GET THE APP

International Research Journals

International Research Journal of Plant Science

All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.

Research Article - International Research Journal of Plant Science ( 2022) Volume 13, Issue 6

Arbuscular Mycorrhizal Fungi in Mizo Bird?s Eye Chilli (Capsicum frutescens L.) from Home Gardens in Aizawl

R. Vanlalmalsawmi1 and John Zothanzama2*
 
1Department of Environmental Science, Mizoram University, Tanhril, 796004, India
2Department of Biotechnology, Mizoram University, Tanrhil, 796004, India
 
*Corresponding Author:
John Zothanzama, Department of Biotechnology, Mizoram University, India, Email: john_zza@yahoo.co.in

Received: 22-Nov-2022, Manuscript No. IRJPS-22-71002; Editor assigned: 23-Nov-2022, Pre QC No. IRJPS-22-71002; Reviewed: 07-Dec-2022, QC No. IRJPS-22-71002; Revised: 23-Dec-2022, Manuscript No. IRJPS-22-71002; Published: 30-Dec-2022, DOI: http:/dx.doi.org/10.14303/irjps.2022.039

Abstract

A study was conducted on the colonization and the diversity of Arbuscular Mycorrhizal Fungi on the roots of the Mizo Bird’s eye chilli Capsicum frutescens L. The study was carried out at three home gardens within Aizawl, Mizoram during the year 2018 - 2019. The study was conducted for different stages of the plant, namely – Juvenile stage, Fruiting stage and Senescence stage. The highest colonization of Arbuscular Mycorrhizal Fungi was found in the roots of the plant in the juvenile stage and the lowest was found in the roots of the plant in the senescence stage. Seven Arbuscular Mycorrhizal fungal taxa belonging to the   genera Acaulospora (3   spp.), Glomus (2   spp.),   Pacispora   (1   sp.) and Funneliformis (1 sp.) were found. Among these, Acaulospora was the dominant genus found at all sites, followed by Glomus. The spore density and root colonization of AMF on Mizo Bird’s Eye Chilli varied significantly among the different stages of the plant.

Keywords

Mizo bird’s eye chilli, Colonization, Juvenile, Fruiting, Senescence, Spore.

Introduction

The Mizo Bird’s Eye Chilli (Capsicum frutescens L.) is located at various places of the world; one of such center of domestication is the Mizoram State of India. In Mizoram, they are locally called ‘Mizo hmarchate’ or Mizo Bird’s eye chilli which belongs to the species C. frutescens and is widely grown in the state of Mizoram. It is mainly used for spicy cuisines, in pickles, chutneys, hot sauces and local medicines and has a very high demand in neighboring state like Assam, Tripura, Manipur and countries like China, Thailand, and Vietnam. The Bird’s Eye Chilli has recently been registered as the rightful Mizo Property under the Geographical Indication (GI) with the name Mizo Chilli or Mizo Bird’s Eye Chilli. Mizoram is known for the presence of considerable diversity of Bird’s eye chilli with respect to fruit shape, size, colour, pungency, plant type, physiological characteristics, reactions to diseases and pests, adaptability and distribution. Three different varieties/qualities – Grade A, Grade B and Grade C of Mizo Hmarchate are being cultivated in the eight districts of Mizoram (Alarcón et al., 2012).

Mycorrhiza is the symbiotic association between plant roots and fungus localized in root-like structure in energy which moves primarily from plants to fungus and inorganic plants to resources from fungus to plant (Lewis, 1973). The term mycorrhiiza was first used by (Francke, 1934) to describe the long - lived association between plant roots and fungal mycelium (Harley, 1969). They are formed between members of the zygomycetes (order, glomales) and the majority of angiosperm species, which includes most agriculturally important crops (Alguacil et al., 2014). AMF are a key functional group for agroecosystems due to their widespread geographical distribution and because they are commonly associated with many important crops (Brundrett, 2009; Alarcon et al., 2012).

AMF are associated with different species and varieties of chili pepper (Capsicum spp.), whose AMF colonization have ranged from 38% to 68% (Castillo et al., 2010; Boonlue et al., 2012; Chen et al., 2012; Vays and Vays, 2012). In addition, some reports have demonstrated significant variations in the composition and in the number of AM fungal spores among Capsicum species (Boonlue et al., 2012; Vays and Vays, 2012).

Materials and Methods

Study Sites

Three study areas, namely Garden 1, Garden 2 and Garden 3 were randomly selected in Aizawl, Mizoram which lies at latitude 23° 44’ 16" N and longitude 92° 39’ 31" E (Garden 1), latitude 23° 43’ 10" N and longitude 92° 43’ 1" E (Garden 2) and latitude 23º 42’ 50" N and longitude 92º 42’ 49" E (Garden 3).

Collection of Samples

The roots and soil samples were taken from a depth of 5 – 15 cm of the rhizosphere portion from three different sites. The soils from the upper layer were scrapped off to remove litter layer. Approximately, 200 grams of rhizospheric soils along with fine roots were collected in a clean plastic box with a tight lid. The soil shaken from the roots were collected, shade dried and stored at room temperature until the soil got dried.

Analysis of Root Colonization

The root samples were washed free of soil and fine roots were cut into segments of 1 cm in length. The root segments were treated in 10% KOH solution and heated for around 15 - 20 minutes after which it was washed again with water and stained using Trypan blue stain. The root segmens were then observed under the microscope and colonization was calculated using the formula given by Giovanetti and Rosse (1980):

food-science-technology

Isolation and Identification of Spores

The spores were isolated from the soil samples of 100 g by wet sieving and decanting technique according to Gendermann and Nicholson (1963). The clean and intact spores were isolated using a needle and were mounted on a glass slide with a drop of Melzer’s reagent. All the spores were examined under the microscope for their morphological characteristics. Spore characterization was mainly done with the help of spore characteristics given by INVAM, 1997.

Result and Discussion

The analysis of mycorrhizal colonization in roots was done using collection of samples from nine plants and grouped into three plant stages, namely - Juvenile stage, Fuiting stage and Senescence stage. The analysis was done on 450 stained segments of fine roots which showed a significant variation between the three stages (Figure 1). The mycorrhizal colonizattion ranged between 30% - 68%. The highest colonization was found in the Juvenile stage,i.e., 57% (± 9.45 SD), followed by the Fruiting stage 38% (± 4.0 SD) and least colonization was found in the Senescence stage 35% (± 5.03 SD).

plant-science-esculentus-juvenile-stage

Figure 1. Percentage AMF Colonization with SD (±) values at ± 4.0, ± 5.03 and ± 9.45 for Fruiting stage, Senescence stage and Juvenile stage respectively.

Seven mycorrhizal spores were identified from the soil samples collected, they are - Acaulospora foveata1, Acaulospora lacunosa2, Acaulospora scrobiculata3, Glomus aggregatum4, Glomus aureum5, Pacispora scintillans6 and Funneliformis geosporum7 (Figure 2)

plant-science-esculentus-juvenile-stage

Figure 2. Mycorrhizal spores found in the soil sample.

The highest colonization of roots was collected from the juvenile stage. Proper addition of natural manures was observed with proper irrigation and proper tillage for air circulation which have increased the plant production thereby facilitating production of new young and fine roots. According to (Oehl, 2004) and Alquacil et al. (2014), intensive agriculture management practices including cultural practices like chemical fertilization, pest control, continuous monoculture, soil tillage, may have significant impacts on the interactions between AMF and plants.

Capsicum frutescens L. is an annual plant which completes its life cycle in one growing season, and then dies. This character of the plant could contribute to the population of AMF communities during the various stages of the plant life cycle. Population of AMF declined during the fruiting stage and least population or colonization was found during senescence period. The senescence period is marked by the gradual deterioration of the functional characteristics of the plants. As the plant reaches maturity or senescence stage, the number of fine roots produced lessens or declines which contributes to the less number of AMF population as AMF infests only the young and fine roots. These findings agree to that of Pawar, J. and Trafdar, J.C. (2006) who attributes the differences to the length of the growing season and the type of root systems of trees, which make the rhizosphere more favourable to spore propagation and AMF colonization (Mohnish Vyas and Anil Vyas, 2012).

(Gashua, et al. 2015) also identified spores belonging to Glomus sp and Gigaspora spp. which were associated with chilli plant. Sánchez-Roque, et al. (2016) also found Glomus spp. and Acaulospora sp associated with chilli plant. Wagner et al., (2019) identified spores belonging to the genera Acaulospora, Glomus, Gigaspora and Funneliformis in association with the rhizosphere of Capsicum frutescens. However, the association of chilli plant with Pascispora scintillans has not been recorded so far in literature (Gerdemann, 1963), (Giovannetti, 1980), (Caputti, 2009). The present record is the first report of the species in chilli plant i.e., the Mizo Bird’s eye chilli.

It may be concluded that the study is significant since it has revealed the AMF association in the Mizo Bird’s Eye Chilli plant as well as a new record of the species Pascispora scintillans from the chilli plant. However, since the work done is not conducted from a larger assemblage of samples with more variation of geographical location, further intensive studies may be conducted to identify more AMF species as well as to find out exact nature and level of the AMF association in the Mizo Bird’s Eye Chilli plant.

References

Alarcón A, Hernández-Cuevas LV, Ferrera-Cerrato R, Franco-Ramírez A. (2012). Diversity and agricultural applications of arbuscular mycorrhizal fungi in Mexico. J Biofertil Biopestici. 3.

Indexed at, Google Scholar, Cross Ref

Alguacil MM, Torrecillas E, García-Orenes F, Roldán A. (2014). Changes in the composition and diversity of AMF communities mediated by management practices in a Mediterranean soil are related with increases in soil biological activity. Soil Biol Biochem. 76: 34-44.

Indexed at, Google Scholar, Cross Ref

Boonlue S, Surapat W, Pukahuta C, Suwanarit P, et al. (2012). Diversity and efficiency of arbuscular mycorrhizal fungi in soils from organic chili (Capsicum frutescens) farms. Mycoscience, 53: 10-16.

Indexed at, Google Scholar, Cross Ref

Brundrett MC. (2009). Mycorrhizal associations and other means of nutrition of vascular plants: understanding the global diversity of host plants by resolving conflicting information and developing reliable means of diagnosis. Plant Soil. 320: 37-77.

Indexed at, Google Scholar, Cross Ref

Castillo Rubio C, Rubio R, Borie F, Sieverding E. (2021). Diversity of arbuscular mycorrhizal fungi in horticultural production systems of southern chile.

Indexed at, Google Scholar, Cross Ref

Caputti G, Corbani RZ, Mazzonetto F, Dalri AB, et al. (2009). Effect of arbuscular mycorrhizal fungi in the development of seedlings of Citrus sinensis grafted on Citrus limonia with different doses of fertilizer monoammonium phosphate on sandy soil. Ecossistema. 105-110.

Indexed at, Google Scholar

Chen K, Weixin L, Guo S. (2012). Diversity of arbuscular mycorrhizal fungi in continuous cropping soils used for pepper production. Afr J Microbiol Res. 6: 2469–2974.

Indexed at, Google Scholar, Cross Ref

Francke HL. (1934). Beiträge zur Kenntnis der Mykorrhiza von Monotropa hypopitys L.: Analyse und Synthese der Symbiose. Flora Allg bot Ztg. 129: 1-52.

Google Scholar

Gashua IB, Abba AM, Gwayo GA. (2015). Occurrence of arbuscular mycorrhizal fungi in chilli peppers (Capsicum annuum L.) grown in sahelian soil. Int j curr microbiol. 4: 419-425.

Indexed at, Google Scholar

Gerdemann JW, Nicolson TH. (1963). Spores of mycorrhizal Endogone species extracted from soil by wet sieving and decanting. Trans Br Mycol. 46: 235-244.

Indexed at, Google Scholar, Cross Ref

Giovannetti M, Mosse B. (1980). An evaluation of techniques for measuring vesicular arbuscular mycorrhizal infection in roots. New Phytol. 489-500.

Indexed at, Google Scholar, Cross Ref

Harley JL. (1969). The biology of mycorrhiza. The biology of mycorrhiza.

Indexed at, Google Scholar, Cross Ref

Lewis DH. (1973). Concepts in fungal nutrition and the origin of biotrophy. Biol Rev. 48: 261-277.

Indexed at, Google Scholar, Cross Ref

Oehl F, Sieverding E, Mäder P, Dubois D, et al. (2004). Impact of long-term conventional and organic farming on the diversity of arbuscular mycorrhizal fungi. Oecologia. 138: 574-583.

Indexed at, Google Scholar, Cross Ref

Rizosfera FMAAA, Dez D. Arbuscular mycorrhizal fungi associated with pepper ten lines rhizosphere chillies capsicum frutescens.

Indexed at, Google Scholar, Cross Ref

Vyas M, Vyas A. (2012). Diversity of arbuscular mycorrhizal fungi associated with rhizosphere of Capsicum annuum in Western Rajasthan. IJPAES. 2: 256-262.

Indexed at, Google Scholar

Citation: Vanlalmalsawmi R, et al (2022). Arbuscular Mycorrhizal Fungi in Mizo Bird�s Eye Chilli (Capsicum frutescens L.) from Home Gardens in Aizawl. IRJPS. 13: 039.