Open Access

First detection of Paenibacillus larvae the causative agent of American Foulbrood in a Ugandan honeybee colony

SpringerPlus20165:1090

https://doi.org/10.1186/s40064-016-2767-3

Received: 16 May 2016

Accepted: 5 July 2016

Published: 15 July 2016

Abstract

Paenibacillus larvae is a highly contagious and often lethal widely distributed pathogen of honeybees, Apis mellifera but has not been reported in eastern Africa to date. We investigated the presence of P. larvae in the eastern and western highland agro-ecological zones of Uganda by collecting brood and honey samples from 67 honeybee colonies in two sampling occasions and cultivated them for P. larvae. Also, 8 honeys imported and locally retailed in Uganda were sampled and cultivated for P. larvae. Our aim was to establish the presence and distribution of P. larvae in honeybee populations in the two highland agro-ecological zones of Uganda and to determine if honeys that were locally retailed contained this lethal pathogen. One honeybee colony without clinical symptoms for P. larvae in an apiary located in a protected area of the western highlands of Uganda was found positive for P. larvae. The strain of this P. larvae was genotyped and found to be ERIC I. In order to compare its virulence with P. larvae reference strains, in vitro infection experiments were conducted with carniolan honeybee larvae from the research laboratory at Ghent University, Belgium. The results show that the virulence of the P. larvae strain found in Uganda was at least equally high. The epidemiological implication of the presence of P. larvae in a protected area is discussed.

Keywords

Apis mellifera Bacterial pathogensEast AfricaHoneybee diseasesPrevalence

Background

Paenibacillus larvae is a spore forming gram-positive bacterial pathogen of the European honeybees, Apis mellifera. P. larvae affects honeybee brood causing American Foulbrood (AFB) which is a highly contagious and often lethal disease in managed honeybee colonies. The disease poses a significant threat to the health of honeybee colonies and to the beekeeping industry because it causes considerable losses to beekeepers (Genersch et al. 2005; Genersch 2010b). Honeybee larvae get infected when they are fed by nurse bees on feed contaminated with spores of P. larvae. Young larvae (<36 h after hatching) are most susceptible to infection (Genersch 2010a). A dose of about 10 spores or fewer is sufficient to successfully infect and kill honeybee larva (Woodrow 1942). Typical clinical symptoms of AFB are the brown, viscous larval remains forming a ropy thread when drawn out with a matchstick (de Graaf et al. 2006). The decaying brood desiccates into hard scales, tightly adhering to the walls of the cells, consisting of millions of bacterial spores which are the infectious stage of the pathogen (Genersch et al. 2006).

AFB is spread both horizontally and vertically (Fries et al. 2006; Lindstrom et al. 2008). However, the most predominant route of spread is via the horizontal routes by both humans and bees. Horizontal transmission of AFB occurs when humans move contaminated honey or beekeeping equipment (Genersch 2010a). In addition, drifting of adult bees between colonies and robbing behavior of foragers can lead to horizontal spread of AFB (Lindstrom et al. 2008).

Paenibacillus larvae has a worldwide distribution (Matheson 1993; Genersch 2010a; Human et al. 2011; Morrissey et al. 2015). However, with the exception of Eritrea, Gambia, Guinea-Bissau, Senegal, South Africa (Matheson 1996; Hansen et al. 2003; Ellis and Munn 2005; de Graaf et al. 2006; Human et al. 2011), Tunisia (Matheson 1993; Hussein 2001; Fries and Raina 2003; Hamdi et al. 2013), Algeria (Adjlane et al. 2014), Libya and Morocco (Hussein 2001; Pirk et al. 2015) there is still doubt whether P. larvae is present in most parts of Africa since no confirmations have been made.

Beekeeping is an important activity in many rural areas of Uganda where it is carried out mainly using traditional beehives and beekeeping practices (UEPB 2005; Chemurot 2011). Beekeepers in Uganda majorly target honey production (UEPB 2005), although beekeeping provides several other benefits to people and the environment: production of propolis, beeswax, bee venom, pollen and pollination service (Jacobs et al. 2006; Genersch 2010b). In doing so, honeybees contribute to food security and biodiversity conservation. However, honeybees are threatened by numerous pathogens like viruses, bacteria, fungi and parasites which can attack them. The most recent honeybee parasite reported in Uganda, is Varroa destructor (Chemurot et al. 2016). In order to develop the beekeeping sector, it is essential to design effective honeybee pest and disease management plans. This requires accurate and adequate information on the distribution of honeybee pathogens in the country.

As part of a bigger project investigating the distribution of honeybee pathogens in selected agro-ecological zones of Uganda, we collected brood and honey samples from honeybee colonies in the eastern and western highland agro-ecological zones (AEZ) of Uganda. We also collected 8 honey samples from imported honeys that are locally retailed in Uganda and cultivated them for P. larvae. The aim of this study was to establish the presence and distribution of P. larvae in honeybee populations in two highland agro-ecological zones of Uganda and to determine if honeys that were locally retailed contained this lethal pathogen. Here we present data showing the presence of P. larvae in one honeybee colony without any clinical symptoms and discuss the epidemiological implication of the findings.

Methods

Study area

The study was conducted in the eastern and western highland agro-ecological zones (AEZ) of Uganda which are approximately 500 km apart (Fig. 1) but have comparable elevation, climatic conditions and land use activities. Altitude in the eastern agro-ecological zone ranges from 1000 to 4000 m above sea level (NEMA 2009) while in the western AEZ, it ranges from 600 to 4500 m (Chemurot et al. 2016). Both AEZs receive bimodal rainfall (900–2100 mm per year in the eastern and 875–1875 mm per year in the western AEZs) (Kajobe et al. 2009; Chemurot et al. 2016). Furthermore, in both AEZs beekeeping activities are practiced in farmlands and protected areas providing conditions for studying the possible influence of human activities on the prevalence of honeybee diseases. For this study, a farmland refers to public or private land under cultivation while protected areas are public owned lands that currently receive government protection because of their recognized natural and ecological values.
Fig. 1

Location of study sites in the agro-ecological zones of Uganda and distribution of P. larvae

In each AEZ, two districts were selected based on having altitudinal gradients and varying land uses in beekeeping areas (Kasese and Kabarole in the western AEZ and Mbale and Kapchorwa in the eastern AEZ). At each district, sub-counties known for beekeeping activities were chosen in consultation with beekeeping extension workers. Then lists of beekeepers were obtained from the District Production Offices and the apiaries sampled were selected based on altitude and land uses. The altitude in the study apiaries ranged from 930–2400 m above sea level. Based on this, we stratified apiaries in each study district according to altitude into four strata; low (900–1100 m), mid-low (1101–1300 m), high (1301–1500 m) and very high (above 1500 m) and at least one apiary was sampled in each strata.

Two honeybee races, Apis mellifera scutellata, and Apis mellifera adonsonii were recently confirmed in Uganda and both races were identified in the eastern and western highland AEZs (Kasangaki et al. in Prep). We sampled a total of 67 honeybee colonies (56 top bar hives, 3 Langstroth and 8 fixed comb hives) from 33 apiaries during two sampling moments (dry and wet seasons) between December 2014 and September 2015 (Table 1). Only three honeybee colonies were sampled twice (during both seasons) because some colonies had either absconded or did not have brood at the time of second sampling. One brood comb from each honeybee colony was collected and frozen as soon as it was possible and later analyzed for P. larvae in the research laboratory at Ghent University, Belgium. During field work, observations on honeybee colony strength and productivity and clinical symptoms of AFB were recorded. Also, eight samples of honey imported and retailed in Uganda were collected directly from supermarkets in Mbale and Kabarole districts.
Table 1

Summary of the number of samples analysed for P. larvae during the two seasons and results obtained

S/N

Source of samples

Dry season

Wet season

Brood

Honey

Brood

Honey

1

Eastern AEZ

23 (0)

10 (0)

2 (0)

2

Western highland AEZ

36 (1)

1 (0)

3 (0)

3

Imported to Uganda

8 (0)

Figures indicate the number of samples analysed; those between brackets indicate the P. larvae positive samples found

Culturing P. larvae

In the laboratory, the culture of P. larvae was performed according to routine protocols (de Graaf et al. 2006). Each brood sample was swabbed using cotton wool swabs (n = 10 cells; 5 on either side of the comb using two swabs) and the cotton wool washed in 5 ml Phosphate Buffered Saline (PBS). The sample was then heated in a water bath for 15 min at 80 °C and 150 µl pipetted onto MYPGP agar containing nalixidic (10 µg/ml) and pipemidic (20 µg/ml) acids. The agar was left to dry before being incubated at 37 °C for 4 days. All agar plates were observed for bacterial growth. Bacterial colonies were observed for similarities with P. larvae reference strain (LMG 9820). Suspicious colonies were subjected to catalase tests and those which were catalase negative were gram stained and examined at 1000× magnification on a microscope. Colonies were confirmed as P. larvae by PCR (Dobbelaere et al. 2001).

PCR for P. larvae

A colony of the suspected bacterial sample was suspended in 50 µl of distilled water and heated to 100 °C for 10 min. The sample was then centrifuged at 13,300 rpm for 5 min and 1 µl of the supernatant was amplified in a 25 µl PCR mixture containing the following: 10× PCR buffer, 2.5 mM MgCl2, 50 pmol of each primer (AFB-F: 5′-CTTGTGTTTCTTTCGGGAGACGCCA-3′ and AFB-R: 5′-TCTTAGAGTGCCCACCTCTGCG-3′) (Dobbelaere et al. 2001), 400 pmol of each deoxynucleoside triphosphate, and 1.25 U of Taq polymerase. The PCR conditions consisted of a 94 °C (5 min) step; 30 cycles of 93 °C (1 min), 55 °C (1/2 min), and 72 °C (1 min); and a final cycle of 72 °C (10 min). As a positive control P. larvae LMG 9820 was used. The molecular weights of the PCR products were compared with those of the Generuler 1 kb plus marker on a 1 % agarose gel stained with ethidium bromide and visualized under ultraviolet light.

ERIC genotyping

We performed ERIC genotyping following the procedures described by Genersch et al. (2006). Briefly, the DNA sequences of the primers used for P. larvae DNA fingerprinting were 5′-ATGTAAGCTCCTGGGGATTCAC-3′ (ERIC1R) and 5′-AAGTAAGTGACTGGGGTGAGCG-3′ (ERIC2). The PCR were carried out in final volumes of 25 µl consisting of 1× reaction buffer (Qiagen) and final concentrations of 2.5 mM MgCl2, 250 mM dNTPs, 10 mM primer and 0.3 U HotStarTaq polymerase (Qiagen). The reaction conditions were: an initial activation step (95 °C for 15 min); 35 cycles at 94 °C for 1 min, 53 °C for 1 min and 72 °C for 2.5 min, followed by a final elongation step at 72 °C for 10 min. A 10 µl sample from the PCR was analysed on a 0.8 % agarose gel. A positive control for each ERIC genotype was used (LMG 9820, R 20833, LMG 16252 and LMG 16247).

Infection assay

The virulence test was conducted at the Laboratory of Molecular Entomology and Bee Pathology (L-MEB), Ghent University following the protocol described by de Graaf et al. (2013) using Apis mellifera carnica larvae. Briefly, plates each consisting of 24-wells were incubated at 34 °C for 24 h. A group of 30 larvae (in 3 wells) was treated with the Ugandan P. larvae isolate, another group of 30 larvae was treated with the P. larvae strain BRL 230010. Six (6) wells were left empty and filled with 1 ml of distilled water to avoid desiccation. Three hundred (300) µl of the spore-contaminated larval diet (20 spores of P. larvae/µl feed) was pipetted into each well of the treatment group. Three wells for the negative control group were left and fed on non-spore contaminated larval diet during the entire experiment. After 24 h of infection, larvae were transferred to a pre-warmed, fresh normal larval diet plate. The grafting tool was decontaminated between each group to avoid reinfection. Every treatment group received fresh larval diet every 24 h and the plates were analyzed each day under a stereo microscope to determine the health status of the larvae. Old feed was removed daily and replaced with pre-warmed fresh larval diet. After defecation (day 8), the larvae were transferred to pupation plates. Larvae were classified as dead when they stopped breathing (movement of tracheal openings stops) and lost body elasticity. The number of dead larvae was recorded every day. To determine whether P. larvae infection caused the death of a larva, dead larvae were plated out on MYPGP plates. Plates were incubated for 3 days at 37 °C to allow the growth of vegetative bacteria. Positive AFB infection was confirmed by growth of P. larvae. Further confirmation was provided by performing P. larvae-specific PCR-analysis of colonies grown from larval remains.

Results

Prevalence of P. larvae

The presence of P. larvae in samples of honeybee brood and honey from the two agro-ecological zones of Uganda is shown in Table 1. A total of 59 brood samples from the two agro-ecological zones were analyzed during the dry season. During the wet season, 11 brood and 13 honey samples were analyzed. No brood sample showed any clinical signs of AFB in the field. None of the honey samples were found to be contaminated with P. larvae spores (Table 1). Of the 59 honeybee brood samples analyzed during the dry season, only one (sample KAS-07) (representing 1.7 %) was confirmed positive for P. larvae (Table 1). As expected, the PCR product banded just above 1000-bp (around 1106-bp) on the Generuler 1 kb plus marker (Fig. 2).
Fig. 2

PCR product image: L = Generuler 1 kb plus marker, 1 = sample KAS-07, 2 = positive control (LMG 9820), N = negative control

ERIC PCR and virulence assay

Genotyping of the P. larvae strain found in this study revealed that it was an ERIC I strain (Fig. 3). The virulence of this P. larvae strain on A. mellifera carnica is shown in Fig. 2. Of the 30 honeybee larvae that were fed with spores, 25 had died by the 6th day (Fig. 4). For the reference ERIC I strain (BRL 230010), only 18 honeybee larvae had died in the same period. However, it is clear that by the 12th day, all honeybee larvae that were fed with P. larvae spores had died. This virulence assay finding confirms that the strain obtained is at least equally virulent when compared to BRL 230010, which was isolated from diseased colonies in the USA and which belongs to the ERIC I genotype (Qin et al. 2006).
Fig. 3

ERIC PCR product image: L = Generuler 1 kb plus marker, 1 = sample KAS-07, 2 = LMG 9820, 3 = R 20833, 4 = LMG 16252, 5 = LMG 16247, N = negative control

Fig. 4

Comparison of the survival of A. mellifera carnica larvae feed on KAS 07 Ugandan P. larvae strain found and ERIC I strain (BRL 230010)

Discussion

In this study, 1.7 % of the honeybee colonies sampled during the dry season were positive for P. larvae. Being the first finding of P. larvae in Uganda, it was necessary to perform ERIC genotyping and virulence tests to compare this strain with reference strains found in some western countries. Moreover, as clinical signs were not observed, we wondered whether this strain had any disease causing potential. We also decided to conduct virulence tests of the P. larvae strain found on A. mellifera carnica of the research laboratory of Ghent University, Belgium as we did not have the facilities nor the required biosafety certificate to perform the experiments in Uganda. The results showed that the strain found was an ERIC I with at least equally high virulence when compared to BRL 230010 from the USA (Qin et al. 2006).

The prevalence (1.7 %) of P. larvae in honeybee colonies and (3.03 %) in apiaries recorded in this study is comparatively much lower than that reported in some Asian countries e.g. 37.3 % in honeybee colonies in Pakistan (Anjum et al. 2015), 24.8 % in honey samples from Taiwan (Chen et al. 2008) and some European countries e.g. 11 % in Belgium (de Graaf et al. 2001), 66 % in France (Mouret et al. 2013) and 5.3–9.8 % in Latvian apiaries (Chauzat et al. 2014; Laurent et al. 2015). However, the prevalence recorded in apiaries in our study sites is in the range of 1–5.7 % in Estonia, 1.5–4.5 % in Greece, 1.6–4.7 % in Poland, 2 % in Sweden, 2.6 % in Slovakia, 2.2–2.7 % in Italy (Chauzat et al. 2014; Laurent et al. 2015) and 1.6–3.2 % in Spain (Garrido-Bailón et al. 2013). Long term epidemiological studies show that the prevalence levels of AFB vary over time. For example, in Uruguay, AFB prevalence levels fluctuated over 12 years after it was first reported (Antúnez et al. 2012) suggesting that the levels recorded in Ugandan apiaries could change over time. Therefore, monitoring programs for this honeybee disease in Uganda should be developed and implemented to ensure that it is detected early and managed.

In Africa, AFB has been confirmed in South Africa (Human et al. 2011), Guinea Bissau (Hussein 2001; Hansen et al. 2003) and Egypt (Masry et al. 2014). P. larvae has also been detected in honey originating from Tunisia (Matheson 1993; Hussein 2001; Fries and Raina 2003; Hamdi et al. 2013), Algeria, Libya and Morocco (Hussein 2001). Despite P. larvae and other honeybee parasites like Varroa destructor being reported in Africa (Human et al. 2011; Muli et al. 2014; Strauss et al. 2015; Chemurot et al. 2016), no major colony losses have been reported yet. This could be associated with the higher levels of disease resistance in African honeybees (Human et al. 2011). However, such a trait may not persist if pathogens accumulate in hives especially with the promotion of frame beehives. Therefore, efforts should be made to prevent loss of the disease resistance in African honeybees.

Behavioral adaptations such as abscondment and swarming among African honeybee races may also explain their low levels of parasite infestation (Chemurot et al. 2016). Two honeybee races, Apis mellifera scutellata, and Apis mellifera adonsonii have been confirmed in Uganda (Kasangaki et al. in Prep). These honeybee races abscond from beehives more frequently when disturbed than other races of A. mellifera (Hansen and Brodsgaard 1997; reviewed in Dietemann et al. 2009). This behavioral trait could result in disinfection in honeybee colonies formally infected by P. larvae (Hansen and Brodsgaard 1997).

The higher levels of hygienic behavior of African honeybees may also reduce the level of AFB infection (Fries and Raina 2003; Human et al. 2011). In addition, the wax moth, Galleria mellonella which is a very common pest in Africa and only affects weak colonies (Strauss et al. 2013) may reduce AFB infestation levels by destroying large amounts of infected combs after colony abscondment (Hansen and Brodsgaard 1997; Human et al. 2011). The overall implication of this is that relatively very low AFB infection levels and extremely rare development of clinical symptoms are observed.

The P. larvae positive sample in this study was from a colony in a protected area suggesting that this pathogen could be present in feral honeybee colonies. Since beekeepers in Uganda rely on natural honeybee colonies to colonize their beehives (Chemurot 2011), P. larvae could spread from feral to managed colonies. On the other hand, absconding and swarming which are common among African honeybee races (Hansen and Brodsgaard 1997) could also spread this pathogen from managed to feral colonies. However, the current predominant use of traditional and top-bar beehives (Chemurot 2011) reduces chances of this pathogen accumulating in honeybee combs since beekeepers harvest the entire comb.

Conclusion

Although honeybee health is an important theme in apiculture, only few attempts have been made to investigate honeybee diseases in Africa. This paper provides the first reported evidence in East Africa of AFB, one of the most serious honeybee diseases. We demonstrate that the pathogen detected is ERIC I strain of P. larvae and compare its virulence with a reference strain. The results suggest that the strain obtained was equally virulent on carniolan honeybees. We recommend regular countrywide monitoring and surveillance for P. larvae to ensure that this pathogen is detected in time and interventions made before it can cause major production losses to beekeepers.

Abbreviations

AEZ: 

Agro-ecological zone

AFB: 

American foulbrood

DNA: 

Deoxyribonucleic acid

ERIC: 

Enterobacterial Repetitive Intergenic Consensus

PCR: 

Polymerase chain reaction

Declarations

Authors’ contributions

MC, AMA and DCD conceived the project. MC carried out sample collection. MC, MB and TD conducted infection experiments and molecular analyses. MC drafted the manuscript. All authors read and approved the final manuscript.

Acknowledgements

We thank I. Mayegu, S. Cherotich, N. Erikibankya, A. Thabulenga and A. Bagonza for fieldwork assistance. The Ministry of Agriculture, Animal Industry and Fisheries, Uganda provided field support while the Uganda National Council for Science and Technology granted research permission for which we are grateful. This research was supported in part by Erasmus Mundus Action 2 (Caribu project) scholarship award to Moses Chemurot.

Competing interests

The authors declare that they have no competing interests.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors’ Affiliations

(1)
Laboratory of Molecular Entomology and Bee Pathology, Ghent University
(2)
Department of Zoology, Entomology and Fisheries Sciences, College of Natural Sciences, Makerere University

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Copyright

© The Author(s) 2016