Prevalence and Serological Detection of Spiroplasma citri, a Cause of Citrus Stubborn Disease in Southern Punjab, Pakistan
Ummad ud Din Umar1, Syed Atif Hasan Naqvi1*, Ishfaq Ahmed1, Ateeq ur Rehman1, Muhammad Asif Zulfiqar2, Sibghat Ullah3, Shah Pasand4, Zehri Khan3 and Abdur Rehman5
1Department of Plant Pathology, BZU, Multan, 60800, Pakistan; 2PARC, Research and Training Station, BZU, Multan. 3PARC, Horticulture Research Institute, Khuzdar, 4PARC, Social Sciences Research Institute, Quetta, 5Plant Protection Department, College of Food and Agriculture Sciences, King Saud University, Riyadh, Saudi Arabia.
Abstract | Spiroplasma citri, a fastidious pathogen, is considered as the main cause of Citrus little leaf disease (Citrus stubborn disease) which is not only responsible for the low citrus production in terms of quality and quantity but also moving the citrus industry to down fall in citrus growing areas throughout the world. Current research was organized to study the distribution of disease using the serological based detection methods by conducting a comprehensive survey in various districts of Southern Punjab. The results of the survey and serology of CSD showed that this destructive disease which causes symptoms mostly similar to citrus greening is present in all areas of South Punjab. Layyah, and Multan showed maximum incidence of CSD with “11.66” and “5.66%” respectively while least incidence was observed in District Bhakkar (03%) and District Khanewal with (02%) incidence. Sweet orange and grape fruit depicted themselves as susceptible ones showing maximum disease with “18.33” and minimum “02%” respectively. Kinnow mandarin and feutral’s early appeared as resistant cultivars against CSD infection in all the surveyed areas. Small acorn shaped, lopsided fruit and leaves with shortened internodes were appeared to be characteristic disease symptoms in Citrus stands of Southern Punjab.
Received | June 01, 2020; Accepted | July 27, 2020; Published | October 06, 2020
*Correspondence | Syed Atif Hasan Naqvi, Department of Plant Pathology, BZU, Multan, 60800, Pakistan; Email: [email protected]
Citation | Umar, U.D.U., S.A.H. Naqvi, I. Ahmed, A. Rehman, M.A. Zulfiqar, S. Ullah, S. Pasand, Z. Khan and A. Rehman. 2020. Prevalence and serological detection of Spiroplasma citri, a cause of citrus stubborn disease in southern Punjab, Pakistan. Pakistan Journal of Agricultural Research, 33(4): 748-753.
DOI | http://dx.doi.org/10.17582/journal.pjar/2020/33.4.748.753
Keywords | Occurrence, Oranges, ELISA, Fastidious, Wall less bacteria
Introduction
Taxonomically citrus belongs to the family “Rutaceae” and considered as important genus from kingdom plantae which originated from South of China and Himalayan countries. Being a vital fruit crop, which is planted in most of the countries around the globe its high yield grants a big profit and economic reward to its growers. Citrus possesses a lot of necessary nutrient compounds such as fibrous compounds, sugary compounds, Vitamin B2, Vitamin B6, Phosphorus, and other phytochemical compounds (Abu-Zeid et al., 1988; Bove et al., 1983). Globally, Pakistan ranks 10th among major citrus producing countries all around the globe in terms of quantity and quality. Among the four provinces of Pakistan, Punjab contributes 94% to Citrus production followed by Khyber Pakhtunkhwa with 3%, Sindh 2.7% and Baluchistan with 1.7%, respectively out of total production. Climatic conditions of Punjab province are highly conducive for this crop and making it as top yielding province in Pakistan especially in its regions like, Sahiwal, Sargodha, Toba Tak Singh and Layyah. As for as export of this fruit commodity is concerned, kinnow mandrin gave its maximum share with 70% enabling Pakistani 5th largest country in terms of citrus export. (Annonymous, 2018). There are a lot of serious issues in citrus’s agroecosystem bringing citrus towards huge loss of production such as infectious diseases (fungal, viral, viroid’s and nematode diseases) insect infestations, and non-infectious problems i.e., various nutrient deficiencies and environmental stresses). Citrus stubborn diseases are a most damaging one among all the infectious diseases under semi-arid conditions where Spiroplasma citri appears destructively in many world’s countries (Bradbury, 1991). Literature has proved that no favor is being provided by low temperature to CSD pathogen and vector, which decides that the disease possesses summer prevalence (Bradbury, 1991). S. citri thrives best in range of high temperature (28-32oC) and may produce non-conspicuous symptoms at cool temperature. Bove et al. (2002) explained the huge perceived impairment due to stubborn in Syria. The series of experiments conducted on same plants each year has proven more mortality at higher temperature (>30oC) as compared to low temperature wherein plants remain asymptomatic (Boonham et al., 2014). The diseases is transmitted by its vector from infected to healthy plants in citrus groves (Gumpf and Calavan, 1981), while S. citri can be transmitted to horse reddish experimentally (Sheta et al., 2004). To the extent of current day literature on CSD, no strain indication has been reported of S. citri. CSD was first ever observed and reported from California, USA upon Navel trees of oranges (Wisler et al., 1992). A characteristic symptom of acorn-morph-formation on infected citrus fruit leads towards the nomination of disease as “acorned disease.” Literature has also reported the same disease from Palestine in 1930 as “Little Leaf Disease” with the proofs of transmission possession of CSD as explained by (Fawcett et al., 1944).
Graft inoculation on indicator plants has been used to detect S. citri, on madame vinous placed at 32 to 27oC day and night temperature respectively (Bove, 1988). Grapefruit, tangelo, sexton and Marsh are some important indicators plants used to detect CSD pathogen where midrib of the leaf has been reported the region where maximum amount of titter can be detected. Symptomatic trees can help to culture S. citri with best seeding material having numerous abortion extent while fruit axis with peduncle end or mottled seasonal leaves gathered in October (Bove, 1988). Since cutlturability of organism declared antisera are easy to grasp. ELISA is the technique applied to detect and identify S. citri from infected plants and insect extract (Clark and Adam, 1977) while rapid detection can also be done using latex agglutination technique (Fletcher and Slack, 1986). Little leaf disease trees also develop acorn fashioned and loped fruits having thin skin on stylar area of fruit leading towards premature breakdown of acorn fashioned fruit. CSD infected fruit appears often greenish to yellowish, bitter/sour tasted/flavored and generally show blue color from inside. Leaves appear erected, trees show shortened internodes and bunchy formation of leaves. Small leaves appear mottled just similar to zinc deficiency symptoms as compared to healthy leaves. Furthermore, CSD infected citrus shrubs produces poor foliage and fruit develops abnormally (Bove et al., 1974). Other symptoms are severe dwarfing of younger trees, short internodal distance and thick shrubbery with cupped, alternative Chlorotic patterned and thickened leaves. Considering the aforementioned facts present research intended to determine the prevalence of the Spiroplasma citri through its serological based detection in the non-core area of Southern Punjab.
Materials and Methods
Study sites
The research was performed at Department of Plant Pathology, Faculty of Agricultural Sciences and Technology, Bahauddin Zakariya University Multan.
Investigation for the assortment of CSD affected specimen
The disease was visualized with characteristic symptoms including bunchy formed growth with reduced internodes usually erect leaves similar to zinc deficiency, acorn and lopsided shaped fruits. Investigation about CSD in different regions of Punjab including Multan, Khanewal, Layyah and Bhakkar was performed and symptomatic specimens of CSD were gathered. The samples were placed in plastic zipper bags in ice box.
Disease incidence/occurrence and cultivar vulnerability
Disease occurrence for all the regions was computed by the formula for disease incidence and the cultivar vulnerability was also evaluated for CSD.
Serological detection of CSD
Clark and Adams in 1977 utilized binary antibody sandwiched (BAS) ELISA for the recognition of S. citri. where Agdia Inc. USA made the antibodies available. Microplate was glazed with coating buffer holding 100ul of arrested antibody thereafter microplate was over nightly incubated at 4oC. Phosphate buffer saline tween PBST pH 7.4 (washing purpose buffer) was utilized to rinse the plate thrice. Antigen or infected plant mass was taken out in 5ml abstraction/ extraction buffer 7.4 pH from 500 mg leaf tissues and individual well of microplate was poured with 0.1ml extract. The incubation was provided overnight at 4oC and the microtiter plate was again rinsed using washing buffer 5 to 6 times. Then microtiter plate was glazed with conjugate/ coupled antibody in conjugate/ coupling buffer and the micro plate was placed at ambient temperature for incubation of 2 hrs. Thereafter the plate’s washing was done 4-5 times with PBST. Substrate buffer was synthesized by dissolving 1mg/ml pNpp tablet and the microplate was glazed 25 minutes at ambient temperature. The absorbance was gauged at 405 nm on ELISA plate observer (Biotek. Inc) U.S.A.
Results and Discussion
Occurrence of Spiroplasma citri in various regions
Citrus stubborn disease (CSD) was founded in all inspected regions of the Punjab. Extreme disease occurrence of CSD was pragmatic in Layyah (11.66%) followed by Multan (5.660%), Bhakkar (3.33%) and District Khanewal with (02%) occurrence. Investigation outcomes exposed highest disease incidence in Layyah and minimum occurrence in District Khanewal (Figure 1).
Cultivar vulnerability in the direction of citrus little leaf disease
Outcomes of cultivar’s vulnerability exposed that maximum value of CSD was present on Citrus sinensis (18.33%) and least was evident on Citrus paradisi (02%) while feutral’s early and kinnow exposed less disease infestation. (Figure 2).
Serological proof of identity of CSD
The ELISA outcomes exposed that specimens from grapefruit and sweet orange (Citrus sinensis) provided positive reply in the direction of the serological finding of CSD. While kinnow, feutral’s early and mandarin exposed colorless means negative. The Maximum range of titer was evaluated in sweet orange (Citrus sinensis) (0.147-0.258) and in grapefruit (Citrus paradisi) (0.171-0.172) (Table 1, Figure 3).
Citrus is very crucial fruiting crop for world’s countries. Top quality citrus from Pakistan is a best cause of foreign exchange. Up till now, Citrus of Pakistan is hampered by a variety of pathosystems which not only affecting quantity but also quality of Citrus fruit and tree. Acorny citrus disease (ACD) etiolated by Spiropalsma citri oozing out as a major hurdle for Citrus growing world’s countries. Low temperature climates discouraging the pathogen as well as its vector which making it obvious that CSD is subtropical situation lover disease.
Table 1: Reaction of citrus tissues in CSD-ELISA tests.
Source Plant |
Reaction |
ELISA Value (A405 n.m.) |
Kinnow Mandrin |
Negative |
0.013-0.017 |
Sweet orange |
Positive |
0.147-0.258 |
Feutral’s early |
Negative |
0.031-0.035 |
Grape fruit |
Positive |
0.171-0.172 |
Positive test sample |
Positive |
0.172-0.257 |
Negative sample |
Negative |
0.027 |
Healthy sample |
Negative |
0.016 |
In present research we described that CSD infection in citrus groves of numerous regions of the South Punjab to determine the prevalence and spread of the CSD through serological and molecular methods. We determined that CSD identified in all investigated regions of Punjab. The collected samples were tested with ELISA and the symptoms were correlated with the results. Maximum disease incidence was recorded in Layyah (11.66%) trailed by Multan (5.66%), Bhakkar (03%) and District Khanewal (02%). Maximum and minimum threshold of disease was founded on sweet orange (18.33%) and grapefruit (2%) while no evidence of disease infestation was recorded on feutral’s early and kinnow mandrin. ELISA results leaded us towards decision of positive reaction formation from sweet orange and grapefruit samples while negative reaction formation from feutral’s early and kinnow samples while these results are also in line with the Bove et al., 1984 who described ELISA as an important technique to detect CSD. Adding to this, outcomes in culturing/ rearing and CSD detection through ELISA has stood much promising in Syria where thirty-eight citrus shrub samples exposed positively colored outcome by methodology of culturing and 38 trees samples founded colorful by ELISA (means positive) out of forty-seven verified CSD infected trees.
To diagnose CSD in the field, most promising and authentic symptoms are fruit symptoms which are more useful and characteristic. Few cases provide evidence of formation of acorned, premature, irregular, and loped fruits on the shrub, thin skin of fruit particularly at stylar helps in breakdown of acorny fruit. Diseased shrub produces acorny and loped fruits which remain greenish to yellowish with false taste as similar symptoms has been observed by Mello et al. (2008). Moreover, Distribution of S. citri exposed graft experimentation as unreliable in plants with low pathogen titer appeared at low temperature as discussed by Gumpf and Calavan, 1981. For this reason, we observed in many years that hot summer season is more effective for inoculum development, collection and sampling for transmission experiments and detection of S. citri. as S. citri was mostly detected from the samples during summer. Hot temperature in greenhouse is essential for symptoms expression in control environments. Day temperature should be in range of (32-38oC) while night temperature should not be less than 27oC. Temperature should not exceed 40oC in any length of time. The epidemiological aspects of CSD are complicated as discussed by researchers conducting their research on wall-less millicutes. Pathogen possesses a with wide range of host including weeds and commercialized crops. It has also a wide range of leaf hopper vectors. All these factors could stimulate the extent of impact of CSD in grooves.
Conclusions and Recommendations
S. citri has the capability to raise economic losses by impacting various host crops which ultimately leads to enhancement of grower’s concern. Insect vector elimination methods are crucial for preventing pathogen spread.
Acknowledgments
The authors are highly grateful to S. Anwar Rizvi, Ph. D. Ex-Senior Staff Officer, USDA-APHIS-PPQ-PHP, Former Area Director – South America, USA for the provision of logistic support for the research work. Special thanks are also due to Agdia, Inc. 52642 County Road 1, Elkhart, IN 46514, USA ([email protected]) for the provision of Antibodies for the detection of Spiroplasma citri for the current research work.
Novelty Statement
Novelty of the research is that it is the first study on the devastating pathogen “Spiroplasma citri” of citrus causing enormous losses to the grooves showing the current status, etiology, symptomatology, cultivar susceptibility and serological detection of the pathogen in the non-core of the Southern Punjab, Pakistan.
Author's Contribution
Ummad ud Din Umar, Syed Atif Hasan Naqvi and Ateeq ur Rehman conceived the idea, experiments were performed by Ishfaq Ahmed, Syed Atif Hasan Naqvi and Abdur Rehman. Statistical analysis was performed by Syed Atif Hasan Naqvi, Sibghat Ullah and Shah Pasand while references were managed by Muhammad Asif, Zulfiqar and Zehri Khan.
Funding
The research was funded by the Office of Research Innovation and Commercialization, Bahauddin Zakariya University, Multan, 60800, Pakistan.
Conflict of interest
The authors have declared no conflict of interest.
References
Abu-Zeid, A., A. Kishtah and E.M. Khalil. 1988. Isolation and culturing of Spìroplasmacitri associated with stubborn disease of citrus in Egypt. J. Phytopathol., 20: 139-140.
Anonymous. 2018. Pakistan Statistical Year Book. Federal Bur. Stat., Statistical Division. Karachi. Pakistan.
Boonham, N., J. Kreuze, S. Winter, R. van der Vlugt, J. Bergervoet, J. Tomlinson and R. Mumford. 2014. Methods in virus diagnostics: From ELISA to next generation sequencing. Virus Res., 186: 20–31. https://doi.org/10.1016/j.virusres.2013.12.007
Bové, J.M., E.C. Calavan, S.P. Capoor, R.E. Cortez and E. Schwarz. 1974. Influence of temperature on symptoms of California stubborn, South Africa greening, India citrus decline and Philippines leaf mottling diseases. In: Conf. Int. Org. Citrus Virol., L.G. Weathers and M. Cohen, eds., Richmond, V.A. pp. 12-15.
Bové, J.M., J. Renaudin, X. Foissac, P. Gaurivaud, P. Carle, F. Laigret, C. Saillard and M. Garnier. 2002. Spiroplasmacitri from functional genomics to genomics. In: Proc. 15th Conf. Int. Organ. Citrus Virol. N. Duran-Villa, R. G. Milne, and J. V. da Graça, eds. IOCV, Riverside, CA. pp. 278-287.
Bové, J.M., R.E. Whitcomb and R.E. McCoy. 1983. Culture techniques forspiroplasmas from plants. In: Methods in Mycoplasmology, J.G. Tully and S. Razin, eds. Academic Press, Inc, N.Y. pp. 225-234. https://doi.org/10.1016/B978-0-12-583802-3.50032-X
Bové, J.M., 1988. Epidemiology of Spiroplasmacitri in the old world. In: Proc. 10th Conf. IOCV, Riverside, IOCV. pp. 295-299.
Bradbury, J.F., 1991. Spiroplasmacitri. CMI Descriptions of Fungi and Bacteria No. 1046. CAB International, Wallingford, UK.
Clark, M.F. and A.N. Adams. 1977. Characteristics of the microplate method of enzyme- linked immunosorbent assay for the detection of plant viruses. J. Gen. Virol. 34: 475-483. https://doi.org/10.1099/0022-1317-34-3-475
Fawcett, H.S., J.C. Perry and J.C. Johnson.1944. The stubborn disease of citrus. Calif.: Citrogr., 29: 140-147.
Fletcher, J. and S.A. Slack. 1986. Latex agglutination as a rapid detection assay for Spiroplasmacitri. Plant Dis., 70: 754-756. https://doi.org/10.1094/PD-70-754
GoP. 2015. Agriculture statistics of Pakistan. Ministry of food, agriculture and livestock. Economic, trade and investment wing. Islamabad, Pakistan.
Gumpf, D.J. and E.C. Calavan. 1981. Stubborn disease of citrus. In: Maramorosch, K. and Raychaudhuri, S.P., eds. Mycoplasma diseases of trees and shrubs. New York, Academic Press. pp. 97-134. https://doi.org/10.1016/B978-0-12-470220-2.50008-0
Mello, A.F.S., R.K. Yokomi, U. Melcher, J.C. Chen, A.C. Wayadande and J. Fletcher. 2008. Genetic diversity of Spiroplasmacitri strains from different regions, hosts, and isolation dates. Phytopathology. 98: 960-968. https://doi.org/10.1094/PHYTO-98-9-0960
Oldfield, G.N., D.A. Sullivan and E.C. Calavan. 1984. Inoculativity of leafhopper vectors of stubborn disease in California. In: Proc. 9th Conf. Int. Organ. Citrus Virol. S.M. Garnsey, L.W. Timmer and J.A. Dodds, eds. IOCV, Riverside, CA. pp. 125-130.
Reichert, I., 1930. Diseases, new to citrus, found in Palestine. Phytopathol., 20: 999-1002.
Sheta, E., S. Salem, A.M. Abou-Zeid, M. Osman, M.A. Shafik and A. El-Hawari. 2004. Development of a citrus certification program in Egypt. Proc. 15th Conf. Int. Org. Citrus Virol. (IOCV), Riverside, 3-6 November 2004, pp. 321-329.
Whiteside, J.O., S.M. Garney and L.W. Timmer. 1988. Compendium of citrus diseases. APS Press, St. Paul. pp. 80.
Wisler, G.C., S.M. Garnsey, L.G. Brown and C.L. Schoulties. 1992. Manual for introduction of citrus germplasm into Florida. Division of Plant Industry P.O. Box 147100 Gainesville, FL 32614-7100.
To share on other social networks, click on any share button. What are these?