Urinary tract infections, bacterial resistance and immunological status: a cross sectional study in pregnant and non-pregnant women at Mbouda Ad-Lucem Hospital.

BACKGROUND: Urinary tract infections (UTI) are frequently encountered medical complications of pregnancy.
OBJECTIVE: This study was aimed at analyzing the bacterial resistance in urogenital tract as well as the immunological profile amongst pregnant and non-pregnant women at Mbouda Ad-Lucem Hospital, Western Region of Cameroon.
METHODS: A cross-sectional study was carried out from December 2015 to May 2016 at Mbouda Ad-Lucem hospital on 104 pregnant women and 24 non-pregnant women. The midstream urine from participants was analysed for the presence, isolation and identification of the uro-pathogens, using selective and specific bacterial culture media. An antibiotic susceptibility tests was carried out using disk diffusion method. Blood samples were collected for C-reactive protein (CRP) dosage, CD4 and CD8 lymphocytes count.
RESULTS: Out of 128 participants in this study, a high prevalence of uro-pathogens and resistance strains was observed. The most prevalent urinary tract pathogens were Staphylococcus sp. with 45% and 38.89% respectively in pregnant and non-pregnant women. Staphylococcus sp. showed resistance to Amoxicillin (AMO; 55.56%) and Chloramphenicol (CHL; 100%) respectively in pregnant and non-pregnant women. Pregnant women had a significantly high average of granulocytes (p=0.009), monocytes (P=0.001), high ratio of CD4/CD8 (p< 0.0001) and significantly low CD8 lymphocytes (p< 0.0001) average compared to non-pregnant women.
CONCLUSION: This study outlines high prevalence of Staphylococcus sp as the main urinary tract infectious pathogen in women at Mbouda Ad-Lucem hospital. It prevalence was accompanied with resistance to the routine antibiotics treatment, and a pronounced lymphocytosis and monocytosis.

Introduction

Pregnant women attending ante-natal visit for check-up of their health and that of their foetuses may not necessarily be presenting any symptoms of illness1. However, urinary tract infections (UTIs) (mostly bacteriuria, vaginitis, cystitis and pyelonephritis) are frequently encountered medical complications of pregnancy2. Although the majority of infections in pregnancy maybe asymptomatic, studies have revealed that they pose high risk of low birth weight, preterm labour, hypertension, maternal anaemia, thrombosis, still birth and abortion2,3. There are hormonal, structural and functional alterations of the urinary tract (UT) during pregnancy4. Pregnancy influences the immune system of pregnant women. This influence makes pregnant women vulnerable and can promote growth of bacteria due to inadequate immune response. During pregnancy, prophylaxis antibiotherapy may lead to the development of resistance in these bacteria4.

Glomerular filtration rate and urinary output increases due to blood-volume expansion5. These predisposes the pregnant women to microbial infection. The microbes present may not be pathogenic except in situations where their growth in the UT is excessive or co-presence with other competing microorganisms. Indeed, it has been shown that frequent antenatal visits may increase the exposure of pregnant women to nosocomial microorganisms and thereby nosocomial associated infections6.

A limited spectrum of organisms cause UTIs. This include E. coli as the major etiologic agent in UTIs. Proteus mirabilis, Klebsiella sp. Pseudomonas aeruginosa and Enterobacter sp. are less frequent causative agents. Enterococci, Gardnerrella vaginalis and U urealyticum are also known agents in UTIs. Gram-positive microorganisms including; Streptococcus, Staphylococcus aureus, Staphylococcus saprophyticus and Staphylococcus haemolyticus have also been pinpointed as UTIs agents7. Antibiotics used for bacterial infection management are usually empirical in some areas in developing world. This can lead to bacterial resistance among pathogens.

Antibiotic-resistant microorganisms pose serious threats to both mother and foetus as treatment becomes more difficult with safe antibiotics. The development of anti-microbial resistance in many bacterial species constitutes one of the most serious problems in the control of infectious diseases. Constant exposure of clinical bacterial isolates to hospital environment and exchange of genetic material among different species, results to acquisition of resistance to numerous antibiotics by various mechanisms1.

UTIs cause high morbidity rates, high financial cost in communities and are the most common bacterial infections8. The immune system of pregnant women is reduced during pregnancy, predisposing them to bacterial infections. The study of immunological parameters, uro-pathogenic bacteria and resistance is necessary to guide the clinicians for the proper management and prevention of UTIs in pregnant women. Therefore, this study is designed to determine the bacterial profile, antibiotic resistant pattern of uro-pathogens and immunological profile among pregnant and non-pregnant women consulting at the Mbouda Ad-Lucem hospital, Western Region of Cameroon. This is to update our knowledge on the area-based prevalence and antibiotic resistant pattern for antibiotics used for the proper management and prevention of UTIs during pregnancy.

Methodology

Study design and area

A cross-sectional study was conducted from December 2015 to May 2016 at the Mbouda Ad-Lucem hospital, located about 700 m from the Mbouda center. Mbouda is found in the Bamboutos Division, Western Region of Cameroun. This hospital is one of the reference Centres in Bamboutos Division.

Ethics approvals

The study was approved by the Ethics Review and Consultancy Committee of the Cameroon Bioethics Initiative (CAMBIN). After obtaining an informed written consent, socio-demographic and clinical data were obtained from each participant. All data obtained in the course of the study were kept confidential and used exclusively for the purpose of the study. The laboratory analysis results of participants in this study were communicated to the clinicians assigned and responsible for ante-natal visit and management at the Mbouda Ad-Lucem hospital for proper treatment.

Study participants

104 asymptomatic pregnant women attending ante-natal visit and 24 symptomatic non-pregnant women coming for UTIs consultation during the study period were enrolled in the study. All socio-demographic and clinical data were taken after obtaining an informed written consent from each participant. Participants treated with antibiotics within the preceding 2 weeks, known anatomic and neurologic urinary tract abnormalities, diabetic, HIV-pregnant women were excluded from the study.

Sample collection

Clean-catch mid-stream urine samples (6–12 ml) were obtained from each participant in a sterile screw-capped wide-mouth container after informing them about proper urine collection method. The containers were labelled with a unique sample number, date and time of collection. The urine samples were processed within an hour after collection in the bacteriological laboratory of Mbouda Ad-Lucem hospital.

Culture and identification of bacterial species

Urine samples were directly inoculated in a prepared nutrient broth and incubated for 24 h at 37°C. Loopful of the inoculated nutrient broth were then cultured by successive streaking on Cystine Lactose Electrolyte Deficient (CLED) agar (Qarad b.v.b.a. (Geel), Belgium), Chapman agar or Mannitol Salt Agar (MSA) (Qarad b.v.b.a. (Geel), Belgium), Eosin Methylene Blue (EMB) Agar (Qarad b.v.b.a. (Geel), Belgium) for the detection of E. coli, Klebsiella sp., Staphylococcus sp., Staphylococcus aureus, Gardnerrella vaginalis, Serratia sp., Aeromonas hydrophilai, Proteus sp.. CLED medium is mostly used in hospital laboratories for the diagnosis of urinary bacterial because it supports the growth of both Gram-positive and Gram-negative urinarypotential pathogens. Nevertheless, it is not possible to differentiate between E. coli and S. aureus. EMB and MSA are also selective media and they can clearly differentiate gram positive from gram negative bacteria. The bacterial isolates were further characterized using standard microbiology techniques such as colony morphology, Gram-staining, catalase test and other biochemical tests which include oxidase, indole, citrate utilization, H2S production, Voges-Proskauer, methyl red, urease and sugar fermentation testes9.

Susceptibility testing

Antibiotics susceptibility test was performed using Kirby-Bauer disc diffusion method10. Bacterial suspensions were prepared using nutrient broth by peaking-up 2–4 colonies from pure culture and adjusting it to 0.5 Mc-Farland standard which is equal to 108 cells/mL. It was then inoculated by swabbing onto Mueller-Hinton Agar (Qarad b.v.b.a. (Geel), Belgium). Antibiotic impregnated discs were placed on the surface of culture medium using a sterile gip. The isolates were tested with Tetracycline (30 ug) (TET), Cephalothin (30 ug) (CEP), Ciprofloxacin (30 ug) (CIP), Streptomycin (10 ug) (STR), Norfloxacin (10 ug) (NOR), Chloramphenicol (30 ug) (CHL), Gentamicin (15 ug) (GEN), Amoxicillin (30 ug) (AMO), Doxycycline (30 ug) (DOX), Netilmicin (30 ug) (NET), and Amoxicillin/Clavulanic acid ((20/10) ug ) (AMC), (Verna Industrial Estate, Verna Goa, India). After 24 hours of incubation at 37°C, zones of growth inhibition were measured to the nearest whole millimetre using a calliper. The zones of inhibition were interpreted according to the Clinical and Laboratory Standards Institute (CLSI) guideline as susceptible (S), intermediate (I) or resistant (R)11. Multidrug resistance (MDR) was defined as the resistance of a bacterium to at least threefamilies of antibiotics12.

Blood Count, CD4, CD8 count and C-reactive protein dosage

Blood was collected in labelled EDTA (Ethylenediaminetetraacetic Acid) tubes and were gently agitated to avoid the formation of clots. Each tube was then introduced into an automated analyzer (Hemascreen 18; Hospitex diagnosis; Firenze, Italie). After 9 seconds, the automat analyzed and posted the concentrations of: white blood cells, lymphocytes, monocytes and granulocytes.

The CD4 and CD8 T-lymphocytes count of all participants was determined using flow Cytometry applied in clinical immunology by the Becton Dickinsons' FACS count method13. The dosage of C-reactive protein (CRP) was done by immune-turbidimetry technique14.

Data analysis

Descriptive statistics were computed and summarised; continuous variables were expressed as means and standard deviations (SD) while categorical variables were expressed as proportions. Significance of differences between pregnant and non-pregnant women means variables were assessed using Student's t-test while chisquared Statistic was employed to determine the proportions of significance resultsbetween groups. The level of statistical significance was set at p < 0.05.

Results

A total of 128 urine specimens were received from the Mbouda Ad-Lucem Hospital with pregnant women (n=104) and non-pregnant women (n=24) (Supplementary Material Table S1 and S2). Bacteriuria was found in 38% of the pregnant women and in 75% of the non-pregnant women. 47.5% (n=19) of pregnant and 55.55% (n=10) of non-pregnant women were aged 30 years and above. No significant difference was observed between ages in pregnancy status, with a Chi-square goodness of fit χ2= 0.326, p= 0.849 (Table 1). Table 1 also shows that, pregnant women had a significantly high granulocytes (p=0.009) and monocytes (P=0.001) average, high ratio of CD4/CD8 (p< 0.0001) and significantly low CD8 lymphocytes (p< 0.0001) average compared to non-pregnant women.

Table 1

Demographic and clinical characteristics by pregnancy status

	Pregnant women	Non pregnant women
Sample characteristic	n (frequency)	n (frequency)
Age group (years)			Chi-square
<20	5 (12.5%)	2 (11.11%)	0.326 (0.849)
20–30	16 (40%)	6 (33.33%)
>30	19 (47.5%)	10(55.55%)
			Probabilities
Blood parameters	Mean±standart deviation	Mean±standart deviation	(p-value)
Leucocytes	6.895±0.453	6.80±0.744	0.904
Lymphocytes	1.644±0.600	1.588±0.142	0.948
Granulocytes	4.130±0.310	3.66±0.61	0.009
Monocytes	1.117±0.197	1.523±0.42	0.001
CD4	724.2±34.9	749.11±60.75	0.506
CD8	458.5±31.1	549.1±33.1	< 0.0001
CD4/CD8	1.781±0.112	1.446±0.147	< 0.0001

n: number

Bacteriuria was observed in 18/24 (75%) non-pregnant and 40/104 (38%) pregnant women (figure 1). Gram-positive bacteria were the most prevalent UT pathogen in both pregnant 60% (n=24) and non-pregnant 55.55% (n=10) women than Gram-negative bacteria 40% (n=16) and 44.44% (n=8) respectively (figure 1). Of the 40 UT pathogens isolates detected in pregnant women, Staphylococcus sp. 45% (n=18), Staphylococcus aureus 15% (n=6) and Escherichia coli 12.5% (n= 5) were the most common isolated bacteria of the UT flora. Interestingly, non-pregnant women, harboured Staphylococcus sp. 38.89% (n=7), Gardnerrella vaginalis 16.67% (n=3), Staphylococcus aureus 16.67% (n=3) and Escherichia coli 11.11% (n=2) as the most prevalent isolated UT bacteria (figure 1).

Figure 1

Distribution of bacterial isolates in relation to pregnancy status

Uro-pathogenics bacterial isolates from UT infected patients revealed high levels of single antibiotics resistances toward commonly prescribed drugs (Table 2). Resistance of Staphylococcus sp. to AMO (P = 0.013) was significantly higher in pregnant women than in non-pregnant women. Resistance of Staphylococcus sp. to CHL (P = 0.047) was significantly higher in non-pregnant women than in pregnant women. Resistance of Escherichia coli to AMO (P < 0.0001), CEP (P <0.0001), GEN (P = 0.022) and to NOR (P= 0.001) was significantly higher in pregnant women than in non-pregnant women, contrary to TET (P = 0.022), DOX (P = 0.022). Resistance of Staphyloccocus aureus to DOX (P = 0.030) was significantly higher in pregnant women than in non-pregnant women. Serratia oderifera showed highly significant resistance to CEP (P <0.0001), STR (P <0.0001), CHL (P <0.0001) in non-pregnant women than in pregnant women contrary to DOX (P <0.0001) (Table 2).

Table 2

Distribution of bacteria resistance among pregnant and non-pregnant women

		Antibiotics (Number (%))
Bacteria	Number of isolate	AMO	AMC	CEP	GEN	STR	NOR	CIP	CHL	TET	DOX
Staphyloccocus sp*	18	10(55.56)	13(72.22)	6(33.33)	5(83.33)	6(33.33)	12(66.67)	6(33.33)	14(77.78)	16(88.89)	12(66.67)
Staphyloccocus sp ii	7	1(14.29)	5(71.43)	1(14.29)	2(28.57)	4(57.41)	6(85.71)	4(57.41)	7(100)	7(100)	6(85.71)
p-value		0.013	0.859	0.206	0.921	0.334	0.346	0.334	0.047	0.261	0.346
Staphyloccocus aureus*	6	4(66.67)	4(66.67)	0 (00)	1(16.67)	1(16.67)	0 (00)	1(16.67)	0 (00)	2(33.33)	2(33.33)
Staphyloccocus aureus**	3	1(33.33)	1(33.33)	0 (00)	1(33.33)	0 (00)	0 (00)	0 (00)	0 (00)	1(33.33)	0 (00)
p-value		0.211	0.211	1.000	0.789	0.100	1.000	0.100	1.000	0.803	0.030
Escherichia coli*	5	4(80)	5(100)	4(80)	2(40)	2(40)	3(60)	1(20)	0 (00)	2(40)	2(40)
Escherichia coli**	2	0 (00)	1(50)	0 (00)	0 (00)	1(50)	0 (00)	0 (00)	0 (00)	2(100)	2(100)
p-value		< 0.0001	0.090	<0.0001	0.022	1.000	0.001	0.094	1.000	0.022	0.022
Serratia mercescens*	0	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)
Serratia mercescens**	1	1(100)	1(100)	1(100)	1(100)	1(100)	1(100)	1(100)	0 (00)	1(100)	1(100)
p-value
Gardnerrella vaginalis*	1	1(100)	1(100)	1(100)	1(100)	1(100)	1(100)	0 (00)	1(100)	1(100)	1(100)
Gardnerrella
vaginalis**	3	3(100)	3(100)	3(100)	3(100)	3(100)	3(100)	1(33.33)	3(100)	3(100)	3(100)
p-value		1.000	1.000	1.000	1.000	1.000	1.000	0.540	1.000	1.000	1.000
Serratia oderiferal*	1	1(100)	1(100)	0 (00)	1(100)	0 (00)	1(100)	0 (00)	0 (00)	1(100)	1(100)
Serratia oderiferal**	1	1(100)	1(100)	1(100)	1(100)	1(100)	1(100)	0 (00)	1(100)	1(100)	0 (00)
p-value		1.000	1.000	< 0.0001	1.000	< 0.0001	1.000		< 0.0001	1.000	< 0.0001
Pseudomonas fluorescens*	1	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)
Pseudomonas fluorescens**	0	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)
p-value
Hafniaalve*	2	2(100)	2(100)	1(50)	2(100)	1(50)	2(100)	1(50)	2(100)	2(100)	2(100)
Hafniaalvei**	0	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)
p-value
Proteus sp*	1	1(100)	1(100)	1(100)	1(100)	0 (00)	1(100)	1(100)	0 (00)	1(100)	1(100)
Proteus sp ii	0	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)
p-value
Aeromonas hydrophila*	1	1(100)	1(100)	1(100)	1(100)	1(100)	1(100)	0 (00)	1(100)	1(100)	1(100)
Aeromonas
hydrophila**	0	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)	0 (00)
Klebsiella sp*	4	3(75)	4(100)	3(75)	3(75)	3(75)	3(75)	3(75)	2(50)	4(100)	4(100)
Klebsiella sp**	1	1(100)	1(100)	1(100)	1(100)	1(100)	0 (00)	0 (00)	1(100)	1(100)	1(100)
p-value		0.564	1.000	0.564	0.564	0.564	< 0.0001	< 0.0001	0.134.	1.000	1.000

Pregnant women,

non pregnant women

TET: Tetracycline, CEP: Cephalothin, CIP: Ciprofloxacin, STR: Streptomycin, NOR: Norfloxacin, CHL: Chloramphenicol, GEN: Gentamicin, AMO: Amoxicillin, DOX: Doxycycline, AMC: Amoxicillin/Clavulanic acid; values in bracket are frequencies.

Uro-pathogenic isolates from UT infected pregnant and non-pregnant women revealed the presence of high levels of multiple antimicrobial resistances against commonly prescribed drugs (Table 3). Multidrug-resistance of Escherichia coli to Quinolones (NOR, CIP) was significantly higher in pregnant women compared to non-pregnant women (P= 0.018). The Escherichia coli isolates were significantly multidrug-resistance in pregnant women than in non-pregnant women (P= 0.018) (Table 3). Klebsiella sp. were only isolated in pregnant women and were more resistant to beta-lactamine (AMO, AMC, and CEP), aminosides (GEN, NET, and STR) and cycline (TET, DOX). The White Blood cells (WBC) involved in the defence of an organism, particularly the lymphocytes, monocytes and granulocytes, were counted. Table 4 compares the principal abnormalities of the WBCs observed among pregnant and non-pregnant women. It could be observed that the pregnant women had a significantly and highly pronounced lymphocytosis and monocytosis than non-pregnant women (Table 4).

Table 3

Bacteria resistance and multidrug resistance among pregnant and non-pregnant women

	Antibiotics families (Number (%))
	Beta-lactamine (AMO, AMC, CEP)	Aminosides (GEN, NET, STR )	Quinolones (NOR, CIP)	Phenicol (CHL)	Cycline (TET, DOX)	Resistance to less than 3 ATB families	Resistance to more than 3 ATB families
Serratiaodorifera*	1(100)	1(100)	1(100)	0(00)	1(100)	0(00)	1(100)
Serratiaodorifera**	1(100)	1(100)	1(100)	1(100)	1(100)	0(00)	1(100)
p-values	0.761	0.761	0.761	0.425	0.761	1.000	0.761
Staphyloccocus sp.*	14(77.8)	13(72.2)	13(72.2)	14(77.8)	16(88.9)	2(11.11)	14(77.8)
Staphyloccocus sp.**	6(85.7)	7(100)	6(85.7)	7(100)	7(100)	0(00)	7(100)
p-values	0.828	0.707	0.975	0.848	0.848	0.070	0.848
Staphyloccocus aereus*	4(66.7)	3(50)	1(16.67)	0(00)	3(50)	3(50)	2(33.33)
Staphyloccocus aereus**	1(33.33)	1(33.33)	0(00)	0(00)	1(100)	2(66.67)	0(00)
p-values	0.428	0.639	0.129	1.000	0.639	0.781	0.070
Gardnerrella Vaginalis*	1(100)	1(100)	1(100)	1(100)	1(100)	0(00)	1(100)
Gardnerrella Vaginalis**	3(100)	3(100)	3(100)	3(100)	3(100)	0(00)	3(100)
p-values	0.157	0.157	0.157	0.157	0.157	1.000	0.157
Escherichia coli*	5(100)	3(60)	4(80)	1(20)	2(40)	1(100)	4(80)
Escherichia coli**	1(50)	1(50)	0(00)	0(00)	2(100)	2(100)	0(00)
p-values	0.276	0.639	0.018	0.129	0.552	0.346	0.018
Hafniaalve**	2(100)	2(100)	2(100)	2(100)	2(100)	0(00)	2(100)
Aeromonas Hydrophila*	1(100)	1(100)	1(100)	0(00)	1(100)	0(00)	1(100)
Proteus sp.*	1(100)	1(100)	1(100)	1(100)	1(100)	0(00)	1(100)
Klebsiella sp.*	4(100)	4(100)	3(75)	2(50)	4(100)	0(00)	4(100)
Serratiamercescens**	1(100)	1(100)	1(100)	1(100)	1(100)	0(00)	1(100)

pregnant women,

non-pregnant women,

TET: Tetracycline, CEP: Cephalothin, CIP: Ciprofloxacin, STR: Streptomycin, NOR: Norfloxacin, CHL: Chloramphenicol, GEN: Gentamicin, AMO: Amoxicillin, DOX: Doxycycline, AMC: Amoxicillin/Clavulanic acid.

Table 4

Principal abnormalities of white blood cells among pregnant and non-pregnant women

Principal anormalities	Pregnant women (n = 40)		Non pregnant women (n=18)
	frequency	Percentage (%)	frequency	Percentage(%)	P-value
Leucopenia	3	7.5	3	16.67	0.415
Granulopenia	3	7.5	5	27.78	0.094
Lymphopenia	22	55.0	7	38.89	0.212
Monopenia	1	2.5	1	5.56	0.761
Leucocytosis	5	12.5	4	22.22	0.446
Granulocytosis	2	5.0	3	16.67	0.270
Lymphocytosis	3	7.5	0	00.00	0.036
monocytosis	13	32.5	11	61.11	0.045
CRP					Chi-square (p-value)
≤6	13	32.5	4	22.22	0.771 (0.680)
6<CRP<40	10	25.0	6	33.33
>40	17	42.5	8	44.44
CD4					Chi-square (p-value)
<500	8	20.0	3	16.67	0.090 (0.764)
>500	32	80.0	15	83.33
CD8>200	40	100.0	18	100.00
CD4/CD8					Chi-square (p-value)
<1	4	10.0	4	22.22	1.560 (0.121)
>1	36	90.0	14	77.78

n: number, CRP: C-reactive protein

Discussion

Bacteriuria in pregnant women is an important causative factor of premature birth, low birth weight, postpartum UTIs and higher foetal mortality rates. Women with bacteriuria have a 20–50-fold increased risk of developing pyelonephritis compared to women who do not have bacteriuria15. In this study, the prevalence of bacteriuria was 38% in pregnant women and 75% in non-pregnant women. The high incidence of UTI in non-pregnant women (75%) is as a result of their symptomatic status when they were included in this study. Low incidence of bacteriuria (38%) in pregnant women can be a result of their asymptomatic status and regular ante-natal visits when they were included in this study.

In this study, a highly significant average value of Monocytes (p=0.001) and granulocytes (p=0.009), high ratio of CD4/CD8 (p<0.0001) and significantly low CD8 lymphocytes average value in pregnant women compared to non-pregnant women was reported. A highly significant average value of Monocytes and granulocytes is due to pregnancy16. Pregnancy is associated with leukocytosis, primarily related to increased circulation of neutrophils. The neutrophil gradually increase as from weeks 6–8 of pregnancy and a plateau attained in the second or third trimester16. In healthy women with normal pregnancies, there is no change in the absolute lymphocyte count and no significant changes in the relative numbers of lymphocytes17.

Pregnancy is associated to some physiological and hormonal changes. At the first and second semester of pregnancy, the ureter begins to dilate and it continues until delivery. Increased progesterone and oestrogens levels normally leads to decrease ureteral and bladder tone. Increased plasma volume during pregnancy leads to decrease urine concentration and increase bladder volume. The combination of these factors leads to urinary stasis and uretero-vesical reflux18. These changes during pregnancy makes it easier for bacteria to travel up the urethra, kidney and causes development of bacteriuria.

Gram-positive bacteria were more prevalent in pregnant women 60% (n=24) (Staphylococcus sp. 45% (n=18), Staphylococcus aureus 15% (n=6)) and non-pregnant women 55.55% (n=10) (Staphylococcus sp. 38.89% (n=7), Staphylococcus aureus 16.67% (n=3)) than Gram-negative bacteria 40% (n=16) and 44.44% (n=8) bacteria in pregnant and non-pregnant women with bacteriuria. These bacteria are those of the digestive flora that often colonizes the maternal genital tract. These varying results may have been due to differences in the areas being studied, in the social habits of the communities being studied, standards of personal hygiene and levels of education of the participants being studied since these factors can influence the spread and bacterial multiplication.

The most commonly isolated bacteria in pregnant women were Staphylococcus sp. 45% (n=18), Staphylococcus aureus 15% (n=6), Escherichia coli 12.5% (n= 5) and Klebsiella sp. 10% (n=4). In non-pregnant women, the most commonly isolated bacteria were Staphylococcus sp. 38.89% (n=7), Gardnerrella vaginalis 16.67% (n=3), Staphylococcus aureus 16.67% (n=3) and Escherichia coli 11.11% (n=2). This finding is consistent with a study conducted by Oko et al.19 who showed that Staphylococcus aureus was the most prevalent uropathogen (29%) in pregnant women attending a tertiary maternity clinic in Northern Nigeria. Amadi et al.20 reported 27.1% and 25.4% for Staphylococcus aureus and Escherichia coli respectively. However, this observation differs from that of Akoachere et al.21 in Bamenda-Cameroon who reported that Klebsiella oxytoca was the most prevalent organism. Variation in geographical location can account for these differences.

This study has, thus, revealed that bacterial agents were significantly associated with increase resistance to antibiotics, such as AMO (55.56%) by Staphylococcus sp., DOX (33.33%) by Staphylococcus aureus, AMO (80%), CEP (80%), GEN (40%), and NOR (60%) by Escherichia coli, and NOR (75%), CIP (75%) by Klebsiella sp. in pregnant women. In non-pregnant women, bacteria resistance was exhibited for; CEP (100%), STR (100%), CHL (100%), by Serratia oderifera, TET (100%), DOX (100%), by Escherichia coli, CHL (100%), by Staphylococcus sp.

The resistance to usually prescribed antibiotics observed in our study can be due to frequent exposure to antibiotics in the locality. It is worth noting that the administration of cephalosporins (CEP ) is relatively safer during pregnancy as compared to quinolones (CIP, NOR…) which are contra-indicated unless there are no other alternatives22. Resistance of Escherichia coli to quinolones (NOR, CIP) was significantly high in pregnant women compared to non-pregnant women (P= 0.018). The Escherichia coli isolates were significantly MDR in pregnant women compared to non-pregnant women (P= 0.018). Klebsiella sp. were only isolated in pregnant women and were more resistant to beta-lactamine (AMO, AMC, CEP), aminosides (GEN, NET, STR) and cyclines (TET, DOX). This may be as a result of the high use of antibiotics by the pregnant women or the bacteria immunity that causes the destruction of any substances that does not allow their growth.

Lymphocytosis and monocytosis were more pronounced in pregnant women than non-pregnant women. This may be as a result of the body building immunity of the foetus and it is achieved by a state of selective immune tolerance, immunosuppression, and immunomodulation in the presence of a strong antimicrobial immunity23. There is also down regulation of potentially dangerous T-cell-mediated immune responses while activating certain components of the innate immune system, such as neutrophils. This unique deregulation between different components of the immune system plays a central role in the maternal adaptation to pregnancy23.

The limitation of this study may be the representation of this findings in the entire pregnant and non-pregnant women population in the studied area; however, the results could be of interest to physicians and other health professionals in Cameroon and worldwide who should apply the findings of this study according to the methodology and especially after comparing the context of the study with their own situation. Further studies will be performed to increase the reliability of these findings.

Conclusion

Urinary tract infection is caused by bacterial colonization of the urethra and the most prevalent agents of urinary tract infection found in this study were Staphylococcus sp. 45%, Staphylococcus aureus 15%, Escherichia coli 12.5% in pregnant women while in non-pregnant women, the most commonly isolated bacteria were Staphylococcus sp. 38.89%, Gardnerrella vaginalis 16.67%, Staphylococcus aureus 16.67% and Escherichia coli 11.11%. Lymphocytosis and monocytosis are more pronounced in pregnant women than non-pregnant women, the prevalence of resistance profile of uropathogens to some antibiotics tested in this study are a serious call for concern. Routine urine culture and antibiotic susceptibility testing and white blood cells count are recommended in pregnancy to identify bacterial causes of urinary tract infections and normal pregnancy for prompt attention and treatment to avoid complications.