Magnitude, risk factors and antimicrobial susceptibility pattern of Shigella and Salmonella, among children with diarrhea in Southern Ethiopia: A Cross-sectional Study.

OBJECTIVE: This study was aimed at identifying Shigella and Salmonella infection, their antibiotic susceptibility pattern and associated risk factors among children with diarrhea who attended Alamura Health Center.
METHOD: A facility-based cross-sectional study was conducted on 263 children aged below 14 years with diarrhea. A structured questionnaire was used to collect socio-demographic and clinical data after obtaining the necessary consent from their parents or caretakers. The culture and sensitivity tests were performed using the standard operating procedure of the microbiology laboratory.
RESULTS: Accordingly, 20/263 (7.6%), 95% confidence interval: 4.4%-11.4% Shigella and 1/263 (0.38%), 95% confidence interval: 0.0%-1.1% Salmonella were isolated. Shigella dysenteriae was dominant 11 (4.2%), followed by Shigella spp. 9 (3.42%) and Salmonella typ 1 (0.38%). The isolates showed 71.4% overall resistance to ampicillin and 61.9% for augmentin and tetracycline, whereas 95.2% of the isolates were sensitive to ciprofloxacin, 85.9% to ceftriaxone and ceftazidime, 81% to gentamycin, 76.2% to chloramphenicol, 66.7% to cefuroxime and 52.4% to cotrimoxazole. The habit of washing hands after toilet use for a while (adjusted odds ratio: 235.1, 95% confidence interval: 20.9-2643.3, p < 0.000) and storing cooked food in an open container for later use (adjusted odds ratio: 36.44, 95% confidence interval: 5.82-228.06, p < 0.000) showed a statistically significant association.
CONCLUSION: High level of Shigella and single Salmonella was isolated. Ampicillin, augmentin and tetracycline were resistant and ciprofloxacin, ceftriaxone, ceftazidime, gentamycin, chloramphenicol, cefuroxime and cotrimoxazole were relatively sensitive. Hand-washing after defecation for some time and storing of foods for later use in an open container were statistically associated. Therefore, to alleviate this infection, the concerned body should focus on imparting health education for hand-wash after defecation and storing food in a closed container for later use is mandatory.

Introduction

Diseases caused by enteric pathogens are of common public health concerns in many parts of the world including Ethiopia.[1,2] Salmonella and Shigella are associated with a high burden of illness among children in the developing world.[3] Children are one of the victims of these infections accounting for approximately 8% of all deaths among children under age 5 worldwide in 2017. This implies that over 1300 young children passed away each day, 480,000 children a year, regardless of the availability of humble active treatment. Most of these deaths are due to diarrhea in South Asia and sub-Saharan Africa.[4] The rates of Shigella and Salmonella in Ethiopia reported from different studies are in the range of 4.3%–45%[5-8] and 1%–12.6%,[7,9,10] respectively.

They are species of particular concerns as they cause enteric fevers, food poisoning and gastroenteritis.[9] They are Gram-negative rods that commonly inhabit the intestinal tracts of humans and many animals.[10] It was estimated that 1.8 million cases of children died from diarrheal illness worldwide, a large proportion of which was attributed to infection by Shigella and Salmonella spp.[11] Different studies have reported that Shigella spp. were associated with majority of cases of bacillary dysentery, which is prevalent mainly in developing nations;[12,13] whereas, Salmonella spp. were the most common cause of food-borne infection outbreaks almost all over the world.[14] In recent years, the emergence and global dissemination of Salmonella and Shigella species resistance to ampicillin, chloramphenicol, tetracycline and co-trimoxazole are increasingly documented in developing countries.[15]

Infections of Shigella and Salmonella can be asymptomatic and can be treated with rehydration solutions unless the infection is by invasive strains.[16] Prescribing antibiotics might shorten the extent of diarrhea and control the organisms, which otherwise might continue to spread among people and in the environment, and furthermore, it would pose a public health concern.[17] Children are at high risk of these infections due to their weakened immune status and ease of contamination.[18] In developing countries, this infection increased due to poor sanitation, personal hygiene and lack of appropriate food supply that leads children to contaminate by themselves.[19] Therefore, this study is aimed at identifying Shigella and Salmonella infections, antibiotic susceptibility and associated risk factors among children with diarrhea who visited Alamura Health Center in Southern Ethiopia.

Materials and methods

Study area and period

The study was conducted in the Southern Nations, Nationalities and Peoples Region (SNNPR) at Hawassa Alamura Health Center from 1 April 2019 to 30 August 2019. Hawassa is the capital city of the SNNPR, located in the Southern part of Ethiopia, on the shores of Lake Hawassa which is one of the Great Rift Valley lakes situated around 270 km from Addis Ababa, the capital city of Ethiopia. The mean annual rainfall is about 950 mm, temperature about 20°C and humidity 70%–80%. The rainy season generally extends from June to October. The human population of Hawassa for 2015 was estimated at 351,469, with an annual growth rate of just over 4%.[20] Hawassa city has 7 sub-cities with 5 private, 1 general and 1 comprehensive specialized hospital and 10 health centers. Alamura Health Center is located in the Tabor sub-city and borderline between Fara and Hitata Kebele near Alamura Mountain.

Study design and population

A facility-based cross-sectional study design was conducted among children with diarrhea at Alamura Health Center. A convenient sampling technique was employed in which diarrheic pediatric patients below the age of 14 years were included. They were considered for the study only after obtaining the necessary consent from their parents or guardian and signing the document. The participants are excluded if their parents are not willing or refuse to sign. All diarrheic pediatric patients who visited Alamura Health Center for the diarrheal case of illness were the source of population.

Sample size determination

The sample size was calculated using a single population proportion formula: n = z2p (1−p)/d2, where n = sample size, z = confidence level at 95% (standard value of 1.96), M = margin of error at 5%, p = estimated prevalence of Shigella and Salmonella from the previous study 22.2%.[21] Therefore, the calculated sample size for this study was 263.

Variable of study

The dependent variables were the presence of Salmonella and Shigella. The independent variables were socio-demographic factors, namely, age, sex, place of residence, educational status of the mothers, marital status, family size, monthly income, occupation of the family. Clinical variables collected include history and type of diarrhea, malnutrition and vaccination status of the children. Another variable considered for the study was behavioral factor, which includes a drinking water source, hand-wash after toilet use, food/drink consumption before illness, storage of cooked food for later use, the habit of hand-washing before and after a meal, washing habit of food containers and history of contact with domestic animals. These were assessed with a structured questionnaire.

Data collection

The socio-demographic and clinical data were collected after informing the parents/caregiver about the aim of the study. A face-to-face interview was conducted to collect the data with a structured questionnaire from parents or caretaker of the children who complained of diarrhea after they signed the consent and the child accepted the assent.

Laboratory diagnosis

The stool was collected using a screw cup container. The parents/caregiver was instructed to bring a fresh stool sample without any contamination before 30 min of collection. All stool specimens were placed into Carry Blair Transport Medium and transported to the Microbiology Laboratory of Hawassa University Comprehensive Specialized Hospital (HUCSH). The stool was inoculated on prepared culture media which is MacConkey, Xylose lysine deoxycholate (XLD) and selenite F-broth (Abtek, UK). The culture plates were incubated aerobically at 37°C for 24 h.

Bacterial identification

The colonies were examined morphologically for size, shape and ability to ferment lactose. Those bacterial colonies with non-lactose fermenting characteristics with H2S for Salmonella and without H2S for Shigella were picked up for biochemical identification. Indole test, urease production, mannitol fermentation, hydrogen sulfide, gas production test, citrate utilization test, motility test, carbohydrate fermentation test, lysine decarboxylase test (LDC) and oxidase test were used to identify the bacteria up to genus/species level.[22]

Antibiotics susceptibility testing

A pure colony of isolated bacteria was mixed with normal saline to make a 0.5 McFarland standard suspension for susceptibility testing and then swabbed on Mueller Hinton agar. The susceptibility pattern of the isolates was determined for ciprofloxacin (CIP; 5 μg), augmentin (AUG; 30 μg), gentamicin (GEN; 10 μg), chloramphenicol (CAF; 30 μg), co-cotrimoxazole (COT; 25 µg), tetracycline (TAT; 30 µg), ampicillin (AMP; 10 µg), ceftriaxone (CRO; 30 µg), cefuroxime (CRX; 30 µg) and ceftazidime (CAZ; 30 µg). After incubation for 24 h at 37°C, the diameter of each zone of inhibition was measured with a ruler in millimeters. The results were then interpreted according to Clinical and Laboratory Standards Institute (CLSI) guidelines antimicrobial susceptibility breaking points 2018 and recorded as sensitive (S), intermediate (I) or resistant (R).[23]

Quality control

A pre-test was conducted on 5% of the questionnaire before conducting the study. The validity and completeness of the data were verified daily. Sterility of culture media and biochemical tests were checked by overnight incubation of un-inoculated media from each batch of preparation. Standard strains of Escherichia coli ATCC 25922 and Pseudomonas aeruginosa ATCC 27853 were used for the culture and antibiotic susceptibility testing of internal quality assurance.

Data analysis

Data were entered into Statistical Package for the Social Sciences (SPSS) version 20 and were analyzed to make inferences on the frequency of occurrence of enteric pathogens associated with diarrhea and to show bacterial resistance pattern to locally prescribed antibiotic substances. Descriptive statistics were performed to get the frequency of dependent and independent variables. Binary logistic regression analysis was conducted to identify real predictor of Shigella and Salmonella. The strength of association was presented by odds ratio at 95% confidence interval (CI) and a p value of ⩽0.05 was considered as a statistically significant association.

Ethical consideration

The study was conducted after obtaining formal permission from the Southern Nations Nationality and People Regional Health Office, Hawassa City Administration Health Office, Alamura Health Center Manager and Laboratory Head. The patients were included in the study only when the parents or caretakers of the patients sign the consent letter. The culture and antimicrobial susceptibility results were communicated to the concerned bodies in the health center within 72 h.

Results

Socio-demographic characteristics of the study subjects

A total of 263 diarrheic pediatric patients from Alamura Health Center were enrolled for the study with a mean and standard deviation of age 6.8 ± 3.7 years. The frequency and percentage of pediatrics age range enrolled for the study were 0–4, 88 (33.5%); 5–9, 103 (39.2%); and 10–14, 72 (27.4%). An almost equal ratio of male to female was enrolled for the study (130:133). Regarding the residence, most of the study subjects 155 (58.9%) were from an urban area and 108 (41.1%) patients were from a rural area. Concerning the educational status of the mothers of pediatric patients, most of them were educated (81%) ranging from reading and writing to university graduate level and the rest 19% were illiterates. The marital status of their mothers: 178 (67.7%) were married, 43 (16.3%) divorced and 41 (15.6%) widowed. The mean and standard deviation of the family size was 5.6 ± 1.9 persons. The average income of the family was 3743.3 ± 2568.1 Ethiopian birr. Most of the study participants have a large family size with a relatively low income of <1500 birr per month and from this number, the diarrhea positive was 12 (57.1%; Table 2).

Table 2.

Bivariate analysis of socio-demographic characteristics and clinical data of diarrheic pediatric patients in the Alamura Health Center, Southern Ethiopia, 2019.

Variables	Frequency (%)	Shigella/Salmonella		COR 95% CI	p value	AOR 95% CI	p value
		Yes (%)	No (%)
Age in group (years)
0–4	88 (33.5)	7 (33.3)	81 (33.5)	1.158 (0.35–3.82)	0.809
5–9	103 (39.2)	9 (42.9)	94 (38.8)	1.283 (0.41–4.00)	0.668
10–14	72 (27.4)	5 (23.8)	67 (27.7)	1
Sex
Male	130 (49.4)	8 (38.1)	122 (50.4)	1
Female	133 (50.6)	13 (61.9)	120 (49.6)	1.652 (0.66–4.13)	0.283
Residence
Rural	108 (41.1)	8 (38.1)	100 (41.3)	1
Urban	155 (58.9)	13 (61.9)	142 (58.7)	0.874 (0.35–2.2)	0.773
Mother’s educational status
No formal education	50 (19.0)	2 (9.5)	48 (19.8)	1.125 (0.10–12.99)	0.925
Read and write	56 (21.3)	9 (42.9)	47 (19.4)	5.170 (0.62–43.05)	0.129
Elementary school	76 (28.9)	5 (23.8)	71 (29.3)	1.901 (0.21–17.03)	0.566
Secondary school	53 (20.2)	4 (19.0)	49 (20.2)	2.204 (0.23–20.7)	0.489
College/university	28 (10.6)	1 (4.8)	27 (11.2)	1
Mother’s marital status
Married	178 (67.7)	14 (67.7)	164 (67.8)	1
Divorced	43 (16.3)	5 (23.2)	38 (15.7)	1.057 (0.37–3.044)	0.919
Widowed	41 (15.6)	2 (9.5)	39 (16.1)	0.560 (0.070–4.468)	0.584
Family size (person)
2–3	23 (8.8)	2 (9.5)	21 (8.7)	1
4–5	129 (49.2)	12 (57.1)	117 (48.5)	1.077 (0.23–5.163)	0.926
⩾ 6	110 (42.0)	7 (33.3)	103 (42.7)	0.714 (0.138–3.679)	0.687
Monthly income birr/ETB
500–1500	51 (19.4)	7 (33.3)	44 (18.2)	1
> 1500	212 (80.6)	14 (66.7)	198 (81.8)	0.444 (0.169–1.166)	0.099
Previous diarrhea
Yes	162 (61.6)	17 (81.0)	145 (59.9)	2.843 (0.928–8.706)	0.067
No	101 (38.4)	4 (19.0)	97 (40.1)	1
Type of diarrhea
Bloody	111 (42.2)	1 (4.8)	100 (43.1)	1
Watery	49 (18.6)	2 (9.5)	47 (20.3)	11.69 (0.99–138.44)	0.051
Mucoid	103 (39.2)	18 (85.7)	85 (36.6)	16.75 (2.13–131.67)	0.007
Frequency of diarrhea
Once	170 (64.6)	11 (52.4)	159 (65.7)	1.038 (0.125–8.598)	0.973
Twice	77 (29.3)	9 (42.9)	68 (28.1)	1.985 (0.234–16.88)	0.530
> 3	16 (6.1)	1 (4.8)	14 (5.8)	1
Malnutrition
Yes	25 (9.5)	3 (14.3)	22 (9.1)	1	0.441
No	238 (90.5)	18 (85.7)	220 (90.9)	1.67 (0.46–6.121)
Vaccination
Yes	202 (76.8)	14 (66.7)	188 (77.7)	0.574 (0.221–1.495)	0.256
No	61 (23.2)	7 (33.3)	54 (223)	1
Drinking H2O sources
Pipe	159 (60.5)	17 (81.0)	142 (58.7)	2.993 (0.978–9.162)	0.055
Other	104 (39.5)	4 (19.0)	100 (41.3)	1
Child’s hand-wash after toilet
Always	221 (84.0)	1 (4.8)	220 (90.9)	1	0.000	235.1 (20.9–2643.3)	0.000
Sometimes	42 (16.0)	20 (95.20	22 (9.1)	200 (25.6–1562.35)
Food taken before illness
Cooked food	82 (31.2)	5 (23.8)	77 (31.8)	0.801 (0.182–3.533)	0.769
Overnight food	77 (29.3)	8 (38.1)	69 (28.5)	1.430 (0.358–5.716)	0.613
Raw vegetable	64 (24.3)	5 (23.8)	59 (24.4)	1.045 (0.236–4.634)	0.954
Raw milk	40 (15.2)	3 (14.3)	37 (15.3)	1
Storage of cooked food
Open containers	40 (15.2)	16 (76.2)	24 (9.9)	29.1 (9.78–86.372)	0.000	36.44	0.000
Closed containers	223 (84.8)	5 (23.8)	218 (90.1)	1
Hand-washing before and after a meal
Yes	85 (32.3)	6 (28.6)	79 (32.6)	1
No	178 (67.7)	15 (71.4)	160 (66.1)	1.212 (0.453–3.242)	0.702
Cleaning of cooking containers
Always	157 (59.7)	4 (19.0)	153 (63.2)	1
Sometimes	106 (40.3)	17 (81.0)	89 (36.8)	7.306 (2.38–22.4)	0.001	4.94 (0.795–30.74)	0.087
Contact with animals
Yes	137 (52.1)	13 (61.9)	124 (51.2)	1.546 (0.62–3.865)	0.351
No	126 (47.9)	8 (38.1)	118 (48.8)	1

COR: crude odds ratio; CI: confidence interval; AOR: adjusted odds ratio; ETB: Ethiopian Birr.

The magnitude of Shigella and Salmonella

The overall magnitude of Shigella and Salmonella among children with diarrhea in Alamura Health Center was 20/263 (7.6%), 95% CI: 4.4%–11.4% and 1/263 (0.38%), 95% CI: 0.0%–1.1%. Shigella dysenteriae was frequently isolated from 4.2% (11/263), 95% CI: 1.9–6.8, from patients followed by other Shigella spp. 3.42% (9/263), 95% CI: 1.5–5.7, and Salmonella spp. 0.38% (1/263), 95% CI: 0.0–1.1. In the rest, 92% (242/263) Shigella and Salmonella were not isolated from diarrheic pediatric patients (Figure 1).

Figure 1.

Magnitude of Shigella spp., Shigella dysenteriae and Salmonella typhi in diarrheic pediatric patients from Alamura Health Center, Southern Ethiopia, 2019.

Salmonella typhi

A single Salmonella typhi was isolated from the patient and it was sensitive to ciprofloxacin, gentamicin, ceftazidime, chloramphenicol, cefuroxime, ceftriaxone and co-trimoxazole and resistant to ampicillin and tetracycline.

Other Shigella species

Shigella spp. isolated were 100.0% sensitive to both ceftriaxone and ciprofloxacin, 77.8% to both ceftazidime and chloramphenicol, 66.7% to cefuroxime and 55.6% to gentamycin. Resistance was seen 81.8% for ampicillin, 72.7% for tetracycline and 55.6% for both co-trimoxazole and augmentin.

Shigella dysenteriae

Shigella dysenteriae isolate was 100% susceptible to gentamicin, 90.9% to ciprofloxacin, 90% to ceftazidime, 72% to both ceftriaxone and chloramphenicol. Resistance was seen for ampicillin (45.5%), 55% for co-trimoxazole, 72.7% for tetracycline and 91% for augmentin (Table 1).

Table 1.

Antimicrobial susceptibility profile of Salmonella typhi, Shigella spp. and Shigella dysenteriae isolated from diarrheic pediatric patients from Alamura Health Center, Southern Ethiopia, 2019.

Antibiotics	Isolates
	S. typhi (1)		Shigella spp. (9)			S. dysentery (11)			Total (21)
	S	R	S	I	R	S	I	R	S (%)	I (%)	R (%)
AMP	0	1	0	4	5	0	2	9	0 (0.0)	6 (28.6)	15 (71.4)
COT	1	—	5	0	4	5	3	3	11 (52.4)	3 (14.3)	7 (33.3)
CIP	1	—	9	0	0	10	1	0	20 (95.2)	1 (4.8)	0 (0.0)
CRO	1	0	9	0	0	8	0	3	18 (85.7)	0 (0.0)	3 (14.3)
CAZ	1	0	7	1	1	10	1	0	18 (85.7)	2 (9.5)	1 (4.8)
GEN	1	0	5	4	0	11	0	0	17 (81.0)	4 (19.0)	0 (0.0)
CAF	1	0	7	1	1	8	2	1	16 (76.2)	3 (14.3)	2 (9.5)
CRX	1	0	6	2	1	7	1	3	14 (66.7)	3 (14.3)	4 (19.0)
AUG	0	1	1	4	4	0	3	8	1 (4.8)	7 (33.7)	13 (61.9)
TAT	0	1	0	5	4	0	3	8	0 (0.0)	8 (38.1)	13 (61.9)

S: sensitive; I: intermediate; R: resistant; AMP: ampicillin; COT: co-cotrimoxazole; CIP: ciprofloxacin; CRO: ceftriaxone; CAZ: ceftazidime; GEN: gentamicin; CAF: chloramphenicol; CRX: cefuroxime; AUG: augmentin; TAT: tetracycline.

Associated risk factors

Among the study participants, 162 (61.6%) patients showed a history of diarrhea; of these, 17 (81.0%) were positive for current infection. Of all diarrheic children, the type of diarrhea was watery for 111 (42.2%), mucoid for 103 (39.2%) and bloody for 49 (18.6%). Children with mucoid diarrhea were more 18 (85.7%) as compared to the rest of the patients. Most of the children, 170 (64.6%), had diarrhea once a day and most of the bacteria, 11 (52.4%), was isolated from these patients. Most of the study subjects used pipe water, 159 (60.5%), for drinking, and the children infected in these categories were more than 17 (81.0%).

Regarding hand-wash, 221 (84.0%) affected children practiced hand-washing after defecation and the rest 42 (16.0%) wash their hands only for some time. Among the 16% of patients who wash their hands only for some time, nearly 95.2% of the patients were affected. Most of the food taken by the children before the illness was cooked food, 82 (31.2%), even if the bacterial infection was dominantly isolated from children who ate food at night, 8 (38.1%). Most of the children enrolled in the study were those who stored their food in closed containers, 223 (84.8%); lack of hand-wash before and after meal, 178 (67.7%); wash food containers, 157 (59.7%); well-nourished, 238 (90.5%); vaccinated, 202 (76.8%); and had animal contact 137 (52.1%). Correspondingly, most of the bacteria were isolated from those who stored food in an open container, 16 (76.2%); lack of hand-wash after or before meal, 15 (71.4%); washing of food container for some time, 17 (81.0%); well-nourished, 18 (85.7%); vaccinated, 14 (66.7%); and had animal contacts, 13 (61.9%) (Table 2).

The bivariate analyses indicate that family with monthly income >1500 (crude odds ratio (COR) = 2.250, 95% CI: 0.86–5.902, p = 0.099), educational status of mother who can read and write (COR = 5.170, 95% CI: 0.62–43.05, p = 0.129), previous history of diarrhea (COR = 0.35, 95% CI: 0.115–0.078, p = 0.067), watery diarrheal type (COR = 11.69, 95% CI: 0.988–138.44, p = 0.051), mucoid (COR = 16.75, 95% CI: 2.130–131.67, p = 0.007) were the candidate variables for multivariable analysis.

Similarly, those who used pipe water source (COR = 2.993, 95% CI: 0.978–9.16, p = 0.055), wash hands of their child after toilet for some time (COR = 200, 95% CI: 25.602–1562.348, p = 0.000), store food in open containers (COR = 29.1, 95% CI: 9.78–86.37, p = 0.000) washing habit of food containers for some time (COR = 7.306, 95% CI: 2.38–22.4, p = 0.001) were candidate variables for multivariable analysis with p value of ⩽0.25 (Table 2).

However, in multivariate analysis, after adjustment, those who had a habit of washing the hands of children after toilet use for some time (adjusted odds ratio (AOR) = 235.1, 95% CI: 20.9–2643.3, p = 0.000) and store cooked food in an open container (AOR = 36.44, 95% CI: 5.82–228.06, p = 0.000) showed a statistically significant association of Shigella and Salmonella infection with p values ⩽0.05. However, factors like the type of diarrhea, history of contact with domestic animals, the habit of hand-washing before and after a meal and washing of food containers were not statistically significant (Table 2).

Discussion

The overall magnitude of Shigella and Salmonella isolated in this study was 8.0% (4.6%–11.4%), which is lower than the studies conducted in Tanzania 42.7%,[24] Mozambique 27.2%,[25] Ethiopia 22.3%,[26] 22.2%[27] and 18.1%.[28] It is comparable with a study reported in Ethiopia from Nekemte 9.2%[28] and Southern Ethiopia 8.3%.[21] The possible reason for such a difference may be the sample size, the method adopted and age variation.[8,21]

In this study, 7.6% (4.6%–11.0%) of Shigella spp. was isolated, which is comparable to the study conducted in Burkina Faso 5.8%,[29] Kenya 7.4%,[30] Nigeria 8%,[31] Ethiopia 8.3%,[32] 9.1%.[33] In contrast to our findings, a lower rate of Shigella infection was reported from China 1.4%,[34] Nekemte 2.1%,[28] Ambo 2.5%,[35] Goba 4.3%,[8] and a higher prevalence of Shigella was reported from Mekelle 13.3%,[36] Botswana 21%.[37] This study identified Shigella dysenteriae from another Shigella spp. with available biochemical tests and accordingly, 11 (4.2%), 95% CI: 1.9%–6.8%, were infected by Shigella dysenteriae. This rate is lower than the report from Nepal 14.5%.[38] However, it is comparable with the findings from Central Africa 3%.[39] The other nine (3.42%), 95% CI: 1.5–5.7, were other species of Shigella and this value is higher compared with the results reported from China 1.4%,[34] Nigeria 1.4%,[40] Addis Ababa 1.3%[41] and Jimma 1.1%.[42] Our findings are lower than the study reported from Jimma 20.1%,[43] Bahir Dar 14.9%,[44] 9.5%,[33] 7.8%,[33] Harar 14.6%,[45] Addis Ababa 9.1%,[32] South Africa 8.5%,[46] Southwest Ethiopia 8.4%,[17] Sudan 8%,[47] Southern Ethiopia 7.0%,[21] Eastern Ethiopia 6.9%[48] and Northern Ethiopia 6.9%.[49] This reported variation may be due to the geographical location, climatic change and age variation of the participant. A comparable result was reported from Gondar 4.6%,[50] Nepal 4.6%,[51] Butajira 4.5%,[52] Kenya 4.0%,[53] Turkey 3.2%[54] and Ethiopia 2.3%.[17]

A single S. typhi 0.4%, 95% CI: 0%–1.1%, isolated in this study was in line with the findings reported from Addis Ababa, 0%,[41] 1.1%.[50] In contrast to our finding, higher rates were reported from Sudan 4.0%,[47] China 4.3%,[34] Addis Ababa 3.95%,[32] Kenya 3.4%,[53] Turkey 3%,[54] Gondar 1.6%[55] and Hawassa 1.5%.[21] This difference might be due to sampling size, climatic condition and age differences.[8,21,41,56]

Our study revealed that the highest rates of antibiotic resistance of Shigella spp. were against Ampicillin 81.8%, which is comparable with the studies from different areas of Ethiopia 70.1% from Jimma,[43] 79.9% from Gonder,[57] 86.7%[28] and 88.9% from Mekelle.[58] Our study also showed relatively low resistance compared to the findings from Nigeria 90.5%,[59] Harar 100%,[48] Jimma 100%,[17] Hawassa 93%.[60] This may be due to widespread resistant strains in the countries. Another antibiotic resistance of Shigella spp. was seen against tetracycline 71.4%, and this was comparable with the findings reported from Harar 70.6%,[48] Jimma 63.6% [43] and Mekelle 77.8%.[49] This result was slightly lower than the studies reported from Butajira 82.4%,[52] Gondar 86%[61] and 86%,[57] Hawassa 90%.[60] This may be due to the nature of the susceptibility of strains to tetracycline. Our results also indicated that 52.4% was resistant against co-trimoxazole and this was comparable with the studies done in Hawassa 56.0%,[50] Addis Ababa 45.7%[62] and Mekelle 55.6%.[49] In contrast to our finding, higher results are reported from Gonder 73.4%.[57] Several factors may contribute for the resistance, which may be related to the potency and quality of antimicrobials and the distribution of resistant strains.[62]

Studies have shown that Shigella is a global problem especially in developing countries.[63,64] It is common in areas where living standards of people are very low and access to safe and adequate drinking water and proper waste disposal systems are often very limited or even absent.[17,32,57,61,65] Deprived access to a good latrine, poor sanitation and hygienic status, hand-washing habit before and after a meal and/or latrine, absence of proper sewage disposal system were responsible for a typhoidal type of Salmonella infections.[17,21,32] Our study assessed risk factors for acquiring Shigella/Salmonella infection. Accordingly, the socio-demographic factors like age group (5–9 years), sex, educational and marital status of mothers; family size (4–5 persons) and monthly income (>1500) were responsible for a higher percentage of infection. However, none of these variables were statistically associated. In agreement with our study, a statistically insignificant association with socio-demographic characteristic was reported from Ethiopia in Addis Ababa[32] and Bahir Dar.[33] In contrast to our study, age range[1-3] from Bale,[8] Burkina Faso[66] and Mekelle Ethiopia;[36] educational status of the family (illiterates) from Gonder;[6] and family income in Thailand[67] were statistically associated with p < 0.05.

The clinical variables showed that there are high rates of infection associated with mucoid diarrhea with a history of diarrhea, no malnutrition. However, none of these variables were statistically associated. Contrasting to our finding, the type of diarrhea with watery consistency from Bahir Dar was with high rates and statistically associated.[33] Similarly, a study from Ambo showed that mucoid diarrhea was with higher rates of infection.[35] Our study also showed that those who have taken vaccination were highly affected, which is in disagreement with the study reported from Ambo, which spells that children who were not vaccinated were at higher risk and significantly associated.[35] Host factors associated with malnutrition, such as a compromised immune system, environmental enteric dysfunction and enteric microbiome may predispose malnourished children to be more severe to disease infection.[68-71] Children with malnutrition may also be more likely to live in households of low socioeconomic status where poor access to clean water,[72,73] sanitation and hygiene may expose them to greater fecal microbial loads and a higher risk of pathogens associated with mortality such as Shigella species.[3] However, in our study, even if it is not statistically associated, high rates of infection were evident from malnourished children.

Behavioral factors such as the source of water from the pipeline, washing of hands after defecation for some time, consumption of food before illness, storing of food in open containers for later use, not washing hands before and after a meal and cleaning of cooking containers for some time constitute associate factors for the infection. However, the multivariate analysis showed that those who had a habit of washing hands for some time as compared to those who practice hand-washing always were at risk of infection. This can be justified that regular hand-washing using detergent is important for the prevention of Shigella and Salmonella transmission. Similarly, those who store cooked food in an open container for later use (34.44 times) are also at risk of infection as compared to those who practice closing the container, with a p value of ⩽0.05, which is in agreement with the studies conducted in Southern Ethiopia Arbaminch.[7,74] This can be explained by the transmission of these infections by flies, cockroaches and rodents in the kitchen and, therefore, exposing food can lead to diarrhea in children through bacterial contamination.[75-79]

Our study does not indicate the total magnitude of Salmonella and Shigella infection in Hawassa town.

It does not identify bacteria at the species level due to a lack of anti-sera in the local market.

Conclusion

Our study indicated that there was a high rate of Shigellosis and incidence of single Salmonella among children with diarrhea. Ampicillin, augmentin and tetracycline were resistant, while ciprofloxacin, ceftriaxone, ceftazidime, gentamycin, chloramphenicol, cefuroxime and cotrimoxazole were relatively sensitive. It was also found that those who practice hand-washing after defecation for some time, and store foods for later use in an open container were at risk of infection. Therefore, to alleviate this infection, the concerned body should be given health education for hand-washing after defecation and storing food in a closed container for later use.

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Supplemental material, sj-pdf-1-smo-10.1177_20503121211009729 for Magnitude, risk factors and antimicrobial susceptibility pattern of Shigella and Salmonella, among children with diarrhea in Southern Ethiopia: A Cross-sectional Study by Manamo Hayamo, Tsegaye Alemayehu, Bereket Tadesse, Enkosilassie Mitiku and Zufan Bedawi in SAGE Open Medicine