, and washed three times with sterile distilled water, then placed on potato dextrose agar plates, incubated at 28 ± 1°C. The cultures were initially gray-white and then developed from gray-brown to dark brown. The colonies developed straight or slightly curved brown conidiophores. Conidia were also brown, 7.0 to 14.5 × 13.1 to 26.8 μm (avg. 10.8 ×21.5 μm) (n= 200) with three septa, curved at the third cell from the base that is longest and darkest of the four cells. The...

The aim of this study was to determine the status of weed Solanum nigrum L. as a transitional host for Meloidogyne enterolobii and its effect on the population base of the nematodes in the next season. The nematode species infecting S. nigrum L. in a fallow field was identified by morphological identification and molecular diagnosis, and parasitic characteristics of the nematodes in S. nigrum L., including development of the nematode in S. nigrum L., the histopathological response of S. nigrum L. to M. enterolobii, and the host suitability of S. nigrum L., were studied. The M. enterolobii soil population density was evaluated before and after S. nigrum L. planting. Species identification revealed that it was M. enterolobii infection. Developmental observation indicated that juveniles of M. enterolobii developed fast in S. nigrum L., establishing feeding sites by 5 days after inoculation (DAI) and forming obvious egg masses on the root at 25 DAI. Histopathological observation showed the typical susceptible response of S. nigrum L., including giant cells with thick cell walls, uniformly dense cytoplasm, and less vacuolation, mainly inside the vascular cylinder. Host suitability assays suggested that S. nigrum L. is a good host for M. enterolobii with an average reproduction factor (RF) of 48.04 ± 14.71. Population densities assays revealed that S. nigrum L. increased the population density of M. enterolobii for two consecutive years from 0.48 ± 0.25 and 0.53 ± 0.31 J2/cm³ to 1.33 ± 0.16 and 1.56 ± 0.43 J2/cm³ of soil. These results indicated that M. enterolobii could reproduce well by infecting S. nigrum L. during the fallow season, and it increased the population base of M. enterolobii to the next season during vegetable production, which suggested a novel direction for the control of root-knot nematodes by controlling weeds as transitional hosts of M. enterolobii in the fallow season.