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. 2018 Oct 17;50(3):413–418. doi: 10.21307/jofnem-2018-020

First Report of Bitylenchus hispaniensis, Pratylenchoides alkani, and Helicotylenchus vulgaris in Association with Cultivated and Wild Olives in Crete, Greece and Molecular Identification of Helicotylenchus microlobus and Merlinius brevidens

Emmanuel A Tzortzakakis 1, Carolina Cantalapiedra-Navarrete 2, Maria Kormpi 3, Maria S Lazanaki 1, Pablo Castillo 2, Antonio Archidona-Yuste 2,*
PMCID: PMC6909313  PMID: 30451424

Abstract

Nematode samplings in cultivated and wild olive in Crete, Greece, yielded the presence of Bitylenchus hispaniensis, Helicotylenchus microlobus, Helicotylenchus vulgaris, Merlinius brevidens, and Pratylenchoides alkani. With the exception of H. microlobus and M. brevidens, reports of these plant-parasitic nematode species constitute new records for Greece. Bitylenchus hispaniensis is also reported for first time in a country outside of Spain, where it was originally described. Pratylenchoides alkani is herein reported for the second time in the Mediterranean area and for the first time in association with olive. Two further populations of H. microlobus and H. vulgaris, from walnut and goji berry from Greece, were identified. Molecular data for all of these nematode species are provided, resulting in the first integrative identification of these Greek populations.

Keywords: 28S rRNA, Detection, New geographic record, ITS

Olive (Olea europaea subsp. europaea L.) is the most common crop on the island of Crete, Greece, while clusters of wild olives (Olea europaea subsp. sylvestris L.) are located also in several non-agricultural areas (Tzortzakakis et al., 2014). Surveys for detection of plant-parasitic nematodes were conducted on both cultivated and wild olives during the period 2013 to 2015. Soil samples were collected with a hoe, discarding the upper 5-cm top soil profile, from 5 to 40 cm depth in the close vicinity of active roots from 2 to 5 olive trees randomly chosen in each from 146 orchards. Similarly, soil samples were also collected from the rhizosphere of individual 36 wild olives distributed in various areas. Furthermore, three additional soil samples, where populations of Helicotylenchus were detected, were included in this study. One sample was from pots where cultivated olive stock plants were maintained for research purposes (Institute of Olive Tree, Subtropical Crops, and Viticulture, Chania, Crete), the second from the roots of walnut (Juglans regia L.) in Evia, Greece, and the third from the roots of goji berry (Lycium barbarum L.) in Thessaly, Greece. Nematodes were extracted from several soil samples of 500 g by the wet-sieving and decanting method (Cobb, 1918). Additional samples were collected later from the same sampling sites to obtain sufficient specimens for morphological and molecular identification. Specimens to be observed under light microscopy (LM) were heat killed by adding hot 4% formaldehyde solution and were processed to pure glycerin using De Grisse’s (1969) method. Microscopical observations were carried out using a Zeiss III compound microscope with Nomarski differential interference contrast at up to ×1,000 magnification. Diagnostic measurements were made using a drawing tube attached to the microscope. Specimens for molecular analysis were preserved in DESS (Yoder et al., 2006). Here, we report five species as identified by morphological and molecular analyses of females: Bitylenchus hispaniensis (Handoo et al., 2014); Helicotylenchus microlobus (Perry et al., 1959); Helicotylenchus vulgaris (Yuen, 1964); Merlinius brevidens (Allen, 1955; Siddiqi, 1970); and Pratylenchoides alkani (Yüksel, 1977; Table 1, Fig. 1). These plant-parasitic nematode species, except H. microlobus and M. brevidens, are new records for Greece. The morphology and morphometry of the isolated nematode species (Table 2) agreed with original and previous descriptions of them, except for minor intraspecific differences (Koliopanos and Vovlas, 1977; Castillo and Gómez Barcina, 1988; Ghaderi et al., 2014; Subbotin et al., 2015; Azizi et al., 2016). Nematode DNA was extracted from single individuals and PCR assays were conducted as described by Castillo et al. (2003). Primers and PCR conditions used in this research were specified in Cantalapiedra-Navarrete et al. (2013), and single amplicons of 800 bp and 1,100 bp in length was obtained by sequencing of the D2-D3 expansion segments of 28S and of ITS rRNA genes, respectively. Sequence alignments for D2-D3 from the Cretan B. hispaniensis, which showed 99 to 100% similarity (differing in 0 to 1 bp, 0 indels) to the Spanish type population, were deposited in NCBI GenBank (accession numbers MG770479, KJ461547, and KJ461545, respectively). The H. microlobus populations from cultivated olive from Crete and walnut from Evia (MG770480–MG770482) showed 99% similarity (differing in 1 to 6 bp, 0 indels) with H. microlobus (KM506793–KM506800) and Helicotylenchus pseudorobustus populations (HM014264, KU722387) deposited in the NCBI. ITS from populations of H. microlobus (MG770406–MG770408) showed 98 to 99% similarity (differing in 13 to 18 bp, 9 indels) to H. microlobus populations (KM506864–KM506867) and only 93% similarity (differing in 68 to 69 bp, 26 indels) to H. pseudorobustus populations (KM506875 and KM506880), which agree with previous data by Subbotin et al. (2015) and which confirmed the integrative diagnosis of our specimens. Similarly, the H. vulgaris populations from wild and cultivated olive, Crete and goji berry, Thessaly (MG770483–MG770484) showed 99 to 100% similarity (differing in 0 to 4 bp, 0 indel) with H. vulgaris populations (FJ485650, KU722388, DQ328759–DQ328761) deposited in NCBI. Intraspecific variability for D2-D3 was low for H. microlobus and H. vulgaris (differing in 5 to 7 bp, 1 indels, and 1 bp, 0 indels, respectively). The D2-D3 sequence of the Cretan population of M. brevidens (MG770485) showed 99% similarity (differing in 4 to 9 bp, 0 to 1 indel) to M. brevidens populations (KJ585416, KP313844, and KP313847). Finally, the D2-D3 28 S expansion segment from the Cretan populations of P. alkani (MG770486) showed 99% similarity to P. alkani (JX261953 and JX261962) and Pratylenchoides ritteri populations (KP313850 and KU855004) (differing in 2–4 bp, 1 to 2 indels, and 4–9 bp, 1–2 indels, respectively). These data support previous suggestions for synonymizing P. alkani and P. ritteri, as suggested by some other researchers (Brzeski, 1998; Karegar, 2006; Ghaderi and Karegar, 2014; Ghaderi et al. 2014; Azizi et al., 2016). Nevertheless, additional studies with other ribosomal and mitochondrial markers on topotype populations of both species are needed to clarify whether the two taxa are conspecific or cryptic species.

Table 1.

Sequenced genes pf plant-parasitic nematodes sampled from cultivated and wild olive in Crete and two other hosts in Evia and Thessaly, Greece.

Nematode species Sample code Host and Locality D2-D3 ITS
Bitylenchus hispaniensis OLI106 Cultivated olive, Episkopi, Crete MG770479 –
B. hispaniensis OLI013 Cultivated olive, Roufas, Crete * –
B. hispaniensis OLE011 Wild olive, Trypiti, Crete *
B. hispaniensis OLE015 Wild olive, Lentas, Crete * –
B. hispaniensis OLE023 Wild olive, Ag. Ioannis, Crete * –
B. hispaniensis OLE029 Wild olive, Ag. Georgios, Crete * –
B. hispaniensis OLE032 Wild olive, Tsoutsouros, Crete * –
Helicotylenchus microlobus OLI066 Cultivated olive, Vori, Crete MG770480 MG770406
H. microlobus OLI002 Cultivated olive, Vori, Crete * –
H. microlobus OLI074 Cultivated olive, Vori, Crete * –
H. microlobus POT017 Potted cultivated olive, Chania, Crete MG770481 MG770407
H. microlobus WAL17 Walnut, Evia, Greece MG770482 MG770408
Helicotylenchus vulgaris OLI004 Cultivated olive, Petrokefali, Crete MG770483 –
H. vulgaris OLI005 Cultivated olive, Petrokefali, Crete * –
H. vulgaris OLI046 Cultivated olive, Gonies, Crete * –
H. vulgaris OLI055 Cultivated olive, Voutes, Crete * –
H. vulgaris OLI071 Cultivated olive, Pentamodi, Crete * –
H. vulgaris OLI129 Cultivated olive, Perama, Crete * –
H. vulgaris OLE026 Wild olive, Agiofarago, Crete * –
H. vulgaris GOBERR Goji berry, Thessaly, Greece MG770484 –
Merlinius brevidens a OLI106 Cultivated olive, Episkopi, Crete MG770485 –
M. brevidens OLE009 Wild olive, Kefali, Crete * –
Pratylenchoides alkani b OLI060 Cultivated olive, Sivas, Crete MG770486 –
P. alkani OLI111 Cultivated olive, Amygdali, Crete * –
P. alkani OLE007 Wild olive, Vathy, Crete * –
P. alkani OLE017 Wild olive, Agiofarago, Crete * –
P. alkani OLE018 Wild olive, Agiofarago, Crete * –
P. alkani OLE031 Wild olive, Listis, Crete * –
P. alkani OLE032 Wild olive, Tsoutsouros, Crete * –
P. alkani OLE036 Wild olive, Agiofarago, Crete * –
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Notes: (*) Sequenced population but not deposited in GenBank database because of its high similarity with previously deposited sequences.

(−) Not obtained.

aFound in 29 further cultivated olive samples (OLI007, OLI010, OLI030, OLI031, OLI033, OLI050, OLI051, OLI066, OLI070, OLI071, OLI080, OLI084, OLI086, OLI097, OLI100, OLI102, OLI103, OLI104, OLI105, OLI108, OLI110, OLI111, OLI114, OLI129, OLI131, OLI134, OLI135, OLI142, and OLI146) and in nine further wild olive samples (OLE011, OLE013, OLE015, OLE021, OLE027, OLE028, OLE029, OLE030, and OLE032).

bMay be a junior synonym of P. ritteri, as supported by phylogenetic analyses by Azizi et al. (2016) and noted by some other researchers (Brzeski, 1998; Ghaderi and Karegar, 2014; Ghaderi et al., 2014).

Fig. 1.

Fig. 1

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Geographic distribution of plant-parasitic nematodes of the genera Bitylenchus, Helicotylenchus, Merlinius and Pratylenchoides in field survey of cultivated and wild olive in Crete, Greece. Numbers of samples for each nematode species are as follows: Bitylenchus hispaniensis (seven samples), Helicotylenchus microlobus (three samples), Helicotylenchus vulgaris (seven samples), Merlinius brevidens (40 samples) and Pratylenchoides alkani (eight samples). 44 sites are presented, as some samples were derived from spatially close (encircled) areas and may therefore not be independent populations.

Table 2.

Morphometrics of Bitylenchus hispaniensis (Handoo, et al., 2014); Helicotylenchus microlobus (Perry et al., 1959); Helicotylenchus vulgaris (Yuen, 1964); Merlinius brevidens (Allen, 1955; Siddiqi, 1970); and Pratylenchoides alkani (Yüksel, 1977) from olive in Crete, Greecea.

B. hispaniensis H. microlobus H. vulgaris M. brevidens P. alkani
Episkopi Vori Petrokefali Episkopi Sivas
Characters/ratiosb Females Females Females Females Females
n 3 4 3 3 3
L 722 ± 47 (670–760) 652 ± 31 (609–680) 672 ± 35 (634–702) 564 ± 116 (490–698) 907 ± 69.1 (840–978)
a 32.3 ± 0.6 (31.9–33.0) 25.4 ± 1.6 (24.2–27.7) 30.6 ± 0.4 (30.2–31.0) 26.3 ± 3.8 (22.9–30.3) 35.3 ± 0.8 (34.7–36.2)
B 6.3 ± 0.4 (6.1–6.8) 4.5 ± 0.4 (4.1–4.9) 5.1 ± 0.02 (5.1–5.2) 4.4 ± 0.6 (4.0–5.1) 6.7 ± 0.2 (6.4–6.8)
C 14.9 ± 0.6 (14.4–15.5) 43.7 ± 8.4 (35.8–55.4) 48.1 ± 1.1 (46.8–48.8) 14.3 ± 2.4 (12.9–17.0) 16.7 ± 0.2 (16.5–16.9)
c′ 3.0 ± 0.2 (2.7–3.2) 1.1 ± 0.2 (0.9–1.4) 1.1 ± 0.0 (1.1–1.1) 3.0 ± 0.1 (2.9–3.2) 3.1 ± 0.2 (2.8–3.2)
V 55.0 ± 1.0 (54.0–56.0) 61.2 ± 1.6 (59.3–63.2) 64.0 ± 2.0 (62.0–66.0) 54.7 ± 3.1 (52.0–58.0) 52.7 ± 1.5 (51.0–54.0)
Stylet length 17.3 ± 0.3 (17.0–17.5) 26.4 ± 1.2 (25.0–28.0) 24.0 ± 1.0 (23.0–25.0) 14.3 ± 1.5 (13.0–16.0) 23.7 ± 0.6 (23.0–24.0)
Pharynx length 114.0 ± 5.3 (110–120) 145.5 ± 7.0 (139–153) 130.7 ± 6.8 (123–136) 127.7 ± 7.2 (123–136) 135.7 ± 11.2 (123–144)
Max. body diam. 22.3 ± 1.2 (21.0–23.0) 25.7 ± 1.5 (24.0–27.0) 22.0 ± 1.0 (21.0–23.0) 21.3 ± 2.1 (19.0–23.0) 25.7 ± 1.5 (24.0–27.0)
Anal body diam. 16.5 ± 2.2 (14.0–18.0) 14.1 ± 1.4 (12.5–16.0) 13.0 ± 1.0 (12.0–14.0) 13.0 ± 1.0 (12.0–14.0) 17.7 ± 0.6 (17.0–18.0)
Tail 48.3 ± 3.1 (45.0–51.0) 15.3 ± 2.4 (12.0–17.0) 14.0 ± 1.0 (13.0–15.0) 39.3 ± 1.5 (38.0–41.0) 54.3 ± 3.5 (51.0–58.0)
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aMeasurements are in µm and in the form of mean ± SD (range).

bAbbreviations are defined in Siddiqi (2000).

Bitylenchus hispaniensis was found in two fields of cultivated olives and five of wild olives in Crete with low population density (1–10 nematodes per 500-cm3 soil). The species is widespread in both cultivated and wild olives in Spain (Handoo et al., 2014; Palomares-Rius et al., 2015), and our report provides the second record of this species for the country. Helicotylenchus microlobus and H. vulgaris are common species in the Mediterranean area (Subbotin et al., 2015; Palomares-Rius et al., 2015). In Crete, low population densities (2–17 nematodes per 500-cm3 soil) of both species were detected in cultivated olive (three fields for H. microlobus and six for H. vulgaris) and the former also in walnut (150 nematodes per 500-cm3 soil, Evia, Greece) and the latter in one wild olive sample (Crete) and one goji berry sample (50 nematodes per 500-cm3 soil, Thessaly, Greece). Helicotylenchus microlobus was previously found in olive in Greece (Hirschmann et al., 1966), but H. vulgaris, despite being a quite common species in Mediterranean area, was not previously reported from Greece. According to our sampling, Merlinius brevidens has a wide distribution in both cultivated (30 fields) and wild (10 plants) olives in Crete with low population density (2–12 nematodes per 500-cm3 soil). It is a cosmopolitan species and has been already reported in olive and pear in Greece (Hirschmann et al., 1966; Koliopanos and Vovlas, 1977) as well as from olive in Cyprus and Spain (Philis and Siddiqi, 1976; Palomares-Rius et al., 2015). Pratylenchoides alkani was found in two fields with cultivated olive and from six wild olives in Crete with low population density (1–22 nematodes per 500-cm3 soil). It was originally described from snap bean in Turkey (Yüksel, 1977), with wheat and almond tree in Iran (Taheri et al., 2013; Ghaderi et al., 2014), and in the only Mediterranean record of it, P. alkani was associated with Aleppo pine (Pinus halepensis L.) in Spain (Castillo and Gómez Barcina, 1988). Thus, the occurrence of this nematode in Crete is the second report for the Mediterranean area and the first one indicating an association of the nematode with cultivated and wild olives.

Acknowledgments

This research was partially funded by grant KBBE 219262 ArimNET-ERANET FP7 2012 to 2015 Project PESTOLIVE “Contribution of olive history for the management of soilborne parasites in the Mediterranean basin” from the Hellenic Agricultural Organization-DEMETER and Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), grant AGR-136 from “Consejería de Economía, Innvovación y Ciencia” from Junta de Andalucía, and Union Europea, Fondo Europeo de Desarrollo regional, “Una manera de hacer Europa.” Maria S. Lazanaki was employed by the ARIMNET-PESTOLIVE project. The authors thank J. Martín Barbarroja and G. León Ropero from IAS-CSIC for the excellent technical assistance, and anonymous reviewers and editor for their helpful suggestions.

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