Introduction

Zea mays belongs to the Poaceae family1 and it is the 3rd most important crop by its production across the world, where rapidly increasing human population has already out-stripped the available food supplies. It plays a major role in food security in many developing countries in Asia and Africa. In Pakistan, maize is classified as the 4th most influential crop after wheat, rice, and cotton and its yield has increased by 6% during 2019–2020 which contributes 0.6% to the gross domestic production of Pakistan2. The 97% volume of the total maize production is achieved from two major provinces of Pakistan where Khyber Pakhtunkhwa (KPK) contributes 57% area and produces 68% of the total yield while in Punjab, maize covers 38% area and shares 30% of total maize yield. On the other side, Sindh and Balochistan provinces contribute only 2–3% of the total maize production3.

In Pakistan, 65% of maize is cultivated on irrigated lands while the rest is grown on dryland4. Maize, being a famous kharif crop (monsoon season crop), is also widely used as forage for domestic animals as well as for poultry5. Maize grains serve as a rich source of vitamins A, and B3, starch, oil, proteins, sugar, fiber, carbohydrates, and ash6. Apart from this, it serves as a raw material to produce corn oil, dextrose, corn syrup, corn flakes, wax, and cosmetics7, ethanol production8, and serves as a major source of calories in animal ingestion and feed sensationalism9.

Maize has a high economic value after rice and wheat and is grown at a large scale due to its ability to survive under various climatic conditions10. Pakistan offers the right set of conditions to enhance maize production, but many limitations impart bad effects on maize production. Many living and non-living factors result in yield losses in maize crops. Among various biotic factors, bacterial stalk rot of maize (BSRM) caused by Dickeya zeae (syn. Erwinia chrysanthemi pv. zeae) is of major concern and causes significant yield losses in maize, adversely affects the quality of the produce if left untreated11,12. Infected stalks produce an unpleasant smell and topple down of plants causing acute yield losses of up to 98.8%13.

Infection caused by D. zeae on maize becomes severe with the change in climatic conditions, and disease incidence increases with the increase in temperature and high humidity14,15. Dickeya zeae has a wide host range and spreads through rainwater from individual plants to the whole maize field16,17. Both high temperature and relative humidity favour the physiological and metabolic activities of the pathogen due to which bacterium grow well and produce sufficient pectolytic enzymes which degrade the plant cell13.

Geographic Information Systems (GIS) together with species distribution modeling (SDM) approaches have already been used in studying species and/or disease distribution as well as their forecasting18,19,20,21,22. Both GIS and SDM are influential tools for a better understanding of spatial disease distribution23. Also, the GIS facilitates the growers to take appropriate action well in time before the disease outbreak24. This technology is widely adopted as an important tool in epidemiological study of plant diseases. Wetwood disease is one of the most influential diseases on elm trees observed in the Northwest of Iran in Tabriz city and become terribly epidemic. The epidemiological assessment of wetwood disease on elm trees was studied by using geographic information system GIS18.

The proposed study aimed at estimating the stalk rot disease incidence, and severity on maize crops cultivated in the Sialkot district, Pakistan. Data collected on the stalk rot of maize and different bioclimatic layers were used in disease predictive modeling and forecasting. Maxent modeling was employed to predict regions with a high chance of disease spread based on disease occurrence and bioclimatic data. This model was further used to forecast the disease spread in coming years25,26. Predictive modeling, high risk of potential distribution, and high chances of BSRM in new areas could help design and adopt the disease management strategies in advance to cope with the potential yield loss due to bacterial stalk rot disease in maize crops. This study is helpful to the farmer community (growers) to understand the stalk rot of maize disease occurrence trends in the coming years and help them devise preventive disease management strategies before the disease outbreak. As no data on the potential distribution of BSRM is available in Pakistan, the current research was carried out to understand the potential distribution of D. zeae in maize-growing areas and predictive modeling for the disease outbreak in the coming years. To our knowledge, this is the first research study on this stated subject from Pakistan.

Materials and methods

Description of the locations of study

The rural areas in the Sialkot district of Punjab, Pakistan were selected for this research study. It is situated at the foot of Kashmir hills, near the river Chenab, in the northeast of Punjab, Pakistan (Fig. 1). Sialkot is bounded on the northeast by the Jammu and Kashmir state, on the north-west by two rivers (Ravi and Chenab) which separate it from the Gujrat, on the west and southeast by Gujranwala and Narowal districts respectively. Sialkot is located at 32.4945° N, 74.5229° E with an elevation of about 840 ft above sea level.

Figure 1
figure 1

Map of Sialkot District, Punjab Pakistan. The area in Sialkot District was divided into a total number of 159 small grid cells each covering an area of 5 × 5 km2.

The average monthly temperature in Sialkot ranges from 11.6 °C in January to 32.2 °C in June27. Monsoon is the source of precipitation in this region, and the mean annual rainfall is 957 mm, over half of which falls in the summer monsoon which often results in flooding28. The study area was divided into 159 grid cells of 5 × 5 km2 (Fig. 1). The major cultivated crops in the district of Sialkot are rice, wheat, and maize29. Kharif (monsoon) season is the main growing season of maize crop. However, it may be planted at any time from March to October.

Field survey for bacterial stalk rot of maize disease assessment

A field survey to assess the occurrence of BSRM was conducted from May to July 2021 in Sialkot district, Pakistan. All four tehsils in district Sialkot including Daska, Pasrur, Sambriyal, and Sialkot were systematically inspected. From each of the selected sites, five fields from every 5 km2 distance were visited. From each field, five points (5 m × 5 m area) were randomly inspected, and maize plants were observed for disease assessment. Field coordinates from each visited location were recorded by using GPS Essentials ArcGIS 10.4 v and MaxEnt v. 3.3 software. Names of the visited areas in Sialkot district along with the GPS coordinates in Degrees, Minutes, and Seconds (DMS) notation are presented as supplementary material.

Disease incidence (DI) and severity (Ds)30 were recorded from each visited location according to the given formulas reported by Tahir et al.30 Disease incidence percentage (DIP) was calculated by using the formula given below:

$$DIP{{ \% }} = { }\frac{{{\text{Total}}\;{\text{ No}}.\;{\text{ of }}\;{\text{Infected }}\;{\text{Plants}}}}{{{\text{Total }}\;{\text{No}}.\;{\text{ of}}\;{\text{ Observed }}\;{\text{Plants}}}}{ }\; \times { }\;100{ }$$

Disease severity was recorded by using the disease severity rating scale31, and the disease severity percentage (DSP) was calculated using the following formula:

$$DSP{{ \% }} = { }\frac{{{\text{Some}}\;{\text{ of}}\;{\text{ the}}\;{\text{ Rating}}}}{{{\text{Total}}\;{\text{ No}}.\;{\text{ of}}\;{\text{ plants}}\;{\text{ observed}}\; \times {\text{Rating}}\;{\text{ scale}}}}{ } \times { }100{ }$$

Isolation of Dickeya zeae from infected plant samples

Maize stalks showing the typical browning and necrosis symptoms were sampled for the isolation of bacteria. Infected segments were surface disinfected in ethanol (70%) for 5 min and 1% NaClO followed by five consecutive washings in sterilized distilled water32. Disinfected plant parts were aseptically crushed in distilled water and streaked on nutrient agar (NA) containing Petri plates and incubated at 26 ± 2 °C for 48h15. After incubation, morphological discrete bacterial colonies were picked aseptically and cultured on freshly prepared NGM medium (23 g of NA, 10 ml of glycerol (1% v/v), and 0.4 g of 2 mM MnCl2.4H2O/1000 ml) carrying Petri plates for detecting the production of characteristic pigments of D. zeae33. All the bacterial strains were preserved at − 80 °C in a solution of NB and 80% glycerol.

Biochemical characterization of Dickeya zeae

The biochemical characterization of D. zeae was carried out following previously reported methodologies: For catalase activity34, a 3% H2O2 on a glass slide, to show the formation of gas bubbles was performed according to Hayward et al.34 The procedure of Dasri et al.35 was followed to test bacterial motility and indole-3-acetic acid production35. Hydrogen sulfide production36 was tested following the methodology of Warren et al. A nutrient gelatin stab method was used for the determination of gelatin liquefication37. Nitrate reduction was assessed with Griess Llosvay reagents38 following the protocol of Choi, et al.38 Starch hydrolysis39, urease activity40, and levan production41 were also tested, for the characterizations of the D. zeae isolates.

Bioclimatic/Environmental variables

A total of 19 bioclimatic layers were obtained from the WorldClim database ver. 1.4 (www. worldclim.org)42. These layers are classified into two categories including temperature variables and precipitation which are presented in Table 1. Future climatic data for the years 2050 and 2070 was downloaded from CliMond43 based on the global climate model, CSIRO-Mk3.0 with the Intergovernmental Panel on Climate Change44.

Table 1 Bioclimatic layers used for predictive modeling of bacterial stalk rot maize disease by Maxent Software45.

Modeling procedure and GIS analyses

A pairwise Pearson correlation analysis was performed to overcome the multicollinearity of the bioclimatic/environmental variables by using ENMTools46. Based on percentage contribution, variables with a lower than 0.8 value were kept for model fitting. However, in the case of variables higher than 0.8 and highest contribution was selected45. The spatial resolution of bioclimatic variables was at 30 arc-seconds (~ 1 km). All these variables were clipped to match the dimensions of district Sialkot, Punjab Pakistan, and saved in ASCII grid format for further use in the MaxEnt program. ArcGIS software v. 10 was used for clipping these bioclimatic layers. The distributions of D. zeae were produced by using MaxEnt software ver.3.3. This software is most influential because it produces and records useful predictions related to species distribution in study area20. All the variables were converted to ASCII files in ArcToolbox 2.0 in ArcGIS47. Data related to stalk rot of maize distribution was also saved in comma-separated value format in an Excel program. The predicted distribution of stalk rot of maize was analyzed and reclassified into different groups. Moreover, the area of distribution was estimated in square kilometers with a zonal statistical analysis program in ArcGIS software.

Model validation and potential habitat prediction

Of all the methods, an area under the curve (AUC) is the most suitable method for evaluating the model accuracy48,49. Jackknife test was performed using the MaxEnt software to determine the predictive performances of all the selected variables by the adopted method from Pearson et al.50. The response curves were generated to observe how each bioclimatic layer affects the Maxent prediction, and how the logistic prediction varies under varying bioclimatic variables48. The values for AUC were theoretically set between 0.5 and 1. AUC value closer to 1.0 indicates a successful model with clear distinction while an AUC value closer to 0.5 reflects a model with no clear distinction51. The model classification index used in this study was: “failure” is 0.50 < AUC < 0.60, “poor” is 0.60 < AUC < 0.70, “fair” is 0.70 < AUC < 0.80, “good” is 0.80 < AUC < 0.90, and “excellent” is 0.90 < AUC < 1.0052,53. Both the curves, such as ROC and AUC were employed for the evaluation of accuracy of the disease distribution model54.

Spatial conservation assessment

The models of current and future distribution were compared with the surveyed areas of BSRM disease in 2021. The accuracy and fitting of models between different periods and all the surveyed areas were also analyzed. The current distribution of stalk rot of maize with future potential distributions in coming years i.e., 2050 and 2070 were combined. For calculating the suitable overlapping areas, the raster calculator was used according to the recently reported methods21,55.

Ethics approval and consent to participate

This study does not include human or animal subjects.

Statement on guidelines

All experimental studies and experimental materials involved in this research are in full compliance with relevant institutional, national and international guidelines and legislation.

Results

Bacterial stalk rot of maize disease assessment survey

All the tehsils in district Sialkot were inspected for BSRM disease assessment recording. The disease data and sampling sites are presented in Fig. 2.

Figure 2
figure 2

Pictorial representation of the data collection sites in district Sialkot, Pakistan.

Symptoms of BSRM were visually recorded from the visited fields. Data on DI and DS showed variations in disease occurrence levels within the villages of all districts in the Sialkot region. Out of 226 visited locations, the highest DI and DS were recorded from Bhoopal Wala (78.5 ± 4.5), Bangla Chowk (76 ± 2.3), Suraj (74 ± 3.2), Bhakhrewali (68.5 ± 2.7), Warsalke (67.5 ± 2.3), Khrolian (67.5 ± 1.8). Whereas, low DI and DS were recorded in Pasrur (20 ± 1), Chawinda (15 ± 2.9), Bun (11 ± 1.4), Head Marala (9 ± 1.1), and Boobkanwala (8.5 ± 1.4) (Table S2). Areas showing the highest and lowest DI percentages are presented in Fig. 3.

Figure 3
figure 3

The highest and lowest maize stalk rot disease incidence and severity were recorded from the surveyed locations.

Biochemical characterization of Dickeya zeae

Different tests such as catalase test, motility test, indole formation, H2S production, gelatin liquefaction, nitrate reduction, starch hydrolase, urease activity, and levan production were performed for the biochemical characterization of D. zeae (Table 2). All bacterial isolates (ERCAR-1, ERCAR-2, ERCAR-3, ERCAR-4, ERCAR-5) were found positive for motility test, able to perform catalase activity and nitrate reduction, but all strains resulted negative for H2S production and urease activity. For indole formation test results were negative with isolates ERCAR-1, ERCAR-2, ERCAR-5, but this assay was not done for ERCAR-3 and ERCAR-4. Of all the tested bacteria displayed gelatin liquefaction ability, except ERCAR-5 which was not tested. Starch hydrolase test results were negative for ERCAR-1, ERCAR-3, ERCAR-4, ERCAR-5 while the test was not performed for ERCAR-2. Similarly, bacterial isolates such as ERCAR-1, ERCAR-2, ERCAR-3, ERCAR-5 were observed negative for levan production while the test was not performed for ERCAR-4.

Table 2 Biochemical characterization of Dickeya zeae strains from Sialkot District, Pakistan, associated with stalk rot of maize.

Environmental variable selection and model performance

Pearson correlation revealed that coefficients between 28 sets of the 19 variables were higher than 0.8. Nineteen variables were selected based on the initial model percentage contribution. Pearson correlation value between every two variables was < 0.8, and the rate of the total contribution of all other variables was 100%. Currently, the most contributing variable bio-16 with a contribution of 25%, followed by bio-2 (11.5%), bio-4 (9.5%), and bio-1 (8.6%) while minimal contributing factors were bio-14 (0.3%), followed by bio-12 (0.1%) and bio-7 with a contribution of 0%. An omission curve on the training data showed a trend similar to the test data. The AUC of the training and test data were 0.871 and 0.765, respectively in the current scenario as shown in Fig. 4a. The accuracy of the current distribution model was observed excellent based on the model evaluation index.

Figure 4
figure 4

Change in receiver operating characteristic curve for (a) current year, (b) 2050, and (c) 2070.

For 2050, the most contributing variable was observed in annual precipitation (bio-12) with a contribution of 29.1%, followed by bio-8 (20.6%), bio-14 (11.1%), and bio-3 (8.3%) while minimal contributing factors were bio-15 (0.3%), followed by bio-7 (0.2%) and the least contributing factor was bio-10 with a contribution of 0.1%. The AUC of the training and test values were 0.856 and 0.766, respectively in 2050 as shown in Fig. 4b.

In the case of 2070, the most contributing variable was bio-12 with a contribution of 29.9%, followed by bio-8 (22.4%), bio-14 (13.6%), and bio-17 (8.6%) while minimal contributing factors were bio-2 (0.3%), and the least contributing factors were bio-15 and bio-16 with 0% contribution. The AUC of the training and test values were 0.853 and 0.784, respectively in the 2070 distribution model as shown in Fig. 4c.

Relationship between the occurrence of Dickeya zeae and bioclimatic variables

Current year

Jackknife analysis displayed that the environmental variable with the highest gain when used in isolation is bio-13 among all bioclimatic layers. Similarly, annual precipitation (bio-12), precipitation seasonality (bio-15), precipitation of wettest quarter (bio-17), and precipitation of warmest quarter (bio-18), were the most influential environmental variables that affect the distribution of D. zeae, with a training gain as presented in Fig. 5a. Precipitation of the coldest quarter (bio-19) and mean temperature of the warmest quarter (bio-10), were also influential bioclimatic variables with training gain. The response curve thresholds of the variables are given in Fig. 5b. Bio-16 ranged from 404 to 946 mm, bio-2 ranged from 14.2 to 15.7 °C, bio-4 ranged from 701 to 756 °C, bio-1 ranged from 22.6 to 23.3 °C, bio-18 ranged from 231 to 455 mm and bio-3 ranged from 41.5 to 44.7 °C while bio-19 ranged from 78 to 182 mm, bio-10 ranged from 30.0 to 31.5 °C, bio-5 ranged from 38.2 to 40.2 °C, bio-6 ranged from 4.1 to 5.2 °C, bio-7 ranged from 31.1 to 36 °C, bio-8 ranged from 28.7 to 29.6 °C, bio-9 ranged from 18.2 to 18.6 °C, bio-10 ranged from 30.0 to 31.5 °C, bio-11 ranged from 12.9 to 13.5 °C, bio-12 ranged from 620 to 1361 mm, bio-13 ranged from 175 to 423 mm, bio-14 ranged from 6 to 10 mm, bio-15 ranged from 108.0 to 119.1 mm, bio-17 ranged from 30 to 69 mm and bio-19 ranged from 78 to 182 mm.

Figure 5
figure 5

(a) Jackknife test of bioclimatic variables which are influential in the distribution of D. zeae in the current year; (b) Response curves of the bioclimatic variables showing how each variable affects the Maxent Prediction for the current year.

For 2050

Jackknife analysis showed that the environmental variable with the highest gain when used in isolation is bio-19 among all bioclimatic layers, which appears to reflect the most useful information by itself. Jackknife's analysis revealed that the omission of bio-14 decreases the gain the most. Which seems to have maximum information that is not present in the other variables.Similarly, mean temperature of wettest quarter (bio-8) annual precipitation (bio-12), precipitation of wettest month (bio-13), precipitation of the driest month (bio-14), precipitation of seasonality (bio-15), precipitation of wettest quarter (bio-16), and precipitation of the driest quarter (bio-17), were the most influential variables that affect the distribution of D. zeae, with a training gain as presented in Fig. 6a. The response curve thresholds of the variables are given in Fig. 6b. The bioclimatic variable values were as follows: bio-16 ranged from 391 to 895 mm, bio-2 ranged from 125 to 139 °C, bio-4 ranged from 7045 to 7391 °C, bio-1 ranged from 249 to 254 °C, bio-18 ranged from 147 to 417 mm and bio-3 ranged from 36 to 38 °C while bio-19 ranged from 91 to 200 mm, bio-10 ranged from 332 to 337 °C, bio-5 ranged from 422 to 427 °C, bio-6 ranged from 65 to 84 °C, bio-7 ranged from 341 to 380 °C, bio-8 ranged from 307 to 314 °C, bio-9 ranged from 201 to 208 °C, bio-10 ranged from 332 to 337 °C, bio-11 ranged from 146 to 156 C, bio-12 ranged from 597 to 1279 mm, bio-13 ranged from 176 to 384 mm, bio-14 ranged from 6 to 9 mm, bio-15 ranged from 103 to 114 mm, bio-17 ranged from 30 to 73 mm and bio-19 ranged from 91 to 200 mm.

Figure 6
figure 6

(a) Jackknife test of bioclimatic variables which are influential in the distribution of D. zeae for 2050; (b) Response curves of the bioclimatic variables showing how each variable affects the Maxent Prediction for 2050.

For 2070

In the case of 2070, Jackknife's analysis revealed that the omission of bio-14 decreases the gain the most. Which seems to have maximum information that is not present in the other variables. However, annual precipitation (bio-12), precipitation of wettest month (bio-13), precipitation of wettest quarter (bio-16), precipitation of driest quarter (bio-17), and precipitation of the coldest quarter (bio-19), were the most influential factors affecting the distribution of D. zeae, with a training gain as presented in Fig. 7a. Response curve thresholds of the variables are presented in Fig. 7b. The bioclimatic variable values were as follows: bio-16 ranged from 401 to 961 mm, bio-2 ranged from 128 to 140 °C, bio-4 ranged from 7002 to 7336 °C, bio-1 ranged from 271 to 277 °C, bio-18 ranged from 147 to 418 mm and bio-3 ranged from 36 to 38 °C while bio-19 ranged from 80 to 169 mm, bio-10 ranged from 354 to 360 °C, bio-5 ranged from 445 to 450 °C, bio-6 ranged from 83 to 103 °C, bio-7 ranged from 344 to 364 °C, bio-8 ranged from 326 to 333 °C, bio-9 ranged from 221 to 229 °C, bio-10 ranged from 354 to 360 °C, bio-11 ranged from 169 to 179 °C, bio-12 ranged from 602 to 1329 mm, bio-13 ranged from 191 to 454 mm, bio-14 ranged from 8 to 13 mm, bio-15 ranged from 108 to 123 mm, bio-17 ranged from 34 to 84 mm and bio-19 ranged from 80 to 169 mm.

Figure 7
figure 7

(a) Jackknife test of bioclimatic variables which are influential in the distribution of D. zeae in 2070; (b) Response curves of the bioclimatic variables showing how each variable affects the Maxent Prediction for 2070.

Modeled distribution and conservation assessment of Dickeya zeae

High suitability areas out of 226 visited locations in the Sialkot region were Bhoopal Wala, Bangla Chowk, Suraj, Bhakhrewali, Warsalke, Khrolian, and Bopal Wala showed the highest DI and DS. Moderate suitability was located in Kobay Chak, Sohedrik, Bajwat, Sialkot Airport Road, and Bdyana. While low-suitability areas were located in Pasrur, Chawinda, Bun, Head Marala, and Boobkanwala. The total suitability area trend increased over time from the current to the 2050s and 2070s. The current distribution of D. zeae increased in the low suitability area, as well as the moderate suitability areas while the trend in the 2050s and 2070s will also increase as shown in Fig. 8.

Figure 8
figure 8

Risk of bacterial stalk rot of maize disease distribution: (a) current, (b) 2050, and (c) 2070.

The overlapping suitability regions were also studied by overlapping the present and future (2050s and 2070s) potential distributions of D. zeae as shown in Fig. 9. The overlapping map indicated that there are chances that the area of BSRM disease progression will increase over the years. The green color indicates a very high risk at the current stage, the blue color indicates a very high risk in the 2050s while the red color indicates a very high risk in the 2070s. Bhoopal wala, Bangla Chowk, Suraj, Bhakhrewali, Warsalke, Khrolian, and Bopal wala were the high suitability areas, with high DI and DS 70–80%. Kobay Chak, Sohedrik, Bajwat, Sialkot Airport Road, and Bdyana were the moderate suitability areas, with 30–50% DI and DS. Pasrur, Chawinda, Bun, Head Marala, and Boobkanwala were the low suitability areas, with 10–20% DI and DS.

Figure 9
figure 9

Overlapping map of the ranges of very high risk of BSRM in the current scenario, 2050 and 2070 predictions.

Discussions

Maize production is vulnerable to the attack of various pathogens resulting into severe yield losses. Of all the major diseases, BSRM caused by D. zeae is of great concern because of significant yield losses. D. zeae is the most destructive plant pathogen that infects maize plants at any growth stage. A comprehensive field survey reflected that out of 226 visited sites in the district Sialkot region, DI ranged from 8.5 to 76% and this variation in the level of disease occurrence could be due to the cultivation of a wide variety of maize hybrids, environmental conditions prevailing in the region, crops rotation and disease management and cultural practices56. Similarly, in another related study, Sharma et al.57 recorded that the grain yield losses due to BSRM ranged from 21 to 98%57. In a study, Kumar et al.13 narrated that under favorable conditions, D. zeae could result in 98.8% crop yield losses, and the wide prevalence and survival of the bacterium is due to the wide host range, high temperature, and moisture (rainy season)13. Our results are similar to the study of Tahir et al.30 where eight maize-growing districts in central and south Punjab, Pakistan were surveyed for BSRM30. Results demonstrated that all the surveyed areas showed 100% prevalence and the highest DI and DS up to 53% and 30.2% respectively.

In the present study, the biochemical attributes of D. zeae, our results contrast with the findings of Jatoth et al.56 where all the tested bacterial strains displayed positive responses for H2S production and indole formation56, meanwhile the strains from the present study, resulted negative in the production of these compounds. Similarly, Kaur et al.58 subjected bacterial isolates to various biochemical tests and found them to show different reactions for utilization of starch and other sugars, gelatin liquefication, and growth at high salt levels58. Biochemical characterization helps to identify bacterial species based on the differential biochemical activities; nevertheless, various strains of D. zeae might demonstrate differences in various biochemical characteristics because of alterations in specific enzymatic activities58.

The Maxent algorithm modeling was employed to predict areas at high risk of disease outbreaks based on occurrence and environmental data in Sialkot; the model was further used to forecast the disease outbreaks in the coming years. In our study, results showed that a total of nineteen bioclimatic variables were selected that were slightly different from the variables used in other studies59,60,61.

Although, the distribution and presence of pathogens may depend upon many factors, here we only focused on bioclimatic factors, because, these factors are biologically meaningful in defining the species distribution62. In many previous studies, these factors were selected for studying the habitats and their implications for the conservation of species as well as for the development of policies20,21, 44. Bioclimatic variables used for modeling by Maxent software have already reported45. Certain variables play a significant role in the distribution of stalk rot of maize. Currently, the precipitation of the wettest quarter, mean diurnal range, temperature seasonality, and annual mean temperature made significant contributions to the model. The AUC of the training and test data were 0.871 and 0.765, respectively in the current distribution model. Jackknife analysis revealed that the environmental variable with the highest gain when used in isolation was bio-13 among all bioclimatic layers.

In the coming years in 2050 the variables of annual precipitation, mean temperature of the wettest quarter, precipitation of the driest month, and isothermality will be crucial. In the 2070s, it was predicted that certain variables such as annual precipitation, mean temperature of wettest quarter, precipitation of driest month, and precipitation of driest quarter would be influential in a disease outbreak. A similar study explained the connection between bioclimatic variables and the potential distribution of Haemaphysalis spinigera associated with Kyasanur forest disease. The study concluded that the average temperature of the warmest quarter, average diurnal temperature range, precipitation of the wettest period, and annual precipitation contribute to affecting the spatial distribution of H. spinigera63.

High suitability areas were Bhoopal wala, Bangla Chowk, Suraj, Bhakhrewali, Warsalke, Khrolian, and Bopal wala showed the highest DI and DS. Moderate suitability was in Kobay Chak, Sohedrik, Bajwat, Sialkot Airport Road, and Bdyana. While low suitability areas were in Pasrur, Chawinda, Bun, Head Marala, and Boobkanwala. The total suitability area trend increased over time from the current to the 2050s and 2070s. The current distribution of D. zeae increased in the low suitability area, as well as the moderate suitability areas while the trend in 2050s and 2070s will also increase. The suitability regions were also identified by overlapping current and future (2050s and 2070s) potential distributions of D. zeae. The overlapping map indicated that there are chances that the area of BSRM disease progression will increase over the years. In another study, environmental conditions linked with the Fusarium solani optimum inoculum density for disease occurrence were accessed and a strong convergence on the environmental requirements of both the host and the disease progress was observed. Among different variables, precipitation and temperature variables were found important for explaining the disease spread64. These results were also similar to the findings of Sallam et al.65 where ecological niche modeling and land cover risk regions for rift valley fever vector, Culex tritaeniorhynchus Giles in Jazan, Saudi Arabia were identified65. Another study in Saudi Arabia on ecological distribution modeling of two malaria mosquito vectors by GIS showed similar results19. The same parameters were used for working with climate data and niche modeling66.

Here, we constructed the maps on the potential distribution of BSRM in Sialkot, Pakistan and these maps can effectively be used in furcating and disease management strategies development. Moreover, our work may be used as a reference to predict other phytopathogenic diseases in major crops and ensure food security.

Conclusion

Bacterial stalk rot of maize caused by D. zeae causes significant yield losses. In this work, isolates of D. zeae from the Sialkot region in Pakistan, were characterized biochemically. During extensive fields surveys, disease incidence was recorded, ranging from 43.5 to 78.5%. Maxent algorithm modeling revealed the areas at risk of disease outbreaks, which also predicted a high risk of BSR outbreak in 2050 and 2070. These results are very important for predicting the spatial distribution trends of BSRM in accordance with the climatic conditions in the coming years. Our findings will be useful in developing and adopting integrated disease management programs to prevent the spreading and control of BSR disease in maize crops.