Effects of temperature, light regime and substrates on the production and germination of Stenocarpella maydis pycnidiospores

Efeito de temperatura, regime de luminosidade e substratos sobre a produção e germinação de picnidioporos de Stenocarpella maydis

Effects of temperature, light regime and substrates on the production and germination of Stenocarpella maydis pycnidiospores

Efeito de temperatura, regime de luminosidade e substratos sobre a produção e germinação de picnidioporos de Stenocarpella maydis

Paulo Roberto Kuhnem Júnior^I*; Ricardo Trezzi Casa^I; Amauri Bogo^II; Lenita Agostineto^I; Jonathan Marcel Bolzan^I; David José Miqueluti^I

^IDepartamento de Agronomia, Centro de Ciências Agroveterinárias, Universidade do Estado de Santa Catarina, Lages, Santa Catarina, Brazil.

IISecretaria de Cooperação Institucional e Internacional, Universidade do Estado de Santa Catarina, Av. Madre Benvenuta, 2007, 88035-001, Florianópolis, Santa Catarina, Brazil. *Author for correspondence. E-mail: [e-mail].

ABSTRACT

This study aimed to evaluate the production and germination of Stenocarpella maydis pycnidiospores under in vitro conditions as affected by substrate composition (sorghum, wheat, black oat or barley), light regime (continuous dark, 12-h light dark^-1 or continuous light conditions), and incubation temperature (21, 24, 27, 30 or 33ºC). Each substrate (20 g of grain) was soaked in 100 mL of water for 24h and sterilized twice for 20 min at 127ºC. Three plugs (5 mm diameter) of a single-spored culture of S. maydis were used as inocula for each substrate. Assessments of pycnidiospore production per gram of grain and percent germination were made 14 days after inoculation. Barley, black oat or wheat grains were the best substrates for the mass production of S. maydis pycnidiospores and the maintenance of high germination rates. The highest pycnidiospore production (67,600 pycnidiospores g^-1) was obtained using barley grain as a substrate with incubation at 27ºC under a 12-h light dark^-1 cycle.

Keywords: Diplodia, ear rot, stalk rot, natural medium.

RESUMO

A produção e a germinação de picnidiosporos de Stenocarpella maydis foram avaliadas in vitro sob a influência da composição de substratos (sorgo, trigo, aveia preta e cevada), regime de luminosidade (escuro contínuo, fotoperíodo de 12h ou luz contínua) e temperatura de inbucação (21, 24, 27, 30 ou 33ºC). Três discos de 5 mm de cultura monospórica de S. maydis foram inoculados em cada substrato. A produção e o percentual de germinação de picnidiosporos foram avaliados aos 14 dias após a inoculação. Grãos de cevada, aveia preta e trigo foram os melhores substratos na produção e germinação de picnidiosporos de S. maydis. A maior concentração (67.600 picnidiosporos g^-1) foi obtida em grãos de cevada, à 27ºC e 12h de fotoperíodo.

Palavras-chave: Diplodia, podridão de grãos, podridão de colmo, meio natural.

Introduction

Stenocarpella maydis (Berk.) Sutton [Syn. Diplodia maydis (Berk.) Sacc.] is an important fungal pathogen of maize (Zea mays L.) and causes both ear and stalk rots (WHITE, 1999). These diseases are distributed worldwide, and in Brazil, they are most prevalent in areas with no-tilled monoculture systems (CASA et al., 2006; ZAMBOLIM et al., 2000). The pathogen survives on maize plant debris and internally in seeds as pycnidia or mycelium (CASA et al., 1998, 2003). Infected ears can cause kernel rot, which downgrades production values for the maize industry (REIS et al., 2004).

In maize breeding programs, pycnidiospore suspensions are mostly used as inocula in experiments to assess the resistance to disease induced by S. maydis under conditions of natural infection or artificial inoculation in the field (ANDERSON; WHITE, 1994; KOEHLER, 1951; MÁRIO; REIS, 2003; PAPPELIS et al., 1973). For the latter, a large amount of inoculum may be necessary (MÁRIO; REIS, 2003; ULLSTRUP, 1970).

Previous research has shown that the viability of pycnidiospores decreases with continued exposure to sunlight (BRUNELLI et al., 2006), and polysaccharides such as dextrose but not cerelose are required for growth (KINSEL, 1937). Species of the Stenocarpella genus usually present fast mycelial growth but reduced sporulation efficiency on artificial media (WHITE, 1999). Culture media such as PDA (potato + dextrose + agar) (MORANT et al., 1993), PSA (potato + sucrose + agar) (CASA et al., 2007), OFA (oat flour + agar) (JONG; EDWARDS, 1991) and malt extract-yeast + agar (BIZZETTO et al., 2000) have been used for Stenocarpella mycelial production but result in very low sporulation rates. Morant et al. (1993) observed that adding biotin to the media has a stimulatory effect on S. macrospora sporulation.

In addition to culture media, environmental factors such as temperature and light exposure are essential for fungal sporulation (DHINGRA; SINCLAIR, 1995). According to Griffin (1994), proteins and enzymes that are responsible for fungus cell maturation are stimulated by temperature. However, light exposure and light quality could inhibit the reproductive capacities of some fungal cells (HAWKER, 1957).

Many substrates that are based on oat, rice, barley, corn, soybean and sorghum grains are reported to improve the mycelial growth rates of many different fungi on artificial media (DHINGRA; SINCLAIR, 1995; HARTMAN et al., 1997; KLINGELFUSS et al., 2007; MELGAR; ROY, 1994; TOLEDO et al., 2004). Although Stenocarpella spp. has been grown on maize stalks (CASA et al., 2007), sorghum grains (ULSTRUP, 1970) and oat grains (MORANT et al., 1993), pycnidiospore production was poor, and the incubation period was longer than 30 days on these substrates.

In plant pathological research, the development of affordable and efficient methods to produce abundant, uniform inocula for artificial inoculations is key. Hence, the objective of this study was to develop such a method by evaluating the effect of natural substrates, temperature and light regimes on the production and germination of S. maydis pycnidiospores under in vitro conditions.

Material and methods

Experiments were carried out at the Centro de Ciências Agroveterinárias (CAV), UDESC (Universidade do Estado de Santa Catarina). Maize kernels infected with S. maydis were obtained in a commercial field located in the Abelardo Luz municipality, Santa Catarina State, Brazil. Kernels were disinfested in 1% NaOCl and plated on potato-dextrose agar (PDA). Plates were maintained under cool, white fluorescent lamps (Philips 15W/75) at 25°C for 5 days until mycelial growth reached approximately 3.0 cm in diameter. A virulent S. maydis isolate (SM1) from the CAV culture collection that was tested in previous studies was used in the experiment.

A factorial experiment with three factors, substrate (sorghum, wheat, black oat or barley grains), light regime (continuous dark, 12-h light dark^-1 cycle or continuous light conditions), and temperature (21, 24, 27, 30 or 33ºC) was designed to evaluate the mass production and percentage of germination of S. maydis pycnidiospores under in vitro conditions.

Twenty grams of each substrate were soaked with 100 mL of sterilized water in 1 L Erlenmeyer flasks for 24h, after which time the excess water was removed, and the substrates were sterilized twice for 25 min. at 127ºC in intervals of 24h. Three plugs (5 mm in diameter) of mycelial growth from PDA medium containing hyphal tips of S. maydis were used to inoculate the substrates, which were incubated for 14 days (FLETT; McLAREN, 2001) for maximum pycnidiospore production. Every 5 days, the flasks were rotated manually and gently for 10 s to homogenize the substrates. Pycnidiospores were harvested by combining 20 mL of distillated water plus 0.05% of Tween-10 and 2 g of the contents of each flask in a 50 mL tube and homogenizing the mixture for 10 s in a vortex at high speed. Four 0.03 mL aliquots of each spore suspension tube were deposited onto a microscope slide. The pycnidiospore concentration per slide was determined using an optical microscope (40 x objective) and converted to the number of spores per gram of substrate. Pycnidiospore germination was determined on a volume of 1 mL of spore suspension in 1% water-agar plates that were incubated for 6h in BOD (biochemical oxygen demand) continuous light systems at 25ºC (CASA et al., 2007), and the percentage of pycnidiospore germination was assessed directly on the plates using an optical microscope (40x objective). A total of 50 pycnidiospores per plate were counted, and the percentage of pycnidiospores showing germ tubes with twice the diameter of the spore, which were considered germinated, was assessed (CASA et al., 2007).

The experiments followed a completely randomized design. The linear model analysis of covariance (ANCOVA) was used to investigate the effects of single and interaction responses of the factors. The two response variables, number of pycnidiospores g^-1 and percentage of pycnidiospore germination, were square root-transformed to normalize the distribution. The comparison of the average value for levels of substrate and light regime were performed using a Bonferroni Test, and the temperature of each substrate and light regime combination was assessed by polynomial regression (STEEL et al., 1997). The statistical analysis of the data was performed by WinStat software (MACHADO; CONCEIÇÃO, 2009), and all tests that were performed considered the minimum level of 1% of the significance bounds range distribution (p = 0.0001).

Results and discussion

Stenocarpella maydis pycnidiospores were produced in all substrates, temperature and light regimes evaluated in this study. However, there were significant effects of light regime, temperature, substrate and their interactions, including a triple interaction, on pycnidiospore production (Table 1).

Stenocarpella maydis responded differently to the qualitative factors of substrate and light regime for pycnidiospore production and percentage of germination (Table 2).

A non-significant difference was observed between the 12-h light dark^-1 and continuous light regimes on pycnidiospore production and the percentage of germination (Table 2). Lower levels of pycnidiospore production and percentage of germination were observed under continuous dark conditions regardless of the temperature or substrate (Table 2). However, the largest numbers of pycnidiospores g^-1 (11,800) and 60% germination efficiency were obtained with the barley grain substrate regardless of the light regime or temperature (Table 2).

The adjusted polynomial regression of all substrates for pycnidiospore production and percentage of germination were significant (p = 0.0001), with the exception of pycnidiospore germination on a wheat substrate with a 12-h light dark^-1 cycle and continuous light and a black oat substrate with a 12-h light dark^-1 cycle (data not shown).

The barley grain substrate at 27ºC under a 12-h light dark^-1 cycle yielded the largest number of pycnidiospores per gram (67,600), 93% of which germinated after 14 days of incubation; therefore, these conditions are recommended for mass inoculum production (Figures 1 and 2).

Hanada et al. (2002) and Brunelli et al. (2006) observed that Mycosphaerella fijiensis (Morelet) Deighton and Cercospora zeae-maydis Tehon & Daniels did not produce conidia in the absence of light. Light exposure has a direct effect on the activation of key enzymes of spore production (MACRAE; YODER, 1988). Nevertheless, some fungal species do not seem to respond to light exposure (PAUL; MUNKVOLD, 2005).

Data from this study corroborate many other reports (BRUNELLI et al., 2006; HANADA et al., 2002; MAFACIOLI et al., 2008; NOZAKI et al., 2004; ULLSTRUP, 1970) in which a temperature between 22 and 27^oC was found to be the optimum interval for inoculum production. Minimum and maximum temperatures of 21 and 33ºC, respectively, resulted in lower S. maydis pycnidiospore production (Figure 1) and percentage of germination (Figure 2) for all substrates tested.

In contrast to our results, Casa et al. (2007) reported a 30% increase in S. macrospora conidia germination on PSA (potato-sucrose-agar) under continuous light compared to continuous dark conditions. The barley grain substrate was best suited for the mass production of pycnidiospores; under these conditions, the pycnidiospores retained 93% of their germination capability. This value is higher than the value found by Morant et al. (1993), who reported S. maydis pycnidiospore germination percentages of 86% and 96% on an oak grain substrate and mineral salt medium, respectively.

When studying mycelial growth and sporulation of S. maydis on sorghum, oak and agar-based substrates, Bizzetto et al. (2000) obtained no more than 10,000 pycnidiospores mL^-1 after 15 days of incubation. Previously, Ullstrup (1970) obtained 1,200,000 pycnidiospores mL^-1 of S. maydis after 6 weeks of incubation at 24ºC under a 12-h light dark^-1 cycle. In contrast, a barley grain substrate at 27ºC under a 12-h light dark^-1 cycle yielded approximately 700,000 pycnidiospores g^-1 after 14 days of incubation, which is slightly more than half of the number produced using Ullstrup’s (1970) method; however, these spores numbers were achieved in a significantly shorter time, demonstrating the efficiency of the present method to produce viable pycnidiospore inocula for experimental research.

Conclusion

The production of large numbers of S. maydis pycnidiospores while maintaining a high germination rate can be achieved using barley grain as a substrate and incubation at 27ºC under a 12-h light dark^-1 cycle. Light was found to be an essential factor for the asexual reproduction of this fungal species.

Acknowledgements

This research was supported by the “PROMOP” fellowship and “PAP” grant programs of Santa Catarina State University.

Received on July 27, 2010. Accepted on February 15, 2011.

License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Publication Dates

• Publication in this collection
  05 Jan 2012
• Date of issue
  Mar 2012

History

• Received
  27 July 2010
• Accepted
  15 Feb 2011