life Article Occurrence and Geographic Distribution of Plant-Parasitic Nematodes Associated with Citrus in Morocco and Their Interaction with Soil Patterns Btissam Zoubi 1,2,3, Fouad Mokrini 2,* , Abdelfattah A. Dababat 4,* , Mohammed Amer 5 , Cherki Ghoulam 3, Rachid Lahlali 6 , Salah-Eddine Laasli 7 , Khalid Khfif 8, Mustafa Imren 9, Oumaima Akachoud 3, Abderrazak Benkebboura 3, Abdelilah Iraqi Housseini 1 and Ahmed Qaddoury 3,* 1 Laboratory of Biotechnology, Environment, Agri-Food, and Health, Faculty of Sciences Dhar El Mahraz, Sidi Mohammed Ben Abdellah University, Fez 30050, Morocco; btissam.zoubi@usmba.ac.ma (B.Z.); abdellah.iraqihousseini@usmba.ac.ma (A.I.H.) 2 Biotechnology Unit, National Institute for Agricultural Research, INRA-Rabat, Rabat 10080, Morocco 3 Center of Agrobiotechnology and Bioengineering, Research Unit Labeled CNRST, Cadi Ayyad University, Marrakech 40000, Morocco; c.ghoulam@gmail.com (C.G.); akachoud.oumaima@gmail.com (O.A.); abderrazakbenkebboura@gmail.com (A.B.) 4 International Maize and Wheat Improvement Center (CIMMYT), Ankara 06810, Turkey 5 Department of Mechanical Engineering, National Yang Ming Chiao Tung University, Hsinchu 30010, Taiwan; mohammedamer.me03g@g2.nctu.edu.tw 6 Phytopathology Unit, Department of Plant Protection, Ecole Nationale d’Agriculture de Meknès, Meknes 50001, Morocco; rlahlali@enameknes.ac.ma 7 Laboratory of Botany, Mycology, and Environment, Faculty of Science, Mohammed V University, Rabat 10080, Morocco; laaslisalaheddine@gmail.com Citation: Zoubi, B.; Mokrini, F.; 8 Research Unit on Nuclear Techniques, Environment, and Quality, National Institute for Agricultural Research, Dababat, A.A.; Amer, M.; Ghoulam, INRA-Tangier, Tangier 90010, Morocco; khalid.khfif@inra.ma C.; Lahlali, R.; Laasli, S.-E.; Khfif, K.; 9 Department of Plant Protection, Faculty of Agriculture, Bolu Abant Izzet Baysal University, Imren, M.; Akachoud, O.; et al. Bolu 14030, Turkey; mustafaimren@ibu.edu.tr Occurrence and Geographic * Correspondence: fmokrini.inra@gmail.com (F.M.); a.dababat@cgiar.org (A.A.D.); Distribution of Plant-Parasitic qadahmed@gmail.com (A.Q.) Nematodes Associated with Citrus in Morocco and Their Interaction with Abstract: Plant-parasitic nematodes (PPNs) are found in citrus plantations throughout the world, but Soil Patterns. Life 2022, 12, 637. they are considered to be the most problematic pest in Morocco. Citrus fruit quality and yield have https://doi.org/10.3390/life been adversely affected by PPNs. Due to data unavailability of nematodes associated with citrus, a 12050637 detailed survey was conducted in the main citrus-growing regions of Morocco during 2020–2021 to assess the occurrence, distribution, and diversity of PPNs associated with rhizospheres of citrus trees. Academic Editors: Fengjuan Pan, In addition, some soil properties have also been assessed for their impact on soil properties. Plant- Yanfeng Hu and Jingsheng Chen parasitic nematode diversity was calculated using two ecological indexes, the Shannon diversity Received: 17 March 2022 index (H′) and the Evenness index (E). The collected soil and root samples were analyzed, and Accepted: 23 April 2022 eleven genera and ten species of plant-parasitic nematodes were identified. The results show that Published: 25 April 2022 the most predominant PPN species were Tylenchulus semipenetrans (88%), Helicotylenchus spp. (75%), Publisher’s Note: MDPI stays neutral Pratylenchus spp. (47%), Tylenchus spp. (51%), and Xiphinema spp. (31%). The results showed that with regard to jurisdictional claims in PPN distributions were correlated with soil physicochemical properties such as soil texture, pH levels, published maps and institutional affil- and mineral content. Based on the obtained result, it was concluded that besides the direct effects iations. of the host plant, physicochemical factors of the soil could greatly affect PPN communities in citrus growing orchards. Keywords: citrus; diversity; Helicotylenchus spp.; nematodes; soil characteristics; Tylenchulus semipenetrans Copyright: © 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons 1. Introduction Attribution (CC BY) license (https:// Citrus (Citrus spp.) is considered one of the most extensively cultivated fruit crops creativecommons.org/licenses/by/ worldwide, specifically in tropical and sub-tropical areas [1]. Citrus production is dom- 4.0/). inated by major producing countries including the United States, China, Brazil, Mexico, Life 2022, 12, 637. https://doi.org/10.3390/life12050637 https://www.mdpi.com/journal/life Life 2022, 12, 637 2 of 17 India, and Spain, with a contribution of approximately 2/3 of the global production [2]. The latter reached 147 million tons in 2017 [2]. Morocco grows citrus as one of its most important fruit crops. The sector represents an important economic element for the coun- try, with an annual production of 1.5 to 2.0 million tons harvested from approximately 125,000 ha [1]. Additionally, the citrus industry provides an important source of foreign exchange, averaging approximately USD 0.296 billion annually [1]. The industry generates approximately 21 million jobs every year including 12 million in related orchards and nine million in packing and processing as well as many other related fields [2]. Backed by real advantages such as the Mediterranean climate, fertile soils, effective agricultural reform programs, and geographic location, Morocco is among the top ten citrus producers in the world [3]. However, the citrus sector faces several constraints that affect its production. For example, the spread of plant-parasitic nematodes (PPNs) harms citrus quality and yield [4]. Several species of PPNs have been found in the rhizosphere of citrus plants [5–8]. Tylenchulus semipenetrans, Radopholus similis, Pratylenchus coffee, Longidorus, Hoplolaimus, Helicotylenchus, Belonolaimus longicaudatus, and Meloidogyne spp. are important pests of citrus responsible for significant economic losses in several regions worldwide [9,10]. Other nematodes are considered less important pests because they rarely cause damage or are restricted to relatively small geographic areas. These include Hemicycliophora arenaria, H. nudata, Paratrichodorus lobatus, P. minor, Pratylenchus brachyurus, P. vulnus, Xiphinema brevicolle, and X. index [6]. The citrus nematode Tylenchulus semipenetrans is a sedentary semi-endoparasitic PPN that attacks more than 75 rutaceous species, mainly citrus [11,12]. It has been found in most citrus-growing regions of the world and in a wide variety of soil types [13,14]. Infested trees show reduced vigor, leaf chlorosis, leaf drop, dieback, and reduced fruit quality and quantity [15]. This nematode accounts for 99.1% of the total nematode community in Egypt [16], 89% in northern Iran, 26% in Florida and California (USA), and 70–90% in Spain [17]. In Morocco, T. semipenetrans has been found to be associated with various rootstocks in many citrus growing regions [7,18]. Nematode infection of citrus roots exacerbates under drought stress where the roots’ ability to absorb water and mineral nutrients are extremely affected [19]. In addition, root injury due to nematode penetration facilitates invasion by other pathogens such as fungi, viruses, and bacteria, which forms a disease complex [20]. Currently, there is limited information on the occurrence, density, and distribution of PPNs in citrus trees in Morocco as well as their relationship with soil physicochemical properties. Given this lack of data and information, the objectives of this study were (i) to provide more information on citrus-associated PPNs and their geographic distribution in the main citrus growing areas in Morocco, and (ii) to explore the affiliation of PPNs to soil physicochemical patterns across citrus orchards. 2. Materials and Methods 2.1. Survey and Sample Collection Sampling was conducted during the 2020–2021 growing season in the main citrus growing areas of Morocco including Souss-Massa, Marrakech-Safi, Beni Mellal-Khenifra, Gharb, and Berkane, as shown in Figure 1. A total of 224 soil and root samples were collected from the rhizosphere of different citrus trees, as clarified in Table 1. A composite representative sample of 1 kg of soil and roots collected in a zigzag path was collected in plastic bags to avoid water loss and stored at 4 ◦C before analysis. Soil texture for each sampled area is summarized in Table 2. Nematological analyses were performed at the laboratory of nematology (INRA, Rabat, Morocco). LLiiffee 22002222,, 1122,, 6x3 F7OR PEER REVIEW  3 3ooff  1177     FFiigguurree 11.. MMaapp ooff tthhee ssuurrvveeyyeedd cciittrruuss‐-ggrroowwiinngg rreeggiioonnss iinn MMoorrooccccoo..  Table 1. Distribution of samples analyzed by prospecting area and citrus rootstocks.  Table 1. Distribution of samples analyzed by prospecting area and citrus rootstocks. Prospecting Area (Region)  Number of Samples  Rootstock Variety  Prospecting Area (Region) Number of Samples Rootstock Variety Carrizo citrange  Souss‐Massa  32  CaSroriuzor ocirtarannggee  Souss-Massa 32 Sour orange mmaaccrroopphhyylllala  Sour orange  Sour orange ‘‘AAuussttrraalliiaann’’s soouur ro roarnagnege  MMaarrrraacckkeecchh-‐SSaafifi  6600  Carrriizzooc citirtarnagnege  Vollkkaammeerirainaana  CC-‐3355 ccitirtraanngegses  SSoouurro orraanngege  CCaarrrriizzooc citirtarnagnege  Beni Mellal-Khenifra 60 Volkameriana Beni Mellal‐Khenifra  60  CV-o3l5kcaimtraenrgiaensa  ‘AustCra‐l3ia5n c’istoraunrgoerasn  ge ‘Australian’ sour orange  Troyer citrange  Gharb  18  Sour orange  Carrizo citrange    Life 2022, 12, 637 4 of 17 Table 1. Cont. Prospecting Area (Region) Number of Samples Rootstock Variety Troyer citrange Gharb 18 Sour orange Carrizo citrange Sour orange Berkane 54 Carrizo citrange ‘Australian’ sour orange Total 224 Table 2. Texture and pH of the soils of the sampled citrus orchards. Region Orchard Soil Texture Soil pH Balfa Sandy loam 7.65 Souss-Massa Taroudant Sandy loam 8.32 Biogra Sandy clay loam 7.86 Souihla Sandy loam 8.57 Marrackech-Safi Es Saada Sandy loam 8.27 Agafai Sandy loam 7.42 Souk Sebt Silty clay 7.89 Beni Mellal-Khenifra Guettaya Silty clay 7.03 M’nasra Sandy 7.43 Allal Tazi Sandy 8.05 Gharb Ouled Azouz Sandy loam 7.64 Sidi Slimane Sandy clay loam 7.81 Sidi Kacem Sandy loam 8.23 Zegzel Sandy clay 8.13 Berkane Aglmine Sandy loam 7.59 2.2. Nematode Extraction and Identification Nematodes were extracted from soil and root samples using the modified Baermann technique [21]. The roots of each sample were completely cleaned in tap water and cut into small fragments (1 cm) of which 20 g was used to extract nematodes [21]. Nematodes were also extracted from each soil sample (100 g) using the same modified Baermann method. After the extraction (usually 72 h), the nematodes were stored for processing. PPN populations were expressed as the number of individuals per 100 g of soil and 20 g of root fragments. Nematodes were identified to the genus level under a stereomicroscope using reliable morphological characteristics [22,23]. The nematode samples obtained were placed in hot formalin–formaldehyde 4% [24]. The nematodes were transferred in liquid I (99 parts 4% formaldehyde + 1 part pure glycerol) to a square watch glass 7 cm in diameter. The latter was stored in a desiccator containing about one-tenths of its volume of 96% ethanol for about 12 h at 40 ◦C. Then, the watch glass containing the nematodes was removed from the desiccator and placed in an incubator at 37 ◦C. The nematodes were then prepared with the dehydration liquid II (95 parts 96% ethanol + 5 parts pure glycerol). Three ml of liquid II was added to the watch glass. The latter was partially covered with a glass slide to let it evaporate slowly. Finally, 2 mL of liquid III (50 parts 96% ethanol + 50 parts pure glycerol) was added and the watch glass was left in the incubator overnight at 37 ◦C. The nematodes were mounted on glass slides for light microscopic identification. Meloidogyne species were identified by preparing the perineal patterns [22]. Root-knot nematode (RKN) females were removed from roots and processed in a solution of sodium chloride (0.9%) for 2 min. The perineal patterns were trimmed and transferred to a drop of glycerin for microscopic examination (×100 magnification). Life 2022, 12, 637 5 of 17 2.3. Nematode Community Assessment Nematode diversity and incidence were determined by calculating prevalence, mean intensity, and maximum density as per the following equations [25]: No. o f Positive Samples Prevalence (%) = × 100 (1) Total no. o f Samples No. o f a particular nematode species in the Positive Samples Mean intensity = × 100 (2) No. o f Positive Samples Maximum density = Maximum no. o f a particular nematode species recovered f rom a sample (3) 2.4. DNA Extraction, PCR, and Sequencing For molecular identification, DNA was extracted from twenty-five individual nema- todes as described by Holterman et al. [26]. The D2–D3 region was amplified with forward primers D2a (5′-ACA AGTACC GTG AGG GAA AGT TG-3′) and reverse primers D3b (5′-TCG GAA GGA ACCAGC TAC TA-3′) according to De Ley et al. [27]. One µL of DNA was added to the PCR reaction mixture containing 22 µL ddH2O, 25 µL 2× DreamTaq PCR Master Mix (Fermentas Life Sciences, Leon-Rot, Germany), and 1 µM of the two primers. The thermocycler program consisted of 5 min at 95 ◦C; 35 cycles of 1 min at 94 ◦C, 45 s at 49 ◦C, and 1 min at 72 ◦C, followed by a final elongation step of 8 min at 72 ◦C. After PCR, 5 µL of each PCR product was mixed with 1 µL of 6× loading buffer (Fermentas Life Sciences, Germany) and loaded onto a 1.5% buffered standard agarose gel (TAE). After electrophoresis (100 V for 40 min), the gel was stained with ethidium bromide (0.1 µg ml−1) for 20 min, visualized, and photographed under UV light. The remaining PCR product was stored at −20 ◦C. The purified PCR products were sequenced in both directions (Macrogen) to obtain overlapping sequences of the forward and reverse DNA strands. Sequences were processed and analyzed using the Chromas 2.00 (Technelysium) and BioEdit 7.0.4.1 [28] software packages. 2.5. Soil Diagnosis All analyses of the soil physicochemical properties were performed on dry and sieved (2 mm) material. Measurements of soil texture (Stxt) were determined on the proportion of clay (0–2 µm), silt (2–50 µm), and sand (50 to >200 µm) according to sedimentation estimation [29]. The pH and electrical conductivity (EC) were measured in the ratio of 1:2.5 (w/v) soil:water suspension as per the methodology described by Richards [30]. Organic matter (OM) and carbon were quantified according to the method by Anne [31]. Sodium (Na), potassium (K), and calcium (Ca) contents were determined by atomic absorption spectrometry. Total (Ptot) and available (Pass) phosphorus content was estimated using the method of Olsen et al. [32]. Total soil nitrogen (N) content was determined by the Kjeldah method [33]. 2.6. Taxonomic Diversity The taxonomic diversity of PPNs was assessed by calculating two nematode indices. The Shannon–Wiener index [34] is given in Equation (4): s H′ = −∑ pi Ln pi (4) i−1 where s is the number of genera; Pi is the proportion belonging to the corresponding number of genera; and H′ is commonly used to characterize species diversity in a community (H′ ranges from 0 to Ln s). The second index is the Evenness index [35], as given in Equation (5): H′ E = (5) Ln s Life 2022, 12, 637 6 of 17 This quantifies the regularity of the genus distribution within the community, E varies between 0 and 1. 2.7. Data Processing A principal component analysis (PCA) was established to define the distribution of nematode genera and the soil characteristics according to their sampling sites. Significant differences among variables were performed using Fisher’s protected least significant difference (LSD) and the Tukey test at p < 0.05. Differences obtained at levels of p < 0.05 were considered to be significant. Molecular data were processed for phylogenetic anal- ysis. The latter relates the Moroccan nematode isolates and published sequences of each species based on the analysis of the ITS region using the maximum likelihood method and Kimura 2-parameter model [36] in MEGAX software [37]. The tree was evaluated via 1000 bootstrap replications. 3. Results 3.1. Distribution and Diversity of Plant-Parasitic Nematode Communities The list of PPN species identified in all of the surveyed citrus orchards is presented in Table 3. Eleven genera and ten species of PPNs were identified morphologically from the collected soil and root samples. The data on prevalence, mean intensity, and maximum density in each studied region are presented in Table 3. Mean intensity and maximum density are quantitative parameters that are calculated to provide information about the specific proportion of plant-parasitic nematodes in soil and root matrices, and to have an idea of how far nematodes can be distributed within the plant environment, respectively. Tylenchulus semipenetrans, Helicotylenchus spp., Pratylenchus spp., Paratylenchus spp., and Tylenchus spp. were found in all the citrus growing regions studied. The dagger nematodes Xiphinema diversicaudatum, X. americanum, and X. pachtaichum were not detected in Gharb, while the root-lesion nematodes Pratylenchus thornei and P. neglectus were encountered only in the Berkane region. The major PPNs found in both soil and root samples were T. semipen- etrans and Helicotylenchus spp. with high prevalence of up to 67 and 75%, respectively, while Pratylenchus spp. represented less than 50% of the total nematode population. Indeed, T. semipenetrans was highly prevalent in Marackech-Safi (62%), Beni Mellal-Khenifra (57%), Gharb (67%), and Berkane (63%), while it was least prevalent in Souss-Massa (28%). In Life 2022, 12, x FOR PEER REVIEW  8  of  17    addition, T. semipenetrans had the highest total density in Beni Mellal with 1114 individuals per soil sample, as shown in Figure 2.   Figure 2. PopulationFdigeunres 2i.t PieopsuolaftiTony ldeenncsihtiuesl uofs Tsyelemncihpueluns estemraipnense(trpanesr (pseori slosila smamppllee)) ini nthet hmeaimn caitirnus cgirtorwu‐s growing ing regions in Morocco. Lower case  letters represent the homogeneous groups based on the pro‐ regions in Morocco.teLctoedw learst csiagsneificlaentt deirffserreencper test eant pt  0.05). The Shannon index was higher in Marrakech-Safi (2.09), Gharb (2.05), and Beni Mellal-Khenifra (2.03) than in Berkane (1.4) and Souss-Massa (1.36). Thus, the citrus growing regions of Marrakech-Safi, Gharb, and Beni Mellal-Khenifra showed a similar trend in nematode abundance. Life 2022, 12, 637 11 of 17 Table 5. Shannon–Wiener diversity (H′), evenness (E), and the number of nematode genera in each of the five surveyed citrus regions. Diversity Parameters Regions Number of PPNs * Shannon Diversity Index (H′) * Evenness (E) * Souss-Massa 2.91 c 1.36 b 0.7 a Marrakech-Safi 12.65 b 2.09 a 0.84 a Beni Mellal-Khenifra 18.05 a 2.03 a 0.88 a Gharb 3.3 c 2.05 a 0.89 a Berkane 3.69 c 1.4 b 0.84 a p <0.05 <0.05 >0.05 * Numbers in the same column followed by different letters were significantly different based on Tukey’s test. 3.3. Physicochemical Properties and Their Interaction with Nematode Communities in Citrus The results of the principal component analysis of the physicochemical properties of the studied soils as depicted in Figure 5 show that the proportion of variance accounted for by the first two axes PC was 24.90% and 21.84% (eigenvalues), respectively. The loading plot of soil factors showed that the PC1 axis was associated with positive PC values with pH and moisture and with negative PC values with nitrogen and electrical conductivity (EC). The PC2 axis was associated with mineral content including calcium (Ca), sodium (Na), potassium (K), and organic matter (OM) in positive PC values and with EC and N in negative PC values. The bi-plot analysis of soil factors in interaction with nematode communities of citrus clearly showed that Trichodorus spp., H. indicus, Longidorus spp., and Tylenchus spp. were associated with moisture and pH. In contrast, T. semipenetrans, X. americanum, Pratylenchus spp., and Helicotylenchus spp. were particularly associated with calcium, carbon, sodium, potassium, and organic matter. However, the following genera, Life 2022, 12, x FOR PEER REVIEW  12  of  17    Meloidogyne, Pratylenchus (P. thornei, P. coffeae, P. vulnus, and P. neglectus), and Xiphinema were associated with soil texture and soil phosphorus (P) content.   Figure 5. PrinciFpigaul rceo 5m. pProinceinptala ncoamlypsoisne(nbti -apnlaolty)soisf (sboi‐ipl lpoht)y osfi csooiclh pehmysicicaolcchhemariaccatl ecrhiasrtiaccsteirnistteircas cintitnegracting  with plant-paraws itihc pnleanmt‐aptaordaesitiacx naeamsastoocdiea tteadxaw asitshocciiattreuds wpiltahn ctistriuns aplllarnetgs ionn asll srteugdioineds .studied.  4. Discussion  4.1. Distribution and Taxonomic Diversity of Plant‐Parasitic Nematodes  To better understand  the distribution of PPNs associated with citrus  trees  in Mo‐ rocco, extensive surveys were conducted in the main citrus growing regions of the coun‐ try. Based on the morphological and morphometric characteristics, eleven genera and ten  species of plant‐parasitic nematodes were  identified. Tylenchulus  semipenetrans was  the  most common PPN in the citrus orchards surveyed, as reported in other citrus growing  areas  in Morocco  [7] and worldwide  including  Iran [38], Egypt  [39,40], and Spain [12].  Indeed, T.  semipenetrans was  the predominant nematode  found  in Souss‐Massa  (88%),  Marackech‐Safi (62%), Beni Mellal‐Khenifra (57%), Gharb (67%), and Berkane (63%). This  species is notable not only for its close association with citrus, but also for the ability of  citrus trees to support very high populations before vigor declines and symptoms appear.  The wide distribution of T. semipenetrans could be attributed to many factors  including  infected  seedlings,  contaminated plant material, organic  fertilizers,  irrigation, and ma‐ chinery [39]. In addition, the high variability of PPN genera observed in this study can be  attributed to the variation in ecological and edaphic factors between and within the dif‐ ferent regions studied [41].  The second most prevalent plant‐parasitic nematode was Helicotylenchus spp., which  varied from 75% in Souss‐Massa to 38% in Beni Mellal‐Kenitra and Gharb. The prevalence  of this genus in Moroccan citrus‐growing regions was higher than that in Spain [12] and  Egypt [40]. On the other hand, a higher prevalence of H. dihystera (80%) was reported by  Kumar and Das in Tinsukia [42]. Four species of Pratylenchus spp. (P. vulnus, P. thornei, P.  neglectus, P. coffeae) were identified in the surveyed regions. Population densities of this  genus ranged from 27 to six nematodes per 100 g soil in Beni Mellal‐Khenitra and Gharb,  respectively, and from 17 to three nematodes per 20 g roots in Berkane and Souss‐Massa,    Life 2022, 12, 637 12 of 17 4. Discussion 4.1. Distribution and Taxonomic Diversity of Plant-Parasitic Nematodes To better understand the distribution of PPNs associated with citrus trees in Morocco, extensive surveys were conducted in the main citrus growing regions of the country. Based on the morphological and morphometric characteristics, eleven genera and ten species of plant-parasitic nematodes were identified. Tylenchulus semipenetrans was the most common PPN in the citrus orchards surveyed, as reported in other citrus growing areas in Morocco [7] and worldwide including Iran [38], Egypt [39,40], and Spain [12]. Indeed, T. semipenetrans was the predominant nematode found in Souss-Massa (88%), Marackech- Safi (62%), Beni Mellal-Khenifra (57%), Gharb (67%), and Berkane (63%). This species is notable not only for its close association with citrus, but also for the ability of citrus trees to support very high populations before vigor declines and symptoms appear. The wide distribution of T. semipenetrans could be attributed to many factors including infected seedlings, contaminated plant material, organic fertilizers, irrigation, and machinery [39]. In addition, the high variability of PPN genera observed in this study can be attributed to the variation in ecological and edaphic factors between and within the different regions studied [41]. The second most prevalent plant-parasitic nematode was Helicotylenchus spp., which varied from 75% in Souss-Massa to 38% in Beni Mellal-Kenitra and Gharb. The prevalence of this genus in Moroccan citrus-growing regions was higher than that in Spain [12] and Egypt [40]. On the other hand, a higher prevalence of H. dihystera (80%) was reported by Kumar and Das in Tinsukia [42]. Four species of Pratylenchus spp. (P. vulnus, P. thornei, P. neglectus, P. coffeae) were identified in the surveyed regions. Population densities of this genus ranged from 27 to six nematodes per 100 g soil in Beni Mellal-Khenitra and Gharb, respectively, and from 17 to three nematodes per 20 g roots in Berkane and Souss-Massa, respectively. Several studies have reported the presence of these nematode species in citrus orchards worldwide. In Brazil, P. coffeae infests about 1% of citrus nurseries and orchards [43], while it has a major trend in Florida, USA [44]. Other RLN species were described to be prominent such as P. vulnus and P. neglectus in Israel [45], and P. vulnus and P. coffeae in Morocco [7]. These species can significantly reduce root weight, which translated into significant yield losses [4]. These nematodes have been reported as one of the main pests limiting raspberry and saffron production in Morocco [46,47]. The dagger nematode Xiphinema spp. is among the ten most economically important PPNs [48]. This genus causes serious problems for organic farming in Egypt [49], raspberry and citrus in Morocco [46,50], and vegetable production in Saudi Arabia [51]. This migratory ectoparasitic nematode is particularly problematic because it can harbor and transmit plant viruses. Thus, even at low densities, these nematode species can be very damaging to plants [52,53]. The distribution of Xiphinema species identified in this study varied considerably among the citrus-growing regions. X. pachtaichum was observed only in Beni Mellal- Khenifra (3.3%) and Berkane (3.7%), X. americanum was found in Marackech-Safi (12%), Beni Mellal-Khenifra (6.7%), and Berkane (1.9%), while X. diversicaudatum, which was first reported in Morocco in May 2012 in the Gharb region, was encountered in Marackech-Safi (6.6%), Beni Mellal-Khenifra (10%), and Berkane (7.4%). According to Mokrini et al. [50], X. diversicaudatum was first reported in Moroccan citrus orchards. This nematode can transmit the Arabis mosaic virus, mainly associated with grapevine fanleaf degeneration disease [50]. On the other hand, X. americanum was reported for the first time ever, associ- ated with citrus in Morocco. This is extremely interesting, giving the economic importance and quarantine aspect of this nematode and its potential damage attributed to citrus crops. The root-knot nematode Meloidogyne spp., attacking citrus crops was not frequently reported due to its limited distribution. In the present study, only a few citrus-growing fields were found to be infested by these nematodes, and had prevalence values of 23, 25, 22, and 13% in Marackech-Safi, Beni Mellal-Khenifra, Gharb, and Berkane, respectively. This prevalence of Meloidogyne spp. was lower than that in Egyptian citrus orchards intercropped with tomato [8], which implies the decent linkage between these nematodes and citrus crops Life 2022, 12, 637 13 of 17 rather than its presence in intercropped trials with native hosts or in weeds. Several studies recorded in Taiwan and India have reported that Meloidogyne spp. could cause elongated galls on citrus roots [11]. Moreover, Some RKN species (e.g., M. incognita, M. javanica, and M. arenaria) were found in the infection zones of Troyer citrange and sour orange rhizospheres, causing small galls without reproduction activity [54]. Many of the nematode genera associated with citrus in the present study have also been previously reported for the same crop worldwide. The needle nematode Longidorus spp., the stubby root nematode Trichodorus spp., the stunt nematode Tylenchorhynchus spp., the ring nematode Criconemoides, and the spiral nematode Rotylenchus spp. are commonly found in the surveyed citrus growing areas. Indeed, Tylenchorhynchus spp. and Longidorus spp. have been detected in Egypt [8], Spain [12], and Tinsukia [42]. In our study, S. bradys and H. indicus were found at low densities that varied between two and four nematodes per 100 g of soil and between two and seven nematodes per 100 g of soil, respectively. According to Kumar and Das [42], H. indicus was very abundant in citrus orchards in Tinsukia. The sheath nematode Hemicycliophora spp. was the least abundant nematode. It was observed in 5% of the sampled citrus plots in the Marackech-Safi region with an average density of two nematodes per 100 g of soil. These results are in agreement with the scientific work of Shanmugam et al. [55], who found that Hemicycliophora spp. was least prevalent in some Indian weeds, shrubs, and herbs. In addition, it has been reported that H. ahvasiensis was isolated from the soil and root matrices of citrus in Egypt. However, the damage amplitude caused by this nematode to the citrus trees have not been documented yet [4]. Therefore, the rare abundance of this nematode could probably be related to the soil’s temperature, irrigation, and aeration, alongside the seasonal attributes [4,17]. The results of the analysis of the Shannon (H′) and evenness (E) diversity indices showed that H′ values were highest in Marrakech-Safi, Gharb, and Beni Mellal-Khenifra, which have extended dry seasons. Freitas et al. [56] indicated that dry season and soil depth (0–10 cm) favored the total population of PPNs associated with citrus plants in Brazil. 4.2. Relationship between Plant-Parasitic Nematode Communities and Soil Physicochemical Factors Understanding the interaction between soil physicochemical properties and plant- parasitic nematodes is critical for effective and environmentally-friendly management. The citrus nematode, T. semipenetrans was positively correlated with soil mineral nutrients (K, Ca, Na, and C) and organic matter content. A strong correlation was found between these parameters and the prevalence of T. semipenetrans in citrus growing areas in Spain [12]. In contrast, Benjlil et al. [57] reported a negative correlation between the prevalence of PPNs parasitizing saffron and soil organic matter. Soil organic matter accumulation could signifi- cantly reduce PPN abundance in wheat via decreasing their vital proprieties [58]. Moreover, the prevalence of Pratylenchus spp., Helicotylenchus spp., and X. americanum was closely related to the mineral content including Fe, Ca, and Na [59,60]. In addition, Francl [61] observed that the population density of Heterodera glycines was positively correlated with magnesium (Mg) content. In this study, most of the identified PPNs showed a negative cor- relation with nitrogen (N), except for Criconemoides, Rotylenchus spp., and Tylenchorhynchus spp. Interestingly, the accumulation of nitrate via nitrification is considered destructive to PPNs [62]. Phosphorus content was positively correlated with the occurrence of Meloidog- yne spp., Xiphinema spp., P. thornei, P. vulnus, and P. neglectus. Nisa et al. [41] reported the same positive correlation between nematode abundance and soil P content. Soil pH also had a strong influence on the abundance of citrus nematodes. Low pH increased nematode abundance and diversity [63,64]. Soils with acidic pH increase the proliferation of the root-knot nematode Meloidogyne spp. [65–67]. In contrast, Salahi Ardakani et al. [68] found that the highest abundance of T. semipenetrans was observed in soils of pH 7. Moreover, Van Gundy and Martin [69] indicated that the density of T. semipenetrans in citrus was four times higher in neutral soils than in acidic soils. Life 2022, 12, 637 14 of 17 Soil texture and structure significantly affect the movement of soil nematodes. Our results indicated that the texture of fine sandy soil positively affects the distribution of nematodes. Salahi Ardakani et al. [68] found that the maximum abundance of the citrus nematode T. semipenetrans was found in clay soils. A recent study by Laasli et al. [70] showed that Aphelenchoides spp., Merlinius spp., and Pratylenchus spp. were associated with sandy and silt soils in wheat fields. In contrast, Longidorus spp., and Xiphinema spp. were more common on soils with higher clay content. Mokrini et al. [46] found that the abundance of several plant-parasitic nematodes affecting raspberries was strongly associated with soil granulometry. Kim et al. [71] indicated that sandy soils favor the growth of nematodes such as M. incognita by promoting their motility and feeding activities. 5. Conclusions This study highlights the main plant-parasitic nematode diversity found in the Mo- roccan citrus-growing areas. The citrus nematode T. semipenetrans was the most abundant nematode identified in the soil and root matrices. This is probably because the local environ- mental and soil conditions are more suitable for its growth. Other economically important nematode species (e.g., P. vulnus, P. thornei, S. bradys, H. indicus, and X. diversicaudatum) were recorded as well as X. Americanum, which has been reported for the first time in citrus orchards. The relationship of these nematodes with edaphic proprieties has been revealed in the sense that it may help farmers to accurately tackle problematic PPNs. Additionally, the results of this study will be of great value to researchers and pest management authorities to control and reduce the spread of PPNs to improve citrus production in Morocco. Author Contributions: Conceptualization, B.Z., F.M., M.A., A.A.D., S.-E.L., A.I.H. and A.Q.; Method- ology, B.Z., F.M., S.-E.L., A.Q., A.I.H., O.A., K.K. and A.A.D.; Software, B.Z., F.M., S.-E.L. and A.B.; Validation, B.Z., F.M., M.A., A.A.D., S.-E.L., A.I.H. and A.Q.; Formal analysis, B.Z., F.M. and S.-E.L.; Investigation, F.M., A.A.D. and M.A.; Resources, M.A, A.A.D., C.G., A.I.H. and A.Q.; Data curation, F.M., S.-E.L. and A.Q.; writing—original draft preparation, B.Z., F.M., S.-E.L., O.A., A.B., A.I.H. and A.Q.; Writing—review and editing, B.Z., F.M., M.A., A.A.D., S.-E.L., A.I.H., M.I. and A.Q.; Visu- alization, A.A.D., M.A., R.L. and C.G.; Supervision, F.M., M.A., A.A.D., A.I.H. and A.Q.; Project administration, F.M., M.A., A.A.D., A.I.H. and A.Q. All authors have read and agreed to the published version of the manuscript. Funding: This research was financially supported by the National Institute of Agricultural Research (INRA). 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